Polmacoxib

Polmacoxib was approved by the Korean Ministry of Food and Drug Safety (MFDS) on Feb 05, 2015. It was originally developed by CrystalGenomics, then it signed an agreement for the commercialization of polmacoxib in South Korea with Dong-A in August. It is marketed as Acelex® in KR.

Polmacoxib is a cyclooxygenase 2 (COX-2) inhibitor, for the treatment of osteoarthritis.

Acelex® is available as capsules for oral use, containing 2 mg of polmacoxib. The recommended dose is 2 mg once daily.

 

General Information

Update Date:2016-03-22

Drug Name:
Polmacoxib
Research Code:
CG-100649
Trade Name:
Acelex®
MOA:
COX-2 inhibitor
Indication:
Osteoarthritis (OA)
Status:
Approved
Company:
CrystalGenomics (Originator) , Dong-A
Sales:
ATC Code:
Approved Countries or Area

Update Date:2016-03-22

Approval Date Approval Type Trade Name Indication Dosage Form Strength Company Review Classification
2015-02-05 First approval Acelex Osteoarthritis (OA) Capsule 2 mg CrystalGenomics
Chemical Structure

Update Date:2016-03-22

Molecular Weight 361.39
Formula C18H16FNO4S
CAS No. 301692-76-2 (Polmacoxib);
Chemical Name Benzenesulfonamide, 4-[3-(3-fluorophenyl)-4,5-dihydro-5,5-dimethyl-4-oxo-2-furanyl]-
Polmacoxib (Free Acid/Base)Parameters:
MW HD HA FRB* PSA* cLogP*
361.39 2 5 3 94.8 1.760±0.591
*:Calculated by ACD/Labs software V11.02.
Related Patents

Update Date:2016-03-29

Synthesis & Impurities

Update Date:2016-05-12


Impurity database is being updated!