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Thiogenesis Therapeutics Corp (TTI) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Tti-0102: Cysteamine-Pantetheine Disulfide, D-MannitolLeigh SyndromePhase IINot Yet RecruitingA Dose-ranging Study of TTI-0102 in Adults and Children With Leigh Syndrome Spectrum (LSS)May 06, 2025―
Tti-0102Melas Syndrome, Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes (Melas)Phase IIRecruitingA Study to Assess TTI-0102 vs Placebo in MELAS PatientsSep 29, 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 Thiogenesis Therapeutics Corp (TSE:TTI) have in its pipeline
Thiogenesis Therapeutics Corp TSE:TTI is currently developing the following