Y- Shaped Pegylated Interferon (YPEG-IFNα-2a) Plus Ribavirin in Egyptian Patients With Untreated Chronic Hepatitis C

NCT ID: NCT01327729

Last Updated: 2011-04-04

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 300 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-11-30
• Study Completion Date: 2013-05-31

Brief Summary

The objective is to assess the efficacy, dosing, safety and tolerance of Y- shaped pegylated interferon (YPEG-IFNα-2a) plus ribavirin in Egyptian patients with chronic hepatitis C and with no prior treatment for hepatitis C virus (HCV).

Methods: Randomized, Open-label trial, in 3 parallel groups (each of 100 patients)

Detailed Description

Methods: Randomized, Open-label trial, in parallel groups (each of 100 patients). Treatment will be given for 48 weeks (positive HCV by polymerase chain reaction (PCR) patients at 24 weeks will be considered non responders) and follow-up for 24 weeks. Total treatment and follow-up duration: 72 weeks. Enrollment duration: 18 months. Total trial duration: 2 years and 9 month, including trial analysis (carried out in the 6 months following the follow-up completion of the last patient). Total number of patients: 300. Precision around the expected efficacy rate (45% in intention-to-treat analysis) will be 9.6% (α = 0.05).

Primary objective: to assess the efficacy, dosing, safety and tolerability of Y- shaped pegylated interferon (YPEG-IFNα-2a) plus ribavirin in Egyptian patients with chronic hepatitis C and with no prior treatment for HCV.

Secondary objective: To assess the plasma level of the YPEG-IFNα-2a in the first 30 patients in each group, to ensure therapeutic plasma level of the drug at 2 hours, 6 hours, 10 hours, 24 hours, 3 days, 5 days, 7 days, 10 days, 14 days and 28 days.

Treatment strategy:

Three groups in which each group will include 100 patients.

The first group will be treated with:

YPEG-IFN α-2a 180mcg/week for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks.

The second group will be treated with:

YPEG-IFN α-2a 180mcg/10 days for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks.

The third group will be treated with:

YPEG-IFN α-2a 180mcg/ 2 weeks for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks. HCV RNA by PCR will be done at 24 weeks and negative PCR patients will continue treatment for another 24 weeks and PCR positive patients will be considered non responders and will be followed up.

Evaluation of the dose efficacy and side effects will be obtained at 4 weeks and 12 weeks of treatment, and any serious side effects or significant dose difference in early virological response in a group will lead to shift of this group to the dose 180 mcg/week.

Main outcome:

Viral clearance by qualitative HCV RNA based on PCR 24 weeks after the end of treatment.

Secondary outcomes:

Evaluation of HCV RNA at 12 and 24 weeks; changes in HCV RNA load during treatment; normalization of ALT during treatment and 24 weeks after the end of treatment; study of side effects; histological changes 24 weeks after the end of treatment: decrease by at least 1 point of the Metavir score.

Conditions

Self Efficacy; Hepatitis C

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

YPEG-IFN α-2a one week

this arm will be treated with: YPEG-IFN α-2a 180mcg/ week for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks

Group Type: ACTIVE_COMPARATOR

pegylated interferon alpha 2a YPEG-IFN α-2a 180mcg

Intervention Type: DRUG

YPEG-IFN α-2a 180mcg dose form: subcutaneous dosage : 180 mcg frequency every week or ten days or 2 weeks according to the group

YPEG-IFN α-2a Ten days

this arm will be treated with: YPEG-IFN α-2a 180mcg/10 days for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks

Group Type: ACTIVE_COMPARATOR

pegylated interferon alpha 2a YPEG-IFN α-2a 180mcg

Intervention Type: DRUG

YPEG-IFN α-2a 180mcg dose form: subcutaneous dosage : 180 mcg frequency every week or ten days or 2 weeks according to the group

YPEG-IFN α-2a two weeks

The third group will be treated with:

YPEG-IFN α-2a 180mcg/ 2 weeks for 48 weeks. Ribavirin 15 mg/kg/day for 48 weeks.

