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Safety of EVG+RTV Administered With Other Antiretroviral Agents for the Treatment of HIV-1 Infection

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00445146
First Posted: March 8, 2007
Last Update Posted: April 25, 2016
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):
Gilead Sciences
  Purpose
The main objective of this study is to observe the long-term safety of elvitegravir (EVG) boosted with ritonavir (RTV) in combination with other antiretroviral (ARV) agents in participants who have completed a prior EVG+RTV treatment study.

Condition Intervention Phase
HIV Infections Drug: EVG Drug: RTV Drug: ARV regimen Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2, Open-Label, Multicenter Study of the Safety of Ritonavir-Boosted GS-9137 (GS-9137/r) Administered in Combination With Other Antiretroviral Agents for the Treatment of HIV-1 Infected Subjects

Resource links provided by NLM:


Further study details as provided by Gilead Sciences:

Primary Outcome Measures:
  • Percentage of Participants Experiencing Any Treatment-Emergent Study Dug-Related Adverse Event [ Time Frame: Up to Week 408 plus 30 days ]

Secondary Outcome Measures:
  • Percentage of Participants Experiencing Treatment-Emergent Adverse Events [ Time Frame: Up to Week 408 plus 30 days ]
    Adverse events (AEs) occurring during treatment and for 30 days following the last dose of study drug were summarized across the participant population. A participant was counted once if they had a qualifying event.

  • Percentage of Participants Experiencing Any Treatment-Emergent Laboratory Abnormality [ Time Frame: Up to Week 408 plus 30 days ]
    Treatment-emergent laboratory abnormalities were defined as values that increase at least one toxicity grade from baseline. The most severe graded abnormality from all tests was counted for each participant.

  • Percentage of Participants Experiencing Any Marked Treatment-Emergent Laboratory Abnormality [ Time Frame: Up to Week 408 plus 30 days ]
    A 'marked abnormality' was defined as a shift from grade 0 (or missing) at baseline to at least grade 3 postbaseline; or grade 1 at baseline to grade 4 postbaseline.

  • Hemoglobin at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Red Blood Cell (RBC) Count at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • White Blood Cell (WBC) Count at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Platelet Count at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Alkaline Phosphatase at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Alanine Aminotransferase (ALT) at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Aspartate Aminotransferase (AST) at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • HIV-1 RNA at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Percentage of Participants With HIV-1 RNA < 400 Copies/mL at Baseline and at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Percentage of Participants With HIV-1 RNA < 50 Copies/mL at Baseline and at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • CD4 Cell Count at Baseline and Change From Baseline at Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 [ Time Frame: Baseline; Weeks 24, 48, 96, 144, 192, 240, 288, 336, and 384 ]
  • Incidence of Mortality [ Time Frame: Up to Week 408 plus 30 days ]
    The percentage of participants who died was summarized.


Enrollment: 192
Study Start Date: February 2007
Study Completion Date: March 2015
Primary Completion Date: March 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: EVG+RTV

EVG 85 mg or 150 mg + RTV + ARV regimen

Participants receiving lopinavir/ritonavir (LPV/r) or atazanavir/ritonavir (ATV/r) as part of their ARV regimen will receive EVG 85 mg and all other participants will receive EVG 150 mg.

Some participants may receive EVG 300 mg during the course of protocol amendment 2.

Drug: EVG
Elvitegravir (EVG) tablet administered orally once daily with food
Other Names:
  • Vitekta®
  • GS-9137
Drug: RTV
Ritonavir (RTV; /r) 100 mg capsule administered orally once daily with food
Other Name: Norvir®
Drug: ARV regimen
The components of the ARV regimen will be selected by the investigator without input from the sponsor. The antiretroviral regimen must consist of at least 2 agents, not including the non-nucleoside reverse transcriptase inhibitors (NNRTIs) efavirenz, nevirapine, or delavirdine; the protease inhibitors saquinavir, nelfinavir, or indinavir; or investigational agents (without sponsor approval).

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Completion of a prior EVG+RTV treatment study without treatment-limiting toxicity.
  • Males and females of childbearing potential must agree to utilize effective contraception methods.
  • Ability to understand and sign a written informed consent form.

