TerminatedPhase 2NCT00211471
Treatment of Rubeosis Iridis With Open-Label Anecortave Acetate Sterile Suspension ( 15 mg.).
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Manhattan Eye, Ear & Throat Hospital
- Principal Investigator
- Lawrence A. Yannuzzi, MDManhattan Eye, Ear & Throat Hospital
- Intervention
- anecortave acetate(drug)
- Eligibility
- 18 years · All sexes
- Timeline
- 2002 – 2007
Study locations (1)
- Manhattan Eye, Ear & Throat Hospital, New York, New York, United States
Collaborators
Alcon Research
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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