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Safety and Efficacy of Cobicistat-boosted Darunavir in HIV Infected Adults

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Janssen, LP
Information provided by (Responsible Party):
Gilead Sciences
ClinicalTrials.gov Identifier:
NCT01440569
First received: September 22, 2011
Last updated: October 23, 2014
Last verified: October 2014
Results First Received: October 23, 2014  
Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Single Group Assignment;   Masking: Open Label;   Primary Purpose: Treatment
Conditions: Acquired Immunodeficiency Syndrome
HIV Infections
Interventions: Drug: COBI
Drug: DRV
Drug: NRTIs

  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
Participants were enrolled at a total of 56 study sites in the United States. The first participant was screened on 22 September 2011. The last participant observation for the Week 48 analysis was on 31 January 2013.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
397 participants were screened and 314 were enrolled; 313 participants were treated, and comprise the Full Analysis Set.

Reporting Groups
  Description
Treatment-Naive Treatment-naive participants received darunavir (DRV; 800 mg; 2 × 400 mg tablets) + cobicistat (COBI; 1 × 150 mg tablet) once daily + two nucleoside analogue reverse transcriptase inhibitors (NRTIs; per prescribing information) for 48 weeks, and may have continued their regimen in the extension period.
Treatment-Experienced Treatment-experienced participants received DRV (800 mg; 2 × 400 mg tablets) + COBI (1 × 150 mg tablet) once daily + two NRTIs (per prescribing information) for 48 weeks, and may have continued their regimen in the extension period.

Participant Flow:   Overall Study
    Treatment-Naive     Treatment-Experienced  
STARTED     296     18  
Enrolled and Treated     295     18  
COMPLETED     0     0  
NOT COMPLETED     296     18  
Enrolled but not treated                 1                 0  
Subjects Still on Study                 261                 14  
Adverse Event                 9                 0  
Pregnancy                 1                 0  
Investigator's Discretion                 1                 1  
Withdrew Consent                 7                 1  
Lost to Follow-up                 12                 2  
Subject Non-Compliance                 3                 0  
Protocol Violation                 1                 0  



  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.
Full Analysis Set: participants who were enrolled into the study and received at least one dose of study drug.

Reporting Groups
  Description
Treatment-Naive Treatment-naive participants received DRV (800 mg; 2 × 400 mg tablets) + COBI (1 × 150 mg tablet) once daily + two NRTIs (per prescribing information) for 48 weeks, and may have continued their regimen in the extension period.
Treatment-Experienced Treatment-experienced participants received DRV (800 mg; 2 × 400 mg tablets) + COBI (1 × 150 mg tablet) once daily + two NRTIs (per prescribing information) for 48 weeks, and may have continued their regimen in the extension period.
Total Total of all reporting groups

Baseline Measures
    Treatment-Naive     Treatment-Experienced     Total  
Number of Participants  
[units: participants]
  295     18     313  
Age  
[units: years]
Mean ± Standard Deviation
  36  ± 10.3     45  ± 10.9     36  ± 10.6  
Gender  
[units: participants]
     
Female     29     5     34  
Male     266     13     279  
Ethnicity (NIH/OMB)  
[units: participants]
     
Hispanic or Latino     64     4     68  
Not Hispanic or Latino     231     14     245  
Unknown or Not Reported     0     0     0  
Race/Ethnicity, Customized  
[units: participants]
     
White     176     11     187  
Black or African Heritage     101     7     108  
American Indian or Alaska Native     4     0     4  
Asian     4     0     4  
Native Hawaiian or Pacific Islander     2     0     2  
Other     8     0     8  
CD4 Count (cells/mm^3)  
[units: cells/mm^3]
Mean ± Standard Deviation
  378.2  ± 199.94     197.8  ± 214.30     367.8  ± 204.79  
HIV-1 RNA (log10 copies/mL)  
[units: log10┬ácopies/mL]
Mean ± Standard Deviation
  4.8  ± 0.76     4.8  ± 1.04     4.8  ± 0.78  
Background Antiretroviral Regimen [1]
[units: participants]
     
FTC/TDF     291     10     301  
AZT+FTC/TDF     0     5     5  
ABC+TDF     2     1     3  
ABC+FTC/TDF     1     1     2  
ABC/3TC     1     0     1  
DDI+FTC     0     1     1  
[1] 3TC, lamivudine (Epivir®); ABC, abacavir; ABC/3TC, abacavir/lamivudine coformulation; AZT, azidothymidine or zidovudine; DDI, didanosine; FTC, emtricitabine (Emtriva®); FTC/TDF, emtricitabine/tenofovir disoproxil fumarate coformulation (Truvada®); TDF, tenofovir disoproxil fumarate (Viread®)



  Outcome Measures
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1.  Primary:   Percentage of Participants With Onset of Any Treatment-emergent Grade 3 or 4 Adverse Event Between Baseline and Week 24   [ Time Frame: Up to 24 weeks ]

2.  Secondary:   Percentage of Participants Achieving HIV-1 RNA < 50 Copies/mL at Week 24 (Snapshot Analysis)   [ Time Frame: Week 24 ]

3.  Secondary:   Percentage of Participants Achieving HIV-1 RNA < 50 Copies/mL at Week 48 (Snapshot Analysis)   [ Time Frame: Week 48 ]

4.  Secondary:   Change From Baseline in CD4+ Cell Count at Week 24   [ Time Frame: Baseline; Week 24 ]

5.  Secondary:   Change From Baseline in CD4+ Cell Count at Week 48   [ Time Frame: Baseline; Week 48 ]

6.  Secondary:   Percentage of Participants Experiencing Any Treatment-emergent Adverse Event and Any Treatment-emergent Adverse Event Leading to Discontinuation of Study Drug Through Week 24   [ Time Frame: Up to 24 weeks ]

7.  Secondary:   Percentage of Participants Experiencing Any Treatment-emergent Adverse Event and Any Treatment-emergent Adverse Event Leading to Discontinuation of Study Drug Through Week 48   [ Time Frame: Up to 48 weeks ]


  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: Clinical Trial Disclosures
Organization: Gilead Sciences, Inc.
e-mail: ClinicalTrialDisclosures@gilead.com


No publications provided


Responsible Party: Gilead Sciences
ClinicalTrials.gov Identifier: NCT01440569     History of Changes
Other Study ID Numbers: GS-US-216-0130, 2011-003501-22
Study First Received: September 22, 2011
Results First Received: October 23, 2014
Last Updated: October 23, 2014
Health Authority: United States: Food and Drug Administration