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Efficacy and Safety of Telbivudine in Treatment naïve Patients With HBeAg-Positive Chronic Hepatitis B (CHB)
This study has been terminated.
Sponsored by: Novartis
Information provided by: Novartis
ClinicalTrials.gov Identifier: NCT00412750
  Purpose

To evaluate the combination of telbivudine and peginterferon alpha-2a for antiviral efficacy in comparison to peginterferon alpha-2a monotherapy.


Condition Intervention Phase
Hepatitis B
Drug: Telbivudine, peginterferon alpha-2a
Phase III

MedlinePlus related topics: Hepatitis Hepatitis B
Drug Information available for: Peginterferon Alfa-2a Hepatitis B Vaccines Telbivudine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Randomized, Open-Label, Controlled, Multi-Center Two-Year Study Comparing Efficacy and Safety of Telbivudine, 600 mg PO in Combination With Peginterferon Alpha-2a sq180 µg With Peginterferon Alpha-2a Monotherapy, and With Telbivudine Monotherapy in Treatment naïve Patients With HBeAg-Positive CHB

Further study details as provided by Novartis:

Primary Outcome Measures:
  • Evaluate the antiviral efficacy of the combination of peginterferon alpha-2a plus telbivudine vs. peginterferon alpha-2a monotherapy assessed by HBV DNA non-detectability at Week 52 in adult patients with HBeAg-positive CHB.

Secondary Outcome Measures:
  • • Evaluate telbivudine monotherapy antiviral efficacy compared to peginterferon alpha-2a monotherapy as shown via PCR non-detectability at Week 52.
  • Assess the antiviral efficacy of the combination of peginterferon alpha-2a plus telbivudine to telbivudine monotherapy at Week 52
  • Assessment of HBV DNA non-detectability, reduction from baseline and sustained reduction in HBV DNA over the course of the study.
  • Assessment of Virologic Breakthrough and treatment emergent HBV resistance at Weeks 48 and 96
  • Assessment of HBeAg loss and HBeAg seroconversion (defined as loss of HBeAg and development of HBeAb).

Estimated Enrollment: 300
Study Start Date: December 2006
Estimated Study Completion Date: December 2009
  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Documented Chronic hepatitis B (CHB) defined by all of the following:

  • Clinical history compatible with CHB
  • Detectable serum HBsAg at the Screening visit and at least 6 months prior
  • HBeAg-positive at the Screening visit
  • HBeAb-negative at the Screening visit
  • History of evidence of chronic liver inflammation,
  • Elevated serum ALT level (1.3 - 10 x upper limit of normal (ULN)) at the Screening visit
  • Serum HBV DNA level ≥ 6 log10 copies/mL,
  • Chronic liver inflammation on previous liver biopsy within the previous 24 months.

Exclusion Criteria:

  • Co-infection with HCV, HDV, or HIV.
  • Has any of the following drug therapy:

    • Previously been treated in a trial with telbivudine
    • Received nucleoside or nucleotide therapy whether approved or investigational
    • Received any immunomodulatory treatment in the 12 months before Screening for this study.
    • Has a medical condition that required prolonged or frequent use of systemic acyclovir or famciclovir.
    • Has a medical condition that requires frequent or prolonged use of systemic corticosteroids although inhaled or intra-articular corticosteroids are allowed.
    • Has a medical condition requiring the chronic or prolonged use of potentially hepatotoxic drugs or nephrotoxic drugs.
    • Is currently abusing alcohol or illicit drugs or has a history of alcohol abuse illicit substance abuse within the preceding two years.
    • Uses other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer.
    • Is currently receiving methadone.
  • Patient has any of the following:

    • History of or clinical signs/symptoms of hepatic decompensation such as ascites, esophageal variceal bleeding, hepatic encephalopathy, or spontaneous bacterial peritonitis.
    • History of malignancy of any organ system, treated or untreated, within the past 5 years whether or not there is evidence of local recurrence or metastases, with the exception of localized basal cell carcinoma of the skin. Patients with previous findings suggestive of possible HCC should have the disease ruled out prior to entrance into the study.
    • One or more additional known primary or secondary causes of liver disease other than hepatitis B, including steatohepatitis.
    • History of clinical and laboratory evidence of chronic pancreatitis, or demonstrates a clinical and laboratory course consistent with current pancreatitis.
  • Has laboratory values during screening visit not within normal limits:
  • Is pregnant or breastfeeding.
  • Is a women of child-bearing potential that is unwilling to practice birth control.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00412750

Locations
United States, California
Novartis
San Francisco, California, United States, 94115
Sponsors and Collaborators
Novartis
  More Information

Responsible Party: novatis ( novartis )
Study ID Numbers: CLDT600A2406
Study First Received: December 15, 2006
Last Updated: June 5, 2008
ClinicalTrials.gov Identifier: NCT00412750  
Health Authority: United States: Food and Drug Administration;   Australia: Therapeutic Goods Administration;   Belgium: Pharmaceutical Inspectorate;   France: Sanitary Safety of Health Products Agency;   Germany: Federal Institute for Drugs and Medical Devices;   Italy: Ministry of Health;   Netherlands: Medicines Evaluation Board;   Spain: Ministry of Health and Consumption;   Switzerland: Agency for Therapeutic Products;   United Kingdom: Medicines and Healthcare Products Regulatory Agency;   Israel: Ministry of Health;   Argentina: National Administration of Drugs, Foods and Medical Technology;   Taiwan: National Laboratories of Foods and Drugs;   Singapore: Health Sciences Authority;   New Zealand: Medicines and Medical Devices Safety Authority;   Hong Kong: Department of Health

Keywords provided by Novartis:
hepatitis B
HBV
chronic hepatitis B
telbivudine
peginterferon

Study placed in the following topic categories:
Interferon-alpha
Liver Diseases
Hepatitis, Chronic
Interferons
Hepatitis, Viral, Human
Hepatitis
Virus Diseases
Digestive System Diseases
Hepatitis B, Chronic
Hepatitis B
Peginterferon alfa-2a
DNA Virus Infections
Interferon Alfa-2a

Additional relevant MeSH terms:
Anti-Infective Agents
Antineoplastic Agents
Growth Substances
Therapeutic Uses
Physiological Effects of Drugs
Growth Inhibitors
Angiogenesis Modulating Agents
Angiogenesis Inhibitors
Antiviral Agents
Hepadnaviridae Infections
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009