Label: RYTELO- imetelstat sodium injection, powder, lyophilized, for solution
- NDC Code(s): 82959-111-01, 82959-112-01
- Packager: Geron Corporation
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated June 11, 2024
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HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use RYTELO safely and effectively. See full prescribing information for RYTELO.
RYTELO (imetelstat) for injection, for intravenous use.
Initial U.S. Approval: 2024INDICATIONS AND USAGE
RYTELO is an oligonucleotide telomerase inhibitor indicated for the treatment of adult patients with low- to intermediate-1 risk myelodysplastic syndromes (MDS) with transfusion-dependent anemia requiring 4 or more red blood cell units over 8 weeks who have not responded to or have lost response to or are ineligible for erythropoiesis-stimulating agents (ESA). (1)
DOSAGE AND ADMINISTRATION
DOSAGE FORMS AND STRENGTHS
CONTRAINDICATIONS
None. (4)
WARNINGS AND PRECAUTIONS
- Thrombocytopenia: Grade 3 and Grade 4 thrombocytopenia occurred; obtain complete blood cell counts prior to initiation of RYTELO, weekly for the first two cycles, and prior to each cycle thereafter to monitor. Delay or dose reduce as recommended. (2.3, 5.1)
- Neutropenia: Grade 3 and Grade 4 neutropenia occurred; obtain complete blood cell counts prior to initiation of RYTELO, weekly for the first two cycles, and prior to each cycle thereafter to monitor. Delay or dose reduce as recommended. (2.3, 5.2)
- Infusion-Related Reactions: Premedicate before infusion. Interrupt, decrease the rate of infusion, or permanently discontinue RYTELO based on severity. (2.2, 2.3, 5.3)
- Embryo-Fetal Toxicity: Can cause embryo-fetal harm. Advise females of reproductive potential of potential risk to a fetus and to use effective contraception. (5.4, 8.1, 8.3)
ADVERSE REACTIONS
Most common adverse reactions (incidence ≥10% with a difference between arms of >5% compared to placebo), including laboratory abnormalities are decreased platelets, decreased white blood cells, decreased neutrophils, increased AST, increased alkaline phosphatase, increased ALT, fatigue, prolonged partial thromboplastin time, arthralgia/myalgia, COVID-19 infections, and headache. (6.1)
To report SUSPECTED ADVERSE REACTIONS, contact Geron Corporation at 1-855-437-6664 (1-855-GERONMI) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
See 17 for PATIENT COUNSELING INFORMATION and Medication Guide.
Revised: 6/2024
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Table of Contents
FULL PRESCRIBING INFORMATION: CONTENTS*
1. INDICATIONS AND USAGE
2. DOSAGE AND ADMINISTRATION
2.1. Recommended Dosage
2.2. Recommended Premedications
2.3. Dosage Modifications for Adverse Reactions
2.4. Preparation and Administration
3. DOSAGE FORMS AND STRENGTHS
4. CONTRAINDICATIONS
5. WARNINGS AND PRECAUTIONS
5.1. Thrombocytopenia
5.2. Neutropenia
5.3. Infusion-Related Reactions
5.4. Embryo-Fetal Toxicity
6. ADVERSE REACTIONS
6.1. Clinical Trials Experience
8. USE IN SPECIFIC POPULATIONS
8.1. Pregnancy
8.2. Lactation
8.3. Females and Males of Reproductive Potential
8.4. Pediatric Use
8.5. Geriatric Use
11. DESCRIPTION
12. CLINICAL PHARMACOLOGY
12.1. Mechanism of Action
12.2. Pharmacodynamics
12.3. Pharmacokinetics
12.6. Immunogenicity
13. NONCLINICAL TOXICOLOGY
13.1. Carcinogenesis, Mutagenesis, Impairment of Fertility
14. CLINICAL STUDIES
14.1. Myelodysplastic Syndromes (MDS)
16. HOW SUPPLIED/STORAGE AND HANDLING
17. PATIENT COUNSELING INFORMATION
- *
- Sections or subsections omitted from the full prescribing information are not listed.
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1. INDICATIONS AND USAGE
RYTELO is indicated for the treatment of adult patients with low- to intermediate-1 risk myelodysplastic syndromes (MDS) with transfusion-dependent anemia requiring 4 or more red blood cell units over 8 weeks who have not responded to or have lost response to or are ineligible for erythropoiesis-stimulating agents (ESA).
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2. DOSAGE AND ADMINISTRATION
2.1. Recommended Dosage
The recommended dosage of RYTELO is 7.1 mg/kg administered as an intravenous infusion over 2 hours every 4 weeks. Discontinue RYTELO if a patient does not experience a decrease in red blood cell (RBC) transfusion burden after 24 weeks of treatment (administration of 6 doses) or if unacceptable toxicity occurs at any time [see Dosage and Administration (2.3)].
2.2. Recommended Premedications
Administer the following pre-treatment medications at least 30 minutes prior to dosing to prevent or reduce potential infusion-related reactions:
- diphenhydramine (or equivalent) 25 mg to 50 mg, intravenously or orally
- hydrocortisone (or equivalent) 100 mg to 200 mg, intravenously or orally
Monitor patients for adverse reactions for at least one hour after the infusion has been completed [see Warnings and Precautions (5.3) and Adverse Reactions (6.1)].
2.3. Dosage Modifications for Adverse Reactions
Recommended dose reductions for Grade 3 and Grade 4 adverse reactions are found in Table 1.
