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Adenoviral Conjunctivitis

4
Pipeline Programs
4
Companies
4
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
4
0
0
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

4 companies ranked by most advanced pipeline stage

Alcon
AlconFORT WORTH, TX
1 program
1
AL-46383A Ophthalmic SolutionPhase 21 trial
Active Trials
NCT00901693Terminated452Est. Jul 2010
IVIEW Therapeutics
IVIEW TherapeuticsNJ - Cranbury
1 program
1
IVIEW-1201Phase 21 trial
Active Trials
NCT03749317Completed135Est. Dec 2024
NicOx
NicOxFrance - Biot
1 program
1
Iota-CarrageenanPhase 21 trial
Active Trials
NCT03009799Withdrawn0Est. Sep 2017
Okogen
OkogenTX - Plano
1 program
1
OKG-0301Phase 21 trial
Active Trials
NCT03856645Unknown219Est. Jun 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
IVIEW TherapeuticsIVIEW-1201
OkogenOKG-0301
NicOxIota-Carrageenan
AlconAL-46383A Ophthalmic Solution

Clinical Trials (4)

Total enrollment: 806 patients across 4 trials

Trial to Evaluate the Efficacy and Safety of IVIEW-1201 in Acute Viral Conjunctivitis

Start: Feb 2023Est. completion: Dec 2024135 patients
Phase 2Completed

OKG-0301 for the Treatment of Acute Adenoviral Conjunctivitis

Start: Feb 2019Est. completion: Jun 2022219 patients
Phase 2Unknown
NCT03009799NicOxIota-Carrageenan

Efficacy and Safety of Iota-Carrageenan Eye Drops (NCX-4240)

Start: Jan 2017Est. completion: Sep 20170
Phase 2Withdrawn
NCT00901693AlconAL-46383A Ophthalmic Solution

An Evaluation of the Efficacy and Safety of AL-46383A Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis

Start: Jun 2009Est. completion: Jul 2010452 patients
Phase 2Terminated

Phase Legend

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

Key Insights

4 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.