Label: KRAZATI- adagrasib tablet, coated

  • NDC Code(s): 80739-812-12, 80739-812-18
  • Packager: Mirati Therapeutics, Inc
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated July 11, 2024

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use KRAZATI safely and effectively. See full prescribing information for KRAZATI.

    KRAZATI® (adagrasib) tablets, for oral use
    Initial U.S. Approval: 2022

    RECENT MAJOR CHANGES

    • Indications and Usage (1.1, 1.2)

    06/2024

    • Dosage and Administration (2.1, 2.2, 2.3)

    06/2024

    • Warnings and Precautions (5.1, 5.2, 5.3, 5.4)

    06/2024

    INDICATIONS AND USAGE

    KRAZATI is an inhibitor of the RAS GTPase family indicated for:

    Non-small cell lung cancer (NSCLC)*

    As a single agent, for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic NSCLC, as determined by an FDA-approved test, who have received at least one prior systemic therapy. (1.1)

    Colorectal cancer (CRC)*

    In combination with cetuximab, for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic CRC, as determined by an FDA-approved test, who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy. (1.2)

    *These indications are approved under accelerated approval based on objective response rate (ORR) and duration of response (DOR). Continued approval for these indications may be contingent upon verification and description of a clinical benefit in confirmatory trials. (1.1, 1.2)

    DOSAGE AND ADMINISTRATION

    Recommended dosage as a single agent for NSCLC and in combination with cetuximab for CRC: 600 mg orally twice daily. (2.2)
    Swallow tablets whole with or without food. (2.2)

    DOSAGE FORMS AND STRENGTHS

    Tablets: 200 mg. (3)

    CONTRAINDICATIONS

    None. (4)

    WARNINGS AND PRECAUTIONS

    Gastrointestinal Adverse Reactions: Monitor patients for diarrhea, nausea and vomiting and provide supportive care as needed. Withhold, reduce the dose or permanently discontinue based on severity. (2.3, 5.1)
    QTc Interval Prolongation: Avoid concomitant use of KRAZATI with other products with a known potential to prolong the QTc interval. Monitor ECG and electrolytes particularly potassium and magnesium, in patients at risk, and in patients taking medications known to prolong the QT interval. Correct electrolyte abnormalities. Withhold, reduce the dose, or permanently discontinue based on severity. (2.3, 5.2)
    Hepatotoxicity: Monitor liver laboratory tests prior to the start of KRAZATI and monthly for 3 months after and as clinically indicated. Reduce the dose, withhold, or permanently discontinue based on severity. (2.3, 5.3)
    Interstitial Lung Disease (ILD) / Pneumonitis: Monitor for new or worsening respiratory symptoms. Withhold KRAZATI for suspected ILD/pneumonitis and permanently discontinue if no other potential causes of ILD/pneumonitis are identified. (2.3, 5.4)

    ADVERSE REACTIONS

    Single agent use in NCSLC: The most common adverse reactions (≥ 25%) were nausea, diarrhea, vomiting, fatigue, musculoskeletal pain, hepatotoxicity, renal impairment, edema, dyspnea, and decreased appetite. The most common (≥ 2%) Grade 3 or 4 laboratory abnormalities were decreased lymphocytes, decreased hemoglobin, increased alanine aminotransferase, increased aspartate aminotransferase, hypokalemia, hyponatremia, increased lipase, decreased leukocytes, decreased neutrophils and increased alkaline phosphatase. (6.1)
    In combination with cetuximab in CRC: The most common adverse reactions (≥ 25%) were rash, nausea, diarrhea, vomiting, fatigue, musculoskeletal pain, hepatotoxicity, headache, dry skin, abdominal pain, decreased appetite, edema, anemia, and cough. The most common (≥ 2%) Grade 3 or 4 laboratory abnormalities were decreased lymphocytes, decreased potassium, decreased magnesium, decreased hemoglobin, increased aspartate aminotransferase, increased lipase, decreased albumin, and increased alanine aminotransferase. (6.1)

    To report SUSPECTED ADVERSE REACTIONS, contact Bristol-Myers Squibb at 1-800-721-5072 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS

    See full prescribing information for clinically significant drug interactions with KRAZATI. (7)

    Strong CYP3A4 Inducers: Avoid concomitant use. (7.1)
    Strong CYP3A4 Inhibitors: Avoid concomitant use until adagrasib concentrations have reached steady state. (7.1)
    Sensitive CYP3A4 Substrates: Avoid concomitant use with sensitive CYP3A4 substrates. (7.2)
    Sensitive CYP2C9 or CYP2D6 Substrates or P-gp Substrates: Avoid concomitant use with sensitive CYP2C9 or CYP2D6 substrates or P-gp substrates where minimal concentration changes may lead to serious adverse reactions. (7.2)
    Drugs That Prolong QT Interval: Avoid concomitant use with KRAZATI. (7.3)

    USE IN SPECIFIC POPULATIONS

    Lactation: Advise not to breastfeed. (8.2)

    See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.

    Revised: 6/2024

  • Table of Contents
  • 1 INDICATIONS AND USAGE

    1.1 KRAS G12C-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

    KRAZATI, as a single-agent, is indicated for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test [see Dosage and Administration (2.1)], who have received at least one prior systemic therapy.

    This indication is approved under accelerated approval based on objective response rate (ORR) and duration of response (DOR) [see Clinical Studies (14.1)]. Continued approval for this indication may be contingent upon verification and description of a clinical benefit in a confirmatory trial.

    1.2 KRAS G12C-Mutated Locally Advanced or Metastatic Colorectal Cancer

    KRAZATI in combination with cetuximab is indicated for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic colorectal cancer (CRC), as determined by an FDA-approved test [see Dosage and Administration (2.1)], who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy.

    This indication is approved under accelerated approval based on ORR and DOR [see Clinical Studies (14.2)]. Continued approval for this indication may be contingent upon verification and description of a clinical benefit in a confirmatory trial.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Patient Selection

    Non-Small Cell Lung Cancer

    Select patients for treatment of locally advanced or metastatic NSCLC with KRAZATI based on the presence of KRAS G12C mutation in plasma or tumor specimens [see Clinical Studies (14.1)]. If no mutation is detected in a plasma specimen, test tumor tissue.

    Colorectal Cancer

    Select patients for treatment of locally advanced or metastatic CRC with KRAZATI based on the presence of KRAS G12C mutation in tumor specimens [see Clinical Studies (14.2)].

    Information on FDA-approved tests for the detection of a KRAS G12C mutation is available at: https://www.fda.gov/CompanionDiagnostics

    2.2 Recommended Dosage

    The recommended dosage of KRAZATI as a single agent or in combination with cetuximab is 600 mg orally twice daily until disease progression or unacceptable toxicity.

    Refer to the cetuximab prescribing information for cetuximab dosage information [see Clinical Studies (14.2)].

    Take KRAZATI at the same time every day with or without food [see Clinical Pharmacology (12.3)]. Swallow tablets whole. Do not chew, crush or split tablets.

    If vomiting occurs after taking KRAZATI, do not take an additional dose. Resume dosing at the next scheduled time.

    If a dose is inadvertently missed, it should be skipped if greater than 4 hours have elapsed from the expected dosing time. Resume dosing at the next scheduled time.

    2.3 Dosage Modifications for Adverse Reactions

    Recommended dose reductions for adverse reactions for use of KRAZATI as a single agent or in combination with cetuximab are outlined in Table 1. If adverse reactions occur, a maximum of two dose reductions are permitted. Permanently discontinue KRAZATI in patients who are unable to tolerate 600 mg once daily.

    Table 1: Recommended KRAZATI Dosage Reductions for Adverse Reactions

    Dose Reduction

    Dosage

    First dose reduction

    400 mg twice daily

    Second dose reduction

    600 mg once daily

    Refer to the cetuximab prescribing information for dose modifications for adverse reactions associated with cetuximab.

