A Randomized SAD and MAD Study Evaluating the Safety and Tolerability of RPh201 in Healthy Subjects and in Adults With Alzheimer's Disease

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

June 30, 2015

Study Completion Date

June 30, 2015

Conditions
Healthy VolunteersModerate to Severe Alzheimer Patients
Interventions
DRUG

RPh201, botanical drug product

SC administration at varying doses

DRUG

Placebo

SC administration at varying doses

Trial Locations (2)

M3B 2S7

Toronto Memory Program, Toronto

M5V 2T3

Kendle Early Stage - Toronto, Toronto

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Syneos Health

OTHER

lead

Regenera Pharma Ltd

INDUSTRY