A Study of MDL 28,574A in HIV-Infected Patients

Completed · Phase 1

Conditions studied: HIV Infections

In brief

To characterize the safety profile of MDL 28574A following both acute and subchronic dosing in HIV-positive patients. To determine the MTD of both acute and subchronic doses of this drug when administered as oral solution. To determine the pharmacokinetic profile of MDL 28574A and castanospermine (from which MDL 28574A is derived) following both acute and subchronic dosing.

Key facts

Study ID

NCT00002329

Run by

Hoechst Marion Roussel

Last updated by the study team

2005-06-24

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must have:
• HIV infection.
• CD4 count >= 500 cells/mm3.
• No evidence of AIDS.
• No antiretroviral therapy within 30 days prior to study entry.
• NOTE:
• Presence of lymphadenopathy in two or more extrainguinal sites, at least 1 cm in diameter for 3 or more months, is permitted.

You may not qualify if…

• Co-existing Condition:
• Patients with the following symptoms or conditions are excluded:
• Clinically significant abnormalities on routine hematology (other than CD4 count and Western blot), serum chemistry, and urinalysis.
• Abnormal EKG.
• Positive stool guaiac.
• Abnormal medical history or physical exam including temperature, heart rate, and blood pressure.
• Clinically significant organ abnormality or disease.
• Positive urine drug screen for illicit drugs.
• Inability to comply with study procedures.
• Concurrent Medication:
• Excluded:
• Routine treatment with nonprescription medications.
• Treatment with other medications except with approval of the investigator.
• Patients with the following prior conditions are excluded:
• Prior participation in this trial.
• Serious physical or mental illness within 1 year prior to study entry that would confound interpretation of data.
• Prior Medication:
• Excluded:
• Antiretroviral therapy within 30 days prior to study entry.
• Known medications that alter renal, hepatic, or hematologic/immunologic function (such as barbiturates, phenothiazines, cimetidine, and immunomodulators) within 14 days prior to study entry.
• Routine treatment with nonprescription medications within 3 days prior to study entry.
• History of alcohol or drug abuse within the past year.

Where it is running

• Saint Francis Mem Hosp — San Francisco, California, United States

Full record on ClinicalTrials.gov

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