drugset / Trial / NCT06527404

A Phase 3, Placebo-controlled, Double-blind Study Assessing Rocatinlimab in Prurigo Nodularis

NCT06527404

Phase 3 Active not recruiting 469 enrolled Amgen
RandomizedParallel-groupDouble-blindTreatment

Summary

The main objective of the study will be to evaluate the efficacy of rocatinlimab compared with placebo at week 24 on the patient-reported outcome (PRO) measure of pruritus and overall clinical assessment score (US only).

Timeline

Start
2024-07-18
Primary completion
2026-04-17
Completion
2027-01-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Rocatinlimab Monoclonal antibody Subcutaneous

Indications