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Study identifier: NCT05162365 Synced from ClinicalTrials.gov · August 06, 2026
● Study status: Terminated

A Safety, Tolerability, and Efficacy Study of IBI314 in Ambulatory Patients With COVID-19

Condition: COVID-19  ·  Sponsor: Innovent Biologics (Suzhou) Co. Ltd.

PhasePhase 1/Phase 2
Planned participants248
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a dose-finding, inferentially seamless Phase 1/2 study evaluating the safety, tolerability and efficacy of IBI314 in Ambulatory Patients with COVID-19.

This description comes directly from the study's public registry record.

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No contact information is available for this study as per the public registry record.

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Locations (19)

SobhAnaheim, California, United States
Long Beach Clinical Trials, LLCLong Beach, California, United States
Acclaim Clinical ResearchSan Diego, California, United States
Herco Research Center, Inc.Coral Gables, Florida, United States
Midland Florida Clinical Research Center - Inf. Disease/InfectiologyDeLand, Florida, United States
Palm Springs Research InstituteHialeah, Florida, United States
Sweet Hope Research Specialty, IncHialeah, Florida, United States
Prestige Clinical Research Center IncMiami, Florida, United States
Cordova Research Institute, LLCMiami, Florida, United States
Clinical Trials of Florida, LLCMiami, Florida, United States
The Clinical Research Institute LLCMiami Gardens, Florida, United States
Pembroke Clinical TrialsPembroke Pines, Florida, United States

+ 7 more locations — full list on the registry record.

Sponsor or site team? See the site landscape for this trial — listed sites, countries, and recruiting-density context.

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