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A Study of Saquinavir Used Alone or in Combination With Other Anti-HIV Drugs in HIV-Infected Patients

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Saquinavir
Sponsored by
Hoffmann-La Roche
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Zalcitabine, Didanosine, Drug Therapy, Combination, Zidovudine, HIV Protease Inhibitors, Saquinavir, Patient Selection, Anti-HIV Agents

Eligibility Criteria

13 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients must have: Sero-positivity for HIV -1 antibody by an ELISA test, with confirmation by an alternative method. CD4 count <= 300 cells/mm3 (within 4 weeks prior to entry). Signed, informed consent from a parent or legal guardian for patients < 18 years of age. Failed previous therapy with or be intolerant to other registered anti-retroviral drugs. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Eligibility for any controlled clinical study of any experimental HIV therapy. Grade 4 hematologic and/or Grade 3 hematologic toxicity at baseline. Patients with the following prior conditions are excluded: Known hypersensitivity to saquinavir or other protease inhibitors. 1. Drugs, such as rifampin and rifabutin, which induce hepatic enzymes are likely to result in decreased levels of saquinavir and, therefore, should be avoided where possible. Concomitant therapy and treatment should be kept at a minimum. Current participation in any study formally excluding concomitant treatment with experimental drugs. 1. Saquinavir can be used in combination with other registered anti-retroviral drugs such as ZDV, ddC and/or ddl. Other not yet registered anti-retroviral drugs can be used in combination with saquinavir when these drugs are widely available in the respective country or when they are allowed in combination treatment in any on-going clinical study. Prophylactic treatment for any opportunistic infections.

Sites / Locations

  • Hoffmann - La Roche Inc

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Hoffmann-La Roche
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1. Study Identification

Unique Protocol Identification Number
NCT00002382
Brief Title
A Study of Saquinavir Used Alone or in Combination With Other Anti-HIV Drugs in HIV-Infected Patients
Official Title
An Open Label International Compassionate Treatment Program for the Use of Saquinavir (R0 31-8959) Either As Monotherapy or in Combination With Other Anti-Retroviral Drugs in Patients With Proven HIV Infection
Study Type
Interventional

2. Study Status

Record Verification Date
June 1997
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Hoffmann-La Roche

4. Oversight

5. Study Description

Brief Summary
To offer an investigational agent (saquinavir) to people with HIV/AIDS who are in need of additional treatment options and are not eligible to enroll in ongoing clinical trials. Patients who no longer benefit from existing antiretroviral therapy and who are not currently enrolled in ongoing saquinavir trials are eligible for this compassionate treatment program.
Detailed Description
Patients who no longer benefit from existing antiretroviral therapy and who are not currently enrolled in ongoing saquinavir trials are eligible for this compassionate treatment program. Patients may be registered with the program through their physicians, who will be responsible for supervising the administration of treatment; following guidelines for saquinavir dose interruption, dose reduction, or discontinuation; and assessing patient progress throughout the duration of the study. Access to saquinavir will be determined by a lottery system; 60 percent of the program slots will be reserved for patients with CD4 counts of 50 or less and the remaining 40 percent of the slots will be devoted to patients with CD4 counts between 51 and 300.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Zalcitabine, Didanosine, Drug Therapy, Combination, Zidovudine, HIV Protease Inhibitors, Saquinavir, Patient Selection, Anti-HIV Agents

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Masking
None (Open Label)
Enrollment
4000 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Saquinavir

10. Eligibility

Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients must have: Sero-positivity for HIV -1 antibody by an ELISA test, with confirmation by an alternative method. CD4 count <= 300 cells/mm3 (within 4 weeks prior to entry). Signed, informed consent from a parent or legal guardian for patients < 18 years of age. Failed previous therapy with or be intolerant to other registered anti-retroviral drugs. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Eligibility for any controlled clinical study of any experimental HIV therapy. Grade 4 hematologic and/or Grade 3 hematologic toxicity at baseline. Patients with the following prior conditions are excluded: Known hypersensitivity to saquinavir or other protease inhibitors. 1. Drugs, such as rifampin and rifabutin, which induce hepatic enzymes are likely to result in decreased levels of saquinavir and, therefore, should be avoided where possible. Concomitant therapy and treatment should be kept at a minimum. Current participation in any study formally excluding concomitant treatment with experimental drugs. 1. Saquinavir can be used in combination with other registered anti-retroviral drugs such as ZDV, ddC and/or ddl. Other not yet registered anti-retroviral drugs can be used in combination with saquinavir when these drugs are widely available in the respective country or when they are allowed in combination treatment in any on-going clinical study. Prophylactic treatment for any opportunistic infections.
Facility Information:
Facility Name
Hoffmann - La Roche Inc
City
Nutley
State/Province
New Jersey
ZIP/Postal Code
071101199
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Study of Saquinavir Used Alone or in Combination With Other Anti-HIV Drugs in HIV-Infected Patients

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