The Effects of Adding TCM-700C on the Standard Combination Treatment for Patients With Genotype 1 Hepatitis C Infection

Chronic Hepatitis C Clinical Trial

— TCM-700C  

Official title:

TCM-700C Phase II Trial The Effects of Adding a Chinese Formulation (TCM-700C) on the Standard Combination Treatment for Patients With Genotype 1 Hepatitis C Infection

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00556504
• Other study ID #: TCM-700-01-04
• Status: Completed
• Phase: Phase 2
• First received: November 8, 2007
• Last updated: August 4, 2014
• Start date: July 2007
• Est. completion date: May 2011

Study information

• Verified date: July 2014
• Source: TCM Biotech International Corp.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationTaiwan : Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to evaluate the effectiveness of TCM-700C as an add-on treatment to the combination drug therapy (Peginterferon α-2b plus Ribavirin) for patients with genotype 1 chronic hepatitis C infections. This will be demonstrated by a higher sustained virologic response rate, defined as the absence of detectable HCV RNA 24 weeks after the termination of combinational drug treatment, compared with the placebo add-on.

Description:

This was a randomized, double-blind, placebo controlled, parallel-group, Phase 2 study to evaluate the effects of adding a Chinese formulation (TCM-700C) on the standard combination treatment for patients with Genotype 1 hepatitis C infection. Patients were screened within 4 weeks before receive the first study drug dose. Eligible patients at baseline were stratified according to baseline HCV RNA (≤800,000 IU/ml vs >800,000 IU/ml) and randomized with an equal chance to receive either TCM-700C or placebo as an add-on to the combination drug therapy. The combination drug therapy was peginterferon α-2b (PEG-INTRON®, Schering-Plough) 1.5 micrograms/kg once weekly injection for 48 weeks plus oral ribavirin (REBETOL®, Shering-Plough) 1000mg-1200mg daily for 48 weeks. The add-on treatment of TCM-700C or placebo was given 2 tablets thrice daily for 48 weeks.

During the 48 week treatment period and 24 week untreated follow-up, patients were assessed at regular intervals for safety and efficacy at weeks 2, 4, 8, 12, 16 and then every 8 weeks thereafter until study completion. Patients who prematurely discontinued test drug therapy had laboratory examination re-taken on the week patient was discontinued from study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 84
• Est. completion date: May 2011
• Est. primary completion date: January 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 65 Years

Eligibility

Inclusion Criteria:

• HCV strain confirmed as genotype I;

• Elevated ALT (=1.5 x upper limit of normal)during last 6 months

• Females of childbearing potential with a negative serum pregnancy test

• Subject must be willing to sign a written informed consent

• Subject must be willing and able to adhere to dose and visit schedule.

Exclusion Criteria:

• Serum AFP levels > 400 ng/ml

• Liver biopsy within 12 months prior to study entry showed liver cirrhosis with METAVIR system fibrosis score of 3-4, or hepatocellular carcinoma (HCC);

• Co-infection with hepatitis B virus (HBV);

• Anti-HIV positive;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Hepatitis C
• Hepatitis
• Hepatitis A
• Hepatitis C
• Hepatitis C, Chronic
• Hepatitis, Chronic

Intervention

Drug:
• TCM-700C
An add-on drug to conventional treatment of Hepatitis C
• Peginterferon alfa-2a
conventional treatment of Hepatitis C
• Ribavirin
conventional treatment of Hepatitis C
• Placebo
Placebo, without acting ingredient.

Locations

Country	Name	City	State
Taiwan	Chang Gung Memorial Hospital	Taoyuan

Sponsors (1)

Lead Sponsor	Collaborator
TCM Biotech International Corp.

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sustained Virologic Response (SVR)	SVR is defined as no detectable HCV RNA in serum of patient at Week 72, which is 24 weeks after the termination of combination drug treatment..; A subject is a sustained responder at a given week, if the subject has negative HCV RNA at that week and all the subsequent weeks through Week 72.; If a patient has a missing value between visits, then the last non-missing HCV RNA is carried forward to fill in the missing value.; If the patient's HCV RNA at last visit, Week 72 is missing or above the limit of detection, then the patient is a non-responder, even if all the previous visits from baseline onwards were undetectable.; Serum HCV RNA will be tested using a commercially available real-time polymerase-chain-reaction (PCR) assay kit (Roche Cobas TaqMan HCV assay kit)	24 weeks after the termination of combinational drug treatment (up to 72 weeks)	No
Secondary	Virologic Response	undetectable HCV RNA at the end of combination drug treatment; Serum HCV RNA will be tested using a commercially available real-time polymerase-chain-reaction (PCR) assay kit (Roche Cobas TaqMan HCV assay kit).	at the end of combination drug treatment (up to 48 weeks)	No
Secondary	ALT Response	An ALT response is defined as normalization of ALT at the end of combination drug treatment.; (ALT normalization is defined as ALT level decreases into within the normal range)	at the end of combination drug treatment (up to 48 weeks)	No
Secondary	Sustained ALT Response	a sustained ALT response is defined as sustained normalization of ALT 24 weeks after cessation of combination drug treatment.	24 weeks after the termination of combinational drug treatment (up to 72 weeks)	No
Secondary	Combined ALT and Virologic Response	Combined ALT and virologic response at the end of combination drug treatment.	at the end of combination drug treatment (up to 48 weeks)	No
Secondary	Immune Cell Normalization	Normalization of immune cells, CD4, CD8 and NK cells at the end of combination drug treatment; (Immune cell normalization is defined as return of CD4, CD8 and NK cells to normal range)	at the end of combination drug treatment (up to 48 weeks)	No
Secondary	Immune Cell Normalization	Normalization of immune cells, CD4, CD8 and NK cells at 24 weeks after cessation of combination drug treatment.	24 weeks after the termination of combinational drug treatment (up to 72 weeks)	No