FDA Approves Pill for all Hepatitis C Forms

Andy Dean/Getty Images
Andy Dean/Getty Images

The US Food and Drug Administration has approved Gilead Sciences’ combination pill Epclusa, the first to treat all major forms of hepatitis C. This is the latest in a series of drug approvals expected to revolutionize treatment of the disease. As Gilead’s pill can be taken by all hepatitis C sufferers, with and without liver damage, it is expected to be easier to use than five other hepatitis drugs recently approved by the FDA, each of which is tailored to different viral strains or stages of liver disease.

The US company’s two earlier drugs already have successfully replaced an older, less effective treatment that involved a mixture of tablets and injections; however, insurers have balked at the high price. 

At $74,760 for a 12-week course of treatment, or about $890 per pill, Epclusa will cost less than the initial cost of $1,125 per pill for Gilead’s second drug, Harvoni. The company’s first hepatitis C drug, Sovaldi, cost roughly $1,000 per pill.

Since 2014, the FDA has approved hepatitis drugs made by AbbVie, Merck & Co and Bristol-Myers Squibb. In January, the European Medicines Agency (EMA) gave the green light for AbbVie's hepatitis C treatment Viekira Pak to be prescribed for patients with the genotype 1 form of hepatitis C. The drug was approved by the US Food and Drug Administration FDA in December 2014.

Gilead and AbbeVie have recently engaged in price wars as they fought for market share. This, observers said, has help made the hepatitis treatment more affordable. Merck & Co earlier this year won a patent dispute against Gilead over sofosbuir, the active ingredient in Gilead’s Solvadi and Harvoni.

Epclusa combines Sovaldi with a new drug that attacks the virus using a different mechanism. It is designed to be used in combination with ribavirin, an older antiviral drug. The new drug is capable of treating all six genetic subtypes of the virus and curing 95% of patients in three months, according to clinical trial data reviewed by the FDA.

IMS Health calculates that Harvoni was the world’s top-selling prescription drug last year, with Sovaldi ranked eighth.

Whitepaper

Excellence in Pharmaceutical Distribution and The Critical Role of Good Distribution Practice (GDP)
Setting the Standard

Excellence in Pharmaceutical Distribution and The Critical Role of Good Distribution Practice (GDP)

Are you ready to elevate your pharmaceutical operations? Download our exclusive whitepaper and discover how compliance with Good Distribution Practice (GDP) is essential for the safety and integrity of pharmaceuticals.

CHEManager Spotlight

Standardization and Harmonization of Digital Chemical and Pharmaceutical Logistics
Creating Interfaces

Standardization and Harmonization of Digital Chemical and Pharmaceutical Logistics

CHEManager Spotlight is an exclusive event tailored for practitioners and decision-makers in the chemical industry. This part of our event series delves into the latest trends and innovations in logistics to streamline your operations and drive efficiency.

most read

Photo
19.03.2025 • NewsInnovation

Data-Driven Enzyme Immobilization

Inseit, based in Bern, develops biocatalysts for industrial setups using enzyme immobilization and biocomputation. Addressing biotech and sustainability challenges, Inseit was selected for Venture Leaders Biotech and won two Nucleate accelerator prizes.

Photo
27.03.2025 • News

J&J to Invest $55 Billion in US Operations

US healthcare giant Johnson & Johnson (J&J) has unveiled plans to invest over $55 billion in the US over the next four years. This significant investment marks a 25% increase compared to the previous four years, the company said.

Photo
24.01.2025 • News

And the Winners are: Cynio, EnaDyne and Green Li-ion

The CHEManager Innovation Pitch, the start-up promotion initiative of CHEManager and CHEManager International, has given more than 100 start-ups from over 15 countries the opportunity to present their innovative ideas, products and technologies to a broad target group since its launch in 2019.