Drugs / Omigapil

Trials 5

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial · 1 met primary
Phase 1 NCT01805024 Dec 2014 → Dec 2017 congenital muscular dystrophy Santhera Pharmaceuticals Completed Met primary
Phase 1/21 trial
Phase 1/2 NCT00407212 Jan 2002 → Nov 2003 Parkinson disease Novartis Completed No outcome recorded
Phase 23 trials
Phase 2 NCT00230074 Nov 2004 → Feb 2005 amyotrophic lateral sclerosis Novartis Completed No outcome recorded
Phase 2 NCT00072709 Sep 2003 → Dec 2004 amyotrophic lateral sclerosis Novartis Pharmaceuticals Completed No outcome recorded
Phase 2 NCT00036413 Jan → Oct 2002 amyotrophic lateral sclerosis Novartis Pharmaceuticals Completed No outcome recorded

Evidence & citations 8 cited values

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

FieldValueCited text
Known as Omigapil ClinicalTrials.gov intervention name — accepted as the source's own label NCT01805024 ↗
Known as Cgp-3466 ChEMBL registry synonym — accepted as the source's own label CHEMBL1232111 ↗
Known as dibenz[b,f]oxepin-10-ylmethyl-prop-2-ynyl-amine, hydrogen maleate salt “TCH346 (dibenz[b,f]oxepin-10-ylmethyl-prop-2-ynyl-amine, hydrogen maleate salt)” NCT00407212 ↗
Known as Omigapilo ChEMBL registry synonym — accepted as the source's own label CHEMBL1232111 ↗
Known as TCH346 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00230074 ↗
3

NCT00407212 ↗

NCT00072709 ↗

NCT00036413 ↗

Action Inhibit “Omigapil is a small molecule which inhibits the GAPDH-Siah1-mediated apoptosis pathway.” PMID 38915423 ↗ May 2024
Modality Small molecule “Omigapil is a small molecule which inhibits the GAPDH-Siah1-mediated apoptosis pathway.” PMID 38915423 ↗ May 2024
1

CHEMBL1232111 ↗

Route Oral “Three Oral Doses (0.5 mg, 2.5 mg and 10 mg Once Daily) of TCH346” NCT00036413 ↗