A First-in-Human Study Evaluating AGA2118 in Men and Postmenopausal Women

PHASE1CompletedINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

June 28, 2022

Primary Completion Date

January 13, 2024

Study Completion Date

January 13, 2024

Conditions
Osteoporosis
Interventions
DRUG

AGA2118

"Part 1 - SAD study: SAD participants in various cohorts will receive various single dose of AGA2118 via either SC or IV.~Part 2 - MAD study: MAD participants in various cohorts will receive various multiple doses of AGA2118 Q4W via SC."

DRUG

Placebo

"Part 1 - SAD study: SAD participants in various cohorts will receive a single dose of placebo via either SC or IV.~Part 2 - MAD study: MAD participants in various cohorts will receive multiple doses of placebo via SC."

Trial Locations (2)

3004

Nucleus Network Pty Ltd., Melbourne

4006

Q-Pharm Pty Ltd, Brisbane

Sponsors
All Listed Sponsors
collaborator

Angitia Australia Pty Ltd

INDUSTRY

lead

Angitia Biopharmaceuticals

INDUSTRY

NCT05225857 - A First-in-Human Study Evaluating AGA2118 in Men and Postmenopausal Women | Biotech Hunter | Biotech Hunter