Trial | Phase | Enrollment | Study Type | Start Date | Status |
A Dose-Volume Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma or Ocular Hypertension [NCT00788541] | Phase 2 | 197 participants (Actual) | Interventional | 2008-12-31 | Terminated(stopped due to Project cancellation) |
An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal Choroidal Neovascularization Due to Exudative Age-Related Macular Degeneration. [NCT00051129] | Phase 3 | 291 participants (Actual) | Interventional | 2007-01-31 | Completed |
A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma [NCT00451152] | Phase 2 | 89 participants (Actual) | Interventional | 2007-03-31 | Completed |
Efficacy and Safety of Posterior Juxtascleral Administrations of Anecortave Acetate for Depot Suspension (15 mg or 30 mg) Versus Sham Administration in Singaporean Patients at Risk for Progressing to Exudative Age-Related Macular Degeneration (AMD) [NCT00333216] | Phase 3 | 24 participants (Actual) | Interventional | 2005-05-31 | Terminated(stopped due to Lack of efficacy) |
[NCT00307398] | Phase 3 | 2,596 participants (Actual) | Interventional | 2004-03-31 | Terminated(stopped due to Management decision) |
A Study of the Safety and Efficacy of Anecortave Acetate for Treatment of Steroid Induced Intraocular Pressure (IOP) Elevation [NCT00315640] | Phase 2 | 70 participants (Actual) | Interventional | 2005-12-31 | Completed |
An Open Label Evaluation of Long Term Efficacy and Safety of Posterior Juxtascleral Injections of Anecortave Acetate 15 mg in Patients With Subfoveal Exudative Age-Related Macular Degeneration (AMD) [NCT00065728] | Phase 3 | 111 participants (Actual) | Interventional | 2003-06-30 | Terminated(stopped due to Management decision) |
A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma or Ocular Hypertension [NCT00691717] | Phase 2/Phase 3 | 201 participants (Actual) | Interventional | 2008-06-30 | Completed |
A Study of the Safety and IOP-Lowering Efficacy of Anecortave Acetate in Patients With Open-Angle Glaucoma [NCT00320203] | Phase 2 | 86 participants (Actual) | Interventional | 2006-03-31 | Completed |
[NCT00211484] | Phase 2 | 5 participants (Actual) | Interventional | 2003-05-31 | Completed |
Compassionate Use of Anecortave Acetate: Clinical Protocol for the Treatment of Corticosteroid-induced Intraocular Pressure (IOP) Increases After Corneal Transplantation [NCT00884039] | | 7 participants (Actual) | Interventional | 2009-05-31 | Terminated(stopped due to Preliminary data analysis showed insufficient efficacy to justify continuation.) |
[NCT00705770] | Phase 2/Phase 3 | 0 participants (Actual) | Interventional | 2008-05-31 | Withdrawn(stopped due to Change in study design) |
[NCT00211328] | Phase 2 | 5 participants (Actual) | Interventional | 2002-03-31 | Completed |
[NCT00211406] | Phase 1 | 0 participants | Interventional | | Terminated |
Treatment of Rubeosis Iridis With Open-Label Anecortave Acetate Sterile Suspension (15mg.). [NCT00211471] | Phase 2 | 0 participants (Actual) | Interventional | 2002-03-31 | Terminated(stopped due to poor enrollment) |
An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal Choroidal Neovascularization Due to Exudative Age-related Macular Degeneration [NCT00058994] | Phase 3 | 0 participants | Interventional | 2003-03-31 | Completed |
Prevention of Steroid-induced Glaucoma Using Anecortave Acetate [NCT00570479] | Phase 1 | 12 participants (Actual) | Interventional | 2006-09-30 | Completed |
[NCT00211367] | Phase 2 | 2 participants (Actual) | Interventional | 2004-04-30 | Terminated(stopped due to poor enrollment) |
Pilot Study of the Combination of Anecortave Acetate 15mg Delivered by Posterior Juxtascleral Injection and Triamcinolone Acetonide 4mg Delivered by Intravitreal Injection for the Treatment of Exudative Age-Related Macular Degeneration (AMD) [NCT00211419] | Phase 1 | 0 participants | Interventional | | Completed |
Treatment of Age-Related Macular Degeneration With Open-label Anecortave Acetate Sterile Suspension (15mg) Following Failed Treatment With Photodynamic Therapy With Visudyne [NCT00211458] | Phase 2 | 0 participants | Interventional | 2005-09-30 | Completed |
Clinical Treatment of Patients With Age-Related Macular Degeneration With Anecortave Acetate Sterile Suspension [NCT00349739] | | 0 participants | Expanded Access | 2003-01-31 | No longer available |
Treatment of Chronic Central Serous Chorioretinopathy With Open-label Anecortave Acetate [NCT00489840] | Phase 1/Phase 2 | 5 participants (Actual) | Interventional | 2007-05-31 | Completed |
Anecortave Acetate Versus Placebo in AMD Patients Following PDT [NCT00346866] | Phase 2 | 136 participants | Interventional | 2000-05-31 | Completed |
[NCT00346957] | Phase 2 | 128 participants (Actual) | Interventional | 1999-04-30 | Completed |
Anterior Juxtascleral Depot of Anecortave Acetate: Intraocular Pressure Reduction in Glaucoma Patients [NCT00533962] | | 30 participants (Actual) | Interventional | 2007-08-31 | Active, not recruiting |
[NCT00211315] | Phase 2 | 4 participants (Actual) | Interventional | 2002-03-31 | Completed |
[NCT00211354] | Phase 2 | 0 participants (Actual) | Interventional | 2002-03-31 | Withdrawn(stopped due to No subjects enrolled) |
[NCT00211432] | Phase 2 | 4 participants (Actual) | Interventional | 2008-04-30 | Completed |
Phase 3 Study to Evaluate Anecortave Acetate vs. Visudyne for the Treatment of the Wet Form of AMD [NCT00041483] | Phase 3 | 530 participants (Actual) | Interventional | 2002-06-30 | Completed |
[NCT00332657] | Phase 3 | 36 participants (Actual) | Interventional | 2006-09-30 | Terminated(stopped due to Management Decision) |
Anecortave Acetate 15 mg Administered Every 3 Months Versus Anecortave Acetate 15 mg Administered Every 6 Months Versus Anecortave Acetate 30 mg Administered Every 6 Months in Patients With Exudative Age-Related Macular Degeneration (AMD) [NCT00299507] | Phase 3 | 240 participants (Actual) | Interventional | 2005-03-31 | Completed |
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |