A Phase 1/2 Study of CF102 in Patients With Chronic Hepatitis C Genotype 1

This is a Phase 1/2, randomized, double-blind, placebo-controlled, dose-escalation study of subjects with chronic hepatitis C genotype 1. Eligible subjects will be assigned in a 3:1 ratio (8 subjects in each cohort) to receive qd or bid treatment for 15 days with oral CF-102 or with placebo. Dose escalation will occur in 2 sequential cohorts.

The decision to continue dosing within a cohort (eg, Subcohort 1a to Subcohort 1b), or to escalate to a new dose level Cohort (eg, Subcohort 1b to Subcohort 2a) will be determined by a blinded independent review of safety data. This review will be conducted by a qualified Safety Review Committee comprising the medical monitor, the consulting toxicologist, and an independent expert clinician.

For the first 2 cohorts, subjects will return to the study center for follow-up assessments on Days 8, 15, and 22. Subjects dosed qd will receive a total of 15 doses of CF-102. Subjects dosed bid will receive a total of 29 doses. The 30th dose has been deleted to accommodate PK sampling on the morning of Day 16, 24 hours after the last dose of CF-102.

For the 3rd cohorts, subjects will return to the study center for follow-up assessments on weeks 2, 4, 8, 12, 16 and 18.

Inclusion criteria

• 18 to 60 years of age
• Body mass index ≤ 30 kg/m2
• Either:

• no evidence of cirrhosis, or liver fibrosis corresponding to Metavir Stages 0 to 31 on a liver biopsy performed within the past 2 years, or
• a score of F0 or F1 on ActiTest-FibroTest performed within the past year.
• Child-Pugh score ≤ 5 at Screening
• Serologic evidence of chronic hepatitis C-infection (anti-HCV in serum)
• HCV plasma RNA ≥ 1 x 105 IU/mL on 2 separate samples obtained during the screening period.
• HCV genotype 1
• The following laboratory values must be documented within the Screening period:

• Hemoglobin > 11.0 g/dL for females and > 12.0 g/dL for males
• Platelet count > 50 x109/L
• Normal serum creatinine
• Aspartic aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 5-fold the upper limit of normal
• International normalized ratio (INR) ≤ 1.3-fold normal
• Serum albumin ≥ 3.6 gm/dL
• Female subjects cannot be pregnant or breastfeeding and must be either postmenopausal, surgically sterile, abstinent, or using 2 proven methods of birth control
• Sexually active male subjects must be practicing acceptable methods of contraception (eg, vasectomy, use of condom plus spermicide, monogamous relationship with a female partner who practices an acceptable method of contraception) during the treatment period
• Negative serum ß-human chorionic gonadotropin (HCG, females of child-bearing potential only)
• Provide informed consent
• Willing to comply with all study requirements

Exclusion criteria

• Positive test at Screening for human immunodeficiency virus
• Uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), angina, myocardial infarction, cerebrovascular accident, coronary/peripheral artery bypass graft surgery, transient ischemic attack, or pulmonary embolism within 3 months prior to initiation of study drug
• History of or ongoing cardiac dysrhythmias requiring treatment, atrial fibrillation of any grade, or persistent prolongation of the corrected QT (QTc) (Fridericia) interval to > 450 msec for males or > 470 msec for females
• Positive results for drugs of abuse at Screening
• Donation or loss of more than 400 mL blood within 2 months prior to anticipated dose administration
• Participation in a clinical study with an investigational drug, biologic, or device within 3 months prior to anticipated dose administration
• Previous exposure to CF102(Cohorts 1 and 2 only)
• Males whose female partner is pregnant
• Serum alpha-feto-protein > 50 ng/mL at screening
• Any severe, acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, may interfere with the informed consent process and/or with compliance with the requirements of the study, or may interfere with the interpretation of study results and, in the investigator's opinion, would make the patient inappropriate for entry into this study.