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Marinomed Biotech AG (93Z) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Eye Drops, Solution In Single-Dose ContainerAllergic Conjunctivitis, Allergic RhinitisPhase IICompletedTherapeutic Effect of Tacrosolv in Patients With Allergic RhinoconjunctivitisAug 21, 2020―
Rhinocort, BudesolvAllergic Conjunctivitis, Allergic Rhinitis, HayfeverPhase IIICompletedDemonstration of Equivalence and Early Onset of a Novel Anti-allergic Nasal Spray Compared to Marketed Nasal SprayNov 21, 2018―

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 Marinomed Biotech AG (DE:93Z) have in its pipeline
Marinomed Biotech AG DE:93Z is currently developing the following drugs: Eye Drops, Solution In Single-Dose Container, Rhinocort, Budesolv. These drug candidates are in various stages of clinical development as the company works toward FDA approval.