Z
Ziad Younes
Publications - 54
Citations - 5265
Ziad Younes is an academic researcher. The author has contributed to research in topics: Ribavirin & Sofosbuvir. The author has an hindex of 22, co-authored 48 publications receiving 4375 citations.
Papers
More filters
Journal ArticleDOI
Ledipasvir and Sofosbuvir for Previously Treated HCV Genotype 1 Infection
Nezam H. Afdhal,K. Rajender Reddy,David R. Nelson,Eric Lawitz,Stuart C. Gordon,Eugene R. Schiff,Ronald Nahass,Reem Ghalib,Norman Gitlin,Robert Herring,Jacob Lalezari,Ziad Younes,Paul J. Pockros,Adrian M. Di Bisceglie,Sanjeev Arora,G. Mani Subramanian,Yanni Zhu,Hadas Dvory-Sobol,Jenny C. Yang,Phillip S. Pang,William T. Symonds,John G. McHutchison,Andrew J. Muir,Mark S. Sulkowski,Paul Y. Kwo +24 more
TL;DR: Treatment with a once-daily, single-tablet regimen of ledipasvir and sofosbuvir resulted in high rates of sustained virologic response among patients with HCV genotype 1 infection who had not had a sustained virologyic response to prior interferon-based treatment.
Journal ArticleDOI
ABT-450/r–Ombitasvir and Dasabuvir with or without Ribavirin for HCV
Peter Ferenci,David E. Bernstein,Jacob Lalezari,Daniel E. Cohen,Yan Luo,Curtis Cooper,Edward Tam,Rui Tato Marinho,Naoky Tsai,A. Nyberg,Terry Box,Ziad Younes,Pedram Enayati,Sinikka Green,Yaacov Baruch,Bal R. Bhandari,Florin Alexandru Caruntu,Thomas Sepe,Vladimir Chulanov,Ewa Janczewska,Giuliano Rizzardini,J. Gervain,Ramon Planas,Christophe Moreno,Tarek Hassanein,Wangang Xie,M. King,Thomas Podsadecki,K. Rajender Reddy +28 more
TL;DR: Twelve weeks of treatment with ABT-450/r-ombitasvir and dasabuvir without ribavirin was associated with high rates of sustained virologic response among previously untreated patients with HCV genotype 1 infection.
Journal ArticleDOI
All-Oral 12-Week Treatment With Daclatasvir Plus Sofosbuvir in Patients With Hepatitis C Virus Genotype 3 Infection: ALLY-3 Phase III Study
David R. Nelson,James N. Cooper,Jacob Lalezari,Eric Lawitz,Paul J. Pockros,Norman Gitlin,B. Freilich,Ziad Younes,William Harlan,Reem Ghalib,Godson Oguchi,Paul J. Thuluvath,Grisell Ortiz-Lasanta,Mordechai Rabinovitz,David E. Bernstein,Michael J. Bennett,Trevor Hawkins,Natarajan Ravendhran,Aasim Sheikh,Peter Varunok,Kris V. Kowdley,Delphine Hennicken,Fiona McPhee,Khurram Rana,Eric Hughes +24 more
TL;DR: A 12‐week regimen of DCV plus SOF achieved SVR12 in 96% of patients with genotype 3 infection without cirrhosis and was well tolerated; there were no adverse events leading to discontinuation and only 1 serious AE on‐treatment, which was unrelated to study medications.
Journal ArticleDOI
Sofosbuvir, velpatasvir, and voxilaprevir for previously treated HCV infection
Marc Bourlière,Stuart C. Gordon,Steven L. Flamm,Curtis Cooper,Alnoor Ramji,Myron J. Tong,Natarajan Ravendhran,John M. Vierling,Tram T. Tran,S. Pianko,Meena B. Bansal,Victor de Ledinghen,Robert H. Hyland,Luisa M. Stamm,Hadas Dvory-Sobol,Evguenia S. Svarovskaia,Jie Zhang,K.C. Huang,G. Mani Subramanian,Diana M. Brainard,John G. McHutchison,Elizabeth C. Verna,Peter Buggisch,Charles S. Landis,Ziad Younes,Michael P. Curry,Simone I. Strasser,Eugene R. Schiff,K. Rajender Reddy,Michael P. Manns,Kris V. Kowdley,Stefan Zeuzem +31 more
TL;DR: Sofosbuvir‐velpatasvir‐voxilaprevir taken for 12 weeks provided high rates of sustained virologic response among patients across HCV genotypes in whom treatment with a DAA regimen had previously failed.
Journal ArticleDOI
Selonsertib for patients with bridging fibrosis or compensated cirrhosis due to NASH: Results from randomized phase III STELLAR trials
Stephen A. Harrison,Vincent Wai-Sun Wong,Takeshi Okanoue,Natalie Bzowej,Raj Vuppalanchi,Ziad Younes,Anita Kohli,Shiv Kumar Sarin,Stephen H. Caldwell,Naim Alkhouri,Mitchell L. Shiffman,Marianne Camargo,Georgia Li,Kathryn Kersey,Catherine Jia,Yanni Zhu,C. Stephen Djedjos,G. Mani Subramanian,Robert P. Myers,Nadege Gunn,Aasim Sheikh,Quentin M. Anstee,Manuel Romero-Gómez,Michael Trauner,Zachary Goodman,Eric Lawitz,Zobair M. Younossi,Stellar,Stellar Investigators +28 more
TL;DR: Although selonsertib led to dose-dependent reductions in hepatic phospho-p38 expression indicative of pharmacodynamic activity, it had no significant effect on liver biochemistry, NITs, progression to cirrhosis, or adjudicated clinical events.