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Double-Blind Comparison of the Efficacy of Continued Zidovudine Versus 2',3'-Dideoxyinosine (ddI) (BMY-40900) for the Treatment of Patients With AIDS or AIDS-Related Complex and Increasing Symptomatology Despite Treatment With Zidovudine

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Zidovudine
Didanosine
Sponsored by
Bristol-Myers Squibb
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Didanosine, Acquired Immunodeficiency Syndrome, AIDS-Related Complex, Zidovudine

Eligibility Criteria

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

Inclusion Criteria Concurrent Medication: Allowed for Hematologic toxicity: Erythropoietin. Colony-Stimulating Factors. Allowed for prophylaxis of Pneumocystis carinii pneumonia (PCP): Aerosolized pentamidine. Trimethoprim/sulfamethoxazole. Dapsone. NOTE: If intravenous pentamidine is required for treatment of PCP, study drug should be suspended until one week after completion of intravenous pentamidine. Allowed: Prophylactic or suppressive therapy begun prior to study entry with the exception of neurotoxic agents (as defined in the protocol). Concurrent Treatment: Allowed: Transfusions for hematologic toxicity. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Active acute AIDS defining infection. Clinical evidence of acute pancreatitis in the last two years or chronic pancreatitis. Dementia of such severity that patient cannot give informed consent. Grade 2 or worse peripheral neuropathy as defined by Targeted Neuropathy Score (Schaumberg). Prior Cytomegalovirus disease requiring ongoing systemic ganciclovir therapy. Extensive Kaposi's sarcoma or other malignancy requiring systemic cytotoxic myelosuppressive or neurotoxic chemotherapy. Cardiomyopathy or the need for antiarrhythmic therapy. Inability to tolerate at least 600 mg per day of zidovudine (AZT). Seizures within the last 6 months or the need for anticonvulsant therapy. Concurrent Medication: Excluded: Ganciclovir (DHPG). Myelosuppressive or neurotoxic chemotherapy. Antiarrhythmic therapy. Anticonvulsant therapy. Neurotoxic agents (as defined in the protocol). NOTE: If intravenous pentamidine is required for treatment of Pneumocystis carinii pneumonia (PCP), study drug should be suspended until 1 week after completion of intravenous pentamidine. Patients with the following are excluded: Symptoms and conditions defined in the Patient Exclusion Co-Existing Conditions field. Average of two sequential CD4 counts from SciCor Clinical Laboratories in the 30 days prior to study entry > 300 cells/mm3. Prior Medication: Excluded, participation in studies using: Dideoxyinosine (ddI). 2',3'-Dideoxy-2',3'-didehydrothymidine (d4T). Dideoxycytidine (ddC). Excluded within one month of study entry: Any other experimental antiretroviral compounds. Patients must: Have documented HIV positivity via ELISA. Meet CDC criteria for AIDS or AIDS related complex (ARC). Have received zidovudine (AZT) for = or > 6 months and tolerated a dose of at least 500 mg per day without significant hematologic toxicity. Have no acute AIDS defining opportunistic infection, but may be receiving suppressive therapy for such infections. Demonstrate at least one of the following criteria for clinical deterioration despite AZT therapy within 4 weeks prior to study entry (8 weeks prior for weight loss): involuntary weight loss of more than 5 percent of the body weight occurring over the 8 week period prior to study entry, Karnofsky score = or > 50 but demonstrating a fall = or > 20 from previous level of functioning (assessment must be persistent on two occasions at least 14 days apart), unexplained fever of = or > 38 degrees C (despite evaluation defined in protocol) for more than 7 days, appearance of newly diagnosed oral hairy leukoplakia or oral candidiasis, or recurrence of a previously quiescent multidermatomal varicella-zoster, appearance of dermatologic afflictions (e.g. psoriasis, molluscum contagiosum, or newly diagnosed seborrheic dermatitis), appearance of chronic herpetic ulcers not responsive to acyclovir therapy. Required: Zidovudine (AZT) for = or > 6 months prior to study entry.