    When KRAZATI is administered in combination with cetuximab, withhold or permanently discontinue cetuximab when KRAZATI is withheld or permanently discontinued.

    Treatment with KRAZATI as a single agent may be continued if cetuximab is permanently discontinued. [see Clinical Pharmacology (12.1), Clinical Studies (14.2)].

    The recommended dosage modifications for adverse reactions are provided in Table 2.

    Table 2: Recommended KRAZATI Dosage Modifications for Adverse Reactions
    ALT = alanine aminotransferase; AST = aspartate aminotransferase; ILD = Interstitial Lung Disease; ULN = upper limit of normal
    *
    Grading defined by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0.
    When KRAZATI is administered in combination with cetuximab, withhold or permanently discontinue treatment with cetuximab when withholding or permanently discontinuing treatment with KRAZATI.

    Adverse Reaction

    Severity*

    Dosage Modification

    Nausea or vomiting despite appropriate supportive care (including anti-emetic therapy)
    [see Warnings and Precautions (5.1)]

    Grade 3 or 4

    Withhold KRAZATI until recovery to ≤ Grade 1 or return to baseline.
    Resume KRAZATI at the next lower dose level.

    Diarrhea despite appropriate supportive care (including anti-diarrheal therapy)
    [see Warnings and Precautions (5.1)]

    Grade 3 or 4

    Withhold KRAZATI until recovery to ≤ Grade 1 or return to baseline.
    Resume KRAZATI at the next lower dose level.

    QTc Interval Prolongation
    [see Warnings and Precautions (5.2)]

    QTc absolute value greater than 500 ms
    or
    Greater than an increase of 60 ms from baseline

    Withhold KRAZATI until QTc interval less than 481 ms or return to baseline.
    Resume KRAZATI at the next lower dose level.

    Torsade de pointes, polymorphic ventricular tachycardia or signs or symptoms of serious or life-threatening arrhythmia

    Permanently discontinue KRAZATI

    Hepatotoxicity
    [see Warnings and Precautions (5.3)]

    Grade 2
    AST or ALT

    Decrease KRAZATI to the next lower dose level.

    Grade 3 or 4
    AST or ALT

    Withhold KRAZATI until recovery to ≤ Grade 1 or return to baseline.
    Resume KRAZATI at the next lower dose level.

    AST or ALT > 3 × ULN with total bilirubin > 2 × ULN in the absence of alternative causes

    Permanently discontinue KRAZATI

    Interstitial Lung Disease / Pneumonitis
    [see Warnings and Precautions (5.4)]

    Any Grade

    Withhold KRAZATI if ILD/pneumonitis is suspected.
    Permanently discontinue KRAZATI if ILD/pneumonitis is confirmed

    Other Adverse Reactions
    [see Adverse Reactions (6.1)]

    Grade 3 or 4

    Withhold KRAZATI until ≤ Grade 1 or return to baseline.
    Resume KRAZATI at the next lower dose level.
  • 3 DOSAGE FORMS AND STRENGTHS

    Tablets: 200 mg, oval shaped, white to off-white, immediate release film coated tablets with "200" on one side and stylized "M" on the opposite side.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Gastrointestinal Adverse Reactions

    KRAZATI can cause severe gastrointestinal adverse reactions.

    In the pooled safety population [see Adverse Reactions (6.1)], who received single-agent KRAZATI, serious gastrointestinal adverse reactions observed were gastrointestinal bleeding in 3.8% including 0.8% Grade 3 or 4, gastrointestinal obstruction in 1.6% including 1.4% Grade 3 or 4, colitis in 0.5% including 0.3% Grade 3, ileus in 0.5%, and stenosis in 0.3%. In addition, nausea, diarrhea, or vomiting occurred in 89% of 366 patients, including 9% Grade 3. Nausea, diarrhea, or vomiting led to dosage interruption or dose reduction in 29% of patients and permanent discontinuation of adagrasib in 0.3%.

    In patients who received KRAZATI in combination with cetuximab [see Adverse Reactions (6.1)], serious gastrointestinal adverse reactions included gastrointestinal bleeding in 8.5% including 1.1% Grade 3 or 4, gastrointestinal obstruction in 5.3% including 5.3% Grade 3 or 4, colitis in 1.1% including 1.1% Grade 3 and ileus in 1.1%. In addition, nausea, diarrhea, or vomiting occurred in 92% of 94 patients, including 6% Grade 3. Nausea, diarrhea, or vomiting led to adagrasib dose interruption or dose reduction in 23% of patients.

    Monitor and manage patients using supportive care, including antidiarrheals, antiemetics, or fluid replacement, as indicated. Withhold, reduce the dose, or permanently discontinue KRAZATI based on severity [see Dosage and Administration (2.3)].

    5.2 QTc Interval Prolongation

    KRAZATI can cause QTc interval prolongation, which can increase the risk for ventricular tachyarrhythmias (e.g., torsades de pointes) or sudden death.

    In the pooled safety population [see Adverse Reactions (6.1)] who received single-agent KRAZATI, 6% of 366 patients with at least one post-baseline electrocardiogram (ECG) assessment had an average QTc ≥ 501 msec and 11% of patients had an increase from baseline of QTc > 60 msec. KRAZATI causes concentration-dependent increases in the QTc interval [see Clinical Pharmacology (12.2)].

    In patients who received KRAZATI in combination with cetuximab [see Adverse Reactions (6.1)], 5% of 93 patients with at least one post-baseline electrocardiogram (ECG) assessment had an average QTc ≥ 501 msec and 16% of patients had an increase from baseline of QTc > 60 msec.

    Avoid concomitant use of KRAZATI with other products with a known potential to prolong the QTc interval [see Drug Interactions (7.3) and Clinical Pharmacology (12.2)]. Avoid use of KRAZATI in patients with congenital long QT syndrome and in patients with concurrent QTc prolongation.

    Monitor ECGs and electrolytes, particularly potassium and magnesium, prior to starting KRAZATI, during concomitant use, and as clinically indicated in patients with congestive heart failure, bradyarrhythmias, electrolyte abnormalities, and in patients who are unable to avoid concomitant medications that are known to prolong the QT interval. Correct electrolyte abnormalities. Withhold, reduce the dose, or permanently discontinue KRAZATI depending on severity [see Dosage and Administration (2.3)].

    5.3 Hepatotoxicity

    KRAZATI can cause hepatotoxicity, which may lead to drug-induced liver injury and hepatitis.

    In the pooled safety population of 366 patients [see Adverse Reactions (6.1)] who received single-agent KRAZATI, drug-induced liver injury was reported in 0.3% of patients, including 0.3% Grade 3. A total of 32% of patients who received adagrasib had increased alanine aminotransferase (ALT)/increased aspartate aminotransferase (AST); 5% were Grade 3 and 0.5% were Grade 4. The median time to first onset of increased ALT/AST was 3 weeks (range: 0.1 to 48). Overall hepatotoxicity occurred in 37%, and 7% were Grade 3 or 4. Hepatotoxicity leading to dose interruption or reduction occurred in 12% of patients. Adagrasib was discontinued due to hepatotoxicity in 0.5% of patients.

    In patients who received KRAZATI in combination with cetuximab [see Adverse Reactions (6.1)], 29% had increased alanine aminotransferase (ALT)/increased aspartate aminotransferase (AST); 5% were Grade 3 and 1.1% were Grade 4. The median time to first onset of increased ALT/AST was 4 weeks (range: 0.1 to 27). Overall hepatotoxicity occurred in 38%, and 10% were Grade 3 or 4. Hepatotoxicity leading to adagrasib dose interruption or reduction occurred in 12% of patients.

    Monitor liver laboratory tests (AST, ALT, alkaline phosphatase and total bilirubin) prior to the start of KRAZATI and monthly for 3 months or as clinically indicated, with more frequent testing in patients who develop transaminase elevations. Reduce the dose, withhold, or permanently discontinue KRAZATI based on severity [see Dosage and Administration (2.3) and Adverse Reactions (6.1)].

