Label: KORSUVA- difelikefalin injection, solution

  • NDC Code(s): 59353-065-01, 59353-065-12
  • Packager: Vifor (International) Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated September 8, 2021

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

    KORSUVA™ (difelikefalin) injection, for intravenous use
    Initial U.S. Approval: 2021

    INDICATIONS AND USAGE

    KORSUVA is a kappa opioid receptor agonist indicated for the treatment of moderate-to-severe pruritus associated with chronic kidney disease (CKD-aP) in adults undergoing hemodialysis (HD). (1)

    Limitation of Use

    Korsuva has not been studied in patients on peritoneal dialysis and is not recommended for use in this population. (1)

    DOSAGE AND ADMINISTRATION

    Recommended dosage is 0.5 mcg/kg. (2.1)
    Administer by intravenous bolus injection into the venous line of the dialysis circuit at the end of each HD treatment. (2.1)
    Do not mix or dilute KORSUVA prior to administration. (2.2)
    Administer within 60 minutes of syringe preparation. (2.3)
    See full prescribing information for additional recommendations on preparation and administration of KORSUVA. (2.2, 2.3)

    DOSAGE FORMS AND STRENGTHS

    Injection: 65 mcg /1.3 mL (50 mcg/mL) of difelikefalin (3)

    CONTRAINDICATIONS

    None (4)

    WARNINGS AND PRECAUTIONS

    Dizziness, Somnolence, Mental Status Changes, and Gait Disturbances: Dizziness, somnolence, mental status changes, and gait disturbances, including falls, have occurred. Centrally-acting depressant medications, sedating antihistamines, and opioid analgesics should be used with caution during treatment with KORSUVA. (5.1)
    Risk of Driving and Operating Machinery: May impair mental or physical abilities. Advise patients not to drive or operate dangerous machinery until the effect of KORSUVA on a patient’s ability to drive or operate machinery is known. (5.2)

    ADVERSE REACTIONS

    The most common adverse reactions (incidence ≥2% and ≥1% higher than placebo) were diarrhea, dizziness, nausea, gait disturbances, including falls, hyperkalemia, headache, somnolence, and mental status change. (6)

    To report SUSPECTED ADVERSE REACTIONS, contact Vifor (International) Inc. at 1-844-835-8277 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    USE IN SPECIFIC POPULATIONS

    Severe Hepatic Impairment: Not recommended in patients with severe hepatic impairment. (8.6)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 8/2021

  • Table of Contents
  • 1 INDICATIONS AND USAGE

    KORSUVA is indicated for the treatment of moderate-to-severe pruritus associated with chronic kidney disease (CKD-aP) in adults undergoing hemodialysis (HD).

    Limitations of Use

    KORSUVA has not been studied in patients on peritoneal dialysis and is not recommended for use in this population.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Dosage

    The recommended dosage of KORSUVA is 0.5 mcg/kg administered by intravenous bolus injection into the venous line of the dialysis circuit at the end of each HD treatment [see Dosage and Administration (2.3)].
    If a regularly scheduled HD treatment is missed, resume KORSUVA at the end of the next HD treatment.

    2.2 Preparation Instructions

    Do not mix or dilute KORSUVA prior to administration.
    Inspect KORSUVA for particulate matter and discoloration prior to administration. The solution should be clear and colorless. Do not use KORSUVA vials if particulate matter or discoloration is observed.
    KORSUVA is supplied in a single-dose vial. Discard any unused product.
    Injection volume to be administered is determined by patient’s target dry body weight in kilograms (one patient may use less than the full contents of the vial or use more than one vial). See Table 1.
    Table 1. KORSUVA Injection Volumes Based on Target Dry Body Weight
    *
    Total Injection Volume (mL) = Patient Target Dry Body Weight (kg) x 0.01, rounded to the nearest tenth (0.1 mL). For patient target dry body weight outside of the ranges in Table 1, use this formula.

