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Daclatasvir and GS-7977

July 2012

Daclatasvir was the first oral HCV NS5A inhibitor to be developed. GS-7977 is a nuke with activity against NS5B. Both drugs have powerful anti-HCV activity when used separately. In study AI444-040, researchers in the U.S. studied different combinations of both drugs in a randomized clinical trial with HCV-positive people infected with the following genotypes:

  • genotype 1a, 1b, 2, and 3

Researchers recruited participants and assigned them to the following six groups:

Group A

  • 15 participants with genotypes 1a and 1b: all received GS-7977 monotherapy for seven days after which daclatasvir was added; dual therapy continued for 23 weeks

Group B

  • 16 participants with genotypes 2 and 3: all received GS-7977 monotherapy for seven days after which daclatasvir 60 mg once daily was added; dual therapy continued for 23 weeks
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Group C

  • 14 participants with genotypes 1a and 1b: all received immediate dual therapy with daclatasvir and GS-7977, both for 24 weeks

Group D

  • 14 participants with genotypes 2 and 3: all received immediate dual therapy with daclatasvir and GS-7977, both for 24 weeks

Group E

  • 15 participants with genotypes 1a and 1b: all received triple therapy with daclatasvir, GS-7977 and ribavirin (dosed between 1,000 and 1,200 mg/day), all for 24 weeks

Group F

  • 14 participants with genotypes 2 and 3: all received triple therapy with daclatasvir, GS-7977 and ribavirin at 800 mg/day, all for 24 weeks

All participants were monitored for an additional 24 weeks once they stopped experimental therapy.

The average profile of participants upon entering the study was as follows:

  • age -- 53 years
  • 50% men, 50% women
  • HCV viral load -- 4 million IU/ml


Results

The decline in HCV levels was faster among participants who received combination therapy immediately rather than delaying combination therapy. Viral suppression was similar in groups C, D, E and F.

Adding ribavirin did not accelerate the decline of HCV viral load.

After four weeks of experimental therapy, 100% of genotype 1 participants had undetectable levels of HCV. The equivalent figure for genotype 2 and3 participants was 91%.

Two participants stopped returning to the study clinic for unknown reason(s). Their last blood samples at weeks 12 and 24 respectively were undetectable.

One participant had his HCV levels rise after first suppressing them.

Another participant (in group B) had his HCV levels rise but doctors enhanced his therapy with interferon + ribavirin and his viral load returned to suppressed levels.


Safety

No deaths occurred.

Two participants left the study because of adverse events: one case of stroke (group C) and one case of fibromyalgia (group F). Researchers considered both incidents to be unrelated to the study.

Serious adverse events occurred in 10 patients, but only three cases were judged to be related to the study medicines and all occurred when patients accidentally took extra doses of daclastavir or GS-7977.

Adverse events in the study that were not related to the experimental treatments were as follows:

  • anxiety -- 2 participants
  • fracture -- 1 participant
  • lung pain -- 1 participant
  • intestinal inflammation -- 1 participant
  • kidney failure -- 1 participant

No cases of severely elevated liver enzymes occurred.

The most common laboratory abnormality was anemia and this occurred in participants who received ribavirin.

In summary, the all-oral regimen of two new drugs without ribavirin cured 100% of genotype 1 participants and at least 90% of genotype 2 and 3 participants.

These very promising findings require confirmation in a larger study.


Reference

Sulkowski M, Gardiner D, Lawitz E, et al. Potent viral suppression with the all oral combination of daclatasvir (NS5A inhibitor) and GS-7977 (nucleotide NS5B inhibitor), +/- ribavirin, in treatment-naive patients with chronic HCV genotype 1,2 or 3. In: Program and abstracts of the 47th annual meeting of the European Association for the Study of the Liver, 18-22 April 2012, Barcelona, Spain.




This article was provided by Canadian AIDS Treatment Information Exchange. It is a part of the publication TreatmentUpdate. Visit CATIE's Web site to find out more about their activities, publications and services.
 

 

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