    5.4 Interstitial Lung Disease / Pneumonitis

    KRAZATI can cause interstitial lung disease (ILD)/pneumonitis, which can be fatal.

    In the pooled safety population [see Adverse Reactions (6.1)] who received single-agent KRAZATI, ILD/pneumonitis occurred in 4.1% of patients, 1.4% were Grade 3 or 4, and one case was fatal. The median time to first onset for ILD/pneumonitis was 12 weeks (range: 5 to 31 weeks). Adagrasib was discontinued due to ILD/pneumonitis in 0.8% of patients.

    In patients who received KRAZATI in combination with cetuximab [see Adverse Reactions (6.1)], Grade 1 ILD/pneumonitis occurred in 1.1% of patients. The time to first onset for ILD/pneumonitis was 38 weeks.

    Monitor patients for new or worsening respiratory symptoms indicative of ILD/pneumonitis (e.g., dyspnea, cough, fever) during treatment with KRAZATI. Withhold KRAZATI in patients with suspected ILD/pneumonitis and permanently discontinue KRAZATI if no other potential causes of ILD/pneumonitis are identified [see Dosage and Administration (2.3)].

  • 6 ADVERSE REACTIONS

    The following clinically significant adverse reactions are described elsewhere in the labeling:

    Gastrointestinal Adverse Reactions [see Warnings and Precautions (5.1)]
    QTc Interval Prolongation [see Warnings and Precautions (5.2)]
    Hepatotoxicity [see Warnings and Precautions (5.3)]
    Interstitial Lung Disease (ILD)/Pneumonitis [see Warnings and Precautions (5.4)]

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    The pooled safety population described in the WARNINGS AND PRECAUTIONS reflect exposure to adagrasib as a single agent at 600 mg orally twice daily in 366 patients with NSCLC and other solid tumors enrolled in KRYSTAL-1 and KRYSTAL-12 (NCT04685135), respectively. Among 366 patients who received adagrasib, 39% of patients were exposed for 6 months or longer and 12% were exposed for greater than one year. In this pooled safety population, the most common (≥ 25%) adverse reactions were nausea (70%), diarrhea (69%), vomiting (57%), fatigue (55%), musculoskeletal pain (38%), hepatotoxicity (37%), renal impairment (33%), edema (30%), dyspnea (26%), and decreased appetite (29%). In this pooled safety population, the most common Grade 3 or 4 (≥ 2%) laboratory abnormalities were decreased lymphocytes (20%), decreased hemoglobin (7%), increased alanine aminotransferase (4.5%), increased aspartate aminotransferase (4.2%), hypokalemia (3.6%), hyponatremia (3.4%), increased lipase (2.5%), decreased leukocytes (2.5%), decreased neutrophils (2.3%), and increased alkaline phosphatase (2.0%).

    The data described in WARNINGS AND PRECAUTIONS and below also reflects exposure to adagrasib in combination with cetuximab in 94 patients with KRAS G12C-mutated, locally advanced or metastatic CRC in KRYSTAL-1.

    Non-Small Cell Lung Cancer

    The safety of adagrasib was evaluated in patients with KRAS G12C-mutated, locally advanced or metastatic NSCLC in KRYSTAL-1 [see Clinical Studies (14.1)]. Patients received adagrasib 600 mg orally twice daily (n = 116). Among patients who received adagrasib, 45% were exposed for 6 months or longer and 4% were exposed for greater than one year.

    The median age of patients who received adagrasib was 64 years (range 25 to 89), 56% female, 84% White, 8% Black or African American, and 4.3% Asian.

    Serious adverse reactions occurred in 57% of patients who received adagrasib. Serious adverse reactions in ≥ 2% of patients were pneumonia (17%), dyspnea (9%), renal impairment (8%), sepsis (5%), hypoxia (4.3%), pleural effusion (4.3%), respiratory failure (4.3%), anemia (3.4%), cardiac failure (3.4%), hyponatremia (3.4%), hypotension (3.4%), muscular weakness (3.4%), pyrexia (3.4%), dehydration (2.6%), diarrhea (2.6%), mental status changes (2.6%), pulmonary embolism (2.6%), and pulmonary hemorrhage (2.6%). Fatal adverse reactions occurred in 11% of patients who received adagrasib due to pneumonia (3.4%), respiratory failure (1.7%), sudden death (1.7%), cardiac failure (0.9%), cerebrovascular accident (0.9%), mental status change (0.9%), pulmonary embolism (0.9%), and pulmonary hemorrhage (0.9%).

    Permanent discontinuation of adagrasib due to an adverse reaction occurred in 13% of patients. Adverse reactions which resulted in permanent discontinuation of adagrasib occurring in two patients each (1.7%) were pneumonia and pneumonitis and occurring in one patient each (0.9%) were cerebrovascular accident, dyspnea, decreased ejection fraction, encephalitis, gastrointestinal obstruction, hemorrhage, hepatotoxicity, hypotension, muscular weakness, pulmonary embolism, pyrexia, respiratory failure and sepsis.

    Dose interruptions of adagrasib due to an adverse reaction occurred in 77% of patients. Adverse reactions requiring dosage interruption in ≥ 2% of patients who received adagrasib included nausea, hepatotoxicity, fatigue, vomiting, pneumonia, renal impairment, diarrhea, QTc interval prolongation, anemia, dyspnea, increased lipase, decreased appetite, dizziness, hyponatremia, muscular weakness, increased amylase, pneumonitis, sepsis and decreased weight.

    Dose reductions of adagrasib due to an adverse reaction occurred in 28% of patients. Adverse reactions which required dose reductions in ≥ 2% of patients who received adagrasib included hepatotoxicity, fatigue, nausea, diarrhea, vomiting, and renal impairment.

    The most common adverse reactions (≥ 20%) were diarrhea, nausea, fatigue, vomiting, musculoskeletal pain, hepatotoxicity, renal impairment, dyspnea, edema, decreased appetite, cough, pneumonia, dizziness, constipation, abdominal pain, and QTc interval prolongation. The most common laboratory abnormalities (≥ 25%) were decreased lymphocytes, increased aspartate aminotransferase, decreased sodium, decreased hemoglobin, increased creatinine, decreased albumin, increased alanine aminotransferase, increased lipase, decreased platelets, decreased magnesium, and decreased potassium.

    Table 3 summarizes the adverse reactions in KRYSTAL-1.

    Table 3: Adverse Reactions (≥ 20%) in Patients with KRAS G12C-mutated NSCLC Who Received Adagrasib in KRYSTAL-1
    *
    Grouped term.
    Hepatotoxicity includes mixed liver injury, blood alkaline phosphatase increased, alanine aminotransferase increased, aspartate aminotransferase increased, liver function test increased, blood bilirubin increased, and bilirubin conjugated increased.
    Renal impairment includes acute kidney injury and increased blood creatinine.

    Adverse Reaction

    Adagrasib
    N = 116

    All Grades
    (%)

    Grade 3 or 4
    (%)

    Gastrointestinal Disorders

      Diarrhea*

    70

    0.9

      Nausea

    69

    4.3

      Vomiting*

    56

    0.9

      Constipation

    22

    0

      Abdominal pain*

    21

    0

    General Disorders and Administration Site Conditions

      Fatigue*

    59

    7

      Edema*

    32

    0

    Musculoskeletal and Connective Tissue Disorders

      Musculoskeletal pain*

    41

    7

    Hepatobiliary Disorders

      Hepatotoxicity*,

    37

    10

    Renal and Urinary Disorders

      Renal impairment*,

    36

    6

    Respiratory

      Dyspnea*

    35

    10

      Cough*

    24

    0.9

    Metabolism and Nutrition Disorders

      Decreased appetite

    30

    4.3

    Infections and Infestations

      Pneumonia*

    24

    17

    Nervous System Disorders

      Dizziness*

    23

    0.9

    Cardiac Disorders

      Electrocardiogram QT prolonged

    20

    6

    Table 4 summarizes the laboratory abnormalities in KRYSTAL-1.

