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Phase 1 Study of MST-168 in Participants With Advanced Solid Malignant Tumors
Sponsor: Mabsoft Therapeutics (Shanghai) Co., Ltd.
Summary
A Phase 1, multiregional, open-label study of MST-168 in participants with target-driven advanced solid tumors. The goal of this clinical trial is to evaluate the safety, tolerability, pharmacokinetics, immunogenicity, pharmacodynamic effects, and preliminary efficacy of MST-168 in participants with target-driven advanced solid tumors. MST-168 is an investigational ADC.
Official title: A Phase 1, Multiregional, Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of MST-168, in Participants With Advanced Solid Malignant Tumors
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
420
Start Date
2026-11-15
Completion Date
2030-06-30
Last Updated
2026-10-14
Healthy Volunteers
No
Conditions
Interventions
MST-168
MST-168 is a proprietary antibody-drug conjugate (ADC) developed by Mabsoft Therapeutics.
Locations (1)
Shanghai Chest Hospital
Shanghai, Shanghai Municipality, China