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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

2025-08-04

Completion Date

2029-12

Last Updated

2026-10-19

Healthy Volunteers

No

Interventions

DRUG

NTS071

Oral administration

Locations (10)

Yale Cancer Center

New Haven, Connecticut, United States

University of Texas MD Anderson Cancer Center

Houston, Texas, United States

NEXT Virginia

Fairfax, Virginia, United States

Peking University People's Hospital

Beijing, China

Beijing Cancer Hospital

Beijing, China

Guangdong Provincial People's Hospital

Guangzhou, China

The First Affiliated Hospital of Nanchang University - Xianghu District

Nanchang, China

Fudan University Shanghai Cancer Center

Shanghai, China

Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, China

The First Affiliated Hospital of Xi'an Jiaotong University

Xi'an, China