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A Prospective Double-Blind Study of Retrovir in Early HIV Infection

Information source: NIH AIDS Clinical Trials Information Service
Information obtained from ClinicalTrials.gov on June 20, 2008
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: HIV Infections

Intervention: Zidovudine (Drug)

Phase: N/A

Status: Completed

Sponsored by: Glaxo Wellcome

Summary

To evaluate the safety and tolerance of chronic administration of Retrovir (AZT) to adult patients with early manifestations of HIV disease. To assess the efficacy of AZT therapy in the treatment of HIV disease in these patients.

(12/01/89) Information supplied by drug company update. Study discontinued due to positive data from ACTG 016.

Clinical Details

Official title: A Prospective Double-Blind Study of Retrovir in Early HIV Infection

Study design: Treatment, Double-Blind

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria

Concurrent Treatment:

Allowed:

- Electron beam therapy to an area of less than 100 cm2.

Patient must have signs and symptoms of HIV infection confined to those of stages WRII-V or CDC groups III IV-A, IV-C-2 (except recurrent Salmonella bacteremia, nocardiosis, or disseminated/extrapulmonary Mycobacterium tuberculosis), and IV-E (except diffuse interstitial lymphoid pneumonitis).

- Patient must be able to give informed consent.

Exclusion Criteria

Co-existing Condition:

Patients with the following are excluded:

- Evidence of nervous system dysfunction caused by factors other than HIV infection,

including chronic alcohol or drug abuse.

- Present or prior known AIDS-defining opportunistic infections, lymphomas, or

malignancies based on CDC criteria.

- Present or prior known systemic opportunistic diseases most recently included in the

expanded CDC definition of AIDS:

- extrapulmonary or disseminated Mycobacterium tuberculosis infections, recurrent

nontyphoidal Salmonella septicemia, coccidioidomycosis, diffuse interstitial lymphoid pneumonitis.

- Evidence of compromised bone marrow function defined by specified lab values.

- Evidence of HIV neurologic disease.

- Evidence of HIV-associated "wasting syndrome".

- Hypersensitivity to zidovudine (AZT).

Concurrent Medication:

Excluded:

- Cytotoxic chemotherapeutic agents.

- Steroids.

- Interferon or immunomodulating agents.

- Any antiretroviral drug including, but not limited to zidovudine (AZT), ribavirin,

HPA23, AL 721, or phosphonoformate.

Patients with the following are excluded:

- Evidence of nervous system dysfunction caused by factors other than HIV infection,

including chronic alcohol or drug abuse. Present or prior known AIDS-defining opportunistic infections, lymphomas, or malignancies based on CDC criteria. Present or prior known systemic opportunistic diseases most recently included in the expanded CDC definition of AIDS:

- extrapulmonary or disseminated Mycobacterium tuberculosis infections, recurrent

nontyphoidal Salmonella septicemia, coccidioidomycosis, diffuse interstitial lymphoid pneumonitis.

- Evidence of compromised bone marrow function defined by specified lab values.

Evidence of HIV neurologic disease.

- Evidence of HIV-associated wasting syndrome.

- Hypersensitivity to retrovir.

Prior Medication:

Excluded within 4 weeks of study entry:

- Interferon.

- Immunomodulating agents.

- Myelosuppressive drugs.

- Nephrotoxic agents.

- Other experimental chemotherapy.

Prior Treatment:

Excluded:

- Treatment with radiation therapy (with the exception of electron beam therapy to an

area of less than 100 cm2).

Chronic alcohol or drug abuse.

Locations and Contacts

Glaxo Wellcome Inc, Research Triangle Park, North Carolina 27709, United States
Additional Information


Last updated: June 23, 2005

Page last updated: June 20, 2008

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