EASL 2015: Gilead Triple Combination Cures Easy-To-Treat Hepatitis C Patients in 6 Weeks

A 6-week regimen of sofosbuvir (Sovaldi) plus 2 experimental direct-acting antivirals being developed by Gilead Sciences cured more than 90% of previously untreated people with genotype 1 hepatitis C virus and no liver cirrhosis, according to a poster presentation at the European Association for the Study of the Liver (EASL) 50th International Liver Congress last month in Vienna. A 4-week regimen was not effective for any group, however, and 6 weeks appears inadequate for harder-to-treat patients. Other studies showed that the new drugs -- GS-5816 (velpatasvir) and GS-9857 -- are also active against other HCV genotypes.

Now that interferon-free direct-acting antiviral (DAA) regimens taken for 12 weeks can cure most people with HCV genotype 1, researchers are working to develop new drugs that work against multiple HCV genotypes (known as "pangenotypic") and that can produce sustained viral suppression with a shorter duration of treatment, which would be more convenient for patients and could potentially lower costs.

Edward Gane from Auckland Clinical Studies in New Zealand and colleagues tested a 3-drug regimen consisting of Gilead's nucleotide HCV NS5B polymerase inhibitor sofosbuvir, the pan-genotypic NS5A inhibitor GS-5816, and the pan-genotypic NS3/4A HCV protease inhibitor GS-9857 taken for 4 or 6 weeks. Combining drugs that attack HCV at 3 different steps of its lifecycle may enable shorter treatment, the researchers hypothesized.

In preclinical and early clinical research presented in posters at the International Liver Congress (abstracts P0861, P0899, P0901), GS-9857 demonstrated potent antiviral activity against HCV genotypes 1-6, an improved resistance profile compared to older HCV protease inhibitors, and good pharmacokinetics and oral bioavailability. Further along in the pipeline, a coformulation of sofosbuvir and GS-5816 has shown promising efficacy in patients with all HCV genotypes and is now being evaluated in the Phase 3 ASTRAL trials (abstract P1332).

This open-label Phase 2 study enrolled 75 participants with HCV genotype 1, stratified according to prior treatment experience and presence or absence of liver cirrhosis. A majority were men, 79% had harder to treat HCV subtype 1a, and 68% had unfavorable IL28B gene variants.

Previously untreated participants without cirrhosis were randomly assigned to receive sofosbuvir/GS-5816 plus GS-9857 for 4 or 6 weeks. Treatment-naive patients with cirrhosis, and treatment-experienced patients (including 17% with cirrhosis) who were not previously cured with interferon-free regimens containing at least 2 DAAs, all received the triple regimen for 6 weeks.

Results

• Using the 6-week regimen, 93% of treatment-naive participants without cirrhosis achieved sustained virological response, or continued undetectable HCV RNA (<15 IU/mL) at 12 weeks after completing therapy (SVR12).
• The SVR12 rate was 87% for treatment-naive patients with cirrhosis, but fell to 67% for treatment-experienced participants.
• Within the treatment-experienced group, cure rates were 68% for people without cirrhosis and 60% for cirrhotics, but the latter subgroup included only 5 patients.
• The 4-week treatment duration did not perform as well: among the 15 treatment-naive non-cirrhotic patients assigned to this regimen, the SVR12 rate was only 27%.
• In all cases, failure to achieve SVR12 was due to relapse after the end of treatment.
• Younger age and lower HCV viral load at baseline were the only factors that predicted SVR12 in a univariate analysis of the treatment-experienced patients.
• A pharmacokinetic substudy found that GS-5816 and GS-9857 drugs levels in the body were similar in people who did and did not achieve sustained response.
• The cure rate was somewhat higher for people who did not have pre-existing HCV NS3 or NS5A resistance-associated variants (RAVs) at baseline compared to patients with these mutations (approximately 60% vs 40%); only 1 person had evidence of NS5B resistance.
• RAVs were rarely observed at the time of relapse, and no one showed resistance to multiple DAA classes.
• Treatment with the triple regimen was generally safe and well-tolerated.
• There were no serious adverse events or drug discontinuations for this reason. The most common side effects were nausea (25%), headache (24%), and fatigue (16%); 4 people (5%) experienced transient, asymptomatic lipase elevations.

Treatment with sofosbuvir/GS-5816 plus GS-9857 for 6 weeks "was highly effective in treatment-naive genotype 1 patients without cirrhosis," but "shortening treatment duration to 4 weeks was associated with a higher relapse rate," the researchers concluded. Treatment-experienced patients and those with cirrhosis "may benefit from treatment for [longer than] 6 weeks."

Recent mathematical modeling research has suggested that 4 weeks of therapy does not lower viral load enough to achieve sustained response even when combining 3 classes of direct-acting antivirals.

Ongoing phase 2 studies are now testing sofosbuvir/GS-5816 plus GS-9857 for treatment durations of 6, 8, and 12 weeks in treatment-naive and treatment-experienced cirrhotic and non-cirrhotic patients with HCV genotypes 1 through 6 -- including hardest-to-treat genotype 3.

5/6/15

References

EJ Gane, RH Hyland, Y Ying, et al. Safety and Efficacy of Short-duration Treatment
with GS-9857 Combined with Sofosbuvir/GS-5816 in Treatment-naive and DAA-experienced Genotype 1 Patients with and without Cirrhosis. 2015 International Liver Congress: 50th Annual Meeting of the European Association for the Study of the Liver (EASL). Vienna, April 22-26, 2015. Abstract LP03.

B Kirby, J Yang, C Yang, et al. Evaluation of the Pan-Genotypic HCV NS3/4A Protease Inhibitor GS-9857 in Healthy Volunteers. 2015 International Liver Congress: 50th Annual Meeting of the European Association for the Study of the Liver (EASL). Vienna, April 22-26, 2015. Abstract P0861.

JG Taylor, T Appleby, O Barauskas, et al. Preclinical Profile of the Pan-genotypic HCV NS3/4A Protease Inhibitor GS-9857. 2015 International Liver Congress: 50th Annual Meeting of the European Association for the Study of the Liver (EASL). Vienna, April 22-26, 2015. Abstract P0899.

M Rodriguez-Torres, S Glass, J Hill, et al. The Pan-genotypic NS3/4A Protease Inhibitor GS-9857 Demonstrates Potent Antiviral Activity in Patients Infected with HCV Genotype 1, 2, 3 or 4 in a 
3-day Monotherapy Study. 2015 International Liver Congress: 50th Annual Meeting of the European Association for the Study of the Liver (EASL). Vienna, April 22-26, 2015. Abstract P0901.

T Asselah, M Charlton, J Feld, et al. The ASTRAL Studies: Evaluation of SOF/GS-5816 Single-Tablet Regimen for the Treatment of Genotype 1-6 HCV Infection. 2015 International Liver Congress: 50th Annual Meeting of the European Association for the Study of the Liver (EASL). Vienna, April 22-26, 2015. Abstract P1332.

Other Source

Gilead Sciences. Gilead Announces Data for Investigational, All-Oral, Pan-Genotypic Three-Drug Regimen of Sofosbuvir, GS-5816 and GS-9857 for Chronic Hepatitis C. Press release. April 23, 2015.