Sites / Locations

  • Univ of Arizona / Health Science Ctr
  • Yale Univ Med School
  • G E Morey Jr
  • VP Med Services / HHCS Research Institute Inc
  • AIDS Research Consortium of Atlanta
  • Edward Hines Veterans Administration Hosp
  • Univ of Kansas School of Medicine
  • Harper Hosp
  • Albany Med College / AIDS Treatment Ctr
  • Med College of Ohio
  • Univ of Pennsylvania / HIV Clinic
  • Univ of Texas Southwestern Med Ctr of Dallas
  • Univ TX Galveston Med Branch
  • Audie L Murphy Veterans Administration Hosp
  • Univ of Utah School of Medicine
  • Dr Stephen L Green
  • Milwaukee County Med Complex
  • UPR School of Medicine

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
August 4, 2011
Sponsor
Bristol-Myers Squibb
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1. Study Identification

Unique Protocol Identification Number
NCT00002035
Brief Title
Double-Blind Comparison of the Efficacy of Continued Zidovudine Versus 2',3'-Dideoxyinosine (ddI) (BMY-40900) for the Treatment of Patients With AIDS or AIDS-Related Complex and Increasing Symptomatology Despite Treatment With Zidovudine
Official Title
Double-Blind Comparison of the Efficacy of Continued Zidovudine Versus 2',3'-Dideoxyinosine (ddI) (BMY-40900) for the Treatment of Patients With AIDS or AIDS-Related Complex and Increasing Symptomatology Despite Treatment With Zidovudine
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 1992 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Bristol-Myers Squibb