    Table 4: Select Laboratory Abnormalities Occurring (≥ 25%) That Worsened from Baseline in Patients with KRAS G12C-mutated NSCLC Who Received Adagrasib in KRYSTAL-1
    *
    Denominator used to calculate the rate varied from 106 to 113 based on the number of patients with a baseline value and at least one post-treatment value.

    Laboratory Abnormality

    Adagrasib*

    All Grades
    (%)

    Grade 3 or 4
    (%)

    Hematology

      Lymphocytes decreased

    64

    25

      Hemoglobin decreased

    51

    8

      Platelets decreased

    27

    0

    Chemistry

      Aspartate aminotransferase increased

    52

    6

      Sodium decreased

    52

    8

      Creatinine increased

    50

    0

      Albumin decreased

    50

    0.9

      Alanine aminotransferase increased

    46

    5

      Lipase increased

    35

    1.8

      Magnesium decreased

    26

    0

      Potassium decreased

    26

    3.5

    Colorectal Cancer

    The safety of adagrasib combined with cetuximab was evaluated in 94 patients with KRAS G12C-mutated, locally advanced or metastatic CRC in KRYSTAL-1 [see Clinical Studies (14.2)]. Patients started treatment with adagrasib 600 mg twice daily in combination with cetuximab weekly (n = 17) or every two weeks (n = 77). Among patients who received adagrasib in combination with cetuximab, 60% were exposed for greater than 6 months and 12% were exposed for greater than 12 months.

    Serious adverse reactions occurred in 30% of patients who received adagrasib in combination with cetuximab. The most common serious adverse reactions (≥ 2%) were pneumonia (4.3%), pleural effusion, pyrexia, acute kidney injury, dehydration, and small intestinal obstruction (2.1% each).

    A fatal adverse reaction of pneumonia occurred in 1 patient who received adagrasib in combination with cetuximab.

    Adverse reactions leading to discontinuation of adagrasib occurred in 2 patients. Adverse reactions which resulted in permanent discontinuation of adagrasib (1 patient each) included abdominal pain and prolonged QT interval.

    Adverse reactions leading to dose interruptions of adagrasib occurred in 62% of patients. The most common adverse reactions or laboratory abnormalities leading to dose interruption in ≥ 2% of patients who received adagrasib included diarrhea, nausea, vomiting, abdominal pain, dizziness, headache, pneumonia, alanine aminotransferase increased, aspartate aminotransferase increased, dyspnea, fatigue, pleural effusion, rash, anemia, electrocardiogram QT prolongation, blood bilirubin increased, blood creatinine increased, decreased appetite, dehydration, hemorrhage, hypomagnesemia, lipase increased, muscular weakness, musculoskeletal pain, and pyrexia.

    Adverse reactions leading to dose reductions of adagrasib occurred in 35% of patients. The most common adverse reactions or laboratory abnormalities leading to dose reductions in ≥ 2% of patients who received adagrasib included fatigue, increased aspartate aminotransferase, increased alanine aminotransferase, nausea, decreased appetite, electrocardiogram QT prolongation, dizziness, acute kidney injury, diarrhea, dysarthria, and vomiting.

    The most common adverse reactions (≥ 20%) were rash, nausea, diarrhea, vomiting, fatigue, musculoskeletal pain, hepatotoxicity, headache, dry skin, abdominal pain, decreased appetite, edema, anemia, dizziness, cough, constipation, and peripheral neuropathy.

    The most common laboratory abnormalities (≥ 25%) were decreased lymphocytes, decreased hemoglobin, decreased leukocytes, increased alanine aminotransferase, decreased magnesium, decreased albumin, increased lipase, decreased potassium, increased aspartate aminotransferase, increased creatinine, decreased sodium, decreased calcium, increased amylase, and increased alkaline phosphatase.

    Table 5 summarizes the adverse reactions in patients with metastatic CRC in KRYSTAL-1.

    Table 5: Adverse Reactions (≥ 20 %) in Patients with KRAS G12C-mutated CRC Received Adagrasib in Combination with Cetuximab in KRYSTAL-1
    *
    Graded per CTCAE version 5.0.
    Grouped term; includes multiple related terms.

    Adverse Reaction*

    Adagrasib in Combination with Cetuximab
    N = 94

    All Grades
    (%)

    Grade 3 or 4
    (%)

    Skin and subcutaneous tissue disorders

      Rash

    84

    4.3

      Dry skin

    36

    0

    Gastrointestinal Disorders

      Nausea

    68

    2.1

      Diarrhea

    65

    5

      Vomiting

    57

    0

      Abdominal pain

    30

    4.3

      Constipation

    23

    0

    General Disorders and Administration Site Conditions

      Fatigue

    57

    3.2

      Musculoskeletal pain

    47

    4.3

      Edema

    28

    0

    Hepatobiliary Disorders

      Hepatotoxicity

    38

    10

    Nervous System Disorders

      Headache

    37

    4.3

      Dizziness

    24

    2.1

      Peripheral neuropathy

    20

    1.1

    Metabolism and Nutrition Disorders

      Decreased appetite

    30

    0

    Blood and lymphatic system disorders

      Anemia

    27

    7

    Respiratory

      Cough

    25

    0

    Other clinically relevant adverse reactions observed in less than 20% of patients were infusion related reactions (15%).

    Table 6 summarizes the laboratory abnormalities in patients with metastatic CRC in KRYSTAL-1.

    Table 6: Selected Laboratory Abnormalities (≥ 25%) in Patients Who Received Adagrasib in Combination with Cetuximab in KRYSTAL-1
    *
    The denominator used to calculate the rate varied from 82 to 92 based on the number of patients with a baseline value and at least one post-treatment value.

    Laboratory Abnormality

    Adagrasib in Combination with Cetuximab*

    All Grades
    (%)

    Grade 3 or 4
    (%)

    Hematology

      Lymphocytes decreased

    63

    17

      Hemoglobin decreased

    48

    5

      Leukocytes decreased

    27

    1.1

    Chemistry

      Alanine aminotransferase increased

    51

    2.2

      Magnesium decreased

    49

    7

      Albumin decreased

    46

    2.2

      Lipase increased

    41

    3.3

      Potassium decreased

    40

    9

      Aspartate aminotransferase increased

    39

    4.3

      Creatinine increased

    30

    1.1

      Sodium decreased

    30

    0

      Calcium decreased

    29

    1.1

      Amylase increased

    29

    0

      Alkaline phosphatase increased

    29

    1.1

  • 7 DRUG INTERACTIONS

    7.1 Effects of Other Drugs on KRAZATI

    Strong CYP3A4 Inducers

    Avoid concomitant use of KRAZATI with strong CYP3A inducers.

    Adagrasib is a CYP3A4 substrate. Concomitant use of KRAZATI with a strong CYP3A inducer reduces adagrasib exposure [see Clinical Pharmacology (12.3)], which may reduce the effectiveness of KRAZATI.

    Strong CYP3A4 Inhibitors

    Avoid concomitant use of KRAZATI with strong CYP3A inhibitors until adagrasib concentrations have reached steady state (after approximately 8 days).

    Adagrasib is a CYP3A4 substrate. If adagrasib concentrations have not reached steady state, concomitant use of a strong CYP3A inhibitor will increase adagrasib concentrations, [see Clinical Pharmacology (12.3)], which may increase the risk of KRAZATI adverse reactions.

    7.2 Effects of KRAZATI on Other Drugs

    Sensitive CYP3A Substrates

    Avoid concomitant use of KRAZATI with sensitive CYP3A substrates unless otherwise recommended in the Prescribing Information for these substrates.

