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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

Interventions

DRUG

HBT-708

bispecific antibody

Locations (1)

Shanghai General Hospital

Shanghai, Shanghai Municipality, China