Ledipasvir/sofosbuvir

Ledipasvir/sofosbuvir
Combination of
Ledipasvir NS5A inhibitor
Sofosbuvir NS5B (RNA polymerase) inhibitor
Clinical data
Trade names Harvoni, Hepcinat-LP, LediHep
AHFS/Drugs.com entry
Pregnancy
category
  • US: B (No risk in non-human studies)
Routes of
administration
Oral
Legal status
Legal status
Identifiers
ATC code J05AX65 (WHO)

Ledipasvir/sofosbuvir (trade name Harvoni) is a two-drug combination for the treatment of hepatitis C. It is administered as a single daily pill containing 90 mg of the viral NS5A inhibitor ledipasvir and 400 mg of sofosbuvir, a nucleotide inhibitor of the viral RNA polymerase.

Ledipasvir/sofosbuvir was developed by the pharmaceutical company Gilead Sciences and first marketed in October 2014. Taken daily for 8–12 weeks, it provides cure rates of 94% to 99% in people infected with genotype 1 (the most common form of hepatitis C in the U.S. and some European countries), irrespective of the presence or absence of liver cirrhosis or prior unsuccessful treatment. In India, Zydus Cadila launched LediHep brand having the same combination at a very economical price. It has also been evaluated for the treatment of infection with other hepatitis C genotypes, and has shown promising results in genotypes 3 and 4.[1][2][3][4]

In the United States, the average cost of treatment with Harvoni is over $90,000.[5] An increasing number of US patients are using drug tourism to countries like India to buy it for as little as 1% of the US cost.[6][7]

Side effects

Common side effects of Harvoni treatment as per Gilead Sciences clinical studies include but are not limited to:

More severe reactions are connected with allergic reactions to the medications and cardiovascular problems.[8] Harvoni side effects are considered relatively mild compared to older interferon-based treatment.

Interactions

In March 2015, Gilead Sciences e-mailed warnings to health care providers about nine patients that began taking its hepatitis C drugs Harvoni (ledipasvir/sofosbuvir) or Sovaldi (sofosbuvir) along with the heart treatments amiodarone, Bristol-Myers Squibb's daclatasvir, or Johnson & Johnson's simeprevir developed abnormally slow heartbeats and one died of cardiac arrest. Three required a pacemaker to be inserted. Gilead said the combinations aren't recommended and product labels will be updated.[9]

References

External links

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