    Target Dry Body Weight Range (kg)

    Injection Volume (mL)*

    36 – 44

    0.4

    45 ‒ 54

    0.5

    55 – 64

    0.6

    65 – 74

    0.7

    75 – 84

    0.8

    85 – 94

    0.9

    95 – 104

    1

    105 – 114

    1.1

    115 – 124

    1.2

    125 – 134

    1.3

    135 – 144

    1.4

    145 – 154

    1.5

    155 – 164

    1.6

    165 – 174

    1.7

    175 – 184

    1.8

    185 – 194

    1.9

    195 – 204

    2

    2.3 Administration Instructions

    KORSUVA is removed by the dialyzer membrane and must be administered after blood is no longer circulating through the dialyzer.
    Administer KORSUVA by intravenous bolus injection into the venous line of the dialysis circuit at the end of each HD session.
    o
    The dose may be given either during or after rinse back of the dialysis circuit.
    o
    If the dose is given after rinse back, administer KORSUVA into the venous line followed by at least 10 mL of normal saline flush.
    o
    If the dose is given during rinse back, no additional normal saline is needed to flush the line.
    The dose must be administered within 60 minutes of the completion of the syringe preparation. Discard any unused product.
  • 3 DOSAGE FORMS AND STRENGTHS

    Injection: 65 mcg/1.3 mL (50 mcg/mL) of difelikefalin as a clear, colorless solution in a single-dose glass vial.

  • 4 CONTRAINDICATIONS

    None

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Dizziness, Somnolence, Mental Status Changes, and Gait Disturbances

    Dizziness, somnolence, mental status changes, and gait disturbances, including falls, have occurred in patients taking KORSUVA and may subside over time with continued treatment [see Adverse Reactions (6.1)]. In Trial 1 and Trial 2, 17.0% of patients randomized to receive KORSUVA reported at least one of these adverse reactions, compared to 12.0% of patients who received placebo. The incidence of somnolence was higher in KORSUVA-treated subjects 65 years of age and older (7.0%) than in KORSUVA-treated subjects less than 65 years of age (2.8%). Concomitant use of centrally-acting depressant medications, sedating antihistamines and opioid analgesics may increase the likelihood of these adverse reactions and should be used with caution during treatment with KORSUVA.

    5.2 Risk of Driving and Operating Machinery

    Dizziness, somnolence, and mental status changes have occurred in patients taking KORSUVA. KORSUVA may impair the mental or physical abilities needed to perform potentially hazardous activities such as driving a car and operating machinery. Advise patients not to drive or operate dangerous machinery until the effect of KORSUVA on a patient’s ability to drive or operate machinery is known.

  • 6 ADVERSE REACTIONS

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

    Dizziness, Somnolence, Mental Status Changes, and Gait Disturbances [see Warnings and Precautions (5.1)]

    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.

    A total of 1306 subjects undergoing HD who had moderate-to-severe pruritus were treated with KORSUVA in placebo-controlled and uncontrolled Phase 3 clinical trials. Of these, 711 were treated for at least 6 months and 400 were treated for at least one year.

    Two placebo-controlled Phase 3 trials (Trial 1 and Trial 2), in subjects undergoing HD who had moderate-to-severe pruritus were pooled to evaluate the safety of KORSUVA in comparison to placebo up to 12 weeks. In total, 848 subjects were evaluated (424 in KORSUVA group and 424 in placebo group). The mean age of the subjects was 59 years (range 22 to 88 years), and 59% of the subjects were male. Of the total subjects, 61% were White, 29% were Black or African American, and 5% were Asian.

    Table 2 summarizes the adverse reactions that occurred at a rate of ≥2% in the KORSUVA group and ≥1% higher than that of the placebo group during the 12-week placebo-controlled period of Trials 1 and 2. The percentage of subjects who discontinued treatment due to any adverse reaction was 2.6% for subjects taking KORSUVA and 0.7% for subjects taking placebo. The most common adverse reactions (≥0.5% of subjects) leading to discontinuation were dizziness (0.9% for KORSUVA and 0.2% for placebo), mental status change (0.7% and 0.2%, respectively), nausea (0.5% and 0%, respectively), and headache (0.5% and 0%, respectively). The percentage of subjects who developed serious adverse reactions was 4.5% in the KORSUVA group and 2.8% in the placebo group.

    Table 2: Adverse Reactions in ≥ 2% of KORSUVA-Treated Subjects with Moderate-to-Severe CKD-aP Undergoing HD and ≥ 1% Higher Than Placebo in Trials 1 and 2
    a Gait disturbances includes: preferred terms of falls and gait disturbances
    b Mental Status Change includes: preferred terms of confusional state and mental status change.

    Adverse Reactions

    Placebo

    (N=424)

    n (%)

    KORSUVA

    (N=424)

    n (%)

    Diarrhea

    24 (5.7)

    38 (9.0)

    Dizziness

    16 (3.8)

    29 (6.8)

    Nausea

    19 (4.5)

    28 (6.6)

    Gait Disturbancesa

    23 (5.4)

    28 (6.6)

    Hyperkalemia

    15 (3.5)

    20 (4.7)

    Headache

    11 (2.6)

    19 (4.5)

    Somnolence

    10 (2.4)

    18 (4.2)

    Mental Status Changeb

    6 (1.4)

    14 (3.3)

    Description of Selected Adverse Reactions

    Gait Disturbances, including Falls

    Gait disturbances, including falls, were reported in 6.6% of subjects receiving KORSUVA compared to 5.4% of subjects who received placebo. Falls were reported as serious adverse reactions in < 1% of subjects receiving KORSUVA and placebo, with one subject discontinuing KORSUVA due to gait disturbance.

    Dizziness

    Dizziness was reported in 6.8% of subjects randomized to KORSUVA compared to 3.8% of subjects who received placebo. Dizziness occurred within the first 3 weeks of treatment and was generally transient. Dizziness was serious in 0.2% of KORSUVA-treated subjects compared to 0% of subjects who received placebo and led to discontinuation in 0.9% of KORSUVA-treated subjects compared to 0.2% of subjects who received placebo.

    Somnolence

    Somnolence was reported in 4.2% of subjects randomized to receive KORSUVA compared to 2.4% of subjects who received placebo. Somnolence occurred within the first 3 weeks of treatment and tended to subside with continued dosing. Somnolence was serious in 0.2% of KORSUVA-treated subjects compared to 0% of subjects who received placebo. There were no subjects who discontinued KORSUVA due to an adverse reaction of somnolence.

    Mental Status Change

    Mental status change (including confusional state) was reported in 3.3% of subjects randomized to receive KORSUVA compared to 1.4% of subjects who received placebo. Most events tended to subside with continued dosing. Mental status change adverse reactions were serious in 1.4% of KORSUVA-treated subjects compared to 0.5% of subjects who received placebo and led to discontinuation in 0.7% of KORSUVA-treated subjects compared to 0.2% of subjects who received placebo.

    Hyperkalemia

    Hyperkalemia was found in 4.7% of subjects who received KORSUVA compared to 3.5% of subjects who received placebo. The incidence of hyperkalemia was higher in subjects who took concomitant opioids regardless of treatment and was almost doubled in the KORSUVA group (11.7%) compared to the placebo group (6.2%). The clinical relevance of this is unknown.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    The limited human data on use of KORSUVA in pregnant women are not sufficient to evaluate a drug-associated risk for major birth defects or miscarriage. In animal reproduction studies, intravenous injection of difelikefalin to pregnant rats and rabbits during the period of organogenesis at doses 711 and 10 times the maximum recommended human dose (MRHD), respectively, resulted in no adverse effects in either rats or rabbits (see Data).

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

    Data

    Animal Data

    In an embryofetal development study, difelikefalin was administered by intravenous injection to pregnant rats at doses of 0.25, 2.5, and 25 mg/kg/day during the period of organogenesis. Difelikefalin was not associated with embryofetal lethality or fetal malformations. Difelikefalin increased the incidences of skeletal variations (wavy ribs and incompletely ossified ribs) at the dose of 25 mg/kg/day (711 times the MRHD based on AUC comparison).

    In an embryofetal development study, difelikefalin was administered by intravenous injection to pregnant rabbits at doses of 0.025, 0.05, and 0.1 mg/kg/day during the period of organogenesis. Maternal toxicity evidenced by decreased maternal body weight gain was noted in all dose groups. Difelikefalin was not associated with embryofetal lethality or fetal malformations at doses up to 0.1 mg/kg/day (10 times the MRHD based on AUC comparison).

