At a glance
ClinicalIndex Comparison RecordPhase 1Completed· 140 enrolled / 140 target
Drug / intervention
Depemokimabbiological
Likely dose
100 milligramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
An Open-Label, Randomized, Single-Dose, Multicenter, Parallel-Group Study to Compare the Pharmacokinetics of Subcutaneous Depemokimab When Delivered With a Safety Syringe Device or an Autoinjector in Healthy Adult Participants
In Brief
A Phase 1 clinical trial evaluating Depemokimab for Asthma. Completed, enrolled 140 participants across 3 sites.
Detailed Summary
This study will compare the pharmacokinetics, safety, tolerability, and immunogenicity of Depemokimab administered via a SSD or autoinjector in healthy participants.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAsthma
CountriesUnited States
CollaboratorsPPD Development, LP
Timeline
Phase 1CompletedFinished
2023202420252026
First PostedNov 2022
Enrollment StartDec 2022
Primary CompletionOct 2023
TodayJul 2026
First PostedNov 1, 2022
Enrollment StartDec 13, 2022
Primary CompletionOct 23, 2023
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 3.7 years ago
Arms & Interventions
Depemokimab via SSDexperimental
Participants received a single subcutaneous dose of 100 milligrams (mg) of depemokimab administered via a Safety Syringe Device (SSD) on Day 1.
Biological: Depemokimab
Depemokimab via autoinjectorexperimental
Participants received a single subcutaneous dose of 100 mg of depemokimab administered via an autoinjector on Day 1.
Biological: Depemokimab
Interventions
Depemokimabbiological
Depemokimab was administered via SSD or autoinjector.