Drugs / AG-270
last change Jan 2025 re-read 3 minutes ago

AG-270

also known as S095033

targets MAT2A via inhibition

Developed for
cancer · lymphoma
Investigated by
Servier

Trials 1

2018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT03435250 Mar 2018 → Apr 2023 cancer, lymphoma Servier Terminated No outcome recorded Stop: Business

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2019-10-27 Agios Pharmaceuticals, Inc. Results Agios Presents Data from Single Agent Dose-Escalation Arm of Phase 1 Study of AG-270, a MAT2A Inhibitor, in Patients with MTAP-Deleted Tumors agios.com ↗
2017-12-26 Agios Pharmaceuticals, Inc. Regulatory Agios Submits New Drug Application to the FDA for Ivosidenib for the Treatment of Patients with Relapsed/Refractory AML and an IDH1 Mutation agios.com ↗
Company Also Announces FDA Clearance of Investigational New Drug Application (IND) for AG-270 Targeting MTAP-Deleted Tumors; Phase 1 Study to Initiate in First Quarter 2018

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as AG-270 ClinicalTrials.gov intervention name — accepted as the source's own label NCT03435250 ↗
Known as S095033 “AG-270/S095033 is an oral, potent, reversible inhibitor of methionine adenosyltransferase 2 A (MAT2A), the enzyme primarily responsible for the synthesis of SAM.” PMID 39762248 ↗ Jan 2025
Action Inhibit “AG-270/S095033 is an oral, potent, reversible inhibitor of methionine adenosyltransferase 2 A (MAT2A), the enzyme primarily responsible for the synthesis of SAM.” PMID 39762248 ↗ Jan 2025
Route Oral “AG-270/S095033 is an oral, potent, reversible inhibitor of methionine adenosyltransferase 2 A (MAT2A), the enzyme primarily responsible for the synthesis of SAM.” PMID 39762248 ↗ Jan 2025
Target MAT2A “AG-270/S095033 is an oral, potent, reversible inhibitor of methionine adenosyltransferase 2 A (MAT2A), the enzyme primarily responsible for the synthesis of SAM.” PMID 39762248 ↗ Jan 2025