Drugs / M3258
last change Oct 2022 re-read 3 minutes ago

M3258

targets PSMB8 via inhibition

Developed for
plasma cell myeloma
Investigated by
EMD Serono Research & Development Institute, Inc. · Merck KGaA, Darmstadt, Germany

Trials 1

2020202120222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT04075721 Sep 2019 → Apr 2021 plasma cell myeloma EMD Serono Research & Development Institute, Inc. Terminated No outcome recorded Stop: Enrollment

Evidence & citations 4 cited values

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

FieldValueCited text
Known as M3258 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04075721 ↗
Action Inhibit “M3258 is an orally bioavailable, potent, selective, reversible inhibitor of the large multifunctional peptidase 7 (LMP7, β5i, PSMB8) proteolytic subunit of the immunoproteasome” PMID 36273822 ↗ Oct 2022
Route Oral “Participants received M3258 at a dose of 10 milligrams (mg) orally” NCT04075721 ↗
Target PSMB8 “M3258 is an orally bioavailable, potent, selective, reversible inhibitor of the large multifunctional peptidase 7 (LMP7, β5i, PSMB8) proteolytic subunit of the immunoproteasome” PMID 36273822 ↗ Oct 2022