A Phase I Safety and Immunogenicity Trial of UBI HIV Lipopeptide Immunotherapeutic P3C541b in HIV-1 Seropositive Human Subjects
Launched by UNITED BIOMEDICAL · Aug 30, 2001
Trial Information
Current as of March 16, 2025
Completed
Keywords
ClinConnect Summary
Patients are randomized to receive P3C541b or placebo within each of two study groups. Enrollment in the first group will be independent of HLA type, whereas all but two of the patients enrolled in group 2 must have one or more HLA types A33, B8, B27, or Bw62. Treatment in group 2 will not begin until those in group 1 have reached day 14 without serious toxicity.
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- Patients must have:
- • HIV positivity.
- • CD4 count \>= 500 cells/mm3.
- • No evidence of AIDS, persistent diarrhea, fever, oral hairy leukoplakia, herpes varicella-zoster (multidermatomal), oral candidiasis, opportunistic infections, severe cytomegalovirus infection, or disseminated or chronic herpes simplex.
- • Successful establishment of EBV transformed B lymphoblastoid cell line.
- NOTE:
- • Most patients in group 2 must possess one or more HLA types A33, B8, B27, or Bw62.
- • Exclusion Criteria
- Co-existing Condition:
- Patients with the following symptoms or conditions are excluded:
- • Active syphilis.
- • Positive circulating hepatitis B virus antigen.
- • Active clinically significant medical problems.
- • Evidence of psychiatric, medical, or substance abuse problems that would affect ability to participate on study.
- • Occupational or other responsibilities that would prevent completion of study.
- Concurrent Medication:
- Excluded:
- • Other HIV immunotherapeutic.
- • Zidovudine or analog.
- • Investigational therapies for HIV.
- Patients with the following prior conditions are excluded:
- • History of cancer unless surgically excised with reasonable assurance of cure.
- • History of anaphylaxis or other serious adverse reactions to vaccines.
- • History of serious allergic reaction to any substance that required hospitalization or emergent medical care (e.g., Stevens-Johnson syndrome, bronchospasms, or hypotension).
- • History of autoimmune disease or use of immunosuppressive medications.
- • History of suicide attempts or past psychosis.
- Prior Medication:
- Excluded within the past 6 months:
- • HIV immunotherapeutic.
- • Zidovudine or analog.
- • Investigational therapies for HIV. Illicit drug use within past 30 days.
About United Biomedical
United Biomedical is a leading clinical trial sponsor dedicated to advancing healthcare through innovative research and development in biotechnology and pharmaceuticals. With a strong focus on immunology and vaccine development, the organization collaborates with academic institutions, healthcare professionals, and industry partners to drive groundbreaking studies that address critical medical needs. United Biomedical is committed to rigorous scientific standards and ethical practices, ensuring that its clinical trials are designed to yield meaningful results that enhance patient care and improve health outcomes globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Boston, Massachusetts, United States
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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