U.S., March 27 -- ClinicalTrials.gov registry received information related to the study (NCT06895499) titled 'Efficacy, Safety, and Tolerability of HB0043 in Hidradenitis Suppurativa Patients.' on March 07.
Brief Summary: The purpose of this study is to assess efficacy safety and tolerability of HB0043 in adult patients with moderate to severe HS.
Study Start Date: March 20
Study Type: INTERVENTIONAL
Condition:
Hidradenitis Suppurativa
Intervention:
DRUG: HB0043
Low dose
DRUG: HB0043
Medium dose
DRUG: HB0043
High dose
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Shanghai Huaota Biopharmaceutical Co., Ltd.
Published by HT Digital Content Services with permission from Health Daily Digest....