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A Study of Pegasys (Peginterferon Alfa-2a) Added to Nucleos(t)Ide Analogue Treatment in Participants With HBeAg-Negative Chronic Hepatitis B Genotype D Showing Stable Hepatitis B Virus (HBV) Deoxyribonucleic Acid (DNA) Suppression

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01706575
First Posted: October 15, 2012
Last Update Posted: February 20, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hoffmann-La Roche
Results First Submitted: June 24, 2016  
Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment;   Masking: None (Open Label);   Primary Purpose: Treatment
Condition: Hepatitis B, Chronic
Interventions: Drug: Pegylated Interferon (Peginterferon) Alfa-2a
Drug: Nucleos(t)ide Analogues (NA)

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
A total of 76 participants started the study and were included in lead-in period. Out of 76 participants, 70 received study drug.

Reporting Groups
  Description
Pegylated Interferon (Peginterferon) Alfa-2a Participants receiving nucleos(t)ide analogues (NA) therapy with Hepatitis B surface Antigen (HBsAg) decline less than <0.5 log 10 international unit/milliliter (IU/ml) at baseline received peginterferon alfa-2a 180 microgram (mcg), subcutaneously (SC) once weekly for 48 weeks along with their NA therapy.

Participant Flow:   Overall Study
    Pegylated Interferon (Peginterferon) Alfa-2a
STARTED   76 
Treated   70 
COMPLETED   64 
NOT COMPLETED   12 
Participant Withdrew Consent                4 
Lost to Follow-up                2 
Started but not Treated                6 



  Baseline Characteristics
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Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
Lead-in participants included all participants enrolled in lead-in period.

Reporting Groups
  Description
Pegylated Interferon (Peginterferon) Alfa-2a Participants receiving nucleos(t)ide analogues (NA) therapy with Hepatitis B surface Antigen (HBsAg) decline less than <0.5 log 10 international unit/milliliter (IU/ml) at baseline received peginterferon alfa-2a 180 microgram (mcg), subcutaneously (SC) once weekly for 48 weeks along with their NA therapy.

Baseline Measures
   Pegylated Interferon (Peginterferon) Alfa-2a 
Overall Participants Analyzed 
[Units: Participants]
 76 
Age 
[Units: Years]
Mean (Standard Deviation)
 49.82  (8.46) 
Gender 
[Units: Participants]
Count of Participants
 
Female      13  17.1% 
Male      63  82.9% 


  Outcome Measures
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1.  Primary:   Efficacy: Percent Change From Baseline in Serum Hepatitis B Surface Antigen (HBsAg) Titer at End of the Combination Treatment (Week 48)   [ Time Frame: Baseline up to Week 48 ]

2.  Primary:   Efficacy: Percentage of Participants With Serum Hepatitis B Surface Antigen (HBsAg) Decrease >/= 50% From Baseline at End of the Combination Treatment (Week 48)   [ Time Frame: Baseline and Week 48 ]

3.  Secondary:   Efficacy: Change From Baseline in Serum Hepatitis B Surface Antigen (HBsAg) Titer at Week 24, 72 and 96   [ Time Frame: Baseline, Week 24, 72 and 96 ]

4.  Secondary:   Efficacy: Percentage of Participants With HBsAg Decrease >/=1 log10 IU/ml From Baseline to Week 48   [ Time Frame: Baseline, Week 48 ]

5.  Secondary:   Efficacy: Number of Participants With Serum HBsAg Loss at Week 12 That Persisted up to Week 96   [ Time Frame: Week 12 up to Week 96 ]

6.  Secondary:   Efficacy: HBsAg Levels According to Interleukin 28B (IL28B) Genotypes   [ Time Frame: Baseline and Week 48 ]

7.  Secondary:   Efficacy: HBsAg Levels According to Interferon-Inducible Protein 10 (IP-10) Serum Levels   [ Time Frame: Baseline and Week 48 ]

8.  Secondary:   Safety: Percentage of Participants With Adverse Events (AE)   [ Time Frame: Baseline up to Week 48 ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Results Point of Contact:  
Name/Title: Medical Communications
Organization: Hoffmann-La Roche
phone: 800 821-8590
e-mail: genentech@druginfo.com



Responsible Party: Hoffmann-La Roche
ClinicalTrials.gov Identifier: NCT01706575     History of Changes
Other Study ID Numbers: ML28262
2012-000080-25 ( EudraCT Number )
First Submitted: October 10, 2012
First Posted: October 15, 2012
Results First Submitted: June 24, 2016
Results First Posted: August 5, 2016
Last Update Posted: February 20, 2017