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Deferiprone Lipomed (deferiprone)

Generic
Region
🇪🇺 EU
Active substance
deferiprone
Company
Lipomed GmbH
Status
Authorised
Therapeutic area
Iron Overload; beta-Thalassemia
CHMP opinion
Thu 26 Jul 2018
EU approval
Wed 19 Sep 2018
Designations
Generic
Application
EMEA/H/C/004710
ATC
V03AC02
Official record
www.ema.europa.eu

Indication

Deferiprone Lipomed monotherapy is indicated for the treatment of iron overload in patients with thalassaemia major when current chelation therapy is contraindicated or inadequate. Deferiprone Lipomed in combination with another chelator is indicated in patients with thalassaemia major when monotherapy with any iron chelator is ineffective, or when prevention or treatment of life-threatening consequences of iron overload justifies rapid or intensive correction.

Regulatory milestones

No milestones recorded in the last year.

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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.