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About
The purpose of this study is to determine the safety and tolerability profile of CD388 Injection, as compared to saline placebo, when dosed by subcutaneous (SQ) administration as a single dose to healthy Japanese adult subjects.
Full description
This is a Phase 1, single-center, prospective, randomized, double-blind study of ascending single doses of CD388 Injection administered SQ to healthy Japanese adult subjects. The goals are to assess safety, tolerability, and pharmacokinetics (PK) of CD388.
Enrollment
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Volunteers
Inclusion criteria
Must be of Japanese descent with Japanese parents and grandparents, as determined by subject's verbal report.
Willing and able to provide written informed consent.
Males and females 18 to 65 years of age, inclusive.
A female subject must meet one of the following criteria:
A woman of childbearing potential must have a negative highly sensitive serum pregnancy test (β-human chorionic gonadotropin) at screening and a negative urine pregnancy test on Day -1 before the first dose of study drug.
A woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for a period of at least 7 months after study drug administration.
A male subject that engages in sexual activity that has the risk of pregnancy must agree to use a double barrier method (e.g., condom and spermicide) and agree to not donate sperm during the study and for at least 7 months after the last dose of the study medication.
Good health and without signs or symptoms of current illness.
Normal clinical examination, including:
Body weight ≥50 kilograms (kg) and body mass index (BMI; calculated as weight in kg divided by height in meters [m] squared) between 18.0 and 30.0 kg/m^2, inclusive.
Willing to refrain from strenuous physical activity that could cause muscle aches or injury, including contact sports, at any time from screening through 30 days after any dose of study drug.
Subject has adequate venous access for blood collection.
Exclusion criteria
History of any hypersensitivity or allergic reaction to zanamivir or other neuraminidase inhibitors (i.e., laninamivir, oseltamivir, peramivir), or to excipients of the CD388 Injection drug formulation; or history of drug-induced exfoliative skin disorders (e.g., Stevens-Johnson syndrome [SJS], erythema multiforme, or toxic epidermal necrolysis [TEN]).
History of any of the following:
Subjects with one or more of the following laboratory abnormalities at screening as defined by the Division of AIDS (DAIDS) Table for Grading the Severity of Adult and Pediatric Adverse Events v2.1 (DAIDS 2017):
Serum creatinine, Grade ≥1 (≥1.1 × upper limit of normal [ULN]).
Pancreatic amylase or lipase, Grade ≥2 (≥1.5 × ULN).
Aspartate aminotransferase (AST) or alanine aminotransferase (ALT), Grade ≥1 (≥1.25 × ULN).
Total bilirubin, Grade ≥1 (≥1.1 × ULN).
Any other toxicity Grade ≥2, except for Grade 2 elevations of triglycerides, low density lipoprotein cholesterol, and/or total cholesterol.
Any other laboratory abnormality considered to be clinically significant by the Investigator.
Alcohol or drug addiction in the past 2 years.
Experiencing symptoms of acute illness or chronic disease within 14 days prior to clinical research unit (CRU) check-in.
At screening, a positive result for hepatitis B virus surface antigen, hepatitis C virus antibody, or human immunodeficiency virus (HIV) antibody.
A positive result at CRU check-in for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by polymerase chain reaction (PCR).
Unwilling to comply with local health policy effective at the time regarding coronavirus disease 2019 (COVID-19). Full COVID-19 vaccination prior to participation is strongly recommended.
Women who are pregnant or nursing.
Received any over-the-counter (OTC) medications or nutritional supplements within 7 days, or any prescription medications within 14 days or <5 half-lives prior to dosing, whichever is longest (except for hormonal contraceptives, acetaminophen, or ibuprofen).
Current nicotine user or has quit habitual nicotine use in the 30 days prior to screening.
Received any vaccines or immunoglobulins within 28 days prior to dosing (90 days in case of intravenous immunoglobulin [IVIg] or biologics, or 14 days for COVID-19 vaccine).
Donated blood (within 56 days of screening) or plasma (within 7 days of screening) or experienced significant blood loss or significant blood draw (blood donation or blood loss ≥500 mL) when participating in non-interventional clinical trials within 30 days prior to dosing.
Received a blood transfusion within 28 days prior to dosing.
Received any biologics within 90 days prior to dosing; or previous participation in another study (including investigational device studies) within 30 days of dosing or 5 half-lives of the study drug, whichever is longer, prior to screening (prior participation at any time in non-invasive methodology trials in which no drugs were given is acceptable).
Previous treatment with CD388.
Preplanned surgery at any time during the study.
The Principal Investigator (PI) considers that the volunteer should not participate in the study.
Primary purpose
Allocation
Interventional model
Masking
28 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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