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Completed Phase 2 Interventional

Safety and Pharmacokinetics of IV CR845 in Hemodialysis Patients, and Its Efficacy in Patients With Uremic Pruritus

ClinicalTrials.gov ID: NCT02229929

Public ClinicalTrials.gov record NCT02229929. 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 Sep 2, 2026, 6:33 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 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Safety and Pharmacokinetics of Intravenous CR845 in Hemodialysis Patients, and Its Safety and Efficacy in Hemodialysis Patients With Uremic Pruritus

Brief summary

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

The primary purpose of this study is to: * Evaluate the safety and pharmacokinetic profile of repeated doses IV CR845 over one week in patients who are undergoing hemodialysis. (Part A) * This study is also investigating whether repeated doses of IV CR845 over two weeks is safe and effective in reducing the intensity of itching in hemodialysis patients with uremic pruritus (Part B).

Study identification

NCT ID
NCT02229929
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cara Therapeutics, Inc.
Industry
Enrollment
89 participants

Conditions and interventions

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
Jun 30, 2014
Primary completion
Jun 30, 2015
Completion
Jun 30, 2015
Last update posted
Aug 9, 2016

2014 – 2015

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
US Renal Care Pine Bluff Arkansas 71603
US Renal Care Chula Vista California 91915
US Renal Care Long Beach California 90806
Valley Renal Medical Group Northridge California 91324
Nephrology Specialists Medical Group, Inc Orange California 92868
North American Research Institute San Dimas California 91773
University of Florida College of Medicine Jacksonville Jacksonville Florida 32209
Orlando Clinical Research Center Orlando Florida 32809
Pines Clinical Research, Inc. Pembroke Pines Florida 33028
Emory Dialysis Center at Northside Atlanta Georgia 30318
Western New England Renal & Transplant Associates, PC Springfield Massachusetts 01107
US Renal Care Gallup New Mexico 87301
Trude Weishaupt Memorial Dialysis Center Fresh Meadows New York 11365
Winthrop University Hospital Mineola New York 11501
Brookview Hills Research Associates, LLC Winston-Salem North Carolina 27103
US Renal Care Aiken South Carolina 29803
Southeast Renal Research Institute Chattanooga Tennessee 37408
Vanderbilt University Medical Center Nashville Tennessee 37232
US Renal Care Grand Prairie Texas 75050
US Renal Care San Antonio Texas 78202

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02229929, 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 Aug 9, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02229929 live on ClinicalTrials.gov.

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