A Study of MDL 28,574A in HIV-Infected Patients
This study has been completed.
Sponsor:
Hoechst Marion Roussel
Information provided by:
NIH AIDS Clinical Trials Information Service
ClinicalTrials.gov Identifier:
NCT00002329
First received: November 2, 1999
Last updated: June 23, 2005
Last verified: May 1995
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Celgosivir hydrochloride |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Pharmacokinetics Study Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Randomized, Placebo-Controlled, Double-Blind, Single and Multiple Oral Dose-Tolerance Study of Oral MDL 28,574A Solution in HIV-Positive Patients |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by NIH AIDS Clinical Trials Information Service:
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria
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.
Exclusion Criteria
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.
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00002329 History of Changes |
| Other Study ID Numbers: | 221A, NDPR0002 |
| Study First Received: | November 2, 1999 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by NIH AIDS Clinical Trials Information Service:
|
MDL 28574 |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome 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 |
ClinicalTrials.gov processed this record on June 17, 2013