    In a prenatal and postnatal development study, difelikefalin was administered by intravenous injection to pregnant rats at doses of 0.6, 2.5, and 10 mg/kg/day beginning on gestation day 7 and continuing through lactation day 20. Persisting effects on decreased maternal body weight and/or maternal body weight gain as well as food consumption were noted at doses greater than or equal to 2.5 mg/kg/day (68 times the MRHD based on AUC comparison). No maternal effects were observed at 0.6 mg/kg/day (14 times the MRHD based on AUC comparison). No difelikefalin-related effects on postnatal developmental, neurobehavioral, or reproductive performance of offspring were noted at doses up to 10 mg/kg/day (282 times the MRHD based on AUC comparison).

    8.2 Lactation

    Risk Summary

    There are no data regarding the presence of KORSUVA in human milk or effects on the breastfed infant or on milk production.

    Studies in rats showed difelikefalin was transferred into the milk in lactating rats. When a drug is present in animal milk, it is likely that the drug will be present in human milk. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for KORSUVA and any potential adverse effects on the breastfed child from KORSUVA or from the underlying maternal condition.

    Data

    Animal Data

    Difelikefalin was administered to lactating rats by intravenous injection at doses of 0.6, 2.5, or 10 mg/kg/day from gestation day 7 through lactation day 14. Difelikefalin was detected in the milk of the lactating rats with the concentration ratio for milk:plasma of 0.04 to 0.05 across the doses. There was no measurable difelikefalin in the plasma of nursing pups.

    8.4 Pediatric Use

    The safety and effectiveness of KORSUVA in pediatric patients have not been established.

    8.5 Geriatric Use

    Of the 848 subjects in the placebo-controlled studies who received KORSUVA, 278 subjects (32.8%) were 65 years of age and older and 98 subjects (11.6%) were 75 years of age and older. No overall differences in safety or effectiveness of KORSUVA have been observed between patients 65 years of age and older and younger adult subjects, with the exception of the incidence of somnolence which was higher in KORSUVA-treated subjects 65 years of age and older (7.0%) than in KORSUVA-treated subjects less than 65 years of age (2.8%), and was comparable in both placebo age groups (3.0% and 2.1%, respectively). No differences in plasma concentrations of KORSUVA were observed between subjects 65 years of age and older and younger adult subjects [see Clinical Pharmacology (12.3)].

    8.6 Hepatic Impairment

    The influence of mild-to-moderate hepatic impairment on the pharmacokinetics of KORSUVA was evaluated in a population pharmacokinetic analysis which concluded that no KORSUVA dosage adjustments are needed in these populations [see Clinical Pharmacology (12.3)]. The influence of severe hepatic impairment on the pharmacokinetics of KORSUVA in subjects undergoing HD has not been evaluated; therefore, use of KORSUVA in this population is not recommended.

  • 10 OVERDOSAGE

    Single doses of KORSUVA up to 12 times and multiple doses of KORSUVA up to 5 times the recommended dosage of 0.5 mcg/kg were administered in clinical studies in subjects undergoing HD. A dose-dependent increase in adverse reactions, including dizziness, somnolence, mental status changes, paresthesia, fatigue, hypertension, and vomiting, were observed.

    In the event of overdosage, provide the appropriate medical attention based on patient’s clinical status. Difelikefalin is primarily eliminated by the kidneys with a low plasma protein binding of approximately 23% to 28% in dialysis patients. Hemodialysis for 4 hours using a high-flux dialyzer effectively cleared approximately 70% to 80% of difelikefalin from plasma, and difelikefalin was not detectable in plasma at the end of the second of two dialysis cycles. [see Clinical Pharmacology (12.3)].