    Adagrasib is a CYP3A inhibitor. Concomitant use with KRAZATI increases exposure of CYP3A substrates [see Clinical Pharmacology (12.3)], which may increase the risk of adverse reactions related to these substrates.

    Sensitive CYP2C9 Substrates

    Avoid concomitant use of KRAZATI with sensitive CYP2C9 substrates where minimal concentration changes may lead to serious adverse reactions unless otherwise recommended in the Prescribing Information for these substrates.

    Adagrasib is a CYP2C9 inhibitor. Concomitant use with KRAZATI increases exposure of CYP2C9 substrates [see Clinical Pharmacology (12.3)], which may increase the risk of adverse reactions related to these substrates.

    Sensitive CYP2D6 Substrates

    Avoid concomitant use of KRAZATI with sensitive CYP2D6 substrates where minimal concentration changes may lead to serious adverse reactions unless otherwise recommended in the Prescribing Information for these substrates.

    Adagrasib is a CYP2D6 inhibitor. Concomitant use with KRAZATI increases exposure of CYP2D6 substrates [see Clinical Pharmacology (12.3)], which may increase the risk of adverse reactions related to these substrates.

    P-gp Substrates

    Avoid concomitant use of KRAZATI with P-gp substrates where minimal concentration changes may lead to serious adverse reactions unless otherwise recommended in the Prescribing Information for these substrates.

    Adagrasib is a P-gp inhibitor. Concomitant use with KRAZATI increases exposure of P-gp substrates [see Clinical Pharmacology (12.3)], which may increase the risk of adverse reactions related to these substrates.

    7.3 Drugs That Prolong QTc Interval

    Avoid concomitant use of KRAZATI with other product(s) with a known potential to prolong the QTc interval. If concomitant use cannot be avoided, monitor electrocardiogram and electrolytes prior to starting KRAZATI, during concomitant use, and as clinically indicated [see Warnings and Precautions (5.2)]. Withhold KRAZATI if the QTc interval is > 500 ms or the change from baseline is > 60 ms [see Dosage and Administration (2.3)].

    Adagrasib causes QTc interval prolongation [see Clinical Pharmacology (12.2)]. Concomitant use of KRAZATI with other products that prolong the QTc interval may result in a greater increase in the QTc interval and adverse reactions associated with QTc interval prolongation, including Torsade de pointes, other serious arrythmias, and sudden death [see Warnings and Precautions (5.2)].

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    There are no available data on the use of KRAZATI in pregnant women. In animal reproduction studies, oral administration of adagrasib to pregnant rats and rabbits during the period of organogenesis did not cause adverse development effects or embryo-fetal lethality at exposures below the human exposure at the recommended dose of 600 mg twice daily (see Data).

    In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

    Data

    Animal Data

    In a rat embryo-fetal development study, once daily oral administration of adagrasib to pregnant rats during the period of organogenesis resulted in maternal toxicity (reduced body weight and food intake, and adverse clinical signs leading to moribund condition and early termination) and lower fetal body weight at 270 mg/kg dose level (approximately 2 times the recommended dose of 600 mg twice daily based on body surface area [BSA]). Adagrasib induced skeletal malformations, such as bent limbs, and skeletal variations, such as bent scapula, wavy ribs, and supernumerary short cervical ribs at 270 mg/kg, which were secondary to maternal toxicity and reduced fetal body weight.

    In a rabbit embryo-fetal development study, once daily oral administration of adagrasib during the period of organogenesis resulted in lower fetal body weight and increased litter frequency of unossified sternebra at 30 mg/kg (approximately 0.11 times the human exposure based on area under the curve [AUC] at the clinical dose of 600 mg twice daily). This skeletal variation was associated with maternal toxicities, including reduced mean body weight and decreased food consumption. Adagrasib exposure did not cause adverse developmental effects and did not affect embryo-fetal survival in rabbits at doses up to 30 mg/kg once daily.

    8.2 Lactation

    Risk Summary

    There are no data on the presence of adagrasib or its metabolites in human milk, the effects on the breastfed child, or on milk production. Because of the potential for serious adverse reactions in breastfed children, advise women not to breastfeed during treatment with KRAZATI and for 1 week after the last dose.

    8.3 Females and Males of Reproductive Potential

    Infertility

    Based on findings from animal studies, KRAZATI may impair fertility in females and males of reproductive potential [see Nonclinical Toxicology (13.1)].

    8.4 Pediatric Use

    The safety and effectiveness of KRAZATI has not been established in pediatric patients.

    8.5 Geriatric Use

    Of 116 patients with metastatic NSCLC who received adagrasib 600 mg orally twice daily in KRYSTAL-1, 49% (57 patients) were ≥ 65 years of age and 13% (15 patients) were ≥ 75 years of age. No overall differences in safety or effectiveness were observed between older and younger patients.

    Of 94 patients with metastatic CRC who received adagrasib 600 mg orally twice daily in combination with cetuximab in KRISTAL-1, 33% (31 patients) were ≥ 65 years of age and 2.1% (2 patients) were ≥ 75 years of age. No overall differences in safety or effectiveness were observed between older and younger patients.

  • 11 DESCRIPTION

    Adagrasib is an irreversible inhibitor of KRAS G12C and belongs to the RAS GTPase family. The molecular formula is C32H35ClFN7O2 and the molecular weight is 604.1 g/mol. The chemical name is {(2S)-4-[7-(8-chloronaphthalen-1-yl)-2-{[(2S)-1-methylpyrrolidin-2-yl]- methoxy}-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-4-yl]-1-(2-fluoroprop-2-enoyl)piperazin-2-yl}acetonitrile. Adagrasib has the following chemical structure:

    Chemical Structure

    Adagrasib is a crystalline solid. The solubility of adagrasib in the aqueous media decreases over the range pH 1.2 to 7.4 from > 262 mg/mL to < 0.010 mg/mL.

    KRAZATI (adagrasib) tablets for oral administration contain 200 mg of adagrasib. The following are inactive ingredients: colloidal silicon dioxide, crospovidone, magnesium stearate (vegetable sourced), mannitol, and microcrystalline cellulose. The tablet film coating contains hypromellose, maltodextrin, medium chain triglycerides (vegetable sourced), polydextrose, talc, and titanium dioxide.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Adagrasib is an irreversible inhibitor of KRAS G12C that covalently binds to the mutant cysteine in KRAS G12C and locks the mutant KRAS protein in its inactive state that prevents downstream signaling without affecting wild-type KRAS protein. Adagrasib inhibited tumor cell growth and viability in cells harboring KRAS G12C mutations and resulted in tumor regression in KRAS G12C-mutated tumor xenograft models with minimal off-target activity. Adagrasib in combination with cetuximab had increased antitumor activity in some cell line-derived and patient-derived KRAS G12C-mutant CRC tumor xenograft models compared to adagrasib or cetuximab alone.

    12.2 Pharmacodynamics

    Adagrasib exposure-response relationships and the time course of pharmacodynamic response are unknown.

    Cardiac Electrophysiology

    Adagrasib increased QTc in a concentration-dependent manner. Based on the concentration-QTcF relationship, the mean (90% CI) QTcF change from baseline (ΔQTcF) was 18 (15, 21) ms at the mean steady-state maximum concentration (Cmax,ss) in patients after administration of adagrasib 600 mg twice daily [see Warnings and Precautions (5.2)].

    12.3 Pharmacokinetics

    The pharmacokinetics of adagrasib were studied in healthy subjects and in patients with KRAS G12C-mutated NSCLC or CRC. Adagrasib pharmacokinetic data are presented as mean (percent coefficient of variation) unless otherwise specified.

    Adagrasib AUC and Cmax increase dose proportionally over the dose range of 400 mg to 600 mg (0.67 to 1 times the approved recommended dose). Adagrasib steady-state was reached within 8 days following administration of the approved recommended dosage and accumulation was approximately 6-fold.

    Absorption

    The median (min, max) Tmax of adagrasib is approximately 6 (6, 12) hours.

