Overview
A Study of Different Doses of Atevirdine Mesylate Plus Zidovudine in HIV-Positive Patients
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
To determine the tolerance and antiviral response of two different doses of atevirdine mesylate (U-87201E) in symptomatic HIV-positive patients with CD4 counts of 50-350 cells/mm3, who also take zidovudine (AZT).Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Pharmacia and UpjohnTreatments:
Atevirdine
Zidovudine
Criteria
Inclusion CriteriaConcurrent Medication:
Allowed:
- Primary or secondary prophylaxis for opportunistic infections.
Patients must have:
- HIV infection.
- Symptoms (currently or prior to enrollment) included in Category B or C of CDC
classification, although THE FOLLOWING CURRENT ACUTE MEDICAL CONDITIONS ARE NOT
ALLOWED:
- Cryptococcosis
- Pneumocystis carinii pneumonia
- Herpes zoster
- Histoplasmosis
- CMV
- Hepatic or renal disease
- Lymphoma.
- CD4 count 50 - 350 cells/mm3 within 14 days prior to study entry.
- Ongoing therapy with AZT at 500 - 600 mg total daily dose for at least 3 months prior
to study entry.
- Consent of parent, guardian, or person with power of attorney if less than 18 years of
age.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions are excluded:
- Intolerance to AZT.
- Current diagnosis of malignancy for which systemic therapy will be required during the
study.
Concurrent Medication:
Excluded:
- Any other investigational drugs.
Prior Medication:
Excluded:
- Cytotoxic chemotherapy within 1 month prior to study entry.
- Prior U-87201E or any other non-nucleoside antiretroviral medications, including but
not limited to nevirapine, TIBO R-82150 or TIBO R-82913, L-697639 or L-696229,
U-90152S, or any protease inhibitors.
- Antiretroviral agents other than AZT within 3 months prior to study entry.
Required:
- AZT for at least 3 months prior to study entry. Present use of excessive alcohol or
illicit drugs.