  • 11 DESCRIPTION

    KORSUVA (difelikefalin) is a kappa opioid receptor agonist. Difelikefalin is a synthetic peptide with a single stereoisomer and is present as an acetate salt. Difelikefalin acetate is a white to off-white powder with a molecular formula of C36H53N7O6•xAcOH (1.0≤ x ≤2.0) and a molecular weight of 679.4 g/mol (mono-isotopic; free base). It is soluble in water. The chemical name of difelikefalin acetate is 4-amino-1-(D-phenylalanyl-D-phenylalanyl-D-leucyl-D-lysyl)piperidine-4-carboxylic acid, acetate salt.

    The chemical structure is:

    Difelikefalin acetate chemical structure

    KORSUVA (difelikefalin) injection is supplied in a single-dose vial containing 65 mcg/1.3 mL (50 mcg/mL) of difelikefalin as a sterile, preservative-free, clear and colorless solution for intravenous injection.

    KORSUVA is formulated as an isotonic 40 mM acetate buffer solution with an osmolality of 250 to 350 mOsm and a pH of 4.5.

    Each milliliter of KORSUVA injection contains 50 mcg of difelikefalin (equivalent to an average of 58.3 mcg of difelikefalin acetate), 1.3 mg of acetic acid, 2.5 mg of sodium acetate trihydrate, 7.2 mg of sodium chloride (to adjust tonicity), and water for injection.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    KORSUVA is a kappa opioid receptor (KOR) agonist. The relevance of KOR activation to therapeutic effectiveness is not known.

    12.2 Pharmacodynamics

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

    Cardiac Electrophysiology

    At a dose 6 times the recommended dosage, difelikefalin does not prolong the QTc interval to any clinically relevant extent.

    12.3 Pharmacokinetics

    The pharmacokinetics of difelikefalin is dose proportional over a single dosage range from 1 to 3 mcg/kg (2 to 6 times the recommended dosage) and multiple intravenous dosage range from 0.5 to 2.5 mcg/kg (1 to 5 times the recommended dosage) in chronic kidney disease patients undergoing HD. Steady-state was reached after the second administered dosage and the mean accumulation ratio was up to 1.6.

    Distribution

    The mean volume of distribution of difelikefalin is approximately 238 mL/kg. Difelikefalin binding to human plasma protein in dialysis patients is 23% to 28%.

    Elimination

    The half-life of difelikefalin in HD subjects prior to dialysis ranged between 23 and 31 hours. Following administration of radiolabeled difelikefalin, >99% of circulating radioactivity was present in plasma as parent. Hemodialysis reduced the difelikefalin plasma concentrations by 70% to 80% and difelikefalin was not detectable in plasma after 2 dialysis cycles.

    Metabolism

    Difelikefalin is not metabolized by cytochrome P450 (CYP) enzymes CYP1A2, CYP2C19, CYP2C8, CYP2C9, CYP2D6 or CYP3A observed in human hepatic microsomes or hepatocytes, in vitro.

    Excretion

    Following administration of difelikefalin to HD patients, 11% of the dosage was excreted in urine, 59% in feces, and 20% in dialysate fluid.

    Specific Populations

    No clinically significant differences in the pharmacokinetics of difelikefalin were observed based on age (25 to 80 years of age), sex, race/ethnicity, or mild-to-moderate hepatic impairment. The effect of severe hepatic impairment on the pharmacokinetics of difelikefalin is unknown [see Use in Specific Populations (8.6)].

    Drug Interaction Studies

    Clinical Studies

    No clinical studies evaluating the drug interaction potential of difelikefalin were conducted.

    In Vitro Studies

    Cytochrome P450 (CYP) Enzymes: Difelikefalin did not inhibit CYP enzymes (CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP3A, or CYP2D6), or induce CYP enzymes (CYP1A2, CYP2B6, or CYP3A) and is not a substrate of CYP450 enzymes (CYP1A2, CYP2C19, CYP2C8, CYP2C9, CYP2D6 or CYP3A).

    Uridine diphosphate (UDP)-glucuronosyl transferase (UGT) Enzymes: Difelikefalin is not an inhibitor of UGT1A3, UGT1A9, or UGT2B7.

