A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple-Ascending Doses of BGB-16673 in Adults With Chronic Spontaneous Urticaria

PHASE1RecruitingINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

July 19, 2025

Primary Completion Date

September 22, 2026

Study Completion Date

September 22, 2026

Conditions
Chronic Spontaneous Urticaria
Interventions
DRUG

BGB-16673

Administered orally

DRUG

Placebo

Administered orally

Trial Locations (10)

100000

RECRUITING

Peking University Third Hospital, Beijing

200443

NOT_YET_RECRUITING

Shanghai Skin Disease Hospital, Shanghai

310006

RECRUITING

Hangzhou First Peoples Hospital, Hangzhou

325000

RECRUITING

The First Affiliated Hospital of Wenzhou Medical University, Wenzhou

410008

NOT_YET_RECRUITING

Xiangya Hospital of Central South University, Changsha

430022

RECRUITING

Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan

510515

NOT_YET_RECRUITING

Nanfang Hospital, Southern Medical University, Guangzhou

610021

NOT_YET_RECRUITING

Chengdu Second Peoples Hospital, Chengdu

630014

NOT_YET_RECRUITING

The First Affiliated Hospital of Chongqing Medical University, Chongqing

Unknown

RECRUITING

Dermatology Hospital of Southern Medical University, Guangzhou

Sponsors

Lead Sponsor

All Listed Sponsors
lead

BeiGene

INDUSTRY