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NOT YET RECRUITING
NCT07060989
PHASE1/PHASE2

A Study of Safety, Tolerability and Preliminary Efficacy of NTS071 in Subjects With Advanced Solid Tumors Harboring a TP53 Y220C Mutation

Sponsor: Nutshell Therapeutics (Shanghai) Co., LTD.

View on ClinicalTrials.gov

Summary

This study is to evaluate the safety, tolerability, PK, and preliminary efficacy of NTS071 in adults with TP53 Y220C-mutated solid tumors.

Official title: A Phase 1/2a Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of NTS071 in Subjects With Advanced Solid Tumors Harboring a TP53 Y220C Mutation

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

220

Start Date

2025-08

Completion Date

2029-12

Last Updated

2025-07-11

Healthy Volunteers

No

Interventions

DRUG

NTS071

Oral administration

Locations (2)

Next Oncology

San Antonio, Texas, United States

Shanghai

Shanghai, China