    Transporter Systems: Difelikefalin did not inhibit BCRP, Pgp, OAT1, OAT3, OCT1, OCT2, OATP1B1, OATP1B3, MATE1, or, MATE2-K human transporters and is not a substrate of OAT1, OAT2, OAT3, OATP1A2, OCT2, OCT3, LAT1, PEPT1, PEPT2, ASBT, BSEP, MRP2, OATP1B1, OATP1B3, OATP2B1, OCT1, OCTN1, OCTN2, Pgp, BCRP, OSTα/β, MATE1, or, MATE2-K.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    In a 2-year carcinogenicity study in rats, difelikefalin was not carcinogenic when administered via subcutaneous injection at doses up to 1.0 mg/kg/day (597 times the MRHD based on AUC comparison). Difelikefalin was not carcinogenic in a 6-month carcinogenicity study in transgenic rasH2 mice at subcutaneous doses up to 30 mg/kg/day.

    Difelikefalin was negative for genotoxicity in a bacterial reverse mutation assay, an in vitro mammalian chromosomal aberration assay, and an in vivo mouse micronucleus assay.

    Difelikefalin administered via intravenous injection caused a significant decrease in the number of estrous cycles per 14 days (i.e., prolonged diestrus) in female rats at doses greater than or equal to 2.5 mg/kg/day (56 times the MRHD based on AUC comparison). Difelikefalin had no effects on mating index, fertility index, or any ovarian or uterine parameters in female rats at doses up to 25 mg/kg/day (635 times the MRHD based on AUC comparison). Difelikefalin did not impair male fertility at doses up to 25 mg/kg/day (971 times the MRHD based on AUC comparison).

  • 14 CLINICAL STUDIES

    The efficacy of KORSUVA was evaluated in two randomized, multicenter, double-blind, placebo-controlled trials (Trial 1 [NCT03422653] and Trial 2 [NCT03636269]) that enrolled a total of 851 subjects 18 years of age and older undergoing HD who had moderate-to-severe pruritus. In both trials, subjects received intravenous bolus injections of KORSUVA 0.5 mcg per kilogram of dry body weight into the venous line of the hemodialysis circuit at the end of each hemodialysis session or placebo three times per week for 12 weeks. In both trials, a 7-day run-in period prior to randomization was used to confirm that each subject had moderate-to-severe pruritus and to establish a baseline itch intensity, as measured by the patient-reported daily 24-hour Worst Itching Intensity Numerical Rating Scale (WI-NRS) scores (0 “no itch” to 10 “worst itch imaginable”).

    The mean (SD) baseline WI-NRS score was 7.1 (1.5) in Trial 1 and 7.2 (1.4) in Trial 2. At baseline in Trial 1, 61% of subjects were male, 49% were White, 42% were Black or African American, the mean age was 57 years (range 22 to 88 years), and 40% of subjects were using prior anti-pruritic medications (including sedating antihistamines) and continued the use throughout the trial. At baseline in Trial 2, 58% of subjects were male, 70% were White, 19% were Black or African American, the mean age was 60 years (range 23 to 90 years), and 36% of subjects were using prior anti-pruritic medications (including sedating antihistamines) and continued the use throughout the trial.

    In each trial, efficacy was assessed based on the proportion of subjects achieving a 4-point or greater improvement (reduction) from baseline in the weekly mean of the daily 24-hour WI-NRS score at Week 12.

    The results of the KORSUVA trials (Trials 1 and 2) are presented in Table 3 and Figure 1.

    Table 3. Efficacy Results of Subjects with Moderate-to-Severe CKD-aP Undergoing HD at Week 12 (Trials 1 & 2)

    Trial 1

    Trial 2

    KORSUVA

    0.5 mcg/kg

    3 times weekly

    N=189

    Placebo

    N=189

    KORSUVA

    0.5 mcg/kg

    3 times weekly

    N=237

    Placebo

    N=236

    Percentage of subjects with ≥4-point improvement from baseline in WI-NRS score

    40%

    21%

    37%

    26%

       Difference from Placebo (95% CI)

    19% (9%, 28%)

    12% (3%, 20%)

    Figure 1: Percentage of Subjects with Moderate-to-Severe CKD-aP Undergoing HD with a ≥4-point Improvement from Baseline on the WI-NRS in Trial 1 and Trial 2