    Effect of Food

    No clinically significant differences in the pharmacokinetics of adagrasib were observed following administration of a high-fat and high-calorie meal (containing approximately 900 to 1000 calories, 50% from fat).

    Distribution

    The apparent volume of distribution of adagrasib is 942 L (57%). Human plasma protein binding of adagrasib is approximately 98% in vitro.

    Elimination

    The adagrasib terminal elimination half-life is 23 hours (16%) and the apparent oral clearance (CL/F) is 37 L/h (54%) in patients.

    Metabolism

    Adagrasib is metabolized primarily by CYP3A4 following single dose administration. Adagrasib inhibits its own CYP3A4 metabolism following multiple dosing to steady-state which permits CYP2C8, CYP1A2, CYP2B6, CYP2C9, and CYP2D6 to contribute to its metabolism at steady-state.

    Excretion

    Following a single oral dose of radiolabeled adagrasib, approximately 75% of the dose was recovered in feces (14% as unchanged) and 4.5% recovered in urine (2% as unchanged).

    Specific Populations

    No clinically significant differences in the pharmacokinetics of adagrasib based on age (19 to 89 years), sex, race (White, Black or African American, or Asian), body weight (36 to 146 kg), ECOG PS (0, 1), tumor type (NSCLC or CRC), or tumor burden. No clinically significant differences in the pharmacokinetics of adagrasib are expected in patients with mild to severe renal impairment (CLcr 15 to < 90 mL/min estimated by Cockcroft-Gault equation) or in patients with mild to severe hepatic impairment (Child-Pugh classes A to C).

    Drug Interaction Studies

    Clinical Studies and Model-Informed Approaches

    The following table describes the effect of other drugs on the pharmacokinetics of adagrasib.

    Table 7: Effect of Other Drugs on Adagrasib
    Cmax = maximum plasma concentration; AUC = area under the plasma concentration-time curve
    *
    Predicted changes in Cmax or AUC of adagrasib.

    Concomitant Drug

    Adagrasib Dosage

    Changes in Cmax or AUC of Adagrasib

    Cmax
    % Decrease

    AUC
    % Decrease

    Rifampin
    (a strong CYP3A inducer)

    600 mg single dose

    88%

    95%

    600 mg multiple doses

    > 61%*

    > 66%*

    Strong CYP3A Inhibitors: Adagrasib Cmax increased by 2.4-fold and AUC increased by 4-fold following concomitant use of a single dose of 200 mg (0.33 times the approved recommended dose) with itraconazole (a strong CYP3A inhibitor). No clinically significant differences in the pharmacokinetics of adagrasib at steady state were predicted when used concomitantly with itraconazole.

    No clinically significant differences in the pharmacokinetics of adagrasib were predicted or observed when used concomitantly with efavirenz (a moderate CYP3A inducer), pantoprazole (a proton pump inhibitor), or rosuvastatin (a BCRP/OATP substrate).

    The following table describes the effect of adagrasib on the pharmacokinetics of other drugs.

    Table 8: Effect of Adagrasib on Other Drugs
    Cmax = maximum plasma concentration; AUC = area under the plasma concentration-time curve
    *
    0.66 times the approved recommended dosage.
    Predicted changes in Cmax or AUC of concomitant drug.

    Concomitant Drug

    Adagrasib Dosage

    Fold Increase of Concomitant Drug

    Cmax

    AUC

    Midazolam
    (a sensitive CYP3A substrate)

    400 mg* twice daily

    4.8-fold

    21-fold

    600 mg twice daily

    3.1-fold

    31-fold

    Warfarin
    (a sensitive CYP2C9 substrate)

    600 mg twice daily

    1.1-fold

    2.9-fold

    Dextromethorphan
    (a sensitive CYP2D6 substrate)

    400 mg* twice daily

    1.9-fold

    1.8-fold

    600 mg twice daily

    1.7-fold

    2.4-fold

    Digoxin
    (a P-gp substrate)

    600 mg twice daily

    1.9-fold

    1.5-fold

    In Vitro Studies

    Cytochrome P450 (CYP) Enzymes: Adagrasib may inhibit CYP2B6.

    Transporter Systems: Adagrasib may be a substrate of BCRP and may inhibit MATE-1/MATE-2K.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenicity studies have not been conducted with adagrasib.

    Adagrasib was not mutagenic in an in vitro bacterial reverse mutation (Ames) assay and was not genotoxic in an in vitro chromosomal aberration assay or an in vivo micronucleus assay in rats.

    Fertility studies were not conducted with adagrasib. In toxicology studies of up to 13-weeks in duration in rats, oral administration of adagrasib induced phospholipidosis which increased vacuolation in female reproductive organs, including vacuolation in ovaries (corpora lutea, macrophage or interstitial cells) and uterus (glandular epithelium), and atrophy with mucification of the vaginal mucosa at doses ≥ 150 mg/kg (approximately equal to or greater than the human exposure at the recommended dose based on area under the curve [AUC]). These findings reversed after cessation of dosing in the 28-day study but in the 13-week study, pigmented macrophage aggregates were observed in the ovaries of female rats after the recovery period. In a 28-day repeat-dose toxicology study, oral administration of adagrasib to male rats induced atrophy and epithelial vacuolation of the prostate gland and seminal vesicles at 300 mg/kg (approximately 1.6 times the human exposure at the recommended dose based on AUC). These findings resolved after cessation of treatment.

    13.2 Animal Toxicology and/or Pharmacology

    Phospholipidosis (vacuolation and/or presence of foamy macrophages) was observed in multiple organs (e.g., lung, trachea, heart, skeletal, ovaries, uterus, adrenal gland, kidney, liver, lymph nodes, spleen, thymus, and thyroid in rats; and heart and lung in dogs) after repeated oral administration of adagrasib in rats and dogs. In toxicology studies of up to 13-week duration in rats, phospholipidosis was observed at doses ≥ 150 mg/kg (approximately ≥ 2 times the human exposure at the recommended dose based on AUC). In a dog 28-day toxicity study, this effect was observed at 25 mg/kg (approximately equal to the human exposure at the recommended dose based on AUC). The extent of vacuolization and the presence of foamy macrophages were more prominent in the rat compared to dogs, and evidence of reversibility after cessation of treatment was noted for most organs. The significance of this finding in humans in unknown.

  • 14 CLINICAL STUDIES

    14.1 Non-Small Cell Lung Cancer

    The efficacy of adagrasib was evaluated in KRYSTAL-1 (NCT03785249), a multicenter, single-arm, open-label expansion cohort study. Eligible patients were required to have locally advanced or metastatic KRAS G12C-mutated NSCLC who previously received treatment with a platinum-based regimen and an immune checkpoint inhibitor, an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1, and at least one measurable lesion as defined by Response Evaluation criteria in Solid Tumors (RECIST v1.1). Identification of a KRAS G12C mutation was prospectively determined by local testing using tissue specimens. Patients received adagrasib 600 mg orally twice daily until unacceptable toxicity or disease progression. Tumor assessments were performed every 6 weeks. The major efficacy outcome measures were confirmed objective response rate (ORR) and duration of response (DOR) as evaluated by blinded independent central review (BICR) according to RECIST v1.1.

    In the efficacy population, KRAS G12C mutation status was determined by prospective local testing using tumor tissue specimens. Of the 112 patients with KRAS G12C mutation, tissue samples from 88% (98/112) patients were tested retrospectively using the QIAGEN therascreen KRAS RGQ PCR Kit. While 89% (87/98) of patients were positive for KRAS G12C mutation, 11% (11/98) did not have a KRAS G12C mutation identified. In addition, plasma samples from 63% (71/112) patients were tested retrospectively using Agilent Resolution ctDx FIRST assay. While 66% (47/71) of patients were positive for KRAS G12C mutation, 34% (24/71) did not have a KRAS G12C mutation identified.

