Treatment of hepatitis delta virus infection
Methods of reducing hepatitis delta virus (HDV) viral loads in a patient are provided. In some embodiments, the method comprises treating the patient with lonafarnib-ritonavir co-therapy. In some embodiments, the method further comprises treating the patient with an interferon.
1. A method of reducing hepatitis delta virus (HDV) viral load in a human patient with an HDV infection, comprising treating the patient with lonafarnib-ritonavir co-therapy.
2. The method of claim 1 , wherein the co-therapy comprises oral administration of lonafarnib at a total daily dose in the range of 50 mg to 150 mg and oral administration of ritonavir at a total daily dose in the range of 100 mg to 200 mg.
3. The method of claim 1 , wherein the patient is treated with lonafarnib-ritonavir co-therapy for at least 60 days.
4. The method of claim 2 , wherein the lonafarnib is administered at a dose of 25 mg BID and the ritonavir is administered at a dose of 100 mg BID.
5. The method of claim 2 , wherein the total daily dose of lonafarnib is 100 mg.
6. The method of claim 5 , wherein the lonafarnib is administered a dose of 50 mg BID and the ritonavir is administered at a dose of 100 mg BID.
7. The method of claim 1 , wherein the lonafarnib and the ritonavir are administered together in a single unit dose form.
8. The method of claim 1 , wherein the patient is treated for at least 24 weeks and the treatment results in normalization of the patient's alanine aminotransferase (ALT) level.
9. The method of claim 1 , wherein the treatment results in a hepatitis flare.
10. The method of claim 1 , further comprising administering interferon to the patient.
11. The method of claim 10 , wherein the interferon is interferon alpha or interferon lambda.
12. The method of claim 11 , wherein the interferon is pegylated interferon alpha-2a or pegylated interferon lambda-1a.
13. The method of claim 12 , wherein the interferon is administered weekly at a dose of 120 micrograms per week or 180 micrograms per week.
14. The method of claim 1 , wherein the lonafarnib-ritonavir co-therapy comprises administering the lonafarnib BID at a first dose for a first treatment period and then administering lonafarnib at a second dose for a second treatment period, wherein the second dose is lower than the first dose.
15. The method of claim 14 , wherein the lonafarnib is administered at a first dose of 50 mg BID for the first treatment period and at a second dose of 25 mg BID for the second treatment period.
16. The method of claim 1 , wherein the lonafarnib and the ritonavir are administered as separate unit dose forms at about the same time.
17. A method of treating a human patient having a hepatitis delta virus (HDV) infection, the method comprising administering lonafarnib-ritonavir co-therapy to the patient, wherein the lonafarnib and the ritonavir are administered as separate unit dose forms, and wherein (i) the lonafarnib is administered a dose of 50 mg BID and the ritonavir is administered at a dose of 100 mg BID, or (ii) the lonafarnib is administered at a dose of 25 mg BID and the ritonavir is administered at a dose of 100 mg BID.
18. A method of treating a human patient having a hepatitis delta virus (HDV) infection, the method comprising administering lonafarnib-ritonavir co-therapy to the patient, wherein the lonafarnib and the ritonavir are administered together in a single unit dose form, and wherein (i) the lonafarnib is administered a dose of 50 mg BID and the ritonavir is administered at a dose of 100 mg BID, or (ii) the lonafarnib is administered at a dose of 25 mg BID and the ritonavir is administered at a dose of 100 mg BID.