The management of Grade 3 and Grade 4 adverse reactions may require temporary dose delay, dose reduction, or treatment discontinuation and are presented in Table 2 and Table 3. RYTELO treatment should be permanently discontinued if the patient cannot tolerate the lowest dose level of 4.4 mg/kg.
Table 1: Recommended Dose Reduction for RYTELO for Grade 3 and Grade 4 Adverse Reactions Dose Reduction Dose Every 4 Weeks First dose reduction 5.6 mg/kg Second dose reduction 4.4 mg/kg Dosage Modifications for Hematologic (Grade 3 and Grade 4) Adverse Reactions
Monitor complete blood cell counts prior to administration of RYTELO, weekly for the first two cycles, prior to each cycle thereafter, and as clinically indicated. Delay the next cycle if absolute neutrophil count is less than 1 × 109/L or platelets are less than 50 × 109/L. Modify dose as described in Table 2.
Table 2: Dosage Modifications for Patients with Hematologic Adverse Reactions (Grade 3 and Grade 4) Adverse Reaction Severity Grade* Occurrence Treatment Modification Abbreviation: ANC = absolute neutrophil count - *
- Severity based on National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03.
Thrombocytopenia
[see Warnings and Precautions (5.1)]Grade 3 First Delay RYTELO until recovery of platelets to 50 × 109/L; restart at same dose level. Second and Third Delay RYTELO until recovery of platelets to 50 × 109/L; restart at one dose level lower. Fourth Discontinue RYTELO. Grade 4 First and Second Delay RYTELO until recovery of platelets to 50 × 109/L; restart at one dose level lower. Third Discontinue RYTELO. Neutropenia
[see Warnings and Precautions (5.2)]Grade 3 First Delay RYTELO until recovery of ANC to 1 × 109/L; restart at same dose level. Second and Third Delay RYTELO until recovery of ANC to 1 × 109/L; restart at one dose level lower. Fourth Discontinue RYTELO. Grade 4 First and Second Delay RYTELO until recovery of ANC to 1 × 109/L; restart at one dose level lower. Third Discontinue RYTELO. Dosage Modifications for Non-hematologic Adverse Reactions
Dosage modifications for infusion-related reactions and other adverse drug reactions, including elevated liver function tests (LFTs), are described in Table 3. Monitor liver function tests prior to administration of RYTELO, weekly for the first cycle, prior to each cycle thereafter, and as clinically indicated.
Table 3: Dosage Modifications for Patients with Non-hematologic Adverse Reactions Adverse Reaction Severity Grade* Occurrence Treatment Modification Abbreviation: LFT = liver function test - *
- Severity based on National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03.
Infusion-Related Reactions
[see Warnings and Precautions (5.3)]Grade 2 or 3 First and Second Interrupt the RYTELO infusion until resolution of the adverse reaction or until the intensity of the reaction decreases to Grade 1; restart infusion at 50% of the infusion rate administered prior to the adverse reaction. Third For Grade 2, stop infusion. May restart at next cycle.
For Grade 3, permanently discontinue RYTELO.Grade 4 First Stop infusion, administer supportive care as appropriate and permanently discontinue RYTELO. Other adverse reactions including elevated LFTs
[see Adverse Reactions (6.1)]Grade 3 or 4 First and Second Delay RYTELO until recovery of adverse reactions to Grade 1 or baseline; restart at one dose level lower. Third Permanently discontinue RYTELO. 2.4. Preparation and Administration
RYTELO is provided as a lyophilized powder in a single-dose vial for intravenous infusion only and must be reconstituted and diluted prior to administration.
Use aseptic technique to prepare RYTELO.
RYTELO does not contain a preservative.
Reconstitution:
- Calculate the dose of RYTELO needed based on the patient's body weight (kg).
- Determine the number of RYTELO vials needed to achieve the required dose (total mg) per Table 4. More than one vial may be needed to achieve a full dose.
- Remove the RYTELO vials from the refrigerator and allow the vials to sit for 10 minutes to 15 minutes (not to exceed 30 minutes) to adjust to room temperature 20°C to 25°C (68°F to 77°F) before use.
- Reconstitute each vial of RYTELO with the volume of 0.9% Sodium Chloride Injection provided in Table 4 directly onto the lyophilized powder to obtain a concentration of 31.4 mg/mL of imetelstat.
Table 4: Reconstitution Volumes Strength* Volume of 0.9% Sodium Chloride Injection for Reconstitution per Vial Final Concentration of Reconstituted Solution per Vial Deliverable Volume per Vial - *
- Recommended to use the appropriate combination of vial strengths to most closely match the intended dose based on the patient's weight.
- †
- Each vial contains an overfill to account for loss of liquid during preparation and extraction of the reconstituted solution, resulting in the final concentration.
47 mg 1.8 mL 31.4 mg/mL† 1.5 mL 188 mg 6.3 mL 31.4 mg/mL† 6 mL - Swirl each vial gently to avoid foaming until the powder is fully reconstituted (not to exceed 15 minutes). Do not shake.
- Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. The reconstituted solution in each vial should appear as a clear to slightly hazy solution, essentially free of visible contaminants, particles and/or particulates. Do not use if discoloration or particulate matter is present.
- Use the reconstituted solution immediately to prepare the RYTELO diluted solution in the infusion bag.
Dilution:
- Calculate the required volume of the reconstituted RYTELO solution needed to obtain the appropriate dose according to the patient's body weight.
- Withdraw a volume equal to the required reconstituted RYTELO solution from a 500 mL infusion bag of 0.9% Sodium Chloride Injection and discard it.
- Add the required volume of reconstituted RYTELO solution into the infusion bag so that the total final volume of RYTELO solution in the bag is approximately 500 mL. Discard any unused portion of the reconstituted solution remaining in each vial.