4. Oversight

5. Study Description

Brief Summary
To compare the efficacy and safety of orally administered didanosine (ddI) with orally administered zidovudine (AZT) in the treatment of patients who exhibit increasing clinical deterioration despite treatment with AZT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Didanosine, Acquired Immunodeficiency Syndrome, AIDS-Related Complex, Zidovudine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
Double
Enrollment
300 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Zidovudine
Intervention Type
Drug
Intervention Name(s)
Didanosine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed for Hematologic toxicity: Erythropoietin. Colony-Stimulating Factors. Allowed for prophylaxis of Pneumocystis carinii pneumonia (PCP): Aerosolized pentamidine. Trimethoprim/sulfamethoxazole. Dapsone. NOTE: If intravenous pentamidine is required for treatment of PCP, study drug should be suspended until one week after completion of intravenous pentamidine. Allowed: Prophylactic or suppressive therapy begun prior to study entry with the exception of neurotoxic agents (as defined in the protocol). Concurrent Treatment: Allowed: Transfusions for hematologic toxicity. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Active acute AIDS defining infection. Clinical evidence of acute pancreatitis in the last two years or chronic pancreatitis. Dementia of such severity that patient cannot give informed consent. Grade 2 or worse peripheral neuropathy as defined by Targeted Neuropathy Score (Schaumberg). Prior Cytomegalovirus disease requiring ongoing systemic ganciclovir therapy. Extensive Kaposi's sarcoma or other malignancy requiring systemic cytotoxic myelosuppressive or neurotoxic chemotherapy. Cardiomyopathy or the need for antiarrhythmic therapy. Inability to tolerate at least 600 mg per day of zidovudine (AZT). Seizures within the last 6 months or the need for anticonvulsant therapy. Concurrent Medication: Excluded: Ganciclovir (DHPG). Myelosuppressive or neurotoxic chemotherapy. Antiarrhythmic therapy. Anticonvulsant therapy. Neurotoxic agents (as defined in the protocol). NOTE: If intravenous pentamidine is required for treatment of Pneumocystis carinii pneumonia (PCP), study drug should be suspended until 1 week after completion of intravenous pentamidine. Patients with the following are excluded: Symptoms and conditions defined in the Patient Exclusion Co-Existing Conditions field. Average of two sequential CD4 counts from SciCor Clinical Laboratories in the 30 days prior to study entry > 300 cells/mm3. Prior Medication: Excluded, participation in studies using: Dideoxyinosine (ddI). 2',3'-Dideoxy-2',3'-didehydrothymidine (d4T). Dideoxycytidine (ddC). Excluded within one month of study entry: Any other experimental antiretroviral compounds. Patients must: Have documented HIV positivity via ELISA. Meet CDC criteria for AIDS or AIDS related complex (ARC). Have received zidovudine (AZT) for = or > 6 months and tolerated a dose of at least 500 mg per day without significant hematologic toxicity. Have no acute AIDS defining opportunistic infection, but may be receiving suppressive therapy for such infections. Demonstrate at least one of the following criteria for clinical deterioration despite AZT therapy within 4 weeks prior to study entry (8 weeks prior for weight loss): involuntary weight loss of more than 5 percent of the body weight occurring over the 8 week period prior to study entry, Karnofsky score = or > 50 but demonstrating a fall = or > 20 from previous level of functioning (assessment must be persistent on two occasions at least 14 days apart), unexplained fever of = or > 38 degrees C (despite evaluation defined in protocol) for more than 7 days, appearance of newly diagnosed oral hairy leukoplakia or oral candidiasis, or recurrence of a previously quiescent multidermatomal varicella-zoster, appearance of dermatologic afflictions (e.g. psoriasis, molluscum contagiosum, or newly diagnosed seborrheic dermatitis), appearance of chronic herpetic ulcers not responsive to acyclovir therapy. Required: Zidovudine (AZT) for = or > 6 months prior to study entry.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bristol-Myers Squibb
Organizational Affiliation
Bristol-Myers Squibb
Official's Role
Study Director
Facility Information:
Facility Name
Univ of Arizona / Health Science Ctr
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States
Facility Name
Yale Univ Med School
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06510
Country
United States
Facility Name
G E Morey Jr
City
Fort Lauderdale
State/Province
Florida
ZIP/Postal Code
33316
Country
United States
Facility Name
VP Med Services / HHCS Research Institute Inc
City
Orlando
State/Province
Florida
ZIP/Postal Code
32806
Country
United States
Facility Name
AIDS Research Consortium of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States
Facility Name
Edward Hines Veterans Administration Hosp
City
Hines
State/Province
Illinois
ZIP/Postal Code
60141
Country
United States
Facility Name
Univ of Kansas School of Medicine
City
Wichita
State/Province
Kansas
ZIP/Postal Code
67214
Country
United States
Facility Name
Harper Hosp
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Albany Med College / AIDS Treatment Ctr
City
Albany
State/Province
New York
ZIP/Postal Code
12203
Country
United States
Facility Name
Med College of Ohio
City
Toledo
State/Province
Ohio
ZIP/Postal Code
43699
Country
United States
Facility Name
Univ of Pennsylvania / HIV Clinic
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Univ of Texas Southwestern Med Ctr of Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Facility Name
Univ TX Galveston Med Branch
City
Galveston
State/Province
Texas
ZIP/Postal Code
775550882
Country
United States
Facility Name
Audie L Murphy Veterans Administration Hosp
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78284
Country
United States
Facility Name
Univ of Utah School of Medicine
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84132
Country
United States
Facility Name
Dr Stephen L Green
City
Hampton
State/Province
Virginia
ZIP/Postal Code
23666
Country
United States
Facility Name
Milwaukee County Med Complex
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States
Facility Name
UPR School of Medicine
City
San Juan
ZIP/Postal Code
009275800
Country
Puerto Rico

12. IPD Sharing Statement

Citations:
Citation
Ruedy N, et al. Results of long term follow-up of a double blind study of ddI vs continued AZT among individuals with CD4s 200-500/mm3. Int Conf AIDS. 1994 Aug 7-12;10(2):16 (abstract no 358B)
Results Reference
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Learn more about this trial

Double-Blind Comparison of the Efficacy of Continued Zidovudine Versus 2',3'-Dideoxyinosine (ddI) (BMY-40900) for the Treatment of Patients With AIDS or AIDS-Related Complex and Increasing Symptomatology Despite Treatment With Zidovudine

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