CClinicalTrials.gg
CompletedNCT00002333Updated Jun 24, 2005

A Study of Saquinavir and Zalcitabine, Used Alone and Together, in the Treatment of Advanced HIV Infection in Patients Who Stopped Taking or Who Cannot Take Zidovudine

A Phase 2 interventional study of Saquinavir and Zalcitabine in HIV Infections, sponsored by Hoffmann-La Roche. Completed at 47 sites in 3 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2005-06-24.

Sponsored by Hoffmann-La Roche · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
900
Ages
18 Years and older
Sex
All
01

Study summary

To compare the safety, tolerance, and efficacy of saquinavir mesylate (Ro 31-8959) alone, zalcitabine (dideoxycytidine; ddC) alone, and both in combination, in patients discontinuing or unable to take zidovudine (AZT).

Read the detailed description

Patients are randomized to one of three treatment regimens: ddC alone, Ro 31-8959 alone, and ddC plus Ro 31-8959. Treatment continues for at least 48 weeks. Patients are stratified by baseline CD4 count. (Per 09/26/94 amendment, a fourth arm, lower dose Ro 31-8959 plus ddC, was discontinued.)

02

Conditions studied

  • HIV Infections

Keywords

  • Zalcitabine
  • Drug Therapy, Combination
  • Acquired Immunodeficiency Syndrome
  • AIDS-Related Complex
  • Saquinavir
  • HIV Protease Inhibitors
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 900 is above the median of 120 across 4,200 interventional studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Hoffmann-La Roche is the lead sponsor of 2,061 studies on the registry; 85 are open to participants now.

Of its 319 completed or terminated interventional studies of FDA-regulated products, 239 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Concurrent Medication:

Allowed:

  • G-CSF and erythropoietin.
  • Prophylaxis or chronic suppression/maintenance therapy with dapsone, aerosolized pentamidine, isoniazid, rifampin, fluoroquinolones, pyrazinamide, ethambutol, fluconazole, itraconazole, acyclovir, clotrimazole, nystatin, trimethoprim/sulfamethoxazole, pyrimethamine, folic acid, sulfadiazine, clindamycin, and fansidar.

Concurrent Treatment:

Allowed:

  • Limited localized radiation therapy to the skin.

Patients must have:

  • Documented HIV infection.
  • CD4 count 50 - 300 cells/mm3.
  • Received prior AZT that has been discontinued at least 28 days prior to study entry.
  • No active opportunistic infection requiring immediate treatment.

Exclusion criteria

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Signs or symptoms of peripheral neuropathy.
  • Malabsorption or inadequate oral intake (defined as unable to eat one or more meals daily because of chronic nausea, emesis, or abdominal/oral-esophageal discomfort.
  • Malignancy, visceral Kaposi's sarcoma, or lymphoma requiring systemic chemotherapy and/or radiotherapy within the next 48 weeks.
  • Any grade 3 or worse laboratory or clinical abnormality.
  • Inability to comply with protocol requirements.

Concurrent Medication:

Excluded:

  • Other antiretroviral drugs.
  • Experimental drugs.
  • Nephrotoxic or hepatotoxic drugs.
  • Drugs likely to cause peripheral neuropathy.
  • Antineoplastic agents.
  • Biologic response modifiers.

Concurrent Treatment:

Excluded:

  • Radiation therapy other than limited localized therapy to skin.

Patients with the following prior conditions are excluded:

  • History of non-Hodgkin's lymphoma.
  • Unexplained fever >= 38.5 C (101.5 F) persisting for 14 days or longer within the 28 days prior to study entry.
  • Unexplained, chronic diarrhea (defined as 3 or more loose stools daily) persisting for 14 days or longer within the 28 days prior to study entry.
  • History of grade 2 or worse peripheral neuropathy.

Prior Medication:

Excluded:

  • Prior HIV proteinase inhibitor.
  • Prior antiretroviral therapy other than AZT.
  • Acute therapy for opportunistic infection within 14 days prior to study entry.

Prior Treatment:

Excluded:

  • More than 3 units of blood in any 21-day period within 3 months prior to study entry.

