Gilead Sciences, Inc. (NASDAQ:GILD) is piling on the phase 3 data for its hepatitis C drug sofosbuvir, announcing two more successful trials for the drug formerly known as GS-7977.
At this point, it looks extremely likely that sofosbuvir will be approved by the FDA. Previous data, released last November, showed the drug worked in patients with genotype 2 or 3 hepatitis C virus. Gilead now has data showing the drug works on genotypes 1 through 6.
Gilead also presented additional data in patients with genotype 2 or 3. In the trial, dubbed Fission, sofosbuvir plus ribavirin only matched the cure rate of ribavirin and Pegasys, but that’s an acceptable result given Pegasys’ side effects. Adverse events observed in greater than 10% of patients — fatigue, headache, nausea, insomnia, and dizziness — all occurred in patients taking Pegasys.
Gilead has one more phase 3 trial, called Fusion, whose results are anticipated later this quarter, and then Gilead will be able to apply for FDA approval. Unless some safety issue crops up, an approval seems all but certain.
Just don’t thnk that sofosbuvir will produce massive sales all on its own. The largest opportunity in the U.S. is in genotype 1 patients, but sales of Incivek continue to fall as patients wait for an all-oral regimen. Remember Gilead only has data combining its drug with Pegasys in that genotype, so don’t expect patients to flock to it just yet.