Vidaza (azacitidine)
- Region
- 🇪🇺 EU
- Active substance
- azacitidine
- Company
- Bristol-Myers Squibb Pharma EEIG
- Status
- Authorised
- Therapeutic area
- Myelodysplastic Syndromes; Leukemia, Myelomonocytic, Chronic; Leukemia, Myeloid, Acute
- CHMP opinion
- Thu 23 Oct 2008
- EU approval
- Wed 17 Dec 2008
- Designations
- Accelerated assessment
- Application
- EMEA/H/C/000978
- ATC
- L01BC07
- Official record
- www.ema.europa.eu
Indication
Vidaza is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (HSCT) with: intermediate 2 and high-risk myelodysplastic syndromes (MDS) according to the International Prognostic Scoring System (IPSS), chronic myelomonocytic leukaemia (CMML) with 10 29 % marrow blasts without myeloproliferative disorder, acute myeloid leukaemia (AML) with 20 30 % blasts and multi-lineage dysplasia, according to World Health Organisation (WHO) classification. Vidaza is indicated for the treatment of adult patients aged 65 years or older who are not eligible for HSCT with AML with >30% marrow blasts according to the WHO classification.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Onureg Authorised · Bristol-Myers Squibb Pharma EEIG
- 🇪🇺 Azacitidine Adienne Application withdrawn · Adienne S.r.l. S.U.
- 🇪🇺 Azacitidine Mylan Authorised · Mylan Pharmaceuticals Limited
- 🇪🇺 Azacitidine Kabi Authorised · Fresenius Kabi Deutschland GmbH
- 🇪🇺 Azacitidine Accord Authorised · Accord Healthcare S.L.U.
- 🇪🇺 Azacitidine betapharm Authorised · betapharm Arzneimittel GmbH
- 🇪🇺 Azacitidine Celgene Withdrawn · Celgene Europe BV
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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.