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Sofosbuvir, velpatasvir, and voxilaprevir for patients with failure of previous direct-acting antiviral therapy for chronic hepatitis C: Results from the German Hepatitis C-Registry (DHC-R).
Vermehren, Johannes; Serfert, Yvonne; Cornberg, Markus; Stoehr, Albrecht; Klinker, Hartwig; Simon, Karl-Georg; Teuber, Gerlinde; Deterding, Katja; Schulze Zur Wiesch, Julian; Jung, Maria-Christina; Manns, Michael P; Zeuzem, Stefan; Wedemeyer, Heiner; Sarrazin, Christoph.
Affiliation
  • Vermehren J; Gastro-Praxis Wiesbaden, Wiesbaden, Germany.
  • Serfert Y; University Hospital Frankfurt, Frankfurt am Main, Germany.
  • Cornberg M; Leberstiftungs-GmbH Deutschland, Hannover, Germany.
  • Stoehr A; Hannover Medical School, Hannover, Germany.
  • Klinker H; ifi-Institute for Interdisciplinary Medicine, Hamburg, Germany.
  • Simon KG; University Hospital Würzburg, Würzburg, Germany.
  • Teuber G; MVZ Dres. Eisenbach, Simon, Schwarz GbR, Leverkusen, Germany.
  • Deterding K; Hepatologische Schwerpunktpraxis, Frankfurt am Main, Germany.
  • Schulze Zur Wiesch J; Hannover Medical School, Hannover, Germany.
  • Jung MC; Essen University Hospital, University of Duisburg-Essen, Essen, Germany.
  • Manns MP; University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany.
  • Zeuzem S; Leberzentrum München, München, Germany.
  • Wedemeyer H; Hannover Medical School, Hannover, Germany.
  • Sarrazin C; University Hospital Frankfurt, Frankfurt am Main, Germany.
Z Gastroenterol ; 58(9): 841-846, 2020 Sep.
Article in En | MEDLINE | ID: mdl-32947629
ABSTRACT
Despite the high effectiveness of direct-acting antivirals for the treatment of hepatitis C, a small proportion of patients do not respond to approved regimens. The combination regimen of SOF/VEL/VOX was recently approved for patients with failure to prior NS5A-based treatment. In this German real-world cohort including patients with cirrhosis (27.3 %) and previous decompensation events, 12 weeks of SOF/VEL/VOX resulted in high virologic response rates irrespective of disease severity and prior DAA regimen. Adverse events were mostly mild or moderate and comparable to those seen in the approval studies.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Sulfonamides / Carbamates / Hepacivirus / Hepatitis C, Chronic / Macrocyclic Compounds / Sofosbuvir / Heterocyclic Compounds, 4 or More Rings Limits: Humans Language: En Journal: Z Gastroenterol Year: 2020 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Sulfonamides / Carbamates / Hepacivirus / Hepatitis C, Chronic / Macrocyclic Compounds / Sofosbuvir / Heterocyclic Compounds, 4 or More Rings Limits: Humans Language: En Journal: Z Gastroenterol Year: 2020 Type: Article Affiliation country: Germany