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Trial · Interventional

CompletedPhase 1Registry data

Study to Evaluate the Pharmacokinetics and Metabolism of [14C] CR845 (Difelikefalin) in Patients With End Stage Renal Disease on Hemodialysis and in Healthy Subjects

Overview

Status
Completed
Phase
Phase 1
Enrollment
12 participants (actual)
Sponsor
Cara Therapeutics, Inc. · Industry
Design
Allocation not applicable · Open label (no masking)
Countries
1 country

United States

Start
17 Jan 2019
Primary completion
6 Apr 2019
Completion
6 Apr 2019
First posted
13 May 2019
Last update posted
24 Jul 2019
Conditions
Hemodialysis · Healthy

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
20192020
  1. Ph 1

    Study to Evaluate the Pharmacokinetics and Metabolism of [14C] CR845 (Difelikefalin) in Patients With End Stage Renal Disease on Hemodialysis and in Healthy Subjects

    NCT03947970

    17 Jan 2019 to 6 Apr 2019

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The objectives of this study are to evaluate the in vivo metabolite profiling and characterization of CR845 administered intravenously (IV) in patients on hemodialysis (HD) and in healthy subjects; and to determine the pharmacokinetics of radiolabeled \[14C\] CR845 administered as a single IV bolus in patients on HD and in healthy subjects.

Interventions

  • [14C] CR845Drug

Arms1

  • Experimental

    [14C] CR845

    Subjects will receive a single dose of \[14C\] CR845 IV solution administered as an IV bolus on Day 1.

Primary outcomes5

Outcomes the sponsor listed as primary.

  1. Measure of the [14C] CR845 and total radioactivity (total [14C] CR845-equivalents) in plasma, urine, feces, and dialysate will be determined.

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

  2. Extent of recovery of [14C] CR845 and radioactivity related to [14C] CR845 in plasma, urine, feces, and dialysate, as applicable, will be derived.

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

  3. Cumulative amount of [14C] CR845 and [14C] CR845-equivalents in urine and feces over the collection period will be calculated.

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

  4. Presence of possible CR845 metabolites will be assessed.

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

  5. Quantitation of possible CR845 metabolites will be assessed.

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

Secondary outcomes(1)
  1. Frequency and severity of adverse events by treatment group

    Time frame · Day 1 to up to 7 days post dose in healthy volunteers and Day 1 to up to 14 days post dose in patients on HD

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Clinical trial · 2023

10 results

Pharmacokinetics, Metabolism, and Excretion of Intravenous [14C]Difelikefalin in Healthy Subjects and Subjects on Hemodialysis.

Stark et al. 2023Clinical pharmacokineticscited by 9

PMID 37369955PMC10450003DOI 10.1007/s40262-023-01262-2PUB-37369955

Free to read · publisher termsCC BY-NC10 results

Eligibility

Who could join, as posted.

Sex
Male
Age
from 18 Years
Healthy volunteers
Accepted
Inclusion and exclusion criteria, as posted
Key Inclusion Criteria for Healthy Subjects * Body mass index (BMI) within the range of 18 to 30 kg/m2, inclusive, and body weight not less than 75 kg; * Vital signs at Screening must be within the following ranges and stable (measured in sitting position after at least 5 minutes' rest); * Systolic blood pressure (SBP) ≥100 and ≤140 mmHg; * Diastolic blood pressure (DBP) ≥50 and ≤90 mmHg; * Heart rate (HR) ≥50 and ≤100 beats per minute (bpm). * Must be in good health as determined by past medical history, physical examination, ECG, vital sign assessments, and clinical laboratory tests at Screening. Any subjects with abnormalities noted at Screening or at any time before dosing on Day 1 must be approved by the Investigator and Medical Monitor. Key Inclusion Criteria for patients on HD * If taking concurrent medications, must be on a stable dose for at least 14 days prior to dosing and the dosing regimen should remain stable for the duration of the study; * Prescription dry body weight of ≥75 kg and ≤135 kg at Screening; * Must be receiving HD 3 times weekly and have been on dialysis for at least 3 months prior to Screening; * For a minimum of 1 month before Day 1, must have stable controlled blood pressure that in the Investigator's opinion will not interfere with study conduct; * Demonstrated adequate dialysis measurements (at least two Kt/V measurements ≥1.2 or two urea reduction ratio \[URR\] measurements ≥65%) during the 3 months prior to Screening Key Exclusion Criteria: * Has a concomitant disease or any medical condition that, in the opinion of the Investigator, could pose undue risk to the patient, impede completion of the study procedures, or would compromise the validity of the study measurements, including, but not limited to: * Known or suspected history of alcohol, narcotic, or other drug abuse, or substance dependence within 12 months prior to Screening; * Significant systolic or diastolic heart failure (eg, New York Heart Association Class IV congestive heart failure \[Appendix 1\]); * Severe mental illness or cognitive impairment (eg, dementia); * Any other relevant acute or chronic medical or neuropsychiatric condition. * History of important drug or other allergy (except for untreated, asymptomatic seasonal allergies at time of dosing) unless deemed not clinically significant by the Investigator; * Use of any beverages and foods containing alcohol, quinine (tonic water), grapefruit, broccoli, Brussels sprouts, Seville oranges, pomegranate, star fruit, char-grilled meat, or caffeine/xanthine from 48 hours prior to dosing with study medication without evaluation and approval by the Investigator; * Use of any over-the-counter (OTC) medication (including nutritional or dietary supplements, herbal preparations, or vitamins, chapparal, comfrey, germander, gin bu huan, kava, pennyroyal, skullcap, St. John's Wort, or valerian) within 7 days prior to dosing with study medication; * Use of any new prescription medication from 14 days prior to dosing with study medication without evaluation and approval by the Investigator; * Has been treated with any known drugs that are moderate or strong inhibitors/inducers of cytochrome P450 (CYP) enzymes (e.g., barbiturates, phenothiazines, cimetidine, carbamazepine) within 30 days prior to dosing with study medication, and that, in the Investigator's judgment, may impact subject safety or the validity of the study results; * Positive results for human immunodeficiency virus (HIV) or hepatitis B surface antigen (HBsAg); * Is a healthy subject with positive results for hepatitis C virus (HCV) antibody at Screening. Note: Subjects with HD who test positive for HCV antibody may be allowed to enroll at the discretion of the Principal Investigator if their liver function tests are not otherwise clinically significant; * Has donated blood or has had an acute loss of blood (˃500 mL) during the 3 months prior to study drug administration; * Previous administration of any \[14C\] labeled drug substance within 1 year of study drug administration; * Has irregular bowel habits. "Irregular" being defined for the purpose of this study as NOT having a bowel movement at least every 2 days.) * Has been involved in an occupation that requires monitoring for radiation exposure (eg, X-ray technician);

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