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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00002170
Other study ID # 259C
Secondary ID Study 518AG1343-
Status Completed
Phase Phase 2
First received November 2, 1999
Last updated June 23, 2005

Study information

Verified date May 1999
Source NIH AIDS Clinical Trials Information Service
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if it is safe and effective to give Viracept to AIDS patients who are being treated for MAC.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years and older
Eligibility Inclusion Criteria

Patients must have:

- HIV infection

- New diagnosis of MAC bacteremia and < 7 days of therapy.

Prior Medication:

Allowed:

Patients no more than 7 days of therapy for MAC disease.

Exclusion Criteria

Prior Medication:

Excluded:

Prior therapy (or less than 2 weeks) with protease inhibitors other than saquinavir.

Study Design

Endpoint Classification: Safety Study, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Nelfinavir mesylate


Locations

Country Name City State
United States Boston VA Med Ctr / 151 Boston Massachusetts
United States Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois
United States Baylor Univ Houston Texas
United States Univ of California / San Diego Treatment Ctr San Diego California
United States Harbor UCLA Med Ctr Torrance California

Sponsors (1)

Lead Sponsor Collaborator
Agouron Pharmaceuticals

Country where clinical trial is conducted

United States, 

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