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A Phase I, Dose-Escalating Safety and Tolerance Study of sCD4-PE40 in HIV-Infected Persons

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Alvircept sudotox
Zidovudine
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Recombinant Proteins, Acquired Immunodeficiency Syndrome, Antigens, CD4, AIDS-Related Complex, Zidovudine

Eligibility Criteria

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

Inclusion Criteria Concurrent Medication: Allowed: PCP prophylaxis with aerosolized pentamidine, trimethoprim / sulfamethoxazole, or dapsone. Clotrimazole troches or nystatin oral suspension for oral candidiasis. Acyclovir (up to 1000 mg/day for 10 days) for herpes lesions. Erythropoietin. Patients must have: Documented HIV infection by ELISA confirmed by a second method. If a prior diagnosis of AIDS has not been established by CDC criteria, a confirmatory test is required. CD4 count = or < 300 cells/mm3 within 4 weeks prior to study entry. Positive p24 antigen. Patients entering the AZT portion of the study only: Must be AZT naive or have had less than 2 months of AZT therapy. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Hemophilia. Acute medical problems (including active opportunistic infections such as active cryptococcosis, Pneumocystis carinii, herpes zoster, histoplasmosis, or CMV or nonopportunistic diseases including liver disease, renal disease, or orthostatic hypotension) at time of study entry. Active pulmonary disease. Chronic active hepatitis B surface antigenemia or unstable hepatitis C. Current diagnosis of malignancy for which systemic therapy would be required during the study. Inadequate intravenous access. Concurrent Medication: Excluded: Hepatotoxic agents. Other antiretroviral or immunomodulator agents (including but not limited to AZT, ddI, ddC, interferon, and steroids). Other investigational drugs. Systemic therapy for malignancy. G-CSF and GM-CSF. Prior Medication: Excluded: Other antiretroviral or immunomodulator agents (including but not limited to AZT, ddI, ddC, interferon, and steroids) within 4 weeks prior to study entry. Ribavirin within 90 days prior to study entry. Cytotoxic chemotherapy within one month prior to study entry. Prior soluble CD4 or CD4-Ig. Excluded in patients entering the AZT portion of the study: More than 2 months of prior AZT therapy. Current active alcoholism or active substance abuse.

Sites / Locations

  • UCLA CARE Center CRS
  • Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU
  • Johns Hopkins Adult AIDS CRS
  • Unc Aids Crs

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 27, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Upjohn, Glaxo Wellcome
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1. Study Identification

Unique Protocol Identification Number
NCT00000743
Brief Title
A Phase I, Dose-Escalating Safety and Tolerance Study of sCD4-PE40 in HIV-Infected Persons
Official Title
A Phase I, Dose-Escalating Safety and Tolerance Study of sCD4-PE40 in HIV-Infected Persons
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 1995 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Upjohn, Glaxo Wellcome

4. Oversight

5. Study Description

Brief Summary
To determine the safety and tolerance of alvircept sudotox (sCD4-PE40) given at various dosing intervals and concentrations. To determine whether frequent dosing alters immunogenicity or toxicity. To obtain preliminary data to ascertain whether sCD4-PE40 has activity against HIV in human subjects. To determine whether there is any additive toxicity with combined use of sCD4-PE40 and zidovudine (AZT). There is some evidence that AZT and sCD4-PE40, an experimental drug with anti-HIV activity previously demonstrated in vitro, may produce increased benefit when used in combination in HIV-infected patients.
Detailed Description
There is some evidence that AZT and sCD4-PE40, an experimental drug with anti-HIV activity previously demonstrated in vitro, may produce increased benefit when used in combination in HIV-infected patients. Cohorts of six patients each receive escalating doses of sCD4-PE40 in a single IV weekly dose for 8 weeks. All six patients at a given dose must complete 2 weeks of therapy without dose-limiting toxicity before dose escalation in subsequent patient cohorts may occur. The MTD is defined as the dose of sCD4-PE40 immediately below that at which two or more of six patients experience grade 3 or higher toxicity or one or more of six patients experience grade 4 toxicity. After the MTD for the once-weekly schedule is reached, subsequent cohorts receive escalated doses of sCD4-PE40 on a 5x weekly schedule for approximately 4 weeks, in an attempt to establish the MTD for that schedule. When an MTD has been determined for the 5x weekly schedule, and if antiretroviral activity is observed, six additional patients receive this dose combined with AZT for 4 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Recombinant Proteins, Acquired Immunodeficiency Syndrome, Antigens, CD4, AIDS-Related Complex, Zidovudine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Masking
None (Open Label)
Enrollment
64 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Alvircept sudotox
Intervention Type
Drug
Intervention Name(s)
Zidovudine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: PCP prophylaxis with aerosolized pentamidine, trimethoprim / sulfamethoxazole, or dapsone. Clotrimazole troches or nystatin oral suspension for oral candidiasis. Acyclovir (up to 1000 mg/day for 10 days) for herpes lesions. Erythropoietin. Patients must have: Documented HIV infection by ELISA confirmed by a second method. If a prior diagnosis of AIDS has not been established by CDC criteria, a confirmatory test is required. CD4 count = or < 300 cells/mm3 within 4 weeks prior to study entry. Positive p24 antigen. Patients entering the AZT portion of the study only: Must be AZT naive or have had less than 2 months of AZT therapy. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Hemophilia. Acute medical problems (including active opportunistic infections such as active cryptococcosis, Pneumocystis carinii, herpes zoster, histoplasmosis, or CMV or nonopportunistic diseases including liver disease, renal disease, or orthostatic hypotension) at time of study entry. Active pulmonary disease. Chronic active hepatitis B surface antigenemia or unstable hepatitis C. Current diagnosis of malignancy for which systemic therapy would be required during the study. Inadequate intravenous access. Concurrent Medication: Excluded: Hepatotoxic agents. Other antiretroviral or immunomodulator agents (including but not limited to AZT, ddI, ddC, interferon, and steroids). Other investigational drugs. Systemic therapy for malignancy. G-CSF and GM-CSF. Prior Medication: Excluded: Other antiretroviral or immunomodulator agents (including but not limited to AZT, ddI, ddC, interferon, and steroids) within 4 weeks prior to study entry. Ribavirin within 90 days prior to study entry. Cytotoxic chemotherapy within one month prior to study entry. Prior soluble CD4 or CD4-Ig. Excluded in patients entering the AZT portion of the study: More than 2 months of prior AZT therapy. Current active alcoholism or active substance abuse.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
van der Horst C
Official's Role
Study Chair
Facility Information:
Facility Name
UCLA CARE Center CRS
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
Facility Name
Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
701122699
Country
United States
Facility Name
Johns Hopkins Adult AIDS CRS
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
Unc Aids Crs
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
275997215
Country
United States

12. IPD Sharing Statement

Citations:
Citation
Alston B, Mitsuyasu R, Lertora J, Flexner C, Timpone J, van der Horst C. Phase I study of sCd4-PE40 in HIV infected persons: (ACTG 201). Int Conf AIDS. 1993 Jun 6-11;9(1):498 (abstract no PO-B29-2178)
Results Reference
background
Citation
Fiscus S, et al. Safety and efficacy of soluble CD4-pseudomonas exotoxin 40 in HIV infected individuals (ACTG 201). Natl Conf Hum Retroviruses Relat Infect (2nd). 1995 Jan 29-Feb 2:70
Results Reference
background

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A Phase I, Dose-Escalating Safety and Tolerance Study of sCD4-PE40 in HIV-Infected Persons

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