Study of the Efficacy and Safety of ICP-332 in Participants With Prurigo Nodularis

NCT07236099 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 135

Last updated 2026-04-09

No results posted yet for this study

Summary

Evaluate the efficacy and safety of ICP-332 in participants with Prurigo Nodularis (PN)

Conditions

  • Prurigo Nodularis (PN)

Interventions

DRUG

ICP-322

ICP-322 Tablets

DRUG

Placebo

ICP-332 Placebo Tablets

Sponsors & Collaborators

  • Beijing InnoCare Pharma Tech Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-27
Primary Completion
2027-03-31
Completion
2027-10-31
FDA Drug
Yes

Countries

  • United States
  • China

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07236099 on ClinicalTrials.gov