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Study identifier: NCT07717905 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, Pharmacodynamics and Clinical Activity of BBT001 Following Intravenous Administration in Participants With Chronic Spontaneous Urticaria (CSU)

Condition: Chronic Spontaneous Urticaria  ·  Sponsor: Bambusa Therapeutics

PhasePhase 1/Phase 2
Planned participants48
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

This is a Phase IIa, randomized, blinded, placebo controlled,Multiple-Ascending Dose study of BBT001 in adult patients with Chronic Spontaneous Urticaria.

This description comes directly from the study's public registry record.

Talk to the study team

Tracy Ji, Study Director  ·  +86 18001322760  ·  tracy.ji@bambusatx.com

Always discuss trial participation with your own doctor first.

Locations (10)

The Second Affiliated Hospital of Wannan Medical CollegeWuhu, Anhui, ChinaNot Yet Recruiting
Peking University People's Hospital, BeijingBeijing, Beijing Municipality, ChinaRecruiting
The Second Affiliated Hospital of Guangzhou Medical UniversityGuangzhou, Guangdong, ChinaNot Yet Recruiting
Dermatology Hospital of Southern Medical UniversityGuangzhou, Guangdong, ChinaNot Yet Recruiting
The First Hospital of Hebei Medical UniversityShijiazhuang, Hebei, ChinaNot Yet Recruiting
Jingzhou Central HospitalJinzhou, Hubei, ChinaNot Yet Recruiting
Wuxi Second People's Hospital,Wuxi, Jiangsu, ChinaNot Yet Recruiting
The Second Hospital of Shanxi Medical UniversityTaiyuan, Shanxi, ChinaNot Yet Recruiting
The Second Affiliated Hospital of Xi'an Jiaotong UniversityXi’an, Shanxi, ChinaNot Yet Recruiting
Hangzhou Third People's HospitalHangzhou, Zhejiang, ChinaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07717905