Drugs / NUMIDARGISTAT

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT03910530 Jul 2019 → Dec 2021 cancer, metastatic neoplasm Incyte Biosciences Japan GK Completed No outcome recorded
Phase 1 NCT02903914 Sep 2016 → Apr 2020 colorectal cancer, gastric cancer, head and neck cancer, lung cancer +5 Incyte Corporation Completed No outcome recorded
Phase 1/23 trials
Phase 1/2 NCT03837509 Sep 2019 → Apr 2022 refractory plasma cell neoplasm Incyte Corporation Terminated No outcome recorded Stop: Enrollment
Phase 1/2 NCT03361228 Mar 2018 → Mar 2019 cancer Incyte Corporation Terminated No outcome recorded
Phase 1/2 NCT03314935 Nov 2017 → Nov 2022 biliary tract cancer, colorectal cancer, endometrial cancer, gastroesophageal cancer +1 Incyte Corporation Completed No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2019-10-01 Molecure S.A. Results First clinical proof-of-concept for arginase inhibitors in cancer immunotherapy molecure.com ↗
INCB1158 was well tolerated and inhibited plasma arginase activity, inducing increased plasma arginine levels at all doses tested.

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as NUMIDARGISTAT ChEMBL registry synonym — accepted as the source's own label CHEMBL4218271 ↗
Known as Arginase inhibitor incb001158 ChEMBL registry synonym — accepted as the source's own label CHEMBL4218271 ↗
Known as CB-1158 ChEMBL registry synonym — accepted as the source's own label CHEMBL4218271 ↗
Known as INCB001158 ClinicalTrials.gov intervention name — accepted as the source's own label NCT03837509 ↗
4

NCT03910530 ↗

NCT02903914 ↗

NCT03314935 ↗

NCT03361228 ↗

Action Inhibit “Consistent with arginase inhibition activity, plasma arginine dose-dependently increased.” PMID 39886141 ↗ May 2024
Modality Small molecule — CHEMBL4218271 ↗
Route Oral “INCB001158 was orally administered two times per day as monotherapy or in combination with intravenous pembrolizumab 200 mg every 3 weeks.” PMID 39886141 ↗ May 2024