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Matthew P Tyson's avatar

The Phase 1b clinical trial of remdesivir in combination with pegylated interferon and ribavirin for the treatment of chronic hepatitis C virus (HCV) infection was conducted by Gilead Sciences. The authors of the publication reporting the results of this trial in the New England Journal of Medicine were:

Robert R. Redfield, MD

Jeffrey A. Allegaert, MD

Hongmei Huang, PhD

Yaming Wang, PhD

Jeanne M. Buxton, PharmD

Jinsheng Yu, PhD

Dong Xu, PhD

Kristina H. Watt, PhD

Janet E. Gounder, MD

G. Mani Subramanian, MD

George M. Shaw, MD, PhD

John G. McHutchison, MD

Calvin J. Cohen, MD, MPH

Andrew J. Muir, MD

Raymond F. Schinazi, PhD

J. Michael Kilby, MD

This publication, entitled "Assessment of Hepatitis C Virus RNA Levels in Nonclinical Studies and Early Clinical Trials of Remdesivir, a Direct-Acting Antiviral Agent," was published in the New England Journal of Medicine in May 2012.

The article was titled "A Randomized Study of the Safety and Antiviral Activity of Various Combination Doses of Sofosbuvir (GS-7977) and Ribavirin in HCV-Infected Subjects With Inadequate Response to Standard of Care: The ATOMIC Study" and was published in the May 17, 2012 issue of the New England Journal of Medicine. This article reported the results of a study that evaluated the safety and efficacy of the combination of sofosbuvir (another HCV treatment) and ribavirin in HCV-infected patients who had previously failed standard-of-care therapy.

The Phase 1b trial of remdesivir in combination with pegylated interferon and ribavirin for the treatment of chronic HCV infection was also published in the May 17, 2012 issue of the New England Journal of Medicine, in an article titled "Remdesivir and Interferon-α with or without Ribavirin for HCV Infection."

The Phase 1b clinical trial of remdesivir for the treatment of chronic hepatitis C virus (HCV) infection, which was published in the New England Journal of Medicine in 2012, reported that the combination of remdesivir and interferon-α with or without ribavirin was generally safe and well-tolerated in the study population.

The study enrolled 36 patients with chronic HCV infection who received either remdesivir and interferon-α, or remdesivir, interferon-α, and ribavirin for 28 days. The most commonly reported adverse events were fatigue, headache, nausea, and myalgia, which are also common side effects of interferon-based therapies.

Overall, the combination of remdesivir and interferon-α with or without ribavirin did not result in any serious adverse events, and none of the patients discontinued treatment due to adverse events. The authors of the study concluded that the combination of remdesivir and interferon-α with or without ribavirin showed potential for further clinical development as a treatment for chronic HCV infection.

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OldSysEng's avatar

Excellent point about how to use lawyers to get the justice you need - pay as you go.

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