| Eligibility |
Inclusion Criteria:
1. Before starting the study, an informed consent form (ICF) approved by the
Institutional Review Board (IRB) is obtained from the subject or his/her legal
representative;
2. Male or female, and 18 to 45 years of age inclusive when signing ICF;
3. Body mass index (BMI) in the range of 18.0 to 35.0kg/m2 and body weight = 40 kg at
Screening;
4. Presence of chronic hepatitis C (CHC) as documented below: (1)A positive anti-HCV
antibody test or positive HCV RNA or positive HCV genotyping test at least 6 months
prior to the Baseline/Day 1 visit or, (2) A liver biopsy or FibroTest performed prior
to the Baseline/Day 1 visit with evidence of chronic HCV infection, such as the
presence of fibrosis and/or inflammation;
5. Positive for anti-HCV antibody at Screening;
6. Presence of an HCV RNA level = 1 x 104 IU/mL at Screening as determined by the Central
Laboratory;
7. Presence of genotype 1a, 1b, or 1a/1b combination HCV-infection at Screening as
determined by the Central Laboratory;
8. HCV treatment naïve defined as no prior therapy with any interferon (IFN), ribavirin
(RBV), or other approved or investigational HCV-specific agent;
9. Without (group 1 to 4) or with (group5 to 6) cirrhosis: (1) Without cirrhosis as
defined as any one of the following: (a) Liver biopsy without showing cirrhosis (e.g.,
Metavir score < F4 or Ishak score < 5) within one year prior to Screening or at
Screening. (b) FibroScan showing cirrhosis or results = 12.5 kPa within six months
prior to Screening or at Screening. (2) With cirrhosis as defined as any one of the
following: (a) Liver biopsy showing cirrhosis (e.g., Metavir score = F4 or Ishak score
= 5) within one year prior to Screening or at Screening. (b) FibroScan showing
cirrhosis or results > 12.5 kPa within six months prior to Screening or at
Screening;NOTICE: If there is liver biopsy, liver biopsy results will supersede
non-invasive testing results and be considered definitive.
10. ECG without clinically significant abnormalities at Screening;
11. Subjects must have the following laboratory parameters at Screening: (1) ALT = 10 ×
the upper limit of normal (ULN). (2) AST = 10 × ULN. (3) Without cirrhosis: Total
bilirubin = 1.5 × ULN except history of Gilbert's syndrome. If Gilbert's syndrome is
the proposed etiology, the total bilirubin must = 2 × ULN. With cirrhosis: Total
bilirubin = 2 × ULN. (4) Platelet count = 90,000 cells/mm3. (5) Absolute neutrophil
count (ANC) = 1,500 cells/mm3. (6) HbA1c = 8.5%. (7) Creatinine clearance (CLcr) = 50
mL /min, as calculated by the Cockcroft-Gault equation. (8) Hemoglobin = 110 g/L for
female subjects; = 120 g/L for male subjects. (9) Without cirrhosis Albumin = 3.5
g/dL;With cirrhosis Albumin =30g/L. (10) Without cirrhosis INR = 1.5 x ULN;With
cirrhosis INR = 1.7 x ULN. (11) Alpha fetoprotein (AFP)<100 ng/mL;20ng/mL=AFP=100ng/mL
need to take Liver Ultrasonic testing to exclude subjects with suspicious liver cancer
cells. (12) Anti-nuclear antibodies (ANA) = 1:320;
12. A female subject is eligible to enter the study if it is confirmed that she is: (1) Of
non-childbearing potential (i.e., women who have had a hysterectomy, have both ovaries
removed or medically documented ovarian failure, or are postmenopausal - women > 50
years of age with cessation (for =12 months) of previously occurring menses), or (2)
Of childbearing potential (Women = 50 years of age with amenorrhea will be considered
to be of childbearing potential). These women must have a negative serum pregnancy
test at Screening and agree to consistently and correctly use an approved
contraceptive method (i.e. abstinence, vaginal ring, cervical cap, contraceptive
diaphragm, or intrauterine devices) from screening until at least 6 months after the
last dose of study drug(s);
13. Male subjects must agree to consistently and correctly use an approved contraceptive
method (i.e. abstinence, condom, or spouses using contraceptive drugs, vaginal ring,
cervical cap, contraceptive diaphragm, or intrauterine devices) from screening until
at least 6 months after the last dose of study drug(s);
14. Male subjects must agree to refrain from sperm donation from screening until at least
6 months after the last dose of study drug(s);
15. Subject must be of generally good health, with the exception of chronic HCV infection,
as determined by Investigator;
16. Subject must be able to comply with the dosing instructions for study drug
administration and able to complete the study schedule of assessments, including all
required post-treatment visits.
Exclusion Criteria:
1. Positive serological test for IgM anti-HAV or anti-HEV antibody at Screening;
2. Positive serological test for HBsAg at Screening;
3. Positive test for HIV-1 or HIV-2 at Screening;
4. Donation or loss of more than 400 mL blood within 3 months prior to Baseline/Day 1;
5. Clinically-relevant drug abuse within 12 months of signing the ICF. A positive drug
screen will exclude subjects unless it can be explained by a prescribed medication;
the diagnosis and prescription must be approved by Investigator;
6. Alcohol misuse as defined by an AUDIT score of = 8;
7. Contraindications to RBV or IFN therapy, including hemoglobinopathies (e.g.,
thalassemia major or sickle-cell anemia);
8. Pregnant or nursing female or male with pregnant female partner;
9. Use of any prohibited medications within 30 days of the Baseline/Day 1 visit;
10. Known hypersensitivity to TG-2349, DAG181, RBV, sulfa drugs, or formulation
excipients;
11. Current or prior history of any of the following: (1) Chronic hepatic disorder not
induced by HCV (including but not limited to Hemochromatosis, Wilson's disease,
alpha-1 antitrypsin deficiency, cholangitis, autoimmune hepatitis, alcoholic liver
disease, drug-induced liver disease. (2) Decompensated liver cirrhosis (Child-Pugh
class B and C). (3) Any dysphagia, malabsorption syndrome, or other gastrointestinal
disturbances affecting drug absorption. (4) Difficulty with blood collection and/or
poor venous access for the purposes of phlebotomy. (5) Central nervous system (CNS)
trauma, seizure disorder, stroke or transient ischemic attack. (6) Solid organ
transplantation. (7) Significant cardiac disease (including but not limited to the
myocardial infarction based on ECG and/or clinical history). (8) Significant pulmonary
disease or porphyria (e.g. lung infiltration or impaired lung function). (9)
Pancreatitis. (10) Autoimmune disease (systemic lupus erythematosus, rheumatoid
arthritis, sarcoidosis, psoriasis). (11) Psychiatric hospitalization, suicide attempt,
and/or a period of disability as a result of their psychiatric illness within the last
5 years. (12) Malignancy within 5 years prior to Screening, with the exception of
specific cancers that are entirely cured by surgical resection (basal cell skin
cancer, etc). Subjects under evaluation for possible malignancy are not eligible. (13)
Serious acute drug allergy (such as anaphylaxis or hepatotoxicity) or serious skin
hypersensitive reaction (such as vesicular rash, Stevens Johnson Syndrome);
12. As determined by Investigator, a subject that would affect the therapy, evaluation or
compliance with the protocol is not suitable to take part in this study.
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