- Gently invert the infusion bag at least 5 times to ensure that the reconstituted RYTELO is well-mixed. Do not shake the infusion bag prior to administration.
Diluted RYTELO Solution Storage:
- If not used immediately, ensure that diluted solution for infusion is used within the total timeframes specified below, according to storage temperature:
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When stored at room temperature 20°C to 25°C (68°F to 77°F):
The total time from the reconstitution of RYTELO to completion of the intravenous infusion should not exceed 18 hours from the time of reconstitution. -
When stored refrigerated 2°C to 8°C (36°F to 46°F):
The total time from the reconstitution of RYTELO to completion of the intravenous infusion should not exceed 48 hours from the time of reconstitution.
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When stored at room temperature 20°C to 25°C (68°F to 77°F):
- 3. DOSAGE FORMS AND STRENGTHS
- 4. CONTRAINDICATIONS
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5. WARNINGS AND PRECAUTIONS
5.1. Thrombocytopenia
RYTELO can cause thrombocytopenia based on laboratory values. In the clinical trial, new or worsening Grade 3 or 4 decreased platelets occurred in 65% of patients with MDS treated with RYTELO [see Adverse Reactions (6.1)].
Median time to onset of first occurrence of Grade 3 or 4 decreased platelets was 6 weeks (range: 2 to 88 weeks) and median time to recovery from each occurrence of Grade 3 or 4 decreased platelets to Grade 2 or lower, or last value available, was 1.3 weeks (range: 0.1 to 13 weeks). Grade 3 or 4 decreased platelets occurred throughout treatment with RYTELO, with 48% of patients experiencing Grade 3 or Grade 4 thrombocytopenia during cycles 1-3, 31% during cycles 4-6, 33% during cycles 7-12, and 24% during cycles 13 and beyond. Grade 3 or 4 bleeding was seen in 2.5% of patients, including gastrointestinal bleeding (1.7%) and hematuria (0.8%).
Monitor patients with thrombocytopenia for bleeding.
Monitor complete blood cell counts prior to initiation of RYTELO, weekly for the first two cycles, prior to each cycle thereafter, and as clinically indicated. Administer platelet transfusions as appropriate. Delay the next cycle and resume at the same or reduced dose, or discontinue as recommended [see Dosage and Administration (2.3)].
5.2. Neutropenia
RYTELO can cause neutropenia based on laboratory values. In the clinical trial, new or worsening Grade 3 or 4 decreased neutrophils occurred in 72% of patients with MDS treated with RYTELO [see Adverse Reactions (6.1)].
Median time to onset of first occurrence of Grade 3 or 4 decreased neutrophils was 4.6 weeks (range: 1 to 81 weeks) and median time to recovery from each occurrence of Grade 3 or 4 decreased neutrophils to Grade 2 or lower, or last value available, was 1.9 weeks (range: 0 to 16 weeks). Grade 3 or 4 decreased neutrophils occurred throughout treatment with RYTELO, with 65% of patients experiencing Grade 3 or Grade 4 neutropenia during cycles 1-3, 35% during cycles 4-6, 32% during cycles 7-12, and 39% during cycles 13 and beyond. Febrile neutropenia occurred in 0.8% and sepsis in 4.2%.
Monitor patients with Grade 3 or 4 neutropenia for infections, including sepsis.
Monitor complete blood cell counts prior to initiation of RYTELO, weekly for the first two cycles, prior to each cycle thereafter, and as clinically indicated. Administer growth factors and anti-infective therapies for treatment or prophylaxis as appropriate. Delay the next cycle and resume at the same or reduced dose, or discontinue as recommended [see Dosage and Administration (2.3)].
5.3. Infusion-Related Reactions
RYTELO can cause infusion-related reactions. In the clinical trial, infusion-related reactions occurred in 8% of patients with MDS treated with RYTELO; Grade 3 or 4 infusion-related reactions occurred in 1.7%, including hypertensive crisis (0.8%). The most common infusion-related reaction was headache (4.2%). Infusion-related reactions usually occur during or shortly after the end of the infusion.
Premedicate patients at least 30 minutes prior to infusion with diphenhydramine and hydrocortisone as recommended and monitor patients for at least one hour following the infusion as recommended [see Dosage and Administration (2.2)]. Manage symptoms of infusion-related reactions with supportive care and infusion interruptions, decrease infusion rate, or permanently discontinue as recommended [see Dosage and Administration (2.3)].
5.4. Embryo-Fetal Toxicity
Based on findings in animals, RYTELO can cause embryo-fetal harm when administered to a pregnant woman. In animal reproduction studies, administration of imetelstat to pregnant mice during the period of organogenesis resulted in embryo-fetal mortality at maternal exposures (AUC) 2.5-times the human exposure at the recommended clinical dose. Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with RYTELO and for 1 week after the last dose [see Use in Specific Populations (8.1, 8.3)].
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6. ADVERSE REACTIONS
The following clinically significant adverse reactions are described elsewhere in the labeling:
- Thrombocytopenia [see Warnings and Precautions (5.1)]
- Neutropenia [see Warnings and Precautions (5.2)]
- Infusion-Related Reactions [see Warnings and Precautions (5.3)]
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.
