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Treatment of Retinal Vein Occlusion (RVO) With Open-Label Anecortave Acetate (15mg.)

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00211354
Enrollment
0
Registered
2005-09-21
Start date
2002-03-31
Completion date
2007-04-30
Last updated
2009-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinal Vein Occlusion

Brief summary

Retinal Vein Occlusion is a blockage of the blood vessels that drain out of the retina. Complications of retinal vein occlusion which threaten vision include neovascularization(growth of new blood vessels)and macular edema ( accumulation of fluid leaking from abnormal blood vessels). Currently, the treatment of retinal vein occlusion is laser photocoagulation. This treatment has found to have limited use in this type of condition.Anecortave Acetate is being considered as an attempt to control the growth of the abnormal blood vessels.

Interventions

ancortave acetate 15 mg. juxtascleral injection every 6 months for 24 months.

Sponsors

Alcon Research
CollaboratorINDUSTRY
Manhattan Eye, Ear & Throat Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Clinical diagnosis of patients Retinal Vein Occlusion. 2. Patients must be 18 years of age or older to receive treatment. 3. Visual acuity of 20/30 to 20/320 Study Eye on the ETDRS visual acuity chart. 4. Visual acuity of 20/800 or better Fellow Eye on the ETDRS visual acuity chart.

Exclusion criteria

1. Patient with significantly compromised visual acuity in the study eye due to concomitant ocular conditions. 2. Patients who have undergone intraocular surgery within last 2 months. 3. Patient participating in any other investigational drug study. 4. Use of an investigational drug or treatment related or unrelated to their condition within 30 days prior to receipt of study medication. 5. Inability to obtain photographs to document CNV (including difficulty with venous access). 6. Patient with significant liver disease or uremia. 7. Patient with known adverse reaction to fluorescein and indocyanine green or iodine. 8. Patient has a history of any medical condition which would preclude scheduled visits or completion of study. 9. Patient has had insertion of scleral buckle in the study eye. 10. Patient has received radiation treatment. 11. Patient is on anticoagulant therapy with the exception of aspirin. 12. Patient is pregnant or nursing.

Design outcomes

Primary

MeasureTime frame
to investigate the use of anecortave acetate for treatment of retinal vein occlusion24 months

Secondary

MeasureTime frame
mean change of VA (ETDRS) from baseline to 24 months24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026