Group Type: ACTIVE_COMPARATOR

pegylated interferon alpha 2a YPEG-IFN α-2a 180mcg

Intervention Type: DRUG

YPEG-IFN α-2a 180mcg dose form: subcutaneous dosage : 180 mcg frequency every week or ten days or 2 weeks according to the group

Interventions

pegylated interferon alpha 2a YPEG-IFN α-2a 180mcg

YPEG-IFN α-2a 180mcg dose form: subcutaneous dosage : 180 mcg frequency every week or ten days or 2 weeks according to the group

Intervention Type: DRUG

Other Intervention Names

YPEG-IFN α-2a 180mcg; YPEG; pegylated interferon

Eligibility Criteria

Inclusion Criteria

• Age > 18 years and < 65 years
• Chronic hepatitis C defined as: HCV antibodies using a third generation test; HCV-RNA positive by PCR; liver biopsy in the past 12 months; METAVIR score of A1 and F0 or higher
• ALT > 1 ULN in the 24 weeks prior to inclusion (W-26; W-2)
• Patients never treated with ribavirin, Interferon or PEG-Interferon
• Normal albumin, prothrombin time > 60%; normal bilirubin
• Alpha-foeto-protein < 3 times the normal range for the laboratory reference
• HBs antigen negative
• Anti Bilharzial antibodies if positive rectal snip shall be done. The examination may be repeated after praziquantel treatment for those with a positive test
• Hemoglobin > 11g/dl, leucocytes > 3000/mm3, neutrophils > 1500/mm3, platelets > 100 000/mm3, blood creatinin < 1.4 mg/dl
• Normal TSH (subjects needing treatment to maintain TSH within a normal range may be included if other eligibility criteria are respected)
• Anti-nuclear antibodies < 1/160
• Fasting blood sugar between 70-115mg/dl ; if glucose intolerance or diabetes, HbA1C < 8.5%
• Normal ophthalmologic examination in patients with history of blood pressure and/or diabetes
• Effective contraception (IUD, diaphragm and spermicide, condoms and spermicides, oral contraceptive, progesterone implants (Norplant), medroxyprogesterone acetate (Depo-provera), tubal ligation, vasectomy) during the treatment period for females. No breastfeeding during the study period
• Signed informed consent

Exclusion Criteria

• Other liver diseases associated with chronic hepatitis C: co-infection with hepatitis B (positive HBs antigen); hemochromatosis; alpha-1 anti-trypsin deficiency; Wilson disease; alcoholism-related liver disease; Gilbert disease
• Alcohol intake > 50g/day for males and 40 g/day for females
• Ongoing intravenous drug use
• Aggravated liver cirrhosis: history or presence of ascitis, oesophageal varicosis, liver encephalopathy
• Hepatocellular carcinoma

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Xiamen Amoytop Biotech Co., Ltd.

INDUSTRY

Sponsor Role: collaborator

BioGeneric Pharma

INDUSTRY

Sponsor Role: lead

Responsible Party

cairo university

Principal Investigators

Gamal Esmat, MD

Role: PRINCIPAL_INVESTIGATOR

cairo university - Kasr alaini school of medicine

Mohamed Karim F Ashour, MD

Role: STUDY_DIRECTOR

Cairo university- Kasr Alaini school of medicine

Locations

Kasr Alaini school of medicne

Cairo, Cairo Governorate, Egypt

Site Status: RECRUITING

Countries

Egypt

Central Contacts

Mohamed Karim f Ashour, MD

Role: CONTACT

drmkarim@gmail.com

0020123130102

Gamal Esmat, MD

Role: CONTACT

g_esmat@yahoo.com

002012455468

Other Identifiers

CHT00234

Identifier Type: -

Identifier Source: org_study_id