CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 258 enrolled
Drug / intervention
Nemolizumab +2 moredrug
Likely dose
Nemolizumab 60 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05075408
NCT05075408Phase 3Completed

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

Galderma R&D·interventional·Posted Oct 12, 2021·Updated May 1, 2026

In Brief

A Phase 3 clinical trial evaluating Nemolizumab and Placebo for Chronic Kidney Disease Associated Moderate to Severe Pruritus. Completed, enrolled 258 participants across 64 sites in 4 countries.

Detailed Summary

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 Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesHungary, Poland, Spain, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20222023202420252026
First PostedOct 12, 2021
Enrollment StartMar 18, 2022
Primary CompletionJan 4, 2024
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 4.7 years ago

Interventions

Nemolizumabdrug

Participants received a loading dose of 60 mg nemolizumab at Baseline followed by 2 Subcutaneous (SC) injections for a total dose of 30 mg nemolizumab once every 4 weeks i.e. at Week 4 and Week 8.

Nemolizumabdrug

Participants received 2 SC injections of 30 mg nemolizumab once every 4 weeks i.e. at Week 4 and Week 8.

Placebodrug

Participants received 2 SC injections of 30 mg placebo-matched to nemolizumab once every 4 weeks i.e. at Week 4 and Week 8.