TipRanks
Go Ultimate55% OFF

Rion Co., Ltd. (6823) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Pep-Tisseel, Tisseel Fibrin Sealant KitChronic Radiation Ulcerphase1AndPhase2Not Yet RecruitingStudy to Evaluate the Safety, Tolerability, and Efficacy of PEP-TISSEEL in Subjects With Chronic Radiation UlcerJan 16, 2025―
Pep (Purified Exosome Product) / TisseelDiabetic Foot UlcerPhase IIActive Not RecruitingPhase 2a Multi-Center Prospective, Randomized Trial to Evaluate the Safety & Efficacy of Topical PEP-TISSEEL for Diabetic Foot Ulcers (DFU)Mar 13, 2024―

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 Rion Co., Ltd. (JP:6823) have in its pipeline
Rion Co., Ltd. JP:6823 is currently developing the following drugs: Pep-Tisseel, Tisseel Fibrin Sealant Kit, Pep (Purified Exosome Product) / Tisseel. These drug candidates are in various stages of clinical development as the company works toward FDA approval.