    A total of 112 patients had at least one measurable lesion at baseline as assessed by BICR according to RECIST v1.1.

    The baseline demographic and disease characteristics in the efficacy population were: median age 64 years (range: 25 to 89), 55% female, 83% White, 8% were Black or African American, 4% Asian, 4% race not reported, 0.9% American Indian or Alaska Native, 16% Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 and 83% ECOG PS 1. Tumor histology was 97% adenocarcinoma and 89% of patients had metastatic disease. Patients received a median of 2 prior systemic therapies (range 1 to 7); 43% received 1 prior line, 35% received 2 prior lines, 10% received 3 prior lines and 12% received 4 or more prior lines, 98% received both prior platinum and prior anti-PD-1/PD-L1 therapy. Sites of extra-thoracic disease included bone 42%, brain 30%, adrenals 21%, and liver 21%.

    Efficacy results are summarized in Table 9.

    Table 9: Efficacy Results for KRYSTAL-1
    CI = Confidence Interval
    *
    Assessed by BICR.
    Estimate using Kaplan-Meier method.
    Observed proportion of patients with duration of response beyond landmark time.

    Efficacy Parameter

    Adagrasib
    (n = 112)

    Objective Response Rate (95% CI)*

    43 (34, 53)

      Complete response rate, %

    0.9

      Partial response rate, %

    42

    Duration of Response*

      Median in months (95% CI)

    8.5 (6.2, 13.8)

      Patients with duration ≥ 6 months, %

    58

    14.2 Colorectal Cancer

    The efficacy of adagrasib in combination with cetuximab was evaluated in KRYSTAL-1, a multicenter, single-arm, open-label expansion cohort study. Eligible patients were required to have locally advanced or metastatic KRAS G12C-mutated CRC and to have previously received therapy with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, a VEGF inhibitor if eligible, and an ECOG PS of 0 or 1.

    Patients initiated treatment with adagrasib 600 mg orally twice daily in combination with cetuximab administered either biweekly (77 patients with 500 mg/m2 every two weeks) or weekly (17 patients with 400 mg/m2 initial dose followed by 250 mg/m2 weekly). Treatment continued until unacceptable toxicity or disease progression. Tumor assessments were performed every 6 weeks. Adagrasib discontinuation required cetuximab discontinuation, however patients could continue to receive adagrasib if cetuximab was discontinued [see Dosage and Administration (2.3)]. Six patients continued with adagrasib single agent therapy after discontinuing cetuximab. The length of time these 6 patients received adagrasib alone ranged from 43 days to 3 years. Patient treatment with adagrasib after disease progression continued if a patient was clinically stable and considered to be deriving clinical benefit by the investigator.

    The major efficacy outcome measures were confirmed ORR and DOR according to RECIST v1.1 as assessed by BICR.

    In the efficacy population, KRAS G12C mutation status was determined by prospective local testing using tumor tissue specimens. Of the 94 patients with KRAS G12C mutation, tissue samples from 79% (74/94) patients were tested retrospectively using the QIAGEN therascreen KRAS RGQ PCR Kit. Of the 74 tissue samples submitted, 81% (60/74) yielded a result with 93% (56/60) positive for KRAS G12C and 7% (4/60) without a KRAS G12C mutation identified.

    The baseline demographic and disease characteristics in the efficacy population were: median age 57 years (range: 24 to 75 years), 53% female, 71% White, 14% were Black or African American, 5% Asian, 1.1% American Indian or Alaska Native, 9% reported as other; 51% ECOG PS 0 and 49% ECOG PS 1. Tumor histology was 100% adenocarcinoma and 99% of patients had metastatic disease. Patients received a median of 3 prior systemic therapies (range 1 to 9); 9% received 1 prior line, 36% received 2 prior lines, 31% received 3 prior lines and 25% received 4 or more prior lines. Sites of metastatic disease included lung (71%), liver (64%) and bone (14%).

    Efficacy results are summarized in Table 10.

    Table 10: Efficacy Results for KRYSTAL-1
    CI = Confidence Interval
    *
    Assessed by BICR.
    Estimate using Kaplan-Meier method.
    Observed proportion of patients with duration of response beyond landmark time.

    Efficacy Parameter

    Adagrasib
    (n = 94)

    Objective Response Rate (95% CI)*

    34 (25, 45)

      Complete response rate, %

    0

      Partial response rate, %

    34.0

    Duration of Response*

      Median in months (95% CI)

    5.8 (4.2, 7.6)

      Patients with duration ≥ 6 months, %

    31

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    How Supplied

    KRAZATI (adagrasib) tablets, 200 mg, oval shaped, white to off-white, immediate release, film coated tablets with "200" on one side and stylized "M" on the other side.

    KRAZATI (adagrasib) tablets are packaged in high-density polyethylene, white opaque, square bottles with desiccant and polypropylene, white, child resistant closures with a tamper-proof heat induction seal.

     
    NDC 80739-812-12: 200 mg, bottle containing 120 tablets.
     
    NDC 80739-812-18: 200 mg, bottle containing 180 tablets.

    Storage and Handling

    Store tablets at room temperature, 20°C to 25°C (68°F to 77°F). Temperature excursions between 15°C and 30°C (59°F to 86°F) are permitted [see USP Controlled Room Temperature].

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Patient Information).

    Gastrointestinal Adverse Reactions

    Advise patients that KRAZATI can cause severe gastrointestinal adverse reactions and to contact their healthcare provider for signs or symptoms of severe or persistent gastrointestinal adverse reactions [see Warnings and Precautions (5.1)].

    QTc Interval Prolongation

    Advise patients that KRAZATI can cause QTc interval prolongation and to contact their healthcare provider for signs or symptoms of arrhythmias [see Warnings and Precautions (5.2)].

    Hepatotoxicity

    Advise patients that KRAZATI can cause hepatotoxicity and to immediately contact their healthcare provider for signs or symptoms of liver dysfunction [see Warnings and Precautions (5.3)].

    Interstitial Lung Disease (ILD)/Pneumonitis

    Advise patients that KRAZATI can cause ILD / pneumonitis and to contact their healthcare provider immediately for new or worsening respiratory symptoms [see Warnings and Precautions (5.4)].

    Drug Interactions

    Advise patients to inform their healthcare providers of all concomitant medications, including prescription medicines, over-the-counter drugs, vitamins, and herbal products [see Drug Interactions (7.1)].

    Missed Dose

    If a dose of KRAZATI is missed by greater than 4 hours, resume dosing at the next scheduled time [see Dosage and Administration (2.2)].

    Lactation

    Advise women not to breastfeed during treatment with KRAZATI and for 1 week after the last dose [see Use in Specific Populations (8.2)].

    Infertility

    Inform patients that KRAZATI may cause infertility [see Use in Specific Populations (8.3)].

  • SPL UNCLASSIFIED SECTION

    KRAZATI (adagrasib)

    Distributed by:
    Bristol-Myers Squibb Company
    Princeton, NJ 08543 U.S.A.

    KRAZATI and the KRAZATI logo are trademarks of Mirati Therapeutics, Inc., a Bristol Myers Squibb company.

  • PATIENT PACKAGE INSERT

    PATIENT INFORMATION
    KRAZATI® (krah zah tee)
    (adagrasib)
    Tablets

    What is KRAZATI?
    KRAZATI is a prescription medicine used in adults:

    o
    alone to treat non-small cell lung cancer (NSCLC)
    o
    that has spread to other parts of the body or cannot be removed by surgery, and
    o
    whose tumor has an abnormal KRAS G12C gene, and
    o
    who have received at least one prior treatment.
    o
    in combination with a medicine called cetuximab to treat colon or rectal cancer (CRC)
    o
    that has spread to other parts of the body or cannot be removed by surgery, and
    o
    whose tumor has an abnormal KRAS G12C gene, and
    o
    who have previously received certain chemotherapy medicines.

