A Phase 1b/2a Study of the Safety and Pharmacokinetics of Rhu-plasma Gelsolin in Hospitalized Subjects With CAP

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

August 28, 2018

Primary Completion Date

April 2, 2019

Study Completion Date

April 2, 2019

Conditions
Community-acquired Pneumonia
Interventions
DRUG

Recombinant Human Plasma Gelsolin

Recombinant human plasma gelsolin lyophilized for reconstitution, reconstituted in sterile water

OTHER

Normal Saline Placebo

Normal saline in volume equivalent to drug

Trial Locations (8)

3011

Footscray Hospital, Footscray

3128

Box Hill Hospital, Box Hill

3300

LTD Geo Hospitals, Mtskheta Multiprofile Medical Center, Mtskheta

3700

JSC Rustavi Central Hospital, Rustavi

4870

Cairns Hospital, Cairns

0160

LTD Central University Clinic After Academic N. Kipshidze, Tbilisi

0179

LTD S. Khechinashvili University Hospital, Tbilisi

0191

LTD 5th Clinical Hospital, Tbilisi

Sponsors
All Listed Sponsors
lead

BioAegis Therapeutics Inc.

INDUSTRY