Low- to Intermediate-Risk Myelodysplastic Syndromes
The safety of RYTELO was evaluated in a randomized, double-blind, placebo-controlled, multicenter trial (IMerge) in 177 adult patients with International Prognostic Scoring System (IPSS) low- to intermediate-1 risk MDS who were transfusion-dependent and relapsed or refractory to or ineligible for ESA treatment [see Clinical Studies (14)]. The safety population included patients who received at least one dose of either RYTELO (n=118) or placebo (n=59) at 7.1 mg/kg as an intravenous infusion administered over two hours every 4 weeks. The median time on treatment with RYTELO was 8 months (range, 0 to 38 months); 69% of patients were exposed to RYTELO for 24 weeks or longer and 45% were exposed for 48 weeks or longer.
The median age of patients who received at least one dose of RYTELO was 72 years (range: 44 to 87 years) with 77% of patients 65 years of age and older and 30% of patients 75 years of age and older. Participants were 60% male, 81% White, 7% Asian, and 0.8% Black.
Serious adverse reactions occurred in 32% of patients who received RYTELO. Serious adverse reactions in > 2% of patients included sepsis (4.2%), fracture (3.4%), cardiac failure (2.5%), and hemorrhage (2.5%). Fatal adverse reactions occurred in 0.8% of patients who received RYTELO, including sepsis (0.8%).
Permanent discontinuation of RYTELO due to an adverse reaction occurred in 15% of patients. Adverse reactions which resulted in permanent discontinuation of RYTELO in > 2% of patients included neutropenia and thrombocytopenia.
Dosage interruptions of RYTELO due to an adverse reaction occurred in 80% of patients. Adverse reactions which required dosage interruption in > 5% of patients included neutropenia, thrombocytopenia and infections.
Dose reductions of RYTELO due to an adverse reaction occurred in 49% of patients. Adverse reactions which required dose reductions in > 2% of patients included neutropenia and thrombocytopenia.
The most common (≥10% with a difference between arms of >5% compared to placebo) adverse reactions, including laboratory abnormalities, were decreased platelets, decreased white blood cells, decreased neutrophils, increased AST, increased alkaline phosphatase, increased ALT, fatigue, prolonged partial thromboplastin time, arthralgia/myalgia, COVID-19 infections, and headache.
Table 5 summarizes the adverse reactions in IMerge.
Table 5: Adverse Reactions (≥5%) in Patients with MDS Who Received RYTELO with a Difference Between Arms of >2% Compared to Placebo in IMerge Adverse Reaction RYTELO
(N=118)Placebo
(N=59)All Grades
%Grades 3 or 4
%All Grades
%Grades 3 or 4
%Graded according to National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03. - *
- Fatigue: asthenia, fatigue, and malaise.
- †
- Arthralgia/myalgia: arthralgia, back pain, bone pain, musculoskeletal pain, myalgia, neck pain, non-cardiac chest pain, pain, pain in extremity, pain in jaw, and pelvic pain.
- ‡
- COVID-19: asymptomatic COVID-19, COVID-19, COVID-19 pneumonia, and SARS-CoV-2 antibody test positive.
- §
- Urinary tract infection: cystitis, Escherichia urinary tract infection, renal abscess, and urinary tract infection.
- ¶
- Syncope: fall, pre-syncope, and syncope.
- #
- Infusion-related reactions: abdominal pain, arthralgia, asthenia, back pain, bone pain, diarrhea, erythema, headache, hypertensive crisis, malaise, non-cardiac chest pain, pruritus, and urticaria. Only events considered related to infusion-related reactions are included.
- Þ
- Atrial arrhythmia: atrial fibrillation and atrial flutter.
- ß
- Fractures: femur fracture, hand fracture, hip fracture, humerus fracture, lumbar vertebral fracture, and thoracic vertebral fracture.
General disorders and administrative site conditions Fatigue* 29 0 20 3.4 Musculoskeletal and connective tissue disorders Arthralgia/myalgia† 25 2.5 19 5 Infections and infestations COVID-19‡ 19 1.7 14 5 Urinary tract infection§ 9 2.5 7 0 Nervous system disorders Headache 13 0.8 5 0 Syncope¶ 7 1.7 1.7 0 Immune system disorders Infusion-related reactions# 8 1.7 3.4 0 Respiratory, thoracic and mediastinal disorders Epistaxis 7 0 0 0 Vascular disorders Hematoma 6 0 0 0 Skin and subcutaneous tissue disorders Pruritus 6 0 1.7 0 Cardiac disorders Atrial arrhythmiaÞ 6 1.7 3.4 1.7 Injury, poisoning and procedural complications Fracturesß 5 3.4 1.7 1.7 Clinically relevant adverse reactions in < 5% of patients who received RYTELO included febrile neutropenia, sepsis, gastrointestinal hemorrhage, and hypertension.
Table 6 summarizes the laboratory abnormalities in IMerge.
Table 6: Select Laboratory Abnormalities (≥10%) That Worsened from Baseline in Patients with MDS Who Received RYTELO with a Difference Between Arms of >2% Compared to Placebo in IMerge Laboratory Abnormality RYTELO* Placebo† All Grades
(%)Grade 3 or 4
(%)All Grades
(%)Grade 3 or 4
(%)Graded according to National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03.
ALP = alkaline phosphatase; ALT = alanine aminotransferase; AST = aspartate aminotransferase; PTT = partial thromboplastin time- *
- The denominator used to calculate the rate varied from 97 to 118 based on the number of patients with a baseline value and at least one post-treatment value.
- †
- The denominator used to calculate the rate varied from 50 to 59 based on the number of patients with a baseline value and at least one post-treatment value.
Hematology Platelet count decreased 97 65 34 8 White blood cell count decreased 94 53 59 1.7 Neutrophil count decreased 92 72 47 7 PTT prolonged 26 1 18 4 Chemistry AST increased 53 0.8 22 1.7 ALP increased 48 0 12 0 ALT increased 43 3.4 37 5 -
8. USE IN SPECIFIC POPULATIONS
8.1. Pregnancy
Risk Summary
Based on findings in animal studies, RYTELO can cause embryo-fetal harm when administered to a pregnant woman. There are no available data on RYTELO use in pregnant women to evaluate for drug-associated risk. In embryo-fetal developmental toxicity studies, administration of imetelstat to pregnant mice and rabbits during the period of organogenesis resulted in embryo-fetal mortality, which in mice occurred at maternal exposures approximately 2.5 times the human exposure at the recommended clinical dose. Advise pregnant women of the potential risk to a fetus [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 embryo-fetal developmental toxicity studies, imetelstat was administered by IV bolus injection at doses of 4.7, 9.4, 14.1 or 28.2 mg/kg/day on gestation days 6, 9, and 12 in mice, or by 2-hour intravenous infusion at doses of 4.7, 14.1, or 28.2 mg/kg on gestation days 6 and 13 in rabbits. In rabbits, the dose of 28.2 mg/kg was maternally toxic. Increased post-implantation loss due to an increase in early resorptions, resulting in a decrease in viable fetuses and litter was noted in mice at 28.2 mg/kg and in rabbits starting at 14.1 mg/kg; corresponding to exposures (based on AUC) that are approximately 2.5-times (mice) or 9.3-times (rabbits) the human exposure at the recommended clinical dose.
8.2. Lactation
Risk Summary
There is no data on the presence of imetelstat in human milk, or the effects RYTELO on the breastfed child, or milk production. Because of the potential for adverse reactions in breastfed children, advise women not to breastfeed during treatment with RYTELO and for 1 week after the last dose.
8.3. Females and Males of Reproductive Potential
Based on findings from animal studies, RYTELO can cause embryo-fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1)].
Pregnancy Testing
Verify the pregnancy status of females of reproductive potential prior to initiating treatment with RYTELO.
Contraception
Females
Advise females of reproductive potential to use effective contraception during treatment with RYTELO and for 1 week after the last dose [see Use in Specific Populations (8.1)].
Infertility
Females
Based on findings in animals, RYTELO may impair fertility in females of reproductive potential. The effect on fertility is reversible [see Nonclinical Toxicology (13.1)].
8.4. Pediatric Use
Safety and effectiveness of RYTELO in pediatric patients have not been established.
8.5. Geriatric Use
Of the 118 patients with low- to intermediate-1 risk myelodysplastic syndromes (MDS) in the clinical trial who received RYTELO, 91 (77.1%) patients were 65 years of age and older and 35 (29.7%) patients 75 years of age and older. No differences in safety or efficacy were observed between older (≥ 65 years) and younger patients.
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11. DESCRIPTION
RYTELO for injection contains imetelstat, an oligonucleotide telomerase inhibitor for intravenous use. Imetelstat sodium is a white to off-white or slightly yellow, amorphous, solid powder. It is highly soluble in aqueous solutions, including in 0.9% Sodium Chloride Injection, at both refrigerated and room temperatures. Imetelstat sodium is hygroscopic.
The chemical name for the imetelstat sodium drug substance is DNA, d(3'-amino-3'-deoxy-P-thio) (T-A-G-G-G-T-T-A-G-A-C-A-A), 5'-[O-[2-hydroxy-3-(hexadecanoylamino)propyl] phosphorothioate], sodium salt (1:13). The molecular formula is C148H198N68O53P13S13Na13 (as sodium salt), which equates to a formula weight of 4896 g/mol. The molecular formula for the free acid form is C148H211N68O53P13S13 which equates to a formula weight of 4610 g/mol. The structural formula for imetelstat sodium is:
RYTELO (imetelstat) for injection is a sterile, preservative-free, white to off-white or slightly yellow lyophilized powder for intravenous infusion after reconstitution and dilution. Each single-dose vial provides either 47 mg of imetelstat (equivalent to 50 mg imetelstat sodium) or 188 mg of imetelstat (equivalent to 200 mg imetelstat sodium). The following inactive ingredients may be added during manufacturing: sodium carbonate anhydrous (for the 47 mg preparation) / sodium carbonate monohydrate (for the 188 mg preparation) or hydrochloric acid (to adjust to pH of 7.0 to 8.5).
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12. CLINICAL PHARMACOLOGY
12.1. Mechanism of Action
Imetelstat is an oligonucleotide human telomerase inhibitor that binds to the template region of the RNA component of human telomerase (hTR), inhibits telomerase enzymatic activity and prevents telomere binding.
Increased telomerase activity and human telomerase reverse transcriptase (hTERT) RNA expression have been reported in MDS and malignant stem and progenitor cells. Nonclinical studies showed imetelstat treatment led to reduction of telomere length, reduction of malignant stem and progenitor cell proliferation, and induction of apoptotic cell death.
12.3. Pharmacokinetics
Imetelstat plasma geometric mean (coefficient of variation [CV] %) maximum concentration (Cmax) is 18.3 µM (27.3%) and the area under the concentration-time curve from time 0 to 28 days (AUC0-28) was 114.2 h*µM (43.2%). Imetelstat does not accumulate between treatment cycles.
Distribution
Following a single intravenous dose of 7.1 mg/kg of RYTELO administered over 2 hours in patients with MDS, the geometric mean (CV%) volume of distribution is approximately 14.1 L (27.2%). In vitro human plasma protein binding is greater than 94%.
Elimination
The imetelstat geometric mean (CV%) apparent plasma half-life is approximately 4.9 hours (43.2%) at the approved recommended dosage.
