About this trial
This is a Phase 1, randomized, double-blind, placebo-controlled, single-dose, first in human safety, tolerability, and pharmacokinetic study of SPY002-072 in healthy participants.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Healthy men and women
Willing and able to attend the necessary visits to the CRU, comply with all testing requirements, remain at the study site unit for the duration of the confinement period and return for the outpatient visits
Disqualifiers
Participation in more than one cohort
Evidence of clinically significant abnormality or disease
Known history of illicit drug use or drug abuse, cannabis/cannabinoid use, harmful alcohol use (at the Investigator's discretion), alcoholism, and/or smoking or nicotine-containing product use within 3 months prior to the first dose of study agent
History of severe allergic reactions or hypersensitivity
Trial design
Sequential
Treatments tested in this trial
SPY002-072
DrugExperimental
Placebo
Other interventionPlacebo
Treatment groups
Trial outcomes
Primary outcomes
Treatment emergent adverse events
Incidence, severity, and causal relationship of TEAEs
Secondary outcomes
Cmax
Maximum concentration after single dose
t1/2
Half life after single dose
Tmax
Time to reach maximum concentration after single dose
ADA
Incidence of anti-drug antibody after single dose
Sponsors and contacts
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Spyre Therapeutics, Inc.
Lead sponsor
Altasciences Company Inc.
Collaborator