
The antiviral drug tenofovir alafenamide (TAF) has been used since 2015 in different combinations for the treatment of HIV and has already been subject to three early benefit assessments for this therapeutic indication by the German Institute for Quality and Efficiency in Health Care (IQWiG).
In January this year, the European Commission granted marketing authorization for US biotech major Gilead Sciences’ (Nasdaq: GILD) Vemlidy (tenofovir alafenamide, TAF) for the treatment of chronic hepatitis B virus (HBV) infection in adults and adolescents. The IQWiG has now examined in a further early benefit assessment whether the drug offers an added benefit for these patients.
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