HIV InfectionsPhase 2NCT00002440
A Study of 1592U89 in Combination With Protease Inhibitors in HIV-Infected Patients Who Have Never Taken Anti-HIV Drugs
A Phase 2 study testing Indinavir sulfate, Ritonavir and Abacavir sulfate in people with HIV Infections, run by Glaxo Wellcome at 8 sites in United States.
Trial summary
The purpose of this study is to see if it is safe and effective to give 1592U89 plus certain protease inhibitors (PIs) to HIV-infected patients who never have been treated with anti-HIV drugs. This study also examines how the body processes these drugs when they are given together. Read more about this study
- Who is it for?
- Ages 16 years and older
- Conditions the study is for
- HIV Infections
- What is being tested?
- Indinavir sulfate, Ritonavir and Abacavir sulfate
- How many people
- 80 participants
- Where
- 8 sitesUnited States
- Study dates
- Start not givento not given
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Concurrent Medication:
- Allowed:
- Local treatment for Kaposi's sarcoma.
- GM-CSF, G-CSF or erythropoietin.
- Patients must have:
- HIV-1 infection documented by a licensed HIV-1 antibody ELISA and confirmed by Western blot detection of HIV-1 antibody or a positive HIV-1 blood culture.
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- CD4+ cell count >= 100 cells/mm3 within 14 days of study drug administration.
- HIV-1 RNA >= 5,000 copies/ml within 14 days of study drug administration.
- No active or ongoing AIDS-defining opportunistic infection or disease.
- Signed, informed consent from parent or legal guardian for patients less than 18 years of age.
- Prior Medication:
- Allowed:
- Local treatment for Kaposi's sarcoma.
Who cannot join
- Co-existing Condition:
- Patients with the following conditions or symptoms are excluded:
- Malabsorption syndrome, or other gastrointestinal dysfunction, that might interfere with drug absorption or render the patient unable to take oral medication.
- Life-threatening infection or other serious medical condition that may compromise a patient's safety.
- Concurrent Medication:
- Excluded:
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- Other investigational agents. NOTE:
- Those available through Treatment IND or expanded access programs are evaluated individually.
- Chemotherapeutic agents for the initial 24 weeks of study (except local treatment for Kaposi's sarcoma).
- Agents with documented anti-HIV activity in vitro.
- Foscarnet.
- Immunomodulating agents such as systemic corticosteroids, interleukins, thalidomide, anti-cytokine agents or interferons.
- Antioxidants.
- Concurrent Treatment:
- Excluded:
- Radiation therapy within the first 24 weeks of study.
- Patients with the following prior conditions are excluded:
- History of clinically relevant pancreatitis or hepatitis within the last 6 months.
- Participation in an investigational HIV-1 vaccine trial.
- Prior Medication:
- Excluded:
- Antiretroviral therapy, including reverse transcriptase inhibitor and protease inhibitor therapy.
- Cytotoxic chemotherapeutic agents within 30 days of study drug administration.
- HIV-1 vaccine dose within the 3 months prior to study drug administration.
- Immunomodulating agents, such as systemic corticosteroids, interleukins or interferons within 30 days of study drug administration.
- Prior Treatment:
- Excluded:
- Radiation therapy within 30 days of study drug administration. Alcohol or illicit drug use that may interfere with patient compliance.
Trial locations and contacts
8 sites in 1 country.
8 sites in 1 country
United States8 sites
Carolinas Med Ctr
Charlotte, North Carolina, 28232
Case Western Reserve Univ / AIDS Clinical Trials Unit
Cleveland, Ohio, 44106
Kansas City AIDS Research Consortium
Kansas City, Missouri, 64111
Vanderbilt Univ Med Ctr
Nashville, Tennessee, 372321302
Yale U / New Haven Med Ctr / AIDS Clinical Trials Unit
New Haven, Connecticut, 065102483
NYU Med Ctr / Dept of Medicine / AIDS Clinical Trial
New York, New York, 10016
Univ of Pittsburgh Med Ctr
Pittsburgh, Pennsylvania, 15213
UCSD Treatment Ctr
San Diego, California, 921036329
About this study
Official title: An Open-Label, Phase II Trial to Evaluate the Steady-State Pharmacokinetics, Safety, and Efficacy of 1592U89 in Combination With Selected HIV-1 Protease Inhibitors in Antiretroviral-Naive, HIV-1-Infected Patients.
The purpose of this study is to see if it is safe and effective to give 1592U89 plus certain protease inhibitors (PIs) to HIV-infected patients who never have been treated with anti-HIV drugs. This study also examines how the body processes these drugs when they are given together.
Read the detailed description
In this Phase II, open-label study patients (16 per treatment group) are randomized to receive 1592U89 in combination with one of five protease inhibitors: indinavir, saquinavir, ritonavir, nelfinavir, or 141W94 for up to 48 weeks.
- Conditions
- HIV Infections
- Being tested
- Indinavir sulfate, Ritonavir, Abacavir sulfate, Amprenavir, Nelfinavir mesylate
- Keywords
- HIV-1, Drug Therapy, Combination, HIV Protease Inhibitors, Mutation, HIV-1 Reverse Transcriptase, HIV Protease, Reverse Transcriptase Inhibitors, Anti-HIV Agents, abacavir
- Medical subject headings
- HIV Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Indinavir sulfateDrug
RitonavirDrug
Abacavir sulfateDrug
AmprenavirDrug
Nelfinavir mesylateDrug
SaquinavirDrug
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Aug 2001 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HIV InfectionsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Enrolment
- 80 participants
Sponsor and investigators
- Lead sponsor
- Glaxo Wellcome
- Sponsor type
- Industry (pharma, biotech, devices)
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00002440
- Sponsor's protocol ID
- 238J
- Other IDs
- CNAA2004
- Status last verified
- Nov 1998
- First submitted
- 2 Nov 1999
- Last updated
- 24 Jun 2005
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2005. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Open-Label, Phase II Trial to Evaluate the Steady-State Pharmacokinetics, Safety, and Efficacy of 1592U89 in Combination With Selected HIV-1 Protease Inhibitors in Antiretroviral-Naive, HIV-1-Infected Patients.
- ClinicalTrials.gov ID
- NCT00002440
- Acronym / sponsor ID
- 238J
- Conditions
- HIV Infections
- Keywords
- HIV-1, Drug Therapy, Combination, HIV Protease Inhibitors, Mutation, HIV-1 Reverse Transcriptase, HIV Protease, Reverse Transcriptase Inhibitors, Anti-HIV Agents
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 80 participants
- Lead sponsor
- Glaxo WellcomeIndustry (pharma, biotech, devices)
- First posted
- 31 Aug 2001 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to see if it is safe and effective to give 1592U89 plus certain protease inhibitors (PIs) to HIV-infected patients who never have been treated with anti-HIV drugs. This study also examines how the body processes these drugs when they are given together.
Detailed description
In this Phase II, open-label study patients (16 per treatment group) are randomized to receive 1592U89 in combination with one of five protease inhibitors: indinavir, saquinavir, ritonavir, nelfinavir, or 141W94 for up to 48 weeks.
Study design
- Primary purpose
- Treatment
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (13 listed)
- Local treatment for Kaposi's sarcoma.
- GM-CSF, G-CSF or erythropoietin.
- HIV-1 infection documented by a licensed HIV-1 antibody ELISA and confirmed by Western blot detection of HIV-1 antibody or a positive HIV-1 blood culture.
- CD4+ cell count >= 100 cells/mm3 within 14 days of study drug administration.
- HIV-1 RNA >= 5,000 copies/ml within 14 days of study drug administration.
Key exclusion criteria (28 listed)
- Malabsorption syndrome, or other gastrointestinal dysfunction, that might interfere with drug absorption or render the patient unable to take oral medication.
- Life-threatening infection or other serious medical condition that may compromise a patient's safety.
- Other investigational agents. NOTE:
- Those available through Treatment IND or expanded access programs are evaluated individually.
- Chemotherapeutic agents for the initial 24 weeks of study (except local treatment for Kaposi's sarcoma).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Indinavir sulfate | Drug | – |
| Ritonavir | Drug | – |
| Abacavir sulfate | Drug | – |
| Amprenavir | Drug | – |
| Nelfinavir mesylate | Drug | – |
| Saquinavir | Drug | – |
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2005.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
8 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Indinavir sulfate, Ritonavir and Abacavir sulfate in people with HIV Infections, run by Glaxo Wellcome at 8 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 13 inclusion and 28 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jun 2005. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 8 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2005.