Completed
The Antiviral Effect of Switching From Hard Capsule Saquinavir (SQVhc) to the Soft Gelatin Capsule of Saquinavir (SQVsc) Versus Switching to Indinavir (IDV) After 1 Year of Saquinavir Use
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-04
144
Participants Needed
16
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
To determine, in HIV-infected patients, whether switching to a new soft gelatin capsule formulation of saquinavir or to indinavir following prolonged use of the original hard capsule formulation of saquinavir results in an acute decrease in plasma HIV RNA. Resistance to anti-HIV agents occurs with increasing duration of use. In vitro studies have shown that cross-resistance occurs among protease inhibitors, although no clinical trials have been conducted to examine antiretroviral activity with sequential use of protease inhibitors or to determine whether saquinavir resistance can be overcome with higher concentrations of the drug.
CONDITIONS
Official Title
The Anti-HIV Effects of Saquinavir Soft Gelatin Capsules Versus Indinavir in Patients Who Have Used Saquinavir Hard Gelatin Capsules for One Year
Who Can Participate
Eligibility Criteria
You may qualify if you...
Inclusion Criteria
Concurrent Medication:
Required:
- PCP prophylaxis if CD4 count <= 200 cells/mm3.
Allowed:
- Intralesional therapy for KS.
- Vitamins.
- Nucleoside RT inhibitors, provided regimen remains stable for first 8 weeks of study.
Concurrent Treatment:
Allowed:
- Acupuncture.
- Visualization techniques.
Patients must have:
- HIV infection.
- Prior hard capsule saquinavir at 1800 mg/day for more than 1 year.
Prior Medication:
Allowed:
- Prior saquinavir.
- Prior antiretrovirals, excluding protease inhibitors other than saquinavir.
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
- Psychological condition or medical instability that would interfere with study evaluation or procedures.
AS PER AMENDMENT 5/7/97:
- Active tuberculosis.
Concurrent Medication:
Excluded:
- Protease inhibitors other than study drugs.
- Non-nucleoside RT inhibitors.
- Interferon.
- Interleukins.
- GM-CSF.
- HIV vaccines.
- Systemic cytotoxic chemotherapy.
- Investigational drugs other than study medications.
- Rifabutin.
- Rifampin.
- Midazolam.
- Triazolam.
- Ketoconazole.
- Delavirdine.
- Cisapride.
- Terfenadine.
- Astemizole.
AS PER AMENDMENT 5/7/97:
- Nevirapine.
Patients with the following prior conditions are excluded:
- Unexplained fever > 38.5 C for any 7 days within 30 days prior to study entry.
- Diarrhea persisting for 15 days within 30 days prior to study entry.
Prior Medication:
Excluded:
- Any prior protease inhibitor other than saquinavir.
Excluded within the past 2 months.
- Change in antiretroviral regimen.
- Systemic chemotherapy for KS.
Excluded within the past month:
- Non-nucleoside RT inhibitors.
- Interferons.
- Interleukins.
- HIV vaccines.
- Experimental therapies.
Excluded within the past 2 weeks:
- Rifabutin.
- Cisapride.
- Terfenadine.
- Astemizole.
- Midazolam.
- Triazolam.
- Oral ketoconazole.
- Delavirdine.
- Acute therapy for infection or other medical illness.
Active substance abuse that would interfere with study evaluation or procedures.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Trial Site Locations
Total: 16 locations
1
Stanford CRS
Palo Alto, California, United States, 94304
Status Unknown
2
Ucsf Aids Crs
San Francisco, California, United States, 94110
Status Unknown
3
Harbor-UCLA Med. Ctr. CRS
Torrance, California, United States, 90502
Status Unknown
4
University of Colorado Hospital CRS
Aurora, Colorado, United States, 80045
Status Unknown
5
Univ. of Miami AIDS CRS
Miami, Florida, United States, 33136
Status Unknown
6
Northwestern University CRS
Chicago, Illinois, United States, 60611
Status Unknown
7
Rush Univ. Med. Ctr. ACTG CRS
Chicago, Illinois, United States, 60612
Status Unknown
8
Massachusetts General Hospital ACTG CRS
Boston, Massachusetts, United States, 02114
Status Unknown
9
Washington U CRS
St Louis, Missouri, United States, 63110
Status Unknown
10
St. Louis ConnectCare, Infectious Diseases Clinic
St Louis, Missouri, United States, 63112
Status Unknown
11
SUNY - Buffalo, Erie County Medical Ctr.
Buffalo, New York, United States, 14260
Status Unknown
12
Beth Israel Med. Ctr. (Mt. Sinai)
New York, New York, United States, 10003
Status Unknown
13
NY Univ. HIV/AIDS CRS
New York, New York, United States, 10016
Status Unknown
14
Univ. of Rochester ACTG CRS
Rochester, New York, United States, 14642
Status Unknown
15
The Ohio State Univ. AIDS CRS
Columbus, Ohio, United States, 43210
Status Unknown
16
University of Washington AIDS CRS
Seattle, Washington, United States, 98104
Status Unknown
How is the study designed?
Study Type
INTERVENTIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
TREATMENT
Number of Arms
0
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Published Research Related To This Trial
Saquinavir switch study stopped.
https://pubmed.ncbi.nlm.nih.gov/11364285Spring cleaning in trial land.
D Gilden
https://pubmed.ncbi.nlm.nih.gov/11364275Methods for investigation of the relationship between drug-susceptibility phenotype and human immunodeficiency virus type 1 genotype with applications to AIDS clinical trials group 333.
A D Sevin, V DeGruttola, M Nijhuis...
https://pubmed.ncbi.nlm.nih.gov/10882582Baseline human immunodeficiency virus type 1 phenotype, genotype, and RNA response after switching from long-term hard-capsule saquinavir to indinavir or soft-gel-capsule saquinavir in AIDS clinical trials group protocol 333.
M F Para, D V Glidden, R W Coombs...
https://pubmed.ncbi.nlm.nih.gov/10950766