Exviera (dasabuvir)
Accelerated assessment
- Region
- 🇪🇺 EU
- Active substance
- dasabuvir
- Company
- AbbVie Limited
- Status
- Withdrawn
- Therapeutic area
- Hepatitis C, Chronic
- CHMP opinion
- Sat 20 Nov 2004
- EU approval
- Wed 14 Jan 2015
- Designations
- Accelerated assessment
- Application
- EMEA/H/C/003837
- ATC
- J05AP09
- Official record
- www.ema.europa.eu
Indication
Exviera is indicated in combination with other medicinal products for the treatment of chronic hepatitis C (CHC) in adults. For hepatitis C virus (HCV) genotype specific activity.
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.