8 Weeks Versus 12 Weeks of Elbasvir/Grazoprevir in Treatment-naïve CHC With Mild Fibrosis

Kaohsiung Medical University

Status and phase

Completed

Phase 3

Conditions

Hepatitis C, Chronic

Treatments

Drug: Zepatier Oral Product

Study type

Interventional

Funder types

Other

Identifiers

NCT03186365

MISP-55740

Details and patient eligibility

About

Grazoprevir plus elbasvir 12 to 16 weeks is now approved for chronic hepatitis C (CHC) genotype 1, 4, or 6 infection regardless liver disease severity. The current study aims to explore the efficacy and safety of 8-week grazoprevir/elbasvir in HCV-1b patients with mild liver fibrosis

Full description

Grazoprevir, an HCV nonstructural protein 3/4A (NS3/4A) inhibitor 100 mg, plus elbasvir, an HCV NS5A inhibitor 50 mg fixed dose combination, Zepatier, achieved high SVR12 rates of > 95 % in treatment-naïve, experienced cirrhotic and non-cirrhotic patients with genotype 1, 4, or 6 infection. Zepatier, 12 to 16 weeks, was approved for the treatment of HCV genotype 1 and 4 in Taiwan in December, 2016. An SVR rate of 93 % was demonstrated in treatment-naive, non-cirrhotic (F0-F3) GT1b-infected patients who received 8 weeks of grazoprevir/elbasvir with or without ribavirin in the pooled analysis of C-WORTHY (PN035) and C-EDGE treatment-naive (PN060) trials. Furthermore, truncated treatment period of 8-week grazoprevir/elbasvir could achieve an even higher SVR rate at > 98% for naive HCV G1b patients with mild fibrosis (Fibrosis score 0-2). The study aims to evaluate the efficacy of 8-week regimen with grazoprevir/elbasvir on naïve, HCV G1b patients with mild fibrosis by a randomized clinical trial.

Enrollment

82 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Treatment naïve, HCV genotype 1b patients
History of chronic HCV infection > 6 months
Aged at least 20 years
HCV RNA of 10,000 IU/mL or greater
Fibroscan examination < 9.5 Kpa
Negative serum or urine pregnancy test result (sensitivity of 25 mIU or better) for women with childbearing potential within the 24-hour period before the first dose of study drugs
Female patients with childbearing potential must agree to use two reliable forms of effective non-hormonal contraception (i.e., condoms, cervical barriers, intrauterine device, spermicides, or sponge), at least 1 of which must be a physical barrier method, during treatment till end of follow up.
A hormonal contraception (in lieu of non-hormonal) plus a physical barrier method can be used after end of treatment. All men with female partners of childbearing potential must use two reliable forms of effective contraception (combined) during treatment and till end of follow up
Ability to participate and willingness to give written informed consent and to comply with the study restrictions.

Exclusion criteria

Prior experience of IFN or direct antiviral agents (DAA)
Hepatitis B virus or HIV co-infection.
Patients with experience of ascites, esophageal varices, or other evidence of hepatic decompensation, and/or hepatocellular carcinoma.
History of organ transplantation, except cornea transplantation.
Hemoglobulin concentration < 11 mg/dl
Platelet count < 75,000/mm3
Albumin < 3 mg/dL
History of active malignancy within the last 5 years, with the exception of localized or in situ carcinoma (e.g., basal or squamous cell carcinoma of the skin)
Poorly controlled diabetes (Hemoglobin A1c value ≥ 8.5%) and endocrine condition.
Total bilirubin >2 mg/dL, unless subject has a documented history of Gilbert's disease.
Pregnant or lactating women.