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An Open-Label, First in Human, Phase 1/2 to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of the CTPS1 Inhibitor STP938 In Adult Subjects With Relapsed/Refractory B-Cell and T-Cell Lymphomas
The Phase 1 part of the study is a dose escalation of STP938 as monotherapy. The Phase 2 part of the study is cohort expansion of STP938 as a monotherapy in 5 different B and T cell lymphomas.
The drug STP938 is an inhibitor of an enzyme called cytidine triphosphate synthase 1 (CTPS1). CTPS1, and a very similar enzyme cytidine triphosphate synthase 2 (CTPS2), control the final step in the production of the cytidine triphosphate (CTP). CTP is an essential building block of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). Studies of people with inherited mutations of the CTPS1 gene indicate that certain types of blood cells required CTPS1 in order to divide rapidly, whereas other cells in the body use the CTPS2 enzyme. Based on these observations, it is expected that blocking CTPS1, using the drug STP938, may be an effective treatment for certain types of cancer that arise from blood cells. The purpose of this study is to see if STP938 is effective at treating different types of lymphoma. STP938 will be given as a tablet. Blood samples will be taken during the study in order to understand the effects of STP938 on the lymphoma and on the rest of the body. The main outcome of the first part of the study is to see if STP938 can be given safely to patients with lymphoma, and to work out the best dose of STP938. The main outcome of the second part of the study is to see if ST938 is effective in treating different types of lymphoma.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Colorado Blood Cancer Institute
Denver, Colorado, United States
Florida Cancer Specialists
Sarasota, Florida, United States
Memorial Sloan Kettering
New York, New York, United States
The Centre Léon Bérard
Lyon, France
Institut Paoli Calmettes
Marseille, France
CHU de Nantes
Nantes, France
Hôpital Saint-Louis
Paris, France
Institut Gustave Roussy
Villejuif, France
University Hospitals of Leicester NHS Trust
Leicester, United Kingdom
Imperial College / Clinical Trials Unit, Hammersmith Hospital
London, United Kingdom
Start Date
August 3, 2022
Primary Completion Date
December 1, 2025
Completion Date
December 1, 2025
Last Updated
April 15, 2025
180
ESTIMATED participants
STP938
DRUG
Lead Sponsor
Step Pharma, SAS
NCT06561048
NCT04161248
Data Source & Attribution
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