Sarizotan

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Sarizotan
Sarizotan.png
Systematic (IUPAC) name
1-[(2R)-3,4-dihydro-2H-chromen-2-yl]-N-([5-(4-fluorophenyl)pyridin-3-yl]methyl)methanamine
Clinical data
Pregnancy
category
  • N/A
Legal status
  • Discontinued
Routes of
administration
Oral
Identifiers
CAS Number 177975-08-5
ATC code none
PubChem CID: 6918388
ChemSpider 2319847
UNII 467LU0UCUW YesY
Chemical data
Formula C22H21FN2O
Molecular mass 348.413 g/mol
  • C1CC2=CC=CC=C2O[C@H]1CNCC3=CN=CC(=C3)C4=CC=C(C=C4)F

Sarizotan (EMD-128,130) is a selective 5-HT1A receptor agonist and D2 receptor antagonist,[1] which has antipsychotic effects,[2][3] and has also shown efficacy in reducing dyskinesias resulting from long-term anti-Parkinsonian treatment with levodopa.[4][5][6][7]

In June 2006, the developer Merck KGaA announced that the development of sarizotan was discontinued, after two sarizotan Phase III studies (PADDY I, PADDY II) failed to meet the primary efficacy endpoint and neither the Phase II findings nor the results from preclinical studies could be confirmed. No statistically significant difference of the primary target variable between sarizotan and placebo could be demonstrated.[8][9]

See also

References

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