Actively Recruiting

Phase 2
Age: 19Years - 65Years
All Genders
NCT06104839

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

Led by NEXTGEN Bioscience · Updated on 2026-04-13

73

Participants Needed

2

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 19Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Men or women between 19 and 65 years of age at the time of informed consent
  • Moderate and severe alopecia areata with a SALT score of 25% to less than 95% at Screening and Day 1/Baseline
  • Current episode of hair loss lasting 6 months or more but less than 8 years
  • Stable disease condition with no significant hair growth in the last 6 months as assessed by the Investigator
  • Willing to keep the same hairstyle and hair color for the duration of the study
Not Eligible

You will not qualify if you...

  • History of alopecia types other than alopecia areata, such as cicatricial/scarring alopecia (including central centrifugal cicatricial alopecia), traction alopecia, androgenic alopecia, or telogen effluvium
  • Active scalp inflammation, infection, psoriasis, or other scalp conditions that may interfere with the SALT assessment
  • Prior use of Janus kinase (JAK) inhibitors (oral or topical) or participation in clinical studies involving JAK inhibitors

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Seoul National University Hospital.

Seoul, South Korea, 03080

Actively Recruiting

2

Kyung Hee University Hospital at Gangdong

Seoul, South Korea, 05278

Actively Recruiting

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Research Team

H

Heesun Kim

CONTACT

Y

YangHye Park

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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