Gilead Sciences, Inc. has announced that two Phase 3 clinical trials (Studies 108 and 110) evaluating investigational use of once-daily tenofovir alafenamide (TAF) 25 mg in treatment-naïve and treatment-experienced adults with HBeAg-negative and HBeAg-positive chronic hepatitis B virus (HBV) infection met their primary objectives. The studies demonstrated that TAF was non-inferior to Gilead's Viread® (tenofovir disoproxil fumarate, TDF) based on the percentage of patients with HBV DNA levels below 29 IU/mL at 48 weeks of therapy. In addition, TAF demonstrated improved renal and bone laboratory safety parameters compared to Viread.
"An estimated 350 million people are living with chronic hepatitis B worldwide, and Viread is an effective treatment option for those appropriate to receive therapy," said Norbert Bischofberger, PhD, Executive Vice President, Research and Development and Chief Scientific Officer, Gilead Sciences. "We are pleased that the TAF Phase 3 study results reflect high efficacy and improved renal and bone safety parameters similar to those seen in clinical studies evaluating TAF-based regimens for HIV. Like HIV, HBV is a chronic condition that requires prolonged therapy and we look forward to the opportunity to offer patients an improved option that has the potential to advance the long-term treatment of HBV."
In Study 108, evaluating HBeAg-negative patients, 94.0 percent (n=268/285) of patients receiving TAF and 92.9 percent (n=130/140; CI -3.6 percent to +7.2 percent, p=0.47) of patients receiving Viread achieved HBV DNA below 29 IU/mL at week 48. In Study 110, evaluating HBeAg-positive patients, 63.9 percent (n=371/581) of TAF patients and 66.8 percent (n=195/292; CI -9.8 percent to +2.6 percent, p=0.25) of Viread patients achieved HBV DNA below 29 IU/mL at week 48. Two criteria were used to evaluate normalization of serum ALT levels: a central laboratory cut-off value and the American Association for the Study of Liver Diseases (AASLD) criteria. In both studies, treatment with TAF showed a statistically significant increase in ALT normalization relative to the Viread arms when using the AASLD criteria. The ALT normalization was not statistically significant using the central laboratory cut-off value, which defines normalization at a higher ALT level. Discontinuations due to adverse events were uncommon in both treatment arms (0.7 percent (n=2) for TAF vs. 0.7 percent (n=1) for Viread in Study 108, and 1.0 percent (n=6) for TAF vs. 1.0 percent (n=3) for Viread in Study 110). The most commonly reported adverse events in both studies included headache, upper respiratory tract infection, nasopharyngitis and cough, and occurred at similar rates in patients receiving either TAF or Viread.
Changes in bone and renal laboratory parameters favored the TAF regimen. In both studies, patients receiving TAF experienced a significantly smaller mean percentage decrease from baseline in hip and spine bone mineral density at week 48 (p
Based on the results of Studies 108 and 110, Gilead plans to submit regulatory applications for TAF for chronic HBV in the United States and the European Union in the first quarter of 2016. Gilead also plans to submit data from both studies for presentation to a scientific conference in 2016.
About Studies 108 and 110
Studies 108 and 110 are randomized, double-blind, 96-week clinical trials among 1,298 treatment-naïve and treatment-experienced patients with chronic HBV. In Study 108, 425 HBeAg-negative patients were randomized 2:1 to receive TAF (n=285) or Viread (n=140). In Study 110, 873 HBeAg-positive patients were randomized 2:1 to receive TAF (n=581) or Viread (n=292).
The primary efficacy endpoint of the studies is the proportion of subjects with plasma HBV DNA levels below 29 IU/mL. Key secondary endpoints include change from baseline in bone mineral density at the hip and spine at week 48, and change from baseline in serum creatinine at week 48. Other secondary endpoints include ALT normalization and change from baseline in eGFR at week 48.
TAF as a single-agent for chronic HBV is an investigational product and its safety and efficacy have not been established.