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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.
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
Conditions
Interventions
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