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Completed Phase 3 Interventional Results available

CR845-CLIN3103: A Global Study to Evaluate the Safety and Efficacy of CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus

ClinicalTrials.gov ID: NCT03636269

Public ClinicalTrials.gov record NCT03636269. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-blind, Randomized, Placebo-controlled Study to Evaluate the Safety and Efficacy of Intravenous CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus, With a 52-Week Open Label Extension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter, international study to evaluate the safety and efficacy of intravenous (IV) CR845 at a dose of 0.5 mcg/kg administered after each dialysis session. The study includes a 12-week randomized, double-blind, placebo-controlled Phase and a 52-week Open-label Extension Phase.

Study identification

NCT ID
NCT03636269
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Cara Therapeutics, Inc.
Industry
Enrollment
473 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2018 (Actual)
Primary completion
Mar 30, 2020 (Actual)
Completion
Mar 30, 2020 (Actual)
Last update posted
Apr 26, 2022

2018 – 2020

United States locations

U.S. sites
29
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
Cara Therapeutics Study Site Chula Vista California 91910 —
Cara Therapeutics Study Site Fountain Valley California 92708 —
Cara Therapeutics Study Site Northridge California 91324 —
Cara Therapeutics Study Site Riverside California 92503 —
Cara Therapeutics Study Site 2 San Dimas California 91773 —
Cara Therapeutics Study Site San Dimas California 91773 —
Cara Therapeutics Study Site Westminster Colorado 80031 —
Cara Therapeutics Study Site Hialeah Florida 33012 —
Cara Therapeutics Study Site Miami Gardens Florida 33169 —
Cara Therapeutics Study Site Orlando Florida 32810 —
Cara Therapeutics Study Site Athens Georgia 30606 —
Cara Therapeutics Study Site Macon Georgia 31201 —
Cara Therapeutics Study Site Baton Rouge Louisiana 70808 —
Cara Therapeutics Study Site Brockton Massachusetts 02301 —
Cara Therapeutics Study Site Kalamazoo Michigan 49007 —
Cara Therapeutics Study Site Roseville Michigan 48066 —
Cara Therapeutics Study Site Saint Clair Michigan 48081 —
Cara Therapeutics Study Site Tupelo Mississippi 38801 —
Cara Therapeutics Study Site St Louis Missouri 63136 —
Cara Therapeutics Study Site Clifton New Jersey 07011 —
Cara Therapeutics Study Site Somerville New Jersey 08876 —
Cara Therapeutics Study Site Albuquerque New Mexico 87109 —
Cara Therapeutics Study Site Long Island City New York 11106 —
Cara Therapeutics Study Site Austin Texas 78758 —
Cara Therapeutics Study Site Dallas Texas 75228 —
Cara Therapeutics Study Site McAllen Texas 78503 —
Cara Therapeutics Study Site San Antonio Texas 78207 —
Cara Therapeutics Study Site St. George Utah 84790 —
Cara Therapeutics Study Site Roanoke Virginia 24014 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03636269, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 26, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03636269 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →