GW873140 to Treat HIV-1 Infected Adults
NCT00076284 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2008-03-04
Summary
This study will determine which of four doses of GW873140 can safely be given to adults to lower the amount of virus (HIV-1) in the body. GW873140 is a new type of anti-HIV drug called a CCR5 receptor antagonist. CCR5 is a receptor on T cells (a type of white blood cell) where HIV-1 enters and then infects the cell. GW873140 is intended to block the CCR5 receptor so that HIV-1 cannot enter the cell.
HIV-1-infected patients 18 years of age and older may be eligible for this study. Candidates are screened with a medical history and physical examination, electrocardiogram, and blood and urine tests. Some of the blood drawn is used to test the patient's HIV-1 type to see if the study drug might lower the amount of HIV-1 in the blood. Women who can become pregnant have a pregnancy test.
Participants are hospitalized for 12 days. They are randomly assigned to take one of the following four treatments for 10 days: 1) 200 mg of GW873140 once a day, or placebo (a look-alike pill with no active ingredient); 2) 200 mg of GW873140 twice a day, or placebo; 3) 400 mg of GW873140 once a day, or placebo; or 600 mg of GW873140 twice a day, or placebo. Participants record the meals they eat on a diary card. In addition, they undergo the following tests and procedures:
During treatment
* Assessment of HIV classification (day 1)
* Review of meal diary cards (days 1,2,3,4,5,8, and 10)
* Review of any HIV-associated conditions, other medications taken besides the study drug, and well-being (days 1,2,3,4,5,8,10, and 11)
* Check of vital signs, including blood pressure, pulse, and temperature (days 1,2,3,4,5,6,7,8,10, and 11)
* Weight assessment (days 1 and 10)
* Electrocardiogram to measure the electrical activity of the heart (days 1,2,3,8, and 10)
* Blood draws for routine laboratory tests, to measure T-cell counts, and to measure HIV levels (days 1,2,5,10, and 11)
* Urine tests (days 1 and 10)
Post-treatment
* Blood tests to monitor the effect of GW873140 on lowering HIV counts (days 12, 15, 17, and 19)
Follow-up visit (2 weeks after last drug dose--day 24)
* Review of medications taken and general well-being
* Check of vital signs
* Physical examination
* Blood and urine tests.
Conditions
- HIV Infections
Interventions
- DRUG
-
GW873140
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Study Design
- Purpose
- TREATMENT
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-01-31
- Completion
- 2005-03-31
Countries
- United States
Study Locations
More Related Trials
-
Safety, Tolerability and Immunogenicity Study of 2 Dose Levels of Trimeric Glycoprotein140 (gp140) in Healthy Adult Volunteers
NCT02304185 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Immunogenicity Study of Ad26-ENVA and Ad35-ENV HIV Vaccines in Healthy HIV-uninfected Adults
NCT01215149 ·Status: COMPLETED ·Phase: PHASE1
-
Safety, Tolerability and Immunogenicity Study of Different Vaccine Regimens of Trivalent Ad26.Mos.HIV or Tetravalent Ad26.Mos4.HIV Along With Clade C Glycoprotein (gp)140 in Healthy Human Immunodeficiency Virus (HIV)-Uninfected Adults
NCT02788045 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Evaluating the Safety, Tolerability, and Pharmacokinetics of an Investigational, Injectable HIV Medicine (GSK1265744) in HIV-Uninfected Adults
NCT02178800 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Immunogenicity of Recombinant HIV Vaccines for HIV/AIDS
NCT01881581 ·Status: UNKNOWN ·Phase: PHASE1
-
A Phase I Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety and Immunogenicity of HIV-1 Recombinant Envelope Glycoprotein gp160
NCT00000745 ·Status: COMPLETED ·Phase: PHASE1
-
Clinical Trial of Recombinant Adenovirus Type 5 AIDS Vaccine
NCT02762045 ·Status: UNKNOWN ·Phase: PHASE1
-
Phase I Protocol for the Evaluation of the Safety and Immunogenicity of Vaccination With Synthetic HIV Envelope Peptides in Patients With Early Human Immunodeficiency Virus Infection
NCT00001386 ·Status: COMPLETED ·Phase: PHASE1
-
A Trial to Evaluate Ad35-GRIN/ENV HIV Vaccine in Healthy Adult Volunteers
NCT00851383 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy of an Antibody to CCR5 in Individuals With HIV Who Are Not Currently on Antiretroviral Therapy
NCT00114699 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety and Immunogenicity of the V3-region Directed Immunogens DV700P-RNA Followed by DV701B1.1-RNA in Adults Without HIV
NCT06919016 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Safety and Immunogenicity Study of 2 Investigational Preventive HIV Vaccines
NCT01264445 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Immune Response to a rAd5 HIV Vaccine Administered in Three Different Ways in Healthy, HIV-Uninfected Adults
NCT01479296 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase I, Multicenter, Randomized Trial to Evaluate the Safety and Immunogenicity of a Recombinant Vaccinia-HIV Envelope Vaccine (HIVAC-1e) in Combination With a Panel of Subunit Recombinant HIV Envelope Vaccines
NCT00000746 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of 2 Different Regimens of Tetravalent Ad26.Mos4.HIV Prime Followed by Boost With Modified Vaccinia Ankara (MVA)-Mosaic OR Ad26.Mos4.HIV Plus a Combination of Mosaic and Clade C gp140 Protein in Human Immunodeficiency Virus (HIV) Type 1 Infected Adults on Suppressive Antiretroviral Treatment
NCT03307915 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of and Immune Response to a DNA HIV Vaccine Followed By Boosting With One of Two Serotypes of Adenoviral Vector HIV Vaccine in Healthy Adults
NCT00472719 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Safety and Immunogenicity of Env (A,B,C,A/E)/Gag (C) DNA and gp120 (A,B,C,A/E) Protein/GLA-SE HIV Vaccines, Given Individually or Co-administered, in Healthy, HIV-1-Uninfected Adults
NCT03409276 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of Recombinant HIV Vaccines in HIV Infected Young Adults on Stable Therapy
NCT00107549 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of and Immune Response to a Modified Vaccinia Ankara (MVA) HIV Vaccine in HIV Uninfected Adults
NCT00376090 ·Status: COMPLETED ·Phase: PHASE1
-
A Clinical Trial to Evaluate the Safety and Immunogenicity of Recombinant HIV-1 Envelope Protein BG505 SOSIP.GT1.1 Gp140 Vaccine, Adjuvanted in Healthy, HIV-uninfected Adults
NCT04224701 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of and Immune Response to a New HIV Vaccine: HIV CTL MEP
NCT00076037 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase I/II Trial of Vaccine Therapy of HIV-1 Infected Individuals With 50-500 CD4 Cells/mm3
NCT00000755 ·Status: COMPLETED ·Phase: PHASE1
-
The Safety and Immunogenicity of a Potential HIV Vaccine
NCT01966900 ·Status: COMPLETED ·Phase: PHASE1
-
Vaccine Treatment for HIV-Infection
NCT00108654 ·Status: COMPLETED ·Phase: PHASE1
-
Study of PRO 140 by Subcutaneous Administration in Adult Subjects With HIV -1 Infection
NCT00642707 ·Status: COMPLETED ·Phase: PHASE2