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Rapid relative effectiveness assessment of new pharmaceuticals for the treatment of chronic Hepatitis C
Subject:
- Active Substance: Sofosbuvir, Ledipasvir/Sofosbuvir, Simeprevir, Daclatasvir, Ombitasvir/Paritaprevir/Ritonavir, Dasabuvir
- Name: SOVALDI®, HARVONI®, OLYSIO™, DAKLINZA™, VIEKIRAX®, EXVIERA®
- Therapeutic area: Hepatitis C
- Pharmaceutical company: Bristol-Myers Squibb GmbH & Co. KGaA, AbbVie Deutschland GmbH & Co. KG, Janssen-Cilag GmbH, Gilead Sciences GmbH
Time table:
- Publication of final assessment: 17.12.2015
Assessment information:
- Title: Rapid relative effectiveness assessment of new pharmaceuticals for the treatment of chronic Hepatitis C
- Author/Co-Author: KCE (Belgium), AAZ (Croatia), UCSC Gemelli (Italy), HVB (Austria)
- Dedicated Reviewers: SNHTA (Switzerland), SAGEM HTA (Turkey), ZIN (Netherlands), AETSA (Spain), AIFA (Italy), MoH Slovak Republic (Slovakia), NIPHNO (Norway), HAS (France), MoH Malta (Malta), NVD (Latvia), FIMEA (Finland), SMC (Scotland), IQWiG (Germany), INFARMED (Portugal)
G-BA assessment available for › Sofosbuvir (D-091), › Ledipasvir/Sofosbuvir (D-143), › Simeprevir (D-113), › Daclatasvir (D-129), › Ombitasvir/Paritaprevir/Ritonavir (D-153), › Dasabuvir (D-152)