A Study Evaluating the Safety and Efficacy of HB0036 in Subjects With Advanced Solid Tumors

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

August 25, 2022

Primary Completion Date

August 1, 2025

Study Completion Date

August 1, 2025

Conditions
Advanced Solid TumorNSCLC
Interventions
DRUG

HB0036

Patients will be assigned to dose regimens in the order of enrollment, and they will receive their assigned fixed dose of HB0036 via intravenous infusion. HB0036 IV every 3 weeks (q3w).

Trial Locations (4)

47905

RECRUITING

Horizon Oncology, Lafayette

78229

RECRUITING

Next Oncology, San Antonio

99216

RECRUITING

Summit Cancer Centers, Spokane

250117

RECRUITING

Shandong Hospital, Jinan

All Listed Sponsors
lead

Shanghai Huaota Biopharmaceutical Co., Ltd.

INDUSTRY