Omigapil

Omigapil
Omigapil
Systematic (IUPAC) name
Dibenzo[b,f]oxepin-10-ylmethyl-methyl-prop-2-ynylamine
Clinical data
Pregnancy cat.  ?
Legal status Investigational
Identifiers
CAS number 181296-84-4
ATC code None
PubChem CID 6419718
UNII 5V14HD0N4Q
Chemical data
Formula C19H17NO 
Mol. mass 275.13 g/mol
SMILES eMolecules & PubChem

Omigapil (TCH346) is a drug that was developed by Novartis and tested in clinical trials for its ability to help treat Parkinson's disease[1] and amyotrophic lateral sclerosis (ALS).[2] The development for ALS has been terminated due to lack of benefit, but Santhera Pharmaceuticals bought the compound for development for the treatment of congenital muscular dystrophy.[3][4]

References

  1. ^ Olanow, C. W.; Schapira, A. H.; Lewitt, P. A.; Kieburtz, K.; Sauer, D.; Olivieri, G.; Pohlmann, H.; Hubble, J. (2006). "TCH346 as a neuroprotective drug in Parkinson's disease: A double-blind, randomised, controlled trial". The Lancet Neurology 5 (12): 1013. doi:10.1016/S1474-4422(06)70602-0.  edit
  2. ^ ClinicalTrials.gov NCT00036413 A 12-Week, Multicenter, Safety and Dose-Ranging Study of 3 Oral Doses of TCH346 in Patients With Amyotrophic Lateral Sclerosis
  3. ^ Santhera to Test Compound in CMD
  4. ^ Meinen, S.; Lin, S.; Thurnherr, R.; Erb, M.; Meier, T.; Rüegg, M. A. (2011). "Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice". EMBO Molecular Medicine 3 (8): 465–479. doi:10.1002/emmm.201100151. PMID 21674808.  edit