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RECRUITING
NCT06993870
PHASE1
Phase I Study of HBT-708 for Patients With Advanced Solid Tumors
Sponsor: Shenyang Sunshine Pharmaceutical Co., LTD.
View on ClinicalTrials.gov
Summary
The purpose of this study will be to evaluate the safety, tolerability, and inital efficacy of HBT-708 in subjects with advanced solid tumors.
Official title: A Phase I Study to Evaluate the Safety, Tolerability, and Initial Efficacy of HBT-708 Monotherapy for Patients With Advanced Solid Tumors
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2025-06-16
Completion Date
2027-06-28
Last Updated
2025-07-11
Healthy Volunteers
No
Conditions
Interventions
DRUG
HBT-708
bispecific antibody
Locations (1)
Shanghai General Hospital
Shanghai, Shanghai Municipality, China