Last reviewed · How we verify
Retaane (anecortave)
At a glance
| Generic name | anecortave |
|---|---|
| Drug class | anecortave |
| Target | Plasminogen activator inhibitor 1 |
| Therapeutic area | Ophthalmology |
| Phase | FDA-approved |
Approved indications
- Exudative age-related macular degeneration
Common side effects
Key clinical trials
- Anecortave Acetate Injection to Treat Steroid-responsive Intraocular Pressure Increase in Cornea Transplant Patients (NA)
- Phase 3 Study to Evaluate Anecortave Acetate vs. Visudyne for the Treatment of the Wet Form of AMD (PHASE3)
- Open-Label Posterior Juxtascleral Injections of Anecortave Acetate 15mg Dose for Long Term Use in Patients With AMD (PHASE3)
- A Dose-Volume Study of a Treatment for Elevated IOP Due to Open-Angle Glaucoma or Ocular Hypertension (PHASE2)
- An Evaluation of Safety and Efficacy of Anecortave Acetate Versus Placebo in Patients With Subfoveal CNV Due to Exudative AMD (PHASE3)
- Anecortave Acetate in Patients With Exudative Age-related Macular Degeneration (AMD) (PHASE3)
- Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension (PHASE2,PHASE3)
- Anecortave Acetate Risk-Reduction Trial (AART) (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Retaane CI brief — competitive landscape report
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- portfolio CI