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A Study of d4T in Patients With AIDS or AIDS-Related Complex Who Cannot Take AZT
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Purpose
To determine the safety and maximum tolerated dose (MTD) of 2',3'-dideoxy-2',3'-didehydrothymidine (d4T) administered to patients with AIDS or AIDS related complex (ARC) who are intolerant of zidovudine (AZT). The study also begins an assessment of the effectiveness of d4T therapy on HIV replication, on plasma levels of p24 antigen, and clinical or immunologic parameters associated with AIDS.
Of the methods that are being evaluated to treat HIV-infected individuals, AZT has produced the best results to date. Toxic effects in approximately 50 percent of patients receiving AZT may limit its usefulness for prolonged treatment. Long-term treatment may be necessary to prevent progression of early stage HIV infection to AIDS and to prevent secondary transmission. Other drugs that may be equally or more effective than AZT and useful in the long- term treatment of HIV infection must be developed and evaluated. Test-tube and animal studies of d4T show that the drug can inhibit replication (reproduction) of HIV at concentrations similar to concentrations of AZT that have anti-HIV activity. These studies also indicate that the drug may stay in the bloodstream longer than AZT. Thus, it may be possible for the drug to be as effective as AZT when taken less frequently than AZT. It also may have a less disturbing effect on other body functions (such as thymidine metabolism).
| Condition | Intervention | Phase |
|---|---|---|
| HIV Infections | Drug: Stavudine | Phase 1 |
| Study Type: | Interventional |
| Study Design: | Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase I Safety Study of BMY-27857 (2',3'-Dideoxy-2',3'-Didehydrothymidine [d4T]) Administered Four Times Daily to AZT-Intolerant Patients With AIDS or AIDS-Related Complex |
| Estimated Enrollment: | 35 |
Of the methods that are being evaluated to treat HIV-infected individuals, AZT has produced the best results to date. Toxic effects in approximately 50 percent of patients receiving AZT may limit its usefulness for prolonged treatment. Long-term treatment may be necessary to prevent progression of early stage HIV infection to AIDS and to prevent secondary transmission. Other drugs that may be equally or more effective than AZT and useful in the long- term treatment of HIV infection must be developed and evaluated. Test-tube and animal studies of d4T show that the drug can inhibit replication (reproduction) of HIV at concentrations similar to concentrations of AZT that have anti-HIV activity. These studies also indicate that the drug may stay in the bloodstream longer than AZT. Thus, it may be possible for the drug to be as effective as AZT when taken less frequently than AZT. It also may have a less disturbing effect on other body functions (such as thymidine metabolism).
Five patients are enrolled at each dose level and receive d4T for 10 weeks at their initial dose level. Escalation to the next higher dose level, using a different group of five patients, occurs after three patients in the preceding group have successfully completed at least 3 weeks of oral dosing.
Eligibility| Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Patients must have:
- Diagnosis of AIDS or AIDS related complex (ARC).
- Previous intolerance to daily doses of up to 1200 mg of zidovudine (AZT) demonstrated by a decrease in hemoglobin levels of 2 - 8.5 g/dl or AZT-related depression of neutrophils of 200 - 750 cells/mm3.
- Ability to provide informed consent.
Prior Medication:
Allowed:
- Zidovudine (AZT).
Exclusion Criteria
Co-existing Condition:
Patients with the following are excluded:
- AIDS-defining opportunistic infection on enrollment.
- Intractable diarrhea.
- History of seizures within past 2 years or currently requiring anticonvulsants for control.
- Any other clinical conditions or prior therapy which in the opinion of the investigator would make the patient unsuitable for study or unable to comply with the dosing requirements.
Concurrent Medication:
Excluded:
- Systemic maintenance or chemoprophylaxis for opportunistic infection (includes dapsone, acyclovir).
- Systemic therapy with this or any other antiretroviral drug (except zidovudine (AZT)) or investigational drug.
- Ribavirin.
- Cytotoxic anticancer therapy.
- Any agent known as a potent inducer or inhibitor of drug-metabolizing enzymes (includes rifampin and barbiturates).
- Trimethoprim / sulfamethoxazole (TMP / SMX).
Patients with the following are excluded:
- AIDS-defining opportunistic infection on enrollment.
- Intractable diarrhea.
- History of seizures within past 2 years or currently requiring anticonvulsants for control.
- Any other clinical conditions or prior therapy which in the opinion of the investigator would make the patient unsuitable for study or unable to comply with the dosing requirements.
Prior Medication:
Excluded within 2 weeks of study entry:
- Any agent known as a potent inducer or inhibitor of drug-metabolizing enzymes (includes rifampin and barbiturates).
Excluded within 1 month of study entry:
- Systemic therapy with this or any other antiretroviral drug (except zidovudine (AZT)) or investigational drug.
Excluded within 3 months of study entry:
- Ribavirin.
- Cytotoxic anticancer therapy.
Active alcohol or drug abuse sufficient in investigator's opinion to prevent adequate compliance with study therapy.
Contacts and LocationsPlease refer to this study by its ClinicalTrials.gov identifier: NCT00000686
| United States, New York | |
| Cornell Univ Med Ctr | |
| New York, New York, United States, 10021 | |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00000686 History of Changes |
| Other Study ID Numbers: |
ACTG 111 AI455-004 |
| Study First Received: | November 2, 1999 |
| Last Updated: | August 25, 2008 |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
|
Drug Evaluation Acquired Immunodeficiency Syndrome AIDS-Related Complex Antiviral Agents Zidovudine |
Additional relevant MeSH terms:
|
HIV Infections AIDS-Related Complex Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
Stavudine Antimetabolites Molecular Mechanisms of Pharmacological Action Reverse Transcriptase Inhibitors Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Anti-HIV Agents |
ClinicalTrials.gov processed this record on June 26, 2017