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Completed Phase 2Phase 3 Interventional Results available

To Evaluate the Efficacy and Safety of Nemolizumab for 12 Weeks in Participants With Chronic Kidney Disease With Associated Moderate to Severe Pruritus

ClinicalTrials.gov ID: NCT05075408

Public ClinicalTrials.gov record NCT05075408. 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 28, 2026, 7:30 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 Efficacy and Safety of Nemolizumab in Subjects With Chronic Kidney Disease With Associated Moderate to Severe Pruritus

Brief summary

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

The purpose of this study was to evaluate the efficacy of nemolizumab compared to placebo at reducing the intensity of pruritus after a 12-week treatment period in adult hemodialysis participants with moderate to severe pruritus.

Study identification

NCT ID
NCT05075408
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Galderma R&D
Industry
Enrollment
258 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
Mar 17, 2022
Primary completion
Jan 3, 2024
Completion
Jan 3, 2024
Last update posted
Apr 30, 2026

2022 – 2024

United States locations

U.S. sites
47
U.S. states
18
U.S. cities
43
Facility City State ZIP Site status
Galderma Investigational Site 9989 Bakersfield California 93309 —
Galderma Investigational Site 9991 Glendale California 91205 —
Galderma Investigational Site 7018 Glendale California 91206 —
Galderma Investigational Site 7015 La Palma California 90623 —
Galderma Investigational Site 9996 Los Angeles California 90048 —
Galderma Investigational Site 9978 Lynwood California 90262 —
Galderma Investigational Site 7017 Riverside California 92505 —
Galderma Investigational Site 9973 Tarzana California 91356 —
Galderma Investigational Site 7028 Victorville California 92392 —
Galderma Investigational Site 9964 Victorville California 92394-1868 —
Galderma Investigational Site 7003 Whittier California 90603 —
Galderma Investigational Site 9971 Denver Colorado 80230 —
Galderma Investigational Site 9988 Bloomfield Connecticut 06002 —
Galderma Investigational Site 9980 Middlebury Connecticut 06762 —
Galderma Investigational Site 9970 Boca Raton Florida 33421 —
Galderma Investigational Site 7037 Coral Gables Florida 33134 —
Galderma Investigational Site 7026 Hollywood Florida 33021 —
Galderma Investigational Site 9965 Miami Florida 33125 —
Galderma Investigational Site7016 Miami Florida 33155 —
Galderma Investigational Site 7032 Sanford Florida 32771 —
Galderma Investigational Site 7004 Tampa Florida 33603 —
Galderma Investigational Site 7025 Tampa Florida 33603 —
Galderma Investigational Site 7027 Columbus Georgia 31904 —
Galderma Investigational Site 9983 Overland Park Kansas 66210 —
Galderma Investigational Site 9972 Wichita Kansas 67214 —
Galderma Investigational Site 9963 Roseville Michigan 48066 —
Galderma Investigational Site 7020 Edina Minnesota 55435 —
Galderma Investigational Site 9982 Minneapolis Minnesota 55404 —
Galderma Investigational Site 7035 Kansas City Missouri 64111 —
Galderma Investigational Site 9962 Las Vegas Nevada 89128 —
Galderma Investigational Site 7038 Fresh Meadows New York 11365 —
Galderma Investigational Site 9998 Great Neck New York 11021 —
Galderma Investigational Site 9995 The Bronx New York 10461 —
Galderma Investigational Site 7007 Winston-Salem North Carolina 27103 —
Galderma Investigational Site 9992 Roseburg Oregon 97471 —
Galderma Investigational Site 9999 Spartanburg South Carolina 29306 —
Galderma Investigational Site 9967 Chattanooga Tennessee 37404 —
Galderma Investigational Site 7039 Arlington Texas 76015 —
Galderma Investigational Site 7040 Dallas Texas 75231 —
Galderma Investigational Site 9966 El Paso Texas 79925 —
Galderma Investigational Site 9977 Greenville Texas 75402 —
Galderma Investigational Site 7011 Houston Texas 77054 —
Galderma Investigational Site 7022 McKinney Texas 75069 —
Galderma Investigational Site 7010 San Antonio Texas 78258 —
Galderma Investigational Site 7019 The Woodlands Texas 77384 —
Galderma Investigational Site 9968 Norfolk Virginia 23502 —
Galderma Investigational Site 9969 Wauwatosa Wisconsin 53226 —

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05075408, 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 30, 2026 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05075408 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →