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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
Conditions
Interventions
DRUG
NTS071
Oral administration
Locations (2)
Next Oncology
San Antonio, Texas, United States
Shanghai
Shanghai, China