Completed

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

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What is being tested

Alvircept sudotox

+ Zidovudine

Drug
Who is being recruted

Blood-Borne Infections+14

+ Urogenital Diseases

+ Genital Diseases

Over 18 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 1
Interventional
See protocol details

Summary

Principal SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Last updated: October 28, 2021
Sourced from a government-validated database.Claim as a partner

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.

Principal SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Last updated: October 28, 2021
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

64 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood-Borne InfectionsUrogenital DiseasesGenital DiseasesCommunicable DiseasesImmunologic Deficiency SyndromesImmune System DiseasesInfectionsRetroviridae InfectionsRNA Virus InfectionsSexually Transmitted DiseasesSlow Virus DiseasesVirus DiseasesSexually Transmitted Diseases, ViralLentivirus InfectionsAcquired Immunodeficiency SyndromeAIDS-Related ComplexHIV Infections

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.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 4 locations

UCLA CARE Center CRS

Los Angeles, United StatesOpen UCLA CARE Center CRS in Google Maps

Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU

New Orleans, United States

Johns Hopkins Adult AIDS CRS

Baltimore, United States

Unc Aids Crs

Chapel Hill, United States
Completed4 Study Centers