Completed
A Multicenter Phase I Clinical Trial of Ribavirin in the Treatment of Patients With AIDS and Advanced AIDS Related Illnesses
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-01
96
Participants Needed
5
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
To determine the maximum long-term dosage of ribavirin (RBV) that is safe and free of serious side effects in patients with AIDS or AIDS related illnesses. Also, to determine what effect different dosage levels have on biologic markers of efficacy, such as the amount of the AIDS virus (HIV) or number of T cells in the patient's blood. RBV is a new drug capable of inhibiting the growth of the AIDS virus in the laboratory with little effect on normal human cells. In earlier tests of RBV in AIDS patients, the drug was well tolerated and safe, and this favorable result suggested that RBV should be more extensively studied in patients with AIDS and advanced AIDS related complex (ARC).
CONDITIONS
Official Title
A Study of Ribavirin in the Treatment of Patients With AIDS and AIDS-Related Problems
Who Can Participate
Eligibility Criteria
You may qualify if you...
Inclusion Criteria
Concurrent Medication:
Allowed:
- Short-course therapy (7 days) with oral acyclovir.
- Short-course therapy (7 days) with ketoconazole.
- Topical medications.
- Aerosolized pentamidine for prophylactic purposes.
Concurrent Treatment:
Allowed:
- Blood transfusions for hemoglobin toxicity.
Patients must have two positive HIV p24 antigen tests with titers = or > 70 picograms at least 72 hours apart and within 1 month prior to entry, the last of which must be within 2 weeks of starting therapy.
Prior Medication:
Allowed:
- Zidovudine (AZT), without cessation of therapy required due to intolerance.
- AZT therapy must be discontinued at least 30 days prior to study entry.
Exclusion Criteria
Co-existing Condition:
Patients with the following are excluded:
- Active opportunistic infection, symptomatic visceral Kaposi's sarcoma (KS) or progression of KS within the month prior to entry into the study, neoplasms other than KS, basal cell carcinoma of the skin, or in situ carcinoma of the cervix. Significant diarrhea, defined as = or > 3 liquid stools per day within the past week.
Concurrent Medication:
Excluded:
- Ongoing systemic therapy and/or prophylaxis for an AIDS-defining opportunistic infection.
- Antineoplastic therapy.
- Other experimental medications.
- Systemic chemoprophylaxis for Pneumocystis carinii pneumonia.
- Chronic (> 7 days) oral acyclovir therapy.
Concurrent Treatment:
Excluded:
- Blood transfusions unless they are for = or > grade 3 hemoglobin toxicity.
Patients with the following are excluded:
- Active opportunistic infection, symptomatic visceral Kaposi's sarcoma (KS) or progression of KS within the month prior to entry into the study, neoplasms other than KS, basal cell carcinoma of the skin, or in situ carcinoma of the cervix. Significant diarrhea, defined as = or > 3 liquid stools per day within the past week.
Prior Medication:
Excluded within 30 days of study entry:
- Antiretroviral agents including zidovudine (AZT).
- Biologic modifiers.
- Systemic corticosteroids.
Prior Treatment:
Excluded within 2 months of study entry:
- Blood transfusion except for those who have taken zidovudine (AZT) who may not have received a transfusion within the previous month.
Active drug or alcohol abuse.
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: 5 locations
1
Univ of California / San Diego Treatment Ctr
San Diego, California, United States, 921036325
Status Unknown
2
San Francisco AIDS Clinic / San Francisco Gen Hosp
San Francisco, California, United States, 941102859
Status Unknown
3
Harvard (Massachusetts Gen Hosp)
Boston, Massachusetts, United States, 02114
Status Unknown
4
Bellevue Hosp / New York Univ Med Ctr
New York, New York, United States, 10016
Status Unknown
5
Univ of North Carolina
Chapel Hill, North Carolina, United States, 275997215
Status Unknown
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
N/A
Model
N/A
Primary Purpose
TREATMENT
Number of Arms
0
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