Required:

  • Prior AZT.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Masking
Double
Enrollment
900 participants

Interventions

  • DrugSaquinavir
  • DrugZalcitabine
06

Study locations

47 sites
  • Kaiser Foundation Hosp
    Harbor City, California 90710, United States
  • UCSD
    La Jolla, California 920930679, United States
  • UCLA School of Medicine
    Los Angeles, California 900121973, United States
  • CARE Ctr / UCLA Med Ctr
    Los Angeles, California 90095, United States
  • UCD
    Sacramento, California 95817, United States
  • UCSF - San Francisco Gen Hosp
    San Francisco, California 94110, United States
  • Davies Med Ctr / c/o HIV Institute
    San Francisco, California 94114, United States
  • Mount Zion Med Ctr / UCSF
    San Francisco, California 94115, United States
  • San Francisco Veterans Administration Med Ctr
    San Francisco, California 94121, United States
  • Pacific Oaks Med Group / Rsch & Scientific Investigation
    Sherman Oaks, California 91403, United States
  • Sunnyvale Med Clinic
    Sunnyvale, California 94086, United States
  • Harbor - UCLA Med Ctr
    Torrance, California 90505, United States
  • Veterans Administration Med Ctr
    Washington, District of Columbia 20422, United States
  • Stratogen of South Florida
    Miami Beach, Florida 33140, United States
  • Miami Veterans Administration Med Ctr
    Miami, Florida 33125, United States
  • Univ of Miami Dept of Medicine
    Miami, Florida 33136, United States
  • AIDS Research Consortium of Atlanta
    Atlanta, Georgia 30308, United States
  • West Paces Clinical Research Incoporated
    Atlanta, Georgia 30327, United States
  • Rush Presbyterian - Saint Luke's Med Ctr
    Chicago, Illinois 60612, United States
  • Univ of Kansas School of Medicine
    Wichita, Kansas 67214, United States
  • Tulane Univ Med School
    New Orleans, Louisiana 70112, United States
  • New England Med Ctr
    Boston, Massachusetts 02111, United States
  • Massachusetts Gen Hosp / Harvard Med School
    Boston, Massachusetts 02114, United States
  • New England Deaconess Hosp
    Boston, Massachusetts 02215, United States
  • Harper Hosp
    Detroit, Michigan 48201, United States
  • Washington Univ School of Medicine
    St. Louis, Missouri 63108, United States
  • UMDNJ - New Jersey Med School / Cooper Hosp
    Camden, New Jersey 08103, United States
  • UMDNJ - New Jersy Med School
    Newark, New Jersey 08103, United States
  • Albany Med College
    Albany, New York 12208, United States
  • Beth Israel Med Ctr
    New York, New York 10003, United States
  • Saint Vincent's Hosp and Med Ctr
    New York, New York 10011, United States
  • Harkness Pavilion
    New York, New York 10032, United States
  • Ohio State Univ Hosp
    Columbus, Ohio 43210, United States
  • Oregon Health Sciences Univ
    Portland, Oregon 97201, United States
  • Thomas Jefferson Med College
    Philadelphia, Pennsylvania 19107, United States
  • Graduate Hosp / Tuttleman Cancer Ctr
    Philadelphia, Pennsylvania 19146, United States
  • Univ of Tennessee
    Memphis, Tennessee 38163, United States
  • Oaklawn Physicians Group
    Dallas, Texas 75219, United States
  • Univ TX Galveston Med Branch
    Galveston, Texas 775550882, United States
  • Baylor College of Medicine
    Houston, Texas 77005, United States
  • Univ of Washington / Harborview Med Ctr
    Seattle, Washington 98104, United States
  • Southern Alberta HIV Clinic
    Calgary, Alberta, Canada
  • McMaster Univ Med Ctr
    Hamilton, Ontario, Canada
  • Sunnybrook Health Science Ctr
    Toronto, Ontario, Canada
  • Clinique Medicale L'Actuele
    Montreal, Quebec, Canada
  • Montreal Gen Hosp
    Montreal, Quebec, Canada
  • San Juan Veterans Administration Med Ctr
    San Juan, 009275800, Puerto Rico
07

References and documents

Publications

  • Revicki D, Swartz C. Quality of life outcomes of saquinavir, zalcitabine and combination saquinavir-zalcitabine therapy for advanced HIV-infection. Conf Retroviruses Opportunistic Infect. 1997 Jan 22-26;4th:113 (abstract no 266)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2005, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00002333
Lead sponsor
Hoffmann-La Roche
First posted
Aug 31, 2001
Last update
Jun 24, 2005
View the source record on ClinicalTrials.gov ↗

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