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RECRUITING
NCT06104839
PHASE2

Safety and Efficacy of Oral NXC-736 in Adult Participants with Moderate and Severe Alopecia Areata

Sponsor: NEXTGEN Bioscience

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the safety and efficacy of NXC-736 monotherapy in participants with severe alopecia areata (AA).

Official title: A Multi-center, Randomized, Double-blind, Placebo-controlled, Phase 2a Study to Evaluate the Efficacy and Safety of NXC736 in Patients with Moderate and Severe Alopecia Areata

Key Details

Gender

All

Age Range

19 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

96

Start Date

2024-09-01

Completion Date

2025-06-30

Last Updated

2024-12-17

Healthy Volunteers

No

Conditions

Interventions

DRUG

NXC736

oral administration

DRUG

Placebo

oral administration

Locations (2)

Seoul National University Hospital.

Seoul, South Korea

Kyung Hee University Hospital at Gangdong

Seoul, South Korea