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Study · Randomized controlled trial · n = 51 · 2012

3 results

Efficacy of thymosin α-1 plus peginterferon α-2a combination therapy compared with peginterferon α-2a monotherapy in HBeAg-positive chronic hepatitis B: a prospective, multicenter, randomized, open-label study.

Kim BH, Lee YJ, Kim W, Yoon JH, Jung EU, Park SJ, Kim YJ, Lee HS

Scandinavian journal of gastroenterology25 Jun 2012Cited by 16 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study3

3 results from studies that gave the peptide. 3 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In HBeAg-positive chronic hepatitis B, combined response at the end of treatment was 15.4% with thymosin alpha‑1 plus peginterferon and 12.0% with peginterferon alone, not significantly different.

    In plain wordsIn HBeAg-positive chronic hepatitis B, adding thymosin alpha‑1 to peginterferon did not give a significantly higher combined response at the end of treatment.

    Outcome
    No significant changeCombined response at end of treatment
    Study

    n = 51

    Comparator
    Peginterferon alfa-2a monotherapy
    Outcome group
    Antiviral activity · Infection
    Studied dose
    1.6 mg twice a week · 12 weeksAs given in this study (human).

    Measurements

    Combined response rate
    15.4%
    combination
    Combined response rate
    12%
    monotherapy

    Source sentences

    Summary
    The rates of the combined response, defined as HBeAg seroconversion, HBV DNA suppression, and normalization of serum ALT, were 4/26 (15.4%) and 3/25 (12.0%) for the combination group and the monotherapy group at the end of treatment (p = 0.725)
    2 context sentences
    Summary · context
    HBeAg-positive CHB patients were enrolled in this prospective, randomized, open-label study.
    Summary · context
    Fifty-one patients were assigned to either combination (26 patients; 180 μg of peginterferon α-2a weekly for 48 weeks and 1.6 mg of thymosin α-1 twice a week for the first 12 weeks) or monotherapy (25 patients; 180 μg of peginterferon α-2a weekly for 48 weeks) groups.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In HBeAg-positive chronic hepatitis B, combined response at the end of follow-up was 23.1% with thymosin alpha‑1 plus peginterferon and 20.0% with peginterferon alone, not significantly different.

    In plain wordsIn HBeAg-positive chronic hepatitis B, adding thymosin alpha‑1 to peginterferon did not give a significantly higher combined response at the end of follow-up.

    Outcome
    No significant changeCombined response at end of follow-up
    Study

    n = 51

    Comparator
    Peginterferon alfa-2a monotherapy
    Outcome group
    Antiviral activity · Infection
    Studied dose
    1.6 mg twice a week · 12 weeksAs given in this study (human).

    Measurements

    Combined response rate
    23.1%
    combination
    Combined response rate
    20%
    monotherapy

    Source sentences

    Summary
    The rates of the combined response, defined as HBeAg seroconversion, HBV DNA suppression, and normalization of serum ALT, were 4/26 (15.4%) and 3/25 (12.0%) for the combination group and the monotherapy group at the end of treatment (p = 0.725), and 6/26 (23.1%) and 5/25 (20.0%) at the end of follow…
    2 context sentences
    Summary · context
    HBeAg-positive CHB patients were enrolled in this prospective, randomized, open-label study.
    Summary · context
    Fifty-one patients were assigned to either combination (26 patients; 180 μg of peginterferon α-2a weekly for 48 weeks and 1.6 mg of thymosin α-1 twice a week for the first 12 weeks) or monotherapy (25 patients; 180 μg of peginterferon α-2a weekly for 48 weeks) groups.
  3. 03HumanRandomized controlled trialSafety outcome

    In HBeAg-positive chronic hepatitis B, adverse events did not differ significantly between thymosin alpha‑1 plus peginterferon and peginterferon alone.

    In plain wordsIn HBeAg-positive chronic hepatitis B, adding thymosin alpha‑1 to peginterferon did not significantly change the rate of side effects.

    Outcome
    No significant changeAdverse events
    Study

    n = 51

    Comparator
    Peginterferon alfa-2a monotherapy
    Outcome group
    Adverse events · Whole body
    Studied dose
    1.6 mg twice a week · 12 weeksAs given in this study (human).

    Source sentences

    Summary
    No significant differences in adverse events were observed.
    2 context sentences
    Summary · context
    HBeAg-positive CHB patients were enrolled in this prospective, randomized, open-label study.
    Summary · context
    Fifty-one patients were assigned to either combination (26 patients; 180 μg of peginterferon α-2a weekly for 48 weeks and 1.6 mg of thymosin α-1 twice a week for the first 12 weeks) or monotherapy (25 patients; 180 μg of peginterferon α-2a weekly for 48 weeks) groups.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 3Current

    9 Oct 2026, 18:17 UTC

    Study results updated

  2. Version 2

    9 Oct 2026, 03:03 UTC

    Study data updated · source update from Europe PMC

  3. Version 1

    9 Oct 2026, 03:02 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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