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Cynata Therapeutics Limited (51S) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Corticosteroids, Cyp-001: Cymerus Induced Pluripotent Stem Cell (Ipsc)-Derived Mesenchymal Stem Cells (Mscs)Graft Versus Host Disease, AcutePhase IIRecruitingA Study of CYP-001 in Combination with Corticosteroids in Adults with High-risk AGvHDNov 29, 2022―
Cyp-006TkDiabetic Foot Ulcer, Cutaneous UlcerPhase ICompletedSafety, Tolerability and Efficacy of CYP-006TK in Adults with Diabetic Foot UlcersOct 18, 2021―
Cyp-001COVID19, Acute Respiratory Distress SyndromePhase ICompletedThe MEseNchymal coviD-19 Trial: MSCs in Adults With Respiratory Failure Due to COVID-19 or Another Underlying CauseAug 25, 2020―
Mesenchymoangioblast-Derived Mesenchymal Stem CellsGraft Vs Host DiseasePhase ICompletedA Study of CYP-001 for the Treatment of Steroid-Resistant Acute Graft Versus Host DiseaseOct 03, 2016―

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 Cynata Therapeutics Limited (DE:51S) have in its pipeline
Cynata Therapeutics Limited DE:51S is currently developing the following drugs: Corticosteroids, Cyp-001: Cymerus Induced Pluripotent Stem Cell (Ipsc)-Derived Mesenchymal Stem Cells (Mscs), Cyp-006Tk, Cyp-001, Mesenchymoangioblast-Derived Mesenchymal Stem Cells. These drug candidates are in various stages of clinical development as the company works toward FDA approval.