A Study of the Safety and Pharmacokinetics of a Human Monoclonal Antibody, VRCHIVMAB0115-00-AB (VRC01.23LS), Administered Intravenously or Subcutaneously to Healthy Adults
Status and phase
Conditions
Treatments
Details and patient eligibility
About
Background:
HIV causes AIDS, a serious disease that can lead to fatal infections. HIV infection can be controlled but not cured, nor is there a vaccine to prevent it. Antibodies may offer a promising new way to prevent HIV infection. Antibodies are proteins that are naturally made by the body to fight germs. One antibody (VRC01.23LS) has been tested in the lab and was found to block HIV-like viruses. Researchers want to find out if it is safe to inject VRC01.23LS into people.
Objective:
To test the safety of VRC01.23LS in healthy adults.
Eligibility:
Healthy people aged 18 to 60 years.
Design:
Participants were divided into 6 groups:
Some got 1 dose of VRC01.23LS. They visited the clinic up to 14 times in 24 weeks.
Some got 3 doses, each 12 weeks apart. They had 25 clinic visits over 48 weeks.
For some participants, the drug was given through a tube attached to a needle inserted into a vein in the arm. This took about 30 to 90 minutes. Others received the drug as an injection under the skin in a fatty area of the belly, arm, or thigh; each dose may have needed up to 3 individual injections.
Participants stayed in the clinic up to 8 hours on the days they received VRC01.23LS.
Participants received a thermometer and measuring tool. They checked their temperature daily for 7 days after they received the study drug. They measured any redness, swelling, or bruising at the injection site.
Full description
Study Design:
This first-in-human, open-label study evaluated VRC01.23LS (VRCHIVMAB0115- 00-AB) in a dose-escalation design to examine safety, tolerability, dose, and pharmacokinetics (PK) in healthy adults. The primary hypothesis was that subcutaneous (SC) and intravenous (IV) administrations of VRC01.23LS will be safe and well-tolerated in healthy adults. A secondary hypothesis was that VRC01.23LS will be detectable in human sera with a definable half-life.
Study Products:
The VRC01.23LS broadly neutralizing monoclonal antibody (bnAb) targets the CD4 binding site in the HIV-1 envelope, is human in origin, and contains two amino acid modifications within the C-terminus of the heavy chain constant region designed to improve the antibody half-life in vivo. VRC01.23LS was developed by the VRC/NIAID/NIH and manufactured under cGMP regulations at the VRC Pilot Plant operated under contract by the Vaccine Clinical Materials Program (VCMP), Leidos Biomedical Research, Inc., Frederick. MD.
Subjects:
Healthy adults, 18-60 years of age
Study Plan:
This open-label study included 6 groups to evaluate VRC01.23LS administered as a single dose or as repeated doses, given 12 weeks apart as shown in the table below. Enrollment began with the 5 mg/kg dose groups, and enrollment in subsequent dose groups proceeded after dose-escalation safety reviews. Assessment of safety included solicited reactogenicity, clinical observation, and monitoring of hematological and metabolic parameters at clinical visits throughout the study.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
- INCLUSION CRITERIA:
A subject must meet all of the following criteria:
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Willing and able to complete the informed consent process.
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Able to provide proof of identity to the satisfaction of the study clinician completing the enrollment process.
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Available for clinical follow-up through the last study visit.
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18 to 60 years of age.
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In good general health without clinically significant medical history.
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Physical examination without clinically significant findings within the 56 days prior to enrollment.
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Adequate venous access if assigned to an IV group or adequate abdominal subcutaneous tissue if assigned to SC group.
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Willing to have blood samples collected, stored indefinitely, and used for research purposes.
Laboratory Criteria within 56 days prior to enrollment:
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White blood cell count (WBC): 2,500-12,000/mm3.
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WBC differential either within institutional normal range or accompanied by the Principal Investigator (PI) or designee approval.
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Platelets: 125,000 - 500,000/mm3.
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Hemoglobin within institutional normal range or accompanied by PI or designee approval.
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Creatinine: <= 1.1 x Upper Limit of Normal (ULN).
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ALT: <= 1.25 x ULN.
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AST: <= 1.25 x ULN.
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Negative for HIV infection by an FDA approved method of detection.
Female-Specific Criteria:
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Agrees to use an effective means of birth control from 21 days prior to enrollment through the duration of study participation.
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Negative Beta-HCG (human chorionic gonadotropin) pregnancy test (urine or serum) on day of enrollment for women presumed to be of reproductive potential.
EXCLUSION CRITERIA:
A subject will be excluded if one or more of the following conditions apply:
- Woman who is breast-feeding or planning to become pregnant during study participation.
- Weight > 115 kg.
- Any history of a severe allergic reaction with generalized urticaria, angioedema or anaphylaxis prior to enrollment that has a reasonable risk of recurrence during the study.
- Hypertension that is not well controlled.
- Receipt of any investigational study product within 28 days prior to enrollment (Note: Emergency Use Authorization of a COVID-19 vaccine is not exclusionary).
- Receipt of an investigational HIV vaccine or anti-HIV monoclonal antibody.
- Receipt of any live attenuated vaccine within 28 days prior to enrollment.
- Receipt of any vaccine within 2 weeks prior to enrollment.
- Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or bleeding difficulties with IM injections or blood draws.
- Any other chronic or clinically significant medical condition that in the opinion of the investigator would jeopardize the safety or rights of the volunteer, including but not limited to: diabetes mellitus type I, chronic hepatitis; OR clinically significant forms of: drug or alcohol abuse, asthma, infectious disease, autoimmune disease, psychiatric disorder, heart disease, or cancer.
Trial design
Primary purpose
Allocation
Interventional model
Masking
23 participants in 6 patient groups
Trial contacts and locations
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Central trial contact
VRC Clinic
Data sourced from clinicaltrials.gov
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