A Double-Blind, Placebo-Controlled, Dose Ranging Study of Xanamem® in Healthy Elderly Volunteers

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

107

Participants

Timeline

Start Date

June 30, 2021

Primary Completion Date

February 11, 2022

Study Completion Date

February 11, 2022

Conditions
Mild Cognitive ImpairmentAlzheimer's Disease
Interventions
DRUG

Xanamem® 5 mg

"Oral Xanamem® (UE2343) capsules 5 mg, administered orally once daily."

DRUG

Placebo

Matching placebo which is identical in appearance to the test product (5 mg, 10 mg Xanamem® QD) except that it contains no active ingredient.

DRUG

Xanamem® 10 mg

"Oral Xanamem® (UE2343) capsules 10 mg, administered orally once daily."

Trial Locations (5)

2148

Paratus Clinical Research Western Sydney, Blacktown

2259

Paratus Clinical Research Central Coast, Kanwal

2617

Paratus Clinical Research Canberra, Bruce

4010

Paratus Clinical Research Brisbane, Albion

4556

USC Clinical Trials, Sippy Downs

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Avance Clinical Pty Ltd.

INDUSTRY

lead

Actinogen Medical

INDUSTRY