On 9 November the US Food and Drug Administration (FDA) approved Heplisav-B, a new vaccine that provides protection against all known subtypes of hepatitis B virus (HBV) with two rather than three doses, which is expected to reduce the number of people who do not complete the vaccine series.
In related news, the American College of Physicians (ACP) and the US Centers for Disease Control and Prevention (CDC) released new guidelines for hepatitis B screening, vaccination and care.
Hepatitis B is a blood-borne disease of the liver. In the US and Europe, it is commonly transmitted through sharing needles to inject drugs or sexual contact. In parts of Asia and Africa, it is endemic and often transmitted from mother to child.
Most people infected with HBV as adults are able to clear the virus naturally and only about 10% develop chronic infection; however, among those infected as infants or young children, around 90% develop chronic infection. Over years or decades, chronic HBV infection can cause severe liver damage including cirrhosis and hepatocellular carcinoma, a type of liver cancer. Hepatitis B can be treated with antiviral drugs but it is seldom cured. The HBV vaccine is now included as a routine infant vaccination in the UK, the US and many other countries.
Heplisav-B, developed by Dynavax Technologies, combines hepatitis B surface antigen (HBsAg) with a toll-like receptor 9 (TLR-9) agonist as an adjuvant to enhance the immune response. The new vaccine is indicated for people aged 18 and older. It is given as two doses administered within one month. It is expected to become available during the first quarter of 2018.
Heplisav-B is the first new HBV vaccine to be approved in the US in more than 25 years. The existing widely used vaccines, GlaxoSmithKline's Engerix B and Merck's Recombivax HB, require three doses given over the course of six months. Experts estimate that nearly half of people who get an initial dose do not complete the full series of three jabs. A combination HBV and hepatitis A vaccine (Twinrix) is also available.
Approval of Heplisav-B was based on data from three phase 3 clinical trials, which together enrolled nearly 10,000 participants, comparing two doses of Heplisav-B versus three doses of Engerix-B. In the largest study, Heplisav-B offered significantly greater protection than Engerix-B (95 vs 81%, respectively). People with diabetes are more susceptible to hepatitis B, and Heplisav-B also worked better than Engerix-B in people with diabetes (90 vs 65%, respectively).
Heplisav-B was generally safe and well tolerated. Across the three trials, the most common adverse events in both the Heplisav-B and Engerix-B arms were injection site pain (23 to 39%), fatigue (11 to 17%) and headache (8 to 17%).
This month's approval comes after two previous rejections as the FDA sought more information on the vaccine's safety and asked for details about post-marketing studies. In the pivotal trials, deaths and serious cardiovascular events such as heart attacks were more common among people who received Heplisav-B, but the overall number of these events was small. The FDA briefing document on Heplisav-B concluded that these findings were likely due to random variation. In July an FDA advisory committee voted 12-1 in favour of the vaccine's safety, with three abstentions. Post-marketing studies focused on cardiovascular events and immune-mediated events will be conducted at Kaiser Permanente Northern California.
"Prevention of hepatitis B in adults through vaccination is more important than ever given the increase in the rate of infections," Prof William Schaffner of Vanderbilt University Medical Center said in a Dynavax press release. "Too many at-risk adults remain unprotected against this virus. A two-dose schedule with higher rates of protection, along with other strategies, may help us move closer to the goal of eliminating hepatitis B as a public health problem in the United States."