Overview

This trial is active, not recruiting.

Condition chronic hepatitis c
Treatments ravidasvir hydrochloride, sofosbuvir, ribavirin
Phase phase 2/phase 3
Sponsor Pharco Pharmaceuticals
Start date January 2015
End date January 2016
Trial size 300 participants
Trial identifier NCT02371408, PPI-668-202

Summary

The study will assess the efficacy of PPI-668 (USAN: ravidasvir hydrochloride) in combination with sofosbuvir, with or without ribavirin, in the following Egyptian HCV gt-4 patient populations:

1. Treatment-naïve patients, with and without cirrhosis (Group 1)

2. Previous non-responders to interferon-based therapies, without cirrhosis (Group 2)

3. Previous non-responders to interferon-based therapies, with cirrhosis (Group 3)

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
PPI-668 + sofosbuvir for 12 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
(Experimental)
PPI-668 + sofosbuvir + ribavirin (RBV) for 12 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
ribavirin
1000 mg - 1200 mg per day, weight-based dosing
(Experimental)
PPI-668 + sofosbuvir for 12 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
(Experimental)
PPI-668 + sofosbuvir + ribavirin for 12 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
ribavirin
1000 mg - 1200 mg per day, weight-based dosing
(Experimental)
PPI-668 + sofosbuvir + ribavirin for 12 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
ribavirin
1000 mg - 1200 mg per day, weight-based dosing
(Experimental)
PPI-668 + sofosbuvir + ribavirin for 16 weeks
ravidasvir hydrochloride PPI-668
200 mg
sofosbuvir
400 mg
ribavirin
1000 mg - 1200 mg per day, weight-based dosing

Primary Outcomes

Measure
Proportions of patients who achieve Sustained Virologic Response at 12 weeks post-treatment (SVR12)
time frame: post-treatment week 12

Secondary Outcomes

Measure
Proportions of patients who achieve Sustained Virologic Response at 4 weeks post-treatment (SVR4)
time frame: post-treatment week 4
Proportions of patients who achieve Sustained Virologic Response at 24 weeks post-treatment (SVR 24)
time frame: post-treatment week 24
Proportion of treated study participants prematurely discontinuing study treatment for any reason, proportion prematurely discontinuing treatment for lack of efficacy or for clinical adverse events or laboratory abnormalities
time frame: during treatment and up to 24 weeks post-treatment
Proportion of patients experiencing treatment-emergent adverse events, and proportion of patients experiencing adverse events considered to be probably or possibly related to one or more of the study drugs
time frame: during treatment and up to 24 weeks post-treatment

Eligibility Criteria

Male or female participants from 18 years up to 65 years old.

Inclusion Criteria: 1. Males or females, ≥ 18 years & ≤ 65 years of age. 2. HCV antibody positive, with serum HCV RNA ≥ 10,000 IU/mL, with clinical history compatible with chronic hepatitis C. 3. HCV genotype-4 infection, confirmed at the central study laboratory 4. Body mass index (BMI) between 18 and 35 kg/m2, inclusive. 5. Both male and female patients who have childbearing potential must agree to practice an acceptable method of birth control during the study and for at least 6 months after the cessation of treatment; such contraceptive methods must include at least one barrier method. 6. Patients for Group 1 must be treatment-naïve - i.e., they have never received any antiviral treatment for their HCV infection, including interferon, pegylated interferon, ribavirin, or other regulatory-approved or investigational HCV antiviral therapies. 7. Patients for Groups 2 and 3 must have previously failed treatment with an interferon-based therapy - i.e., interferon or pegylated interferon, with or without ribavirin, with no other previous HCV antiviral therapies. Patients for Group 2 must be non-cirrhotic diagnosed on screening visit by both Fibroscan™ liver stiffness measurement < 12.5 kPa and FIB-4 score < 3.25 if the results of Fibroscan and FIB-4 score are not matching; liver biopsy will be used for detection of cirrhosis. In case that the liver biopsy is not applicable, hepatic imaging or ultrasound reports could be used for determination of cirrhosis. Patients for Group 3 must have underlying cirrhosis diagnosed on screening visit by both Fibroscan liver stiffness measurement > 12.5 kPa and FIB-4 score > 3.25, if the results of Fibroscan and FIB-4 score are not matching liver biopsy will be used for detection of cirrhosis. In case that the liver biopsy is not applicable, hepatic imaging or ultrasound reports could be used for determination of cirrhosis. 8. Willing and able to give informed consent 9. Willing and able to complete all study visits and procedures, including compliance with the requirements and restrictions listed in the consent form. Exclusion Criteria: 1. Mixed genotype or non-typable HCV genotype infection, 2. Positive test for HBsAg or HIV antibody, or IgM antibody to HAV or HEV 3. History of schistosomiasis or positive test for schistosoma surface antigen at Screen. 4. Serum alpha-fetoprotein (AFP) >100ng/ml. Patients with an AFP between 50 and 100ng/ml may be included as long as a liver ultrasound within 3 months of Screening, or at Screening, shows no evidence of potential hepatocellular cancer. 5. History of treatment with any investigational or regulatory-approved direct-acting antiviral (DAA) agent for HCV infection - nucleos(t)ide or non-nucleosidic HCV polymerase inhibitor, HCV protease inhibitor, NS5A inhibitor, or other antiviral agent for HCV infection other than pegylated -interferon and/or ribavirin Previous pegylated interferon and/or ribavirin treatment is allowed for Groups 2 and 3 but prohibited for group 1, as noted above in Inclusion criterion 6) 6. Evidence of a medical condition other than HCV that is contributing to liver disease 7. History of, or clinical signs of, hepatic decompensation or portal hypertension: Variceal bleeding, or documented esophageal or GI varices (at investigator discretion, patients suspected of having esophageal varices should be evaluated by endoscopy, and varices excluded) Ascites by history or on physical examination Documented or suspected hepatic encephalopathy Physical signs of portal hypertension: Clinically significant splenomegaly Spider angiomata History of porto-systemic shunt procedure(s) 8. Uncontrolled diabetes mellitus as evidenced by HgbA1C ≥ 8.5% at Screening. 9. Hemoglobin < 11g/dL for females and < 12 g/dL for males 10. WBC count < 3,500/mm3 OR absolute neutrophil count (ANC) < 1800/mm 11. Platelet count < 75,000/mm3 12. Serum creatinine > 1.3 x ULN OR creatinine clearance (GFR) < 50 mL/minute 13. Serum ALT or AST >10x ULN 14. Serum albumin ≤ 3.2 g/dl 15. Direct serum bilirubin > 2xULN 16. INR > 1.7. 17. History of poorly controlled asthma, with one or more hospitalizations or emergency room visits in the previous 6 months 18. History of any malignancy within the last 5 years (except prostate cancer still within Glisson's capsule or basal cell carcinoma of the skin). 19. History of alcohol abuse as assessed by the investigator within the past 2 years, or an alcohol use pattern that may interfere with the patient's study compliance. Patients must have abstained from alcohol for at least 6 months prior to study start. 20. History of drug abuse as assessed by the investigator within the last 2 years. 21. Pregnancy, including current lactation in female patients, male patients with partners who are pregnant, or female patients intending to become pregnant. 22. Major surgery requiring overnight hospitalization within 3 months prior to Screening 23. Participation in another clinical trial of an investigational drug or device within 6 months prior to Screening 24. Current use or history of use within the preceding 6 months of immunosuppressive or immune-modulating agents, including: azathioprine, systemic corticosteroids (prednisone or prednisone equivalent of more than 10mg/day for more than 10 days), or other immunosuppressive agents. Use of inhaled steroids for mild/moderate asthma and topical steroids for minor skin conditions is allowed. 25. History of solid organ or bone marrow transplantation. 26. History of use of medications associated with QT prolongation concurrently or within the 30 days prior to Screening Visit, including: macrolides, antiarrhythmic agents, azoles, fluoroquinolones, and tricyclic anti-depressants. 27. correction, or a personal or family history of Torsades de Pointe. 28. Cardiac ischemia with history of recurrent angina, clinically symptomatic cardiac abnormalities, or requirement for cardiac pacemaker 29. History of a known allergy to ribavirin (RBV), or any excipient in the investigational product, or history of drug or other allergy that, in the opinion of the investigator, mitigates against study participation

Additional Information

Official title A Phase IIb/IIIa, Randomized Study to Evaluate the Efficacy and Safety of PPI-668 (NS5A Inhibitor) Plus Sofosbuvir, With or Without Ribavirin, in Patients With Chronic Hepatitis C Genotype-4
Principal investigator Gamal Esmat, M.D.
Trial information was received from ClinicalTrials.gov and was last updated in April 2016.
Information provided to ClinicalTrials.gov by Pharco Pharmaceuticals.