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Ocular Inflammation

5
Pipeline Programs
3
Companies
2
Clinical Trials
1 recruiting
3
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
1
0
1
3
Early DiscoveryClinical DevelopmentMarket

On Market (3)

Approved therapies currently available

Bausch + Lomb
LOTEMAX SMApproved
loteprednol etabonate
Bausch + Lomb
ophthalmic2019
21M Part D
Bausch + Lomb
ALREXApproved
loteprednol etabonate
Bausch + Lomb
ophthalmic1998
11M Part D
Bausch + Lomb
LOTEMAXApproved
loteprednol etabonate
Bausch + Lomb
ophthalmic1998
11M Part D

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Bausch + Lomb
Bausch + LombNJ - Bridgewater
1 program
1
1
LOTEMAX SM(loteprednol etabonate)Phase 3
EMS
EMSBrazil - Hortolândia
1 program
1
SATURNO II associationPhase 21 trial
Active Trials
NCT03580473Completed118Est. Mar 2022
Thea Pharma
Thea PharmaMA - Waltham
1 program
HydrocortisonePHASE_31 trial
Active Trials
NCT05668455RecruitingEst. Jul 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Thea PharmaHydrocortisone
EMSSATURNO II association

Clinical Trials (2)

Total enrollment: 118 patients across 2 trials

Comparison of Topical Treatment for Inflammatory Secretions of the Conjonctiva (Patients With Ocular Prostheses)

Start: May 2023Est. completion: Jul 2026
Phase 3Recruiting
NCT03580473EMSSATURNO II association

Efficacy and Safety of Saturno IIB Association on the Control of Ocular Inflammation Post-phacoemulsification

Start: Feb 2020Est. completion: Mar 2022118 patients
Phase 2Completed

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

1 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 118 patients
3 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.