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Axitinib Accord (axitinib)

Generic
Region
🇪🇺 EU
Active substance
axitinib
Company
Accord Healthcare S.L.U.
Status
Authorised
Therapeutic area
Carcinoma, Renal Cell
CHMP opinion
Thu 25 Jul 2024
EU approval
Thu 19 Sep 2024
Designations
Generic
Application
EMEA/H/C/006206
ATC
L01EK01
Official record
www.ema.europa.eu

Indication

Axitinib Accord is indicated for the treatment of adult patients with advanced renal cell carcinoma (RCC) after failure of prior treatment with sunitinib or a cytokine.

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.