    Figure 1: Percentage of Subjects with Moderate-to-Severe CKD-aP Undergoing HD with a ≥4-point Improvement from Baseline on the WI-NRS in Trial 1 and Trial 2

    Itch reduction was seen by Week 4 and sustained through Week 12.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    How Supplied

    KORSUVA (difelikefalin) injection is supplied as a sterile, clear and colorless solution in 1.3 mL single-dose, glass vials:

     
    NDC 59353-065-01: 65 mcg/1.3 mL (50 mcg/mL) single-dose vial

    NDC 59353-065-12: Carton containing 12 vials

    Storage and Handling

    Store vials at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP

    Controlled Room Temperature]. Do not freeze.

    KORSUVA injection must be administered within 60 minutes of syringe preparation; prepared syringes can be stored at ambient temperature 20°C to 25°C (68°F to 77°F) until dosing [see Dosage and Administration (2.2, 2.3)].

    KORSUVA injection is supplied in a single-dose vial. Any unused drug remaining after injection must be discarded.

  • 17 PATIENT COUNSELING INFORMATION

    Dizziness, Somnolence, Mental Status Changes, and Gait Disturbances

    Inform patients that dizziness, somnolence, mental status changes, and gait disturbances, including falls, can occur during treatment with KORSUVA [see Adverse Reactions (6.1)]. Somnolence is more likely to happen to patients who are age 65 years or older.

    Inform patients that concomitant treatment with centrally-acting depressants, sedating antihistamines and opioid analgesics may increase the likelihood of these adverse reactions and these medications should be used with caution during treatment with KORSUVA [see Warnings and Precautions (5.1)].

    Driving or Operating Machinery

    Inform patients that KORSUVA may impair the ability to perform potentially hazardous activities such as driving a car or operating heavy machinery. Advise patients not to drive or operate machinery until they know how they will react to KORSUVA [see Warnings and Precautions (5.2)].

    Manufactured for:
    Cara Therapeutics, Inc.
    Stamford, CT 06902

    Marketed by:
    Vifor (International) Inc.,
    Rechenstrasse 37, 9014 St. Gallen, Switzerland

    KORSUVA is a trademark of Cara Therapeutics, Inc.

    For patent information:
    www.caratherapeutics.com/innovation/patents

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – carton label

    KORSUVA - difelikefalin injection, solution

    KORSUVA
    (difelikefalin) Injection

    65 mcg/1.3 mL (50mcg/mL)

    NDC 59353-065-12

    Rx only

    For Intravenous Use after Hemodialysis
    Single-dose vial, Discard unused portion
    Store at 20°C to 25 °C (65°F to 77°F), excursions
    permitted to 15°C to 30°C [see USP controlled Room Temperature], Do not freeze
    Sterile, preservative-free solution.

    12 x 1,3 mL Single-dose Vials

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – container label

    KORSUVA - difelikefalin injection, solution

    KORSUVA
    (difelikefalin) Injection

    65 mcg/1.3 mL (50mcg/mL)

    NDC 59353-065-01

    Rx only

    For IV Use Only

    1.3 mL Single-dose vial. Discard unused portion

  • INGREDIENTS AND APPEARANCE
    KORSUVA 
    difelikefalin injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:59353-065
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIFELIKEFALIN ACETATE (UNII: 0P70AR5BYB) (DIFELIKEFALIN - UNII:NA1U919MRO) DIFELIKEFALIN50 ug  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    SODIUM ACETATE (UNII: 4550K0SC9B)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59353-065-1212 in 1 TRAY01/11/2021
    1NDC:59353-065-011.3 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21491601/11/2021
    Labeler - Vifor (International) Inc. (482603065)
    Establishment
    NameAddressID/FEIBusiness Operations
    Patheon Manufacturing Services LLC079415560ANALYSIS(59353-065) , MANUFACTURE(59353-065) , PACK(59353-065)
    Establishment
    NameAddressID/FEIBusiness Operations
    Patheon Italia S.p.A237710418ANALYSIS(59353-065) , MANUFACTURE(59353-065) , PACK(59353-065)