Exclusion Criteria:

  • Females who are pregnant or breastfeeding.
  • Participation in any other clinical trial without prior approval from the Sponsor.
  • Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the subject unsuitable for the study.
  • Subjects receiving ongoing therapy with contraindicated drugs.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00445146


  Hide Study Locations
Locations
United States, Arizona
Pheonix, Arizona, United States, 85006
United States, Arkansas
Little Rock, Arkansas, United States, 72207
United States, California
Beverly Hills, California, United States, 90211
Costa Mesa, California, United States, 92626
Fountain Valley, California, United States, 92708
Long Beach, California, United States, 90813
Los Angeles, California, United States, 90033
Newport Beach, California, United States, 92663
Palo Alto, California, United States, 94305
San Diego, California, United States, 92103
San Francisco, California, United States, 94110
United States, Connecticut
Norwalk, Connecticut, United States, 06851
United States, District of Columbia
Washington, District of Columbia, United States, 20037
United States, Florida
Atlantis, Florida, United States, 33462
Fort Lauderdale, Florida, United States, 33308
Manors, Florida, United States, 33305
Miami, Florida, United States, 33136
North Miami Beach, Florida, United States, 33169
North Palm Beach, Florida, United States, 33408
Orlando, Florida, United States, 32803
Sarasota, Florida, United States, 34239
Tampa, Florida, United States, 33602
United States, Georgia
Decatur, Georgia, United States, 30033
Macon, Georgia, United States, 31201
United States, Illinois
Chicago, Illinois, United States, 60657
United States, Maryland
Baltimore, Maryland, United States, 21205
United States, Massachusetts
Boston, Massachusetts, United States, 02215
West Springfield, Massachusetts, United States, 01107
United States, Michigan
St. Louis, Michigan, United States, 63108
United States, Nevada
Henderson, Nevada, United States, 89074
United States, New Jersey
Hillsborough, New Jersey, United States, 08844
United States, New Mexico
Santa Fe, New Mexico, United States, 87505
United States, New York
Albany, New York, United States, 12208
Bronx, New York, United States, 11030
Manhasset, New York, United States, 11030
New York, New York, United States, 10016
Stonybrook, New York, United States, 11794
United States, North Carolina
Durham, North Carolina, United States, 27110
Huntersville, North Carolina, United States, 28078
United States, Pennsylvania
Hershey, Pennsylvania, United States, 17033
Philadelphia, Pennsylvania, United States, 19107
United States, Tennessee
Memphis, Tennessee, United States, 38105
United States, Texas
Dallas, Texas, United States, 75204
Houston, Texas, United States, 77030
United States, Virginia
Annandale, Virginia, United States, 22003
United States, Washington
Seattle, Washington, United States, 98101
Tacoma, Washington, United States, 98405
Puerto Rico
Santurce, Puerto Rico, 00921
Sponsors and Collaborators
Gilead Sciences
Investigators
Study Director: Martin Rhee, MD Gilead Sciences
  More Information

Responsible Party: Gilead Sciences
ClinicalTrials.gov Identifier: NCT00445146     History of Changes
Other Study ID Numbers: GS-US-183-0130
First Submitted: February 28, 2007
First Posted: March 8, 2007
Results First Submitted: March 23, 2016
Results First Posted: April 25, 2016
Last Update Posted: April 25, 2016
Last Verified: March 2016

Keywords provided by Gilead Sciences:
Phase 2
Open-label
Rollover
Integrase Inhibitor
Antiretroviral Agents
Highly Active Antiretroviral Activity
HAART
HIV, HIV-1, AIDS virus, Human Immunodeficiency Virus
Acquired Immune Deficiency Syndrome Virus
treatment experienced

Additional relevant MeSH terms:
Infection
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Ritonavir
Anti-Retroviral Agents
HIV Protease Inhibitors
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Anti-HIV Agents
Antiviral Agents
Anti-Infective Agents
Cytochrome P-450 CYP3A Inhibitors
Cytochrome P-450 Enzyme Inhibitors