A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

May 31, 2014

Primary Completion Date

December 31, 2014

Study Completion Date

January 31, 2015

Conditions
Healthy Volunteers
Interventions
DRUG

AGN-223575 Formulation A

One drop of AGN-223575 Formulation A administered in the study eye(s) per protocol.

DRUG

AGN-223575 Formulation B

One drop of AGN-223575 Formulation B in both eyes on day 1, followed by one drop of AGN-223575 Formulation B twice daily in both eyes for 13 days, and a single drop of AGN-223575 Formulation B in both eyes on day 15.

DRUG

AGN-223575 Formulation C

One drop of AGN-223575 Formulation C in both eyes on day 1, followed by one drop of AGN-223575 Formulation C twice daily in both eyes for 13 days, and a single drop of AGN-223575 Formulation C in both eyes on day 15.

DRUG

AGN-223575 Vehicle

One drop of AGN-223575 vehicle administered in the study eye(s) per protocol.

Trial Locations (1)

Unknown

Newport Beach

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allergan

INDUSTRY

NCT02155543 - A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Healthy Subjects | Biotech Hunter | Biotech Hunter