Specific populations
No clinically significant differences in the pharmacokinetics of imetelstat were observed based on age (21 to 87 years), sex, race (81% White, 4% Asian, 7% Black, 8% other/unknown), mild to moderate renal impairment (CLcr 30 to < 90 mL/min), mild hepatic impairment (total bilirubin ≤ ULN and AST > ULN, or total bilirubin > 1× to 1.5× ULN and any AST), or moderate hepatic impairment (total bilirubin > 1.5× to 3× ULN and any AST). The effect of severe renal impairment (CLcr 15 to < 30 mL/min), end-stage renal disease, or severe hepatic impairment (total bilirubin > 3× ULN and any AST) has not been established.
12.6. Immunogenicity
The observed incidence of anti-drug antibodies (ADA) is highly dependent on the sensitivity and specificity of the assay. Differences in assay methods preclude meaningful comparisons of the incidence of anti-drug antibodies in the studies described below with the incidence of anti-drug antibodies in other studies, including those of RYTELO.
Seventeen percent (28/166) of evaluable patients with low- or intermediate-1 risk MDS tested positive for imetelstat anti-drug antibodies, with a median onset of 38 weeks following the study drug dosage of RYTELO for a median duration of treatment of 35 weeks in Phase 2 and Phase 3 of the IMerge study. There was no clinically significant effect of ADA on the PK, safety, or efficacy of RYTELO among the study participants who developed anti-drug antibodies.
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13. NONCLINICAL TOXICOLOGY
13.1. Carcinogenesis, Mutagenesis, Impairment of Fertility
Carcinogenicity studies have not been conducted with imetelstat.
In vitro, imetelstat was not mutagenic in the bacterial mutagenicity assay (Ames test) or clastogenic in the chromosomal aberrations assay using cultured human peripheral blood lymphocytes. Imetelstat was not genotoxic in an in vivo mouse micronucleus assay at intravenous dose levels up to approximately 104 mg/kg.
Fertility studies have not been conducted with imetelstat. Female monkeys given 14.1 mg/kg once weekly for 9 months exhibited uterine endometrial atrophy in a general toxicology study. This effect was observed at a mean exposure (based on AUC) that is approximately 14.4-times the human exposure at the recommended clinical dose. This finding was not present in animals following a 14-week recovery period.
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14. CLINICAL STUDIES
14.1. Myelodysplastic Syndromes (MDS)
The efficacy of RYTELO was evaluated in a randomized, double-blind, placebo-controlled, multicenter trial (IMerge; NCT02598661) in 178 patients enrolled with International Prognostic Scoring System (IPSS) low- or intermediate-1 risk MDS who were transfusion-dependent (requiring ≥ 4 red blood cell (RBC) units over an 8-week period during the 16 weeks prior to randomization). Eligible patients were required to have failed to respond or have lost response or be ineligible for erythropoiesis-stimulating agents (ESAs); and had an absolute neutrophil count of 1.5 × 109/L or greater and platelets 75 × 109/L or greater. Patients were ineligible if they had del(5q) cytogenetic abnormality or had received prior treatment with lenalidomide or hypomethylating agents.
Participants were randomized in a 2:1 ratio to receive an intravenous infusion of RYTELO (n=118) 7.1 mg/kg or placebo (n=60) in 28-day treatment cycles until disease progression, unacceptable toxicity, or withdrawal from the study. Randomization was stratified by prior RBC transfusion burden and by IPSS risk group. All patients received supportive care, which included RBC transfusions.
Of the 178 patients enrolled, the median age was 72 years (range: 39 to 87 years), with 62% male, and 80% White, 6% Asian, 1.7% Black, 12% other or not reported. The key baseline disease characteristics of the efficacy population are shown in Table 7.
Table 7: Baseline Disease Characteristics of Patients with MDS in IMerge Disease Characteristic RYTELO
(N=118)Placebo
(N=60)Abbreviations: ECOG = Eastern Cooperative Oncology Group; ESA = erythropoietin stimulating agents; IPSS = International Prognostic Scoring System; RBC = Red Blood Cell; MDS = myelodysplastic syndromes; sEPO = serum erythropoietin; WHO = World Health Organization - *
- Prior RBC transfusion burden is defined as the maximum number of RBC units transfused over an 8-week period during the 16 weeks prior to randomization.
- †
- RS+ includes refractory anemia with ring sideroblasts (RARS)/refractory cytopenia with multilineage dysplasia and ≥ 15% ringed sideroblasts (RCMD-RS).
- ‡
- RS˗ includes others.
Time since original diagnosis Median years (range) 3.5 (0.1, 26.7) 2.8 (0.2, 25.7) ECOG Score (0, 1, 2), n (%) 0: Asymptomatic 42 (35.6) 21 (35) 1: Symptomatic fully ambulatory 70 (59.3) 39 (65) 2: Symptomatic in bed less than 50% of the day 6 (5.1) 0 IPSS Risk Classification, n (%) Low 80 (67.8) 39 (65) Intermediate-1 38 (32.2) 21 (35) Prior RBC transfusion burden*, n (%) 4 to 6 units 62 (52.5) 33 (55) > 6 units 56 (47.5) 27 (45) WHO Classification (2008), n (%) RS+† 73 (61.9) 37 (61.7) RS˗‡ 44 (37.3) 23 (38.3) Missing 1 (0.8) 0 Baseline sEPO, n (%) ≤ 500 mU/mL 87 (73.7) 36 (60) > 500 mU/mL 26 (22) 22 (36.7) Missing 5 (4.2) 2 (3.3) Prior ESA Use, n (%) Yes 108 (91.5) 52 (86.7) No 10 (8.5) 8 (13.3) Baseline blood counts, median Neutrophils (cells/L) 2.6 × 109 2.7 × 109 Hemoglobin (g/dL) 7.9 7.8 Platelets (cells/L) 230 × 109 230 × 109 Efficacy was established after a median follow up time of 19.5 months (range: 1.4 to 36.2) in the imetelstat group and 17.5 months (range: 0.7 to 34.3) in the placebo group based upon the proportion of patients who achieved ≥ 8-week and ≥ 24-week RBC-TI, defined as the absence of RBC transfusion(s) during any consecutive 8 weeks (56 days) period, and during any consecutive 24 weeks (168 days) period, respectively, from randomization until the start of subsequent anti-cancer therapy (if any). The efficacy results are summarized in Table 8.
