Drugs / dirucotide

Trials 4

20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 2/33 trials
Phase 2/3 NCT00870155 Feb 2007 → Sep 2009 secondary progressive multiple sclerosis Eli Lilly and Company Terminated No outcome recorded
Phase 2/3 NCT00869986 Nov 2006 → Sep 2009 relapsing-remitting multiple sclerosis Eli Lilly and Company Completed No outcome recorded
Phase 2/3 NCT00869726 Dec 2004 → May 2009 secondary progressive multiple sclerosis Eli Lilly and Company Completed No outcome recorded
Phase 31 trial · 1 missed
Phase 3 NCT00468611 Jun 2007 → Jul 2009 secondary progressive multiple sclerosis BioMS Technology Corp. Terminated Missed primary

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2009-07-27 Eli Lilly and Company Results Dirucotide Does Not Meet Primary Endpoint in Phase III MAESTRO-01 Trial in Secondary Progressive Multiple Sclerosis lilly.com ↗
In addition, there were no statistically significant differences between dirucotide and placebo on the secondary endpoints of the study.

All press releases naming this drug 1 release

DateIssuerRelease

Evidence & citations 8 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as Dirucotide ClinicalTrials.gov intervention name — accepted as the source's own label NCT00869726 ↗
2

NCT00870155 ↗

NCT00869986 ↗

Known as Dirucotida ChEMBL registry synonym — accepted as the source's own label CHEMBL2105639 ↗
Known as DIRUCOTIDE ACETATE ChEMBL registry synonym — accepted as the source's own label CHEMBL2105639 ↗
Known as MBP8298 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00468611 ↗
Known as MBP8298 PEPTIDE ChEMBL registry synonym — accepted as the source's own label CHEMBL2105639 ↗
Known as SF-328 ChEMBL registry synonym — accepted as the source's own label CHEMBL2105639 ↗
Modality Protein / enzyme biologic — CHEMBL2105639 ↗
Route Intravenous “500mg MBP8298 IV every six months for a period of two years” NCT00468611 ↗