Status:
COMPLETED
A COVID-19 Study to Evaluate Safety and Pharmacokinetics of COVID-HIGIV Administered in Healthy Adults
Lead Sponsor:
Emergent BioSolutions
Collaborating Sponsors:
United States Department of Defense
Conditions:
COVID-19
Eligibility:
All Genders
18-60 years
Phase:
PHASE1
Brief Summary
This study is designed to evaluate three dose levels of Anti-SARS-CoV-2 Immunoglobulin Intravenous (Human) (COVID-HIGIV) for safety and pharmacokinetics (PK) in healthy adults. Twenty-eight healthy ad...
Detailed Description
This study will be a Phase 1, single-center, randomized, double-blind, placebo-controlled design to assess safety and PK of COVID-HIGIV in healthy adults. In total, 28 healthy adult subjects are to b...
Eligibility Criteria
Inclusion
- Able and willing to provide written informed consent (voluntarily signed by the subject) prior to performing study procedures.
- Females and males 18-60 years of age, inclusive.
- Have a body mass index (BMI) less than or equal to 35.0 kg/m2.
- Women who are either:
- A) Not of childbearing potential: either surgically sterile (at least six weeks post bilateral tubal ligation, bilateral oophorectomy or hysterectomy); or post-menopausal (defined as ≥50 years of age with a history of ≥12 months without menses prior to randomization in the absence of other pathologic or physiologic causes, following cessation of exogenous sex-hormonal treatment); OR
- B) Women of childbearing potential (WOCBP) who are not planning to be pregnant during the study period and meet all of the following criteria:
- Negative serum pregnancy test (PT) at Screening; and Negative PT prior to dosing at Day 1; and
- Use of a highly effective contraception during the study period:
- Hormonal contraceptives (e.g., implants, pills, patches) initiated ≥30 days prior to Day 1; or
- Intrauterine device (IUD) inserted ≥30 days prior to Day 1; or
- Double barrier type of birth control (e.g., male condom with female diaphragm, male condom with cervical cap).
- Subject understands and agrees to comply with planned study procedures.
- Healthy as determined by the Principal Investigator based on medical history, physical exam, vital signs, urinalysis, blood chemistry and hematology test results at Screening and evidence of no prior exposure to SARS-CoV-2 (i.e., Reverse transcription polymerase chain reaction \[RT-PCR\] negative for SARS-CoV-2 and negative for SARS-CoV-2 antibodies) at Screening.
Exclusion
- Use of any investigational product, within 30 days prior to Screening, or use of investigational SARS-CoV-2 vaccines, SARS-CoV-2 monoclonal antibodies or COVID-19 convalescent plasma at any time prior to Screening or during the study follow-up period, or subject plans to participate in another clinical study during the study period.
- Screening clinical laboratory test result greater than the laboratory's upper limit of normal (ULN) for alanine aminotransferase (ALT), aspartate aminotransferase (AST), random glucose, total and/or bilirubin, blood urea nitrogen (BUN), or creatinine. Other serum chemistry parameters that are not within the reference range will not be considered exclusionary unless deemed clinically significant by the Principal Investigator.
- History of allergy or hypersensitivity to blood or plasma products or to COVID-HIGIV excipients (proline, PS80).
- History of allergy to latex or rubber.
- History of hemolytic anemia.
- History of Immunoglobulin A (IgA) deficiency.
- Receipt of any blood product within the past 12 months.
- Plasma donation within 7 days or significant blood loss or blood donation within 56 days of randomization/dosing.
- History of known congenital or acquired immunodeficiency or receipt of immunosuppressive therapy (e.g., prednisone or equivalent for more than two consecutive weeks within the past three months).
- History of thrombosis or hypercoagulable state with increased risk of thrombosis.
- History of clinically significant chronic illness (e.g., requiring hospitalization in the past three months) such as cardiac, pulmonary, renal, hepatic or other chronic conditions.
- Receipt of a live vaccine within 28 days prior to screening or anticipated receipt of a live vaccine during the study period.
- Currently pregnant, breastfeeding, or planning to become pregnant during the study.
- History of, or suspected substance abuse problem (including alcohol).
- Other medical condition which may place subject at increased risk due to participation in the study as determined by the investigator.
- Any planned elective surgery during the study period.
- An opinion of the investigator that it would be unwise to allow the individual to be randomized into the study.
Key Trial Info
Start Date :
December 24 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 27 2021
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT04661839
Start Date
December 24 2020
End Date
July 27 2021
Last Update
June 8 2025
Active Locations (1)
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1
Icahn School of Medicine at Mount Sinai
New York, New York, United States, 10029