Product logins

Find logins to all Clarivate products below.


The Golden Age of Interferon-Free HCV Therapies | Physician & Payer Forum | US | 2015

How Will Healthcare Reform and Payer-Led Cost-Containment Strategies Impact U.S. Prescribing?

The market opportunity for hepatitis C virus (HCV) features a large prevalent population, a significant proportion of which is at risk of advancing liver disease. The primary goal of HCV treatment is to completely eliminate the virus from the patient’s body and thereby reduce or halt the progression of liver fibrosis, preventing further complications, such as cirrhosis and hepatocellular carcinoma. Previous treatment strategies for HCV included the prescribing of suboptimal interferon (IFN)-based therapies (Roche’s Pegasys or Merck’s PegIntron), which were associated with significant tolerability issues, efficacy limitations, and long treatment durations. The HCV treatment landscape in the United States has been dramatically altered by the approval of novel antiviral therapies, including Gilead’s Sovaldi (sofosbuvir) and Harvoni (sofosbuvir/ledipasvir), Janssen’s Olysio (simeprevir), and AbbVie’s Viekira Pak (paritaprevir/ombitasvir/ritonavir plus dasabuvir), ushering in the era of IFN-free therapy for HCV. These therapies are typically highly efficacious and well tolerated, making it difficult for pharmaceutical companies to differentiate their products from competitors. An important battleground in the future will be duration of treatment, where genotype-1 market leader Harvoni holds the potential to reduce treatment duration to 8 weeks from the current standard of 12-24 weeks for genotype-1 patients. In addition, pan-genotypic activity and elimination of ribavirin (Roche’s Copegus; Merck’s Rebetol; generics) from treatment regimens represent key unmet needs in the HCV space. Marketers of HCV therapies also face an increasingly competitive landscape and maneuver to secure formulary inclusion and preferred status through exclusive deals, rebates, and discounts. U.S. payers and prescribers are challenged with incorporating these highly desirable but costly new therapies into medical practice.

Related Market Assessment Reports

Report
Asthma – Current Treatment – Treatment Algorithms: Claims Data Analysis – Pediatric Asthma (US)
Pediatric asthma is treated using two types of pharmacotherapies: rescue therapy for acute symptoms via bronchodilation (e.g., a SABA such as Teva’s ProAir HFA) and maintenance therapy to prevent…
Report
Acute Coronary Syndrome – Unmet Need – Unmet Need – Acute Coronary Syndrome: Secondary Prevention, on Top of Statin Treatment (US/EU)
This report covers the 12-month post-hospital management of secondary prevention in ACS patients. Reducing cardiovascular (CV) residual risk and achieving guideline-recommended LDL-C targets…
Report
Beta Thalassemia – Landscape & Forecast – Niche & Rare Disease Landscape & Forecast (US/EU5)
Beta thalassemia (BT) is a rare genetic disorder characterized by the reduced production of hemoglobin. BT minor is caused by a mutation in one hemoglobin beta (HBB) gene, and transfusion-dependent…
Report
Multiple Sclerosis – Unmet Need – Unmet Need – Multiple Sclerosis: Nonrelapsing Secondary-Progressive Multiple Sclerosis (US/EU)
No treatments are approved for nonrelapsing secondary-progressive multiple sclerosis (nrSP-MS), an MS disease course in which physical disability accumulates in the absence of superimposed relapses…
Report
Osteoarthritic Pain – Current Treatment – Treatment Algorithms: Claims Data Analysis – Osteoarthritic Pain (US)
Osteoarthritic (OA) pain affects more than 30 million people in the United States, and the aging population and rising obesity rates are expected to drive further increases. Current treatments,…