Last reviewed · How we verify
AGN-210669 ophthalmic solution, 0.05%
AGN-210669 ophthalmic solution, 0.05% is a Corticosteroid Small molecule drug developed by Allergan. It is currently in Phase 2 development for Treatment of non-infectious uveitis affecting the posterior segment of the eye.
AGN-210669 ophthalmic solution is a corticosteroid used to reduce inflammation in the eye.
AGN-210669 ophthalmic solution is a small molecule used to treat conditions such as open-angle glaucoma and ocular hypertension. It is compared to bimatoprost ophthalmic solution in clinical trials for its safety and efficacy.
-
Baseline phase 2 → approval rate
+15.3pp
Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2031–2034 | — |
| EMA | EU | 2032–2035 | +0.7 yr |
| MHRA | GB | 2032–2035 | +0.7 yr |
| Health Canada | CA | 2032–2036 | +0.9 yr |
| TGA | AU | 2032–2036 | +1.2 yr |
| PMDA | JP | 2032–2036 | +1.5 yr |
| NMPA | CN | 2033–2037 | +2.3 yr |
| MFDS | KR | 2032–2036 | +1.4 yr |
| CDSCO | IN | 2032–2037 | +1.8 yr |
| ANVISA | BR | 2033–2037 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | AGN-210669 ophthalmic solution, 0.05% |
|---|---|
| Sponsor | Allergan |
| Drug class | Corticosteroid |
| Modality | Small molecule |
| Therapeutic area | Ophthalmology |
| Phase | Phase 2 |
Mechanism of action
Corticosteroids like AGN-210669 work by inhibiting the production of inflammatory mediators, thereby reducing swelling and pain in the eye. This is achieved through the suppression of phospholipase A2, an enzyme involved in the production of prostaglandins and leukotrienes, which are key players in the inflammatory response.
Approved indications
- Treatment of non-infectious uveitis affecting the posterior segment of the eye
Common side effects
- Increased intraocular pressure
Key clinical trials
- Safety and Efficacy of AGN-210669 Ophthalmic Solution Compared With Bimatoprost Ophthalmic Solution in Patients With Open-Angle Glaucoma or Ocular Hypertension (PHASE2)
- Safety and Efficacy of AGN 210669 Ophthalmic Solution in Patients With Ocular Hypertension or Primary Open-Angle Glaucoma (PHASE1, PHASE2)
- Safety and Efficacy of Three Formulations of AGN-210669 Ophthalmic Solution Compared With Bimatoprost Ophthalmic Solution (PHASE2)
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:
- AGN-210669 ophthalmic solution, 0.05% CI brief — competitive landscape report
- AGN-210669 ophthalmic solution, 0.05% updates RSS · CI watch RSS
- Allergan portfolio CI
Frequently asked questions about AGN-210669 ophthalmic solution, 0.05%
What is AGN-210669 ophthalmic solution, 0.05%?
How does AGN-210669 ophthalmic solution, 0.05% work?
What is AGN-210669 ophthalmic solution, 0.05% used for?
Who makes AGN-210669 ophthalmic solution, 0.05%?
What drug class is AGN-210669 ophthalmic solution, 0.05% in?
What development phase is AGN-210669 ophthalmic solution, 0.05% in?
What are the side effects of AGN-210669 ophthalmic solution, 0.05%?
Related
- Drug class: All Corticosteroid drugs
- Manufacturer: Allergan — full pipeline
- Therapeutic area: All drugs in Ophthalmology
- Indication: Drugs for Treatment of non-infectious uveitis affecting the posterior segment of the eye
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing