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Aldeyra Therapeutics (ALDX) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Adx-629Alcohol HepatitisPhase IICompletedA Clinical Trial Investigating the Safety and Efficacy of Subjects With Alcohol Associated Hepatitis (Part 1)Nov 11, 2024
Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%)Dry Eye DiseasePhase IIICompletedA Trial to Assess the Safety and Efficacy of Subjects With Dry Eye DiseaseJul 02, 2024―
Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%)Dry Eye DiseasePhase IIICompletedA Clinical Trial to Assess the Safety and Efficacy of Subjects With Dry Eye DiseaseMay 17, 2024―
Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%)Dry Eye DiseasePhase IIICompletedA Clinical Trial to Assess the Efficacy and Safety of Subjects With Dry Eye DiseaseApr 25, 2024―
Adx-629 (Open-Label)Atopic DermatitisPhase IICompletedA Clinical Trial in Subjects With Atopic Dermatitis (Part 1)Jan 25, 2023―
Adx-629Ethanol Intoxicationphase1AndPhase2CompletedA Clinical Trial to Evaluate the Safety and Efficacy of ADX-629 in in Subjects With Elevated Ethanol LevelsAug 02, 2022―
Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%)Dry Eye SyndromesPhase IICompletedA Clinical Trial to Evaluate the Safety and Efficacy of Rreproxalap in Adults With Dry Eye DiseaseJun 15, 2022―
Adx-629Chronic CoughPhase IICompletedA Clinical Trial to Evaluate the Safety and Efficacy in Subjects With Chronic CoughMay 05, 2022―
Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%)Allergic ConjunctivitisPhase IIICompletedThe INVIGORATE 2 Trial: A Clinical Trial to Assess the Efficacy and Safety of Subjects With Seasonal Allergic ConjunctivitisFeb 01, 2022―
Reproxalap Ophthalmic Solution (0.25%), Xiidra (5% Lifitegrast Ophthalmic Solution)Dry EyePhase IICompletedAn Exploratory Crossover Clinical Trial to Compare the Activity of Reproxalap and Lifitegrast in a Dry Eye Disease ChamberOct 18, 2021―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Aldeyra Therapeutics (ALDX) have in its pipeline
Aldeyra Therapeutics ALDX is currently developing the following drugs: Adx-629, Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%), Adx-629 (Open-Label), Reproxalap Ophthalmic Solution (0.25%), Xiidra (5% Lifitegrast Ophthalmic Solution), Reproxalap Ophthalmic Solution (0.25%), Reproxalap Ophthalmic Solution (0.25%), Vehicle Opthalmic Solution, Adx-2191 (Intravitreal Methotrexate 0.8%), Standard Surgical Care Procedure, Reproxalap Ophthalmic Solution (0.25% Novel Formulation) Qid To Bid, Vehicle Ophthalmic Solution (0.25% Novel Formulation) Qid To Bid, Reproxalap Ophthalmic Solution (0.25%) Qid, Vehicle Ophthalmic Solution Qid, Reproxalap Ophthalmic Solution (0.25%) Qid To Bid, Vehicle Ophthalmic Solution Qid To Bid, Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%), Reproxalap Ophthalmic Solution (0.5%), Adx-102 1% Topical Dermal Cream (Reproxalap), Vehicle Of Adx-102 Topical Dermal Cream, Vehicle Ophthalmic Solution, Reproxalap Ophthalmic Solution (0.25%), Reproxalap Ophthalmic Solution (0.1%), Adx-102 Ophthalmic Solution (0.5%), Adx-102 Ophthalmic Solution (0.1%), Adx-102 Ophthalmic Lipid Solution (0.5%), Adx-102 Ophthalmic Solution (0.5%), Vehicle Of Adx-102 Ophthalmic Solution. These drug candidates are in various stages of clinical development as the company works toward FDA approval.