MSD Announces Results from its Pivotal Phase III C-EDGE Programme and C-SURFER Trial
MSD has announced the first presentation of data from the C-SURFER trial, the first to investigate an all-oral, once-daily, Ribavirin-Free Hepatitis C treatment regimen of grazoprevir (100 mg) and elbasvir (50 mg) in treatment-naïve and treatment-experienced patients infected with chronic hepatitis C virus (HCV) genotype 1 and advanced chronic kidney disease (CKD), demonstrating sustained virologic response (SVR) 12 rates of 99%.
In addition, results from the C-EDGE clinical trial programme were announced, including data sets evaluating treatment-naïve, treatment-experienced and HIV co-infected patients with chronic hepatitis C virus genotypes 1, 4 or 6 Infection, demonstrating SVR 12 rates of 92–97% These data were presented at The International Liver Congress 2015 – the 50th annual congress of the European Association for the Study of the Liver.
Dr Kosh Agarwal, Consultant Hepatologist and Transplant Physician at the Institute of Liver Studies, King's College Hospital, stated: “Data from the C-SURFER and C-EDGE trials are extremely encouraging given they provide well-tolerated treatment options for 'more difficult to treat patient populations', such as cirrhotics. Specifically, those patients with co-morbidities, such as CKD, demonstrate high efficacy and favourable tolerability within a well conducted trial design.”
The C-SURFER phase II/III clinical trial is evaluating patients infected with chronic HCV genotype 1 with advanced CKD stages 4 and 5 with or without liver cirrhosis, including treatment-naïve patients and patients who failed prior pegylated interferon HCV therapy. Following 12 weeks of immediate treatment with grazoprevir and elbasvir, in the modified full analysis set‡, 99% of patients receiving grazoprevir plus elbasvir achieved a sustained virologic response 12 weeks after completion of treatment (SVR12).
Dr Kosh Agarwal continued: “At present, there is limited treatment options for patients with advanced CKD including those on haemodialysis. The initial C-SURFER data demonstrates high cure rates without the need for ribavirin and interferon and favourable tolerability. This combination could improve patient care and access to renal transplantation.”
Data sets from the ongoing C-EDGE Phase III clinical trial programme include treatment-naïve, treatment-experienced and HIV co-infected patients with chronic hepatitis C virus genotypes 1, 4 or 6 Infection. Patients in both the HCV infected treatment-naïve (C-EDGE TN) and HIV/HCV co-infected treatment-naïve (C-EDGE CO-INFXN) trials treated for 12 weeks achieved rates of sustained virologic response 12 weeks after the completion of treatment (SVR12) of 95%. In addition, HCV infected treatment-experienced patients (C-EDGE TE) treated with or without ribavirin (RBV) for 12 weeks achieved SVR12 rates of 94% and 92%, respectively, and those treated for 16 weeks achieved SVR12 rates of 97% and 92%, respectively.
Further, patients with cirrhosis in C-EDGE TN and C-EDGE CO-INFXN trials treated for 12 weeks achieved SVR12 rates of 97 percent and 100 percent respectively.2,3 In addition, HCV infected treatment-experienced patients (C-EDGE TE) with cirrhosis treated with or without ribavirin (RBV) for 12 weeks achieved SVR12 rates of 89%, respectively, and those treated for 16 weeks achieved SVR12 rates of 92& and 100%, respectively.
Dr Mark Toms, Medical Director, MSD UK, commented: “The data from the C-SURFER trial and C-EDGE programme show that we are progressing towards being able to achieve our ultimate goal: helping to eliminate hepatitis C. Having demonstrated consistently high rates of SVR12 in a diverse population of patients infected with chronic HCV, including the more difficult to treat patients with co-morbidities such as advanced chronic kidney disease, physicians could hopefully soon have another treatment option in their armamentarium. This is great news for the estimated 214,000 people in the UK living with hepatitis C, many of which remain undiagnosed.”
Related News
-
News CPHI Podcast Series: The power of proteins in antibody drug development
In the latest episode of the CPHI Podcast Series, Lucy Chard is joined by Thomas Cornell from Abzena to discuss protein engineering for drug design and development. -
News Amgen sues Samsung biologics unit over biosimilar for bone disease
Samsung Bioepis, the biologics unit of Samsung, has been issued a lawsuit brought forth by Amgen over proposed biosimilars of Amgen’s bone drugs Prolia and Xgeva. -
News CPHI Podcast Series: Why we need to consider women in clinical trials
The latest episode of the CPHI Podcast Series with Lucy Chard covers women's health, specifically women's representation in clinical trials, the associated bias, and the impacts on health for this population. -
News US FDA does not approve MDMA therapy for PTSD, requests more data
The MDMA-based therapeutic developed by Lykos Therapeutics, a California-based Public Benefit Corporation (PBC), has been reviewed and unapproved by the US FDA. The regulator has requested additional phase III trial data for further safety and efficacy... -
News Novartis and Viatris latest facing lawsuit over HeLa cell misuse
Global pharmaceutical companies Novartis and Viatris are the latest hit with a lawsuit claim pertaining to alleged misuse of the ‘HeLa’ cell line from the estate of woman whose cancerous tissue cells were taken without consent. -
News Sanofi invests billions into Frankfurt insulin production site
French pharmaceutical company Sanofi have announced an investment of EUR1.3 billion at their existing BioCampus site in Frankfurt am Main for the expansion of insulin production. -
News Novel oral Type 1 diabetes drug gains US FDA IND designation
A University of Alabama at Birmingham startup has gained FDA clearance for Investigational New Drug clinical trials for an oral Type 1 diabetes drug, a milestone for diabetes treatment. -
News A Day in the Life of a Vice President in R&D & Engineering
In the Day in the Life of Series, we've already had the chance to get to know a range of people in various roles in the pharma industry. In the latest interview we get a glimpse into the R&D side of things from Jennifer Sorrells, Vice Presiden...
Position your company at the heart of the global Pharma industry with a CPHI Online membership
-
Your products and solutions visible to thousands of visitors within the largest Pharma marketplace
-
Generate high-quality, engaged leads for your business, all year round
-
Promote your business as the industry’s thought-leader by hosting your reports, brochures and videos within your profile
-
Your company’s profile boosted at all participating CPHI events
-
An easy-to-use platform with a detailed dashboard showing your leads and performance