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A Study of Viracept in AIDS Patients with Cytomegalovirus Retinitis



A Study of Viracept in AIDS Patients with Cytomegalovirus Retinitis

For Condition: Cytomegalovirus Retinitis,HIV Infections
Status: Completed
Sponsor(s): Agouron Pharmaceuticals ,
Synopsis: The purpose of this study is to see if it is safe and effective to give Viracept to AIDS patients who are already being treated for cytomegalovirus (CMV) retinitis.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Placebo Control, Safety Study
Minimum Age/Maximum Age: 13 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria Patients must have: - HIV infection. - Newly diagnosed or first progression of CMV retinitis. Exclusion Criteria Prior Medication: Excluded: Prior therapy (or less than 2 weeks) with protease inhibitor other than saquinavir.
Total Enrollment: 

Location and Contact Information:

Northwestern Univ / SOCA
Chicago,  Illinois,  60611
United States
 

Baylor Univ
Houston,  Texas,  77009
United States
 

Univ of California / UCI Med Ctr
Orange,  California,  92868
United States
 

Univ of California / San Diego Treatment Ctr
San Diego,  California,  92103
United States
 

Univ of Texas Med Branch
Galveston,  Texas,  77555
United States
 

George Washington Univ
Washington D.C.,  District of Columbia,  20037
United States
 

Harbor UCLA Med Ctr
Torrance,  California,  90502
United States
 

Univ of Southern California / LA County USC Med Cntr
Los Angeles,  California,  90033
United States
 


Additional Information:
Study ID Numbers:
  259A;  Study 517,AG1343-517
Study Start Date: 
Record last reviewed: May 1999
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00002169

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