An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant in Patients With Retinitis Pigmentosa

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

July 31, 2008

Primary Completion Date

December 31, 2009

Study Completion Date

May 31, 2010

Conditions
Retinitis Pigmentosa
Interventions
DRUG

400 µg Brimonidine Tartrate Implant

400 µg brimonidine tartrate implant in the study eye on Day 1.

DRUG

200 µg Brimonidine Tartrate Implant

200 µg brimonidine tartrate implant in the study eye on Day 1.

DRUG

100 µg Brimonidine Tartrate Implant

100 µg brimonidine tartrate implant in the study eye on Day 1.

OTHER

Sham (no implant)

Sham in the fellow eye on Day 1.

Trial Locations (4)

Unknown

Arlington

Paris

Tübingen

Coimbra

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Allergan

INDUSTRY

NCT00661479 - An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant in Patients With Retinitis Pigmentosa | Biotech Hunter | Biotech Hunter