    Your healthcare provider will perform a test to make sure that KRAZATI is right for you.
    It is not known if KRAZATI is safe and effective in children.

    Before taking KRAZATI, tell your healthcare provider about all of your medical conditions, including if you:

    o
    have any heart problems, including heart failure and congenital long QT syndrome.
    o
    have liver problems.
    o
    are pregnant or plan to become pregnant. It is not known if KRAZATI can harm your unborn baby.
    o
    are breastfeeding or plan to breastfeed. It is not known if KRAZATI passes into your breastmilk. Do not breastfeed during treatment and for 1 week after your last dose of KRAZATI.

    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. KRAZATI can affect the way other medicines work, and other medicines can affect how KRAZATI works.

    How should I take KRAZATI?

    o
    Take KRAZATI exactly as your healthcare provider tells you to take it. Do not change your dose or stop taking KRAZATI unless your healthcare provider tells you to.
    o
    Your healthcare provider may change your dose, or temporarily or permanently stop treatment with KRAZATI if you develop certain side effects.
    o
    For colon or rectal cancer, you will also receive cetuximab through a vein in your arm (intravenously) given by your healthcare provider. Your healthcare provider will permanently or temporarily stop your treatment with cetuximab if your treatment with KRAZATI is permanently or temporarily stopped.
    o
    Take your prescribed dose of KRAZATI 2 times each day, at about the same time each day.
    o
    Take KRAZATI either with food or without food.
    o
    Swallow KRAZATI tablets whole. Do not chew, crush or split tablets.
    o
    If you vomit after taking a dose of KRAZATI, do not take an extra dose. Take your next dose at your next scheduled time.
    o
    If you miss a dose of KRAZATI, take the dose as soon as you remember. If it has been more than 4 hours, do not take the dose. Take your next dose of KRAZATI at your next scheduled time. Do not take 2 doses at the same time to make up for a missed dose.

    What are possible side effects of KRAZATI?
    KRAZATI can cause serious side effects, including:

    o
    Stomach and intestinal (gastrointestinal) problems. Stomach and intestinal side effects including nausea, diarrhea, or vomiting, are common with KRAZATI but can also sometimes be severe. KRAZATI can also cause serious stomach and intestinal side effects such as bleeding, obstruction, inflammation of the colon (colitis), and narrowing (stenosis).
    o
    Call your healthcare provider if you develop any of the signs or symptoms of stomach or intestinal problems listed above during treatment with KRAZATI.
    o
    Your healthcare provider may prescribe an antidiarrheal medicine or anti-nausea medicine, or other treatment, as needed.
    o
    Changes in the electrical activity of your heart called QTc prolongation. Certain changes can occur in the electrical activity of your heart during treatment with KRAZATI and can be seen on a test called an electrocardiogram (ECG or EKG). QTc prolongation can increase your risk for irregular heartbeats that can be life-threatening, such as torsades de pointes, and can lead to sudden death.
    o
    You should not take KRAZATI if you have congenital long QT syndrome or if you currently have QTc prolongation. See "Before taking KRAZATI, tell your healthcare provider about all of your medical conditions, including if you:"
    Your healthcare provider should monitor the electrical activity of your heart and the levels of body salts in your blood (electrolytes) especially potassium and magnesium before starting and during treatment with KRAZATI if you have heart failure, a slow heart rate, abnormal levels of electrolytes in your blood, or if you take a medicine that can prolong the QT interval of your heartbeat.
    Tell your healthcare provider if you feel dizzy, lightheaded, or faint, or if you get abnormal heartbeats during treatment with KRAZATI.
    o
    Liver problems. Abnormal liver blood test results are common with KRAZATI and can sometimes be severe. Your healthcare provider should do blood tests before starting and during treatment with KRAZATI to check your liver function. Tell your healthcare provider right away if you develop any signs or symptoms of liver problems, including:
    o
    your skin or the white part of your eyes turns yellow (jaundice)
    o
    dark or "tea-colored" urine
    o
    light-colored stools (bowel movements)
    o
    tiredness or weakness
    o
    nausea or vomiting
    o
    bleeding or bruising
    o
    loss of appetite
    o
    pain, aching or tenderness on the right side of your stomach area (abdomen)
    o
    Lung or breathing problems. KRAZATI may cause inflammation of the lungs that can lead to death. Tell your healthcare provider or get emergency medical help right away if you have new or worsening shortness of breath, cough, or fever.

    The most common side effects of KRAZATI when used alone for NSCLC include:

    o
    nausea
    o
    diarrhea
    o
    vomiting
    o
    tiredness
    o
    muscle and bone pain
    o
    kidney problems
    o
    swelling
    o
    decreased appetite
    o
    trouble breathing

    The most common side effects of KRAZATI when used in combination with cetuximab for CRC include:

    o
    skin rash
    o
    nausea
    o
    diarrhea
    o
    vomiting
    o
    tiredness
    o
    muscle and bone pain
    o
    headache
    o
    dry skin
    o
    stomach pain
    o
    decreased appetite
    o
    swelling
    o
    low red blood cell count
    o
    cough
    o
    dizziness
    o
    constipation
    o
    nerve damage in the arms and legs

    Certain abnormal blood test results are common during treatment with KRAZATI, when used alone or in combination with cetuximab. Your healthcare provider will monitor you for abnormal blood tests and treat you if needed.

    KRAZATI may cause fertility problems in males and females, which may affect your ability to have children. Talk to your healthcare provider if this is a concern for you.
    These are not all of the possible side effects of KRAZATI.
    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

    How should I store KRAZATI?

    o
    Store KRAZATI at room temperature between 68°F to 77°F (20°C to 25°C).
    o
    KRAZATI comes in a child-resistant container.
    o
    KRAZATI comes with a desiccant (drying agent) in the container to keep the medicine dry. Do not remove the desiccant from the container after opening. Do not eat or swallow the desiccant.

    Keep KRAZATI and all medicines out of the reach of children.

    General information about the safe and effective use of KRAZATI.
    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use KRAZATI for a condition for which it was not prescribed. Do not give KRAZATI to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about KRAZATI that is written for health professionals.

    What are the ingredients in KRAZATI?
    Active ingredient: adagrasib
    Inactive ingredients: colloidal silicon dioxide, crospovidone, magnesium stearate (vegetable sourced), mannitol, and microcrystalline cellulose. The tablet film coating contains hypromellose, maltodextrin, medium chain triglycerides (vegetable sourced), polydextrose, talc, and titanium dioxide.
    Distributed by: Bristol-Myers Squibb Company, Princeton, NJ 08543 U.S.A.
    KRAZATI and the KRAZATI logo are trademarks of Mirati Therapeutics, Inc., a Bristol Myers Squibb company.
    For more information, go to www.KRAZATI.com or call 1-866-4-KRAZATI (1-866-457-2928).

    This Patient Information has been approved by the U.S. Food and Drug Administration.                         Revised: 07/2024

  • PRINCIPAL DISPLAY PANEL - 180 Tablet Bottle Carton

    NDC 80739-812-18

    Rx Only

    KRAZATI®
    (adagrasib tablets)

    200 mg

    180 tablets

    Bristol Myers Squibb®

    PRINCIPAL DISPLAY PANEL - 180 Tablet Bottle Carton
  • INGREDIENTS AND APPEARANCE
    KRAZATI 
    adagrasib tablet, coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:80739-812
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADAGRASIB (UNII: 8EOO6HQF8Y) (ADAGRASIB - UNII:8EOO6HQF8Y) ADAGRASIB200 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MANNITOL (UNII: 3OWL53L36A)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYDEXTROSE (UNII: VH2XOU12IE)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize16mm
    FlavorImprint Code 200;M
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80739-812-121 in 1 CARTON12/12/2022
    1120 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:80739-812-181 in 1 CARTON12/12/2022
    2180 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21634012/12/2022
    Labeler - Mirati Therapeutics, Inc (078870124)