Table 8: Efficacy Results of RYTELO in IMerge RYTELO
(N=118)Placebo
(N=60)% Difference
(95% CI)*p-value† Abbreviations: CI = Confidence Interval; RBC = Red Blood Cell; TI = Transfusion Independence Rate of ≥ 8-week RBC TI ≥ 8-week RBC TI, n (%) 47 (39.8) 9 (15.0) 24.8
(9.9, 36.9)< 0.001 95% CI for response rate (%)‡ (30.9, 49.3) (7.1, 26.6) Rate of ≥ 24-week RBC TI ≥ 24-week RBC TI, n (%) 33 (28.0) 2 (3.3) 24.6 95% CI for response rate (%)‡ (20.1, 37.0) (0.4, 11.5) (12.6, 34.2) < 0.001 - 16. HOW SUPPLIED/STORAGE AND HANDLING
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17. PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling (Medication Guide).
Discuss the following with patients prior to and during treatment with RYTELO.
Thrombocytopenia
Advise patients of the risk of thrombocytopenia with RYTELO, and that their blood counts will be monitored routinely while on treatment and dose of RYTELO delayed or reduced as needed. Instruct patients to notify a healthcare provider immediately if they show signs or symptoms of thrombocytopenia such as unusual bleeding or bruising [see Warnings and Precautions (5.1)].
Neutropenia
Advise patients of the risk of neutropenia with RYTELO and that their blood counts will be monitored routinely while on treatment and the dose of RYTELO may be delayed or reduced as needed. Instruct patients to notify a healthcare provider immediately if they show signs or symptoms of neutropenia, such as fever or infection [see Warnings and Precautions (5.2)].
Infusion-Related Reactions
Inform patients that infusion-related reactions can occur during treatment with RYTELO and premedications will be given prior to each infusion. Patients will be monitored by their healthcare provider for at least an hour after the infusion [see Dosage and Administration (2.2) and Warnings and Precautions (5.3)].
Advise patients that their healthcare provider may decide to give RYTELO more slowly or stop the infusion if an infusion-related reaction occurs [see Adverse Reactions (6.1)]
Embryo-Fetal Toxicity
Advise pregnant women and females of reproductive potential of the potential risk to a fetus. Advise females of reproductive potential to inform their healthcare provider if they are pregnant or become pregnant [see Warnings and Precautions (5.4) and Use in Specific Populations (8.1)]. Advise females of reproductive potential to use effective contraception during treatment with RYTELO and for 1 week after the last dose [see Use in Specific Populations (8.3)].
Lactation
Advise women not to breastfeed during treatment with RYTELO and for 1 week after the last dose [see Use in Specific Populations (8.2)].
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SPL UNCLASSIFIED SECTION
Manufactured for:
Geron Corporation
919 E. Hillsdale Blvd., Suite 250
Foster City, CA 94404Manufactured by (188 mg vials):
Catalent Indiana, LLC
1300 S Patterson Drive
Bloomington, IN 47403Manufactured by (47 mg vials):
Patheon Italia, S.p.A
2° Trav. SX Via Morolense, 5
03013 Ferentino (FR), ItalyGER005-01
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MEDICATION GUIDE
This Medication Guide has been approved by the U.S. Food and Drug Administration. Issued: 6/2024 MEDICATION GUIDE
RYTELO™ (ri-TEL-o)
(imetelstat)
for injection, for intravenous useWhat is the most important information I should know about RYTELO?
RYTELO may cause serious side effects, including:- Low platelet counts (thrombocytopenia). Low platelet counts are common during treatment with RYTELO and can also be severe. Low platelet counts can increase your risk for bleeding. Your healthcare provider may give you platelet transfusions to reduce the risk of bleeding if you develop a low platelet count during treatment with RYTELO. Tell your healthcare provider right away if you develop any signs or symptoms of bleeding, including:
- unusual bleeding or bruising
- bleeding that lasts a long time
- nosebleeds
- vomiting blood
- blood in your stool or black tarry stool
- Low neutrophil counts (neutropenia). Low counts of a type of white blood cell called neutrophils are common during treatment with RYTELO and can also be severe. Low neutrophil counts can increase your risk for infections, including serious infections and sepsis. Your healthcare provider may give you medicines before you start treatment to help prevent neutropenia and infections and may treat you with medicines if you develop these problems during treatment with RYTELO. Tell your healthcare provider right away if you develop any signs or symptoms of infection during treatment with RYTELO, including:
- fever
- shortness of breath or trouble breathing
- cough
- chills
- pain or burning when you urinate
Your healthcare provider will do blood tests to check your platelet and neutrophil counts before starting treatment with RYTELO, weekly for the first 2 cycles of treatment, before you receive each additional cycle, and as needed during your treatment.
Your healthcare provider may delay your next treatment, decrease your dose, or stop treatment with RYTELO if you develop thrombocytopenia or neutropenia during treatment.
See "What are the possible side effects of RYTELO?" for more information about side effects.What is RYTELO?
RYTELO is a prescription medicine used to treat a condition called low- to intermediate-1 risk myelodysplastic syndromes (MDS) in adults:- with anemia (low red blood cell counts) who need blood transfusions of 4 or more red blood cell units over 8 weeks and
- who have not responded to, have stopped responding to, or cannot be treated with other medicines called erythropoiesis-stimulating agents (ESAs).
Before receiving RYTELO, tell your healthcare provider about all of your medical conditions, including if you: - are pregnant or plan to become pregnant. RYTELO may harm your unborn baby and may cause loss of pregnancy (miscarriage). Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with RYTELO.
Females who are able to become pregnant:- Your healthcare provider will perform a pregnancy test before you are given RYTELO.
- You should use effective birth control (contraception) during treatment with RYTELO and for 1 week after your last dose.
- are breastfeeding or plan to breastfeed. It is not known if RYTELO passes into your breastmilk. Do not breastfeed during treatment with RYTELO and for 1 week after your last dose.
How will I receive RYTELO? - RYTELO will be given as an intravenous infusion into your vein over a period of 2 hours by your healthcare provider.
- RYTELO is usually given every 4 weeks.
- Your healthcare provider will prescribe RYTELO in a dose that is right for you and may change your dose, change your dosing schedule, or stop treatment depending on how you respond to RYTELO.
- Your healthcare provider will do certain blood tests during treatment with RYTELO to check for side effects and to see how well you respond to treatment.
- Your healthcare provider will decide how long you will continue treatment with RYTELO.
What are the possible side effects of RYTELO?
RYTELO may cause serious side effects, including:- See "What is the most important information I should know about RYTELO?"
- Infusion-related reactions. RYTELO can cause infusion-related reactions during or after your infusion that can be severe, including a severe sudden increase in blood pressure called hypertensive crisis. Your healthcare provider will give you medicines before each RYTELO infusion to help prevent or lessen infusion-related reactions and will watch you for at least 1 hour after your infusion. If you develop infusion-related reactions, your healthcare provider may infuse RYTELO more slowly, temporarily stop, or permanently stop your treatment. Tell your healthcare provider if you develop any signs or symptoms of infusion-related reactions, including:
- stomach pain
- joint pain
- weakness and tiredness
- back and bone pain
- diarrhea
- redness
- headache
- high blood pressure
- not feeling well
- chest pain that is not related to your heart
- itching
- hives
The most common side effects of RYTELO include: - decreased platelet counts
- decreased white blood cell counts
- decreased neutrophil counts
- increased liver enzymes (AST, alkaline phosphatase, and ALT)
- tiredness
- longer than usual blood clotting times
- joint, bone and muscle pain
- Covid-19 infections
- headache
RYTELO may cause fertility problems in females. This could affect your ability to get pregnant. Talk to your healthcare provider if this is a concern for you.
These are not all of the possible side effects of RYTELO. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.General information about the safe and effective use of RYTELO.
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. You can ask your pharmacist or healthcare provider for information about RYTELO that is written for health professionals.What are the ingredients in RYTELO?
Active ingredient: imetelstat
Inactive ingredients:- 47 mg: sodium carbonate anhydrous or hydrochloric acid may be added during manufacturing to adjust the pH
- 188 mg: sodium carbonate monohydrate or hydrochloric acid may be added during manufacturing to adjust the pH
Manufactured for: Geron Corporation, 919 E. Hillsdale Blvd., Suite 250, Foster City, CA 94404
Manufactured by (47 mg vials):
Patheon Italia, S.p.A, 2° Trav. SX Via Morolense, 5, 03013 Ferentino (FR), Italy
Manufactured by (188 mg vials):
Catalent Indiana, LLC, 1300 S Patterson Drive, Bloomington, IN 47403
GER006-01
For more information about RYTELO, go to www.RYTELO.com or call 1-866-471-0921. - PRINCIPAL DISPLAY PANEL - 47 mg Vial Label
- PRINCIPAL DISPLAY PANEL - 47 mg Vial Carton
- PRINCIPAL DISPLAY PANEL - 188 mg Vial Label
- PRINCIPAL DISPLAY PANEL - 188 mg Vial Carton
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INGREDIENTS AND APPEARANCE
RYTELO
imetelstat sodium injection, powder, lyophilized, for solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:82959-112 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength imetelstat sodium (UNII: 2AW48LAZ4I) (imetelstat - UNII:F60NE4XB53) imetelstat 47 mg Inactive Ingredients Ingredient Name Strength sodium carbonate (UNII: 45P3261C7T) hydrochloric acid (UNII: QTT17582CB) Product Characteristics Color WHITE (white to off-white or slightly yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82959-112-01 1 in 1 CARTON 06/06/2024 1 1 in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA217779 06/06/2024 RYTELO
imetelstat sodium injection, powder, lyophilized, for solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:82959-111 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength imetelstat sodium (UNII: 2AW48LAZ4I) (imetelstat - UNII:F60NE4XB53) imetelstat 188 mg Inactive Ingredients Ingredient Name Strength sodium carbonate monohydrate (UNII: 2A1Q1Q3557) hydrochloric acid (UNII: QTT17582CB) Product Characteristics Color WHITE (white to off-white or slightly yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82959-111-01 1 in 1 CARTON 06/06/2024 1 1 in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA217779 06/06/2024 Labeler - Geron Corporation (858854490)
