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RECRUITING
NCT07644650
PHASE1

Phase 1 Study of MST-168 in Participants With Advanced Solid Malignant Tumors

Sponsor: Mabsoft Therapeutics (Shanghai) Co., Ltd.

View on ClinicalTrials.gov

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

BIOLOGICAL

MST-168

MST-168 is a proprietary antibody-drug conjugate (ADC) developed by Mabsoft Therapeutics.

Locations (1)

Shanghai Chest Hospital

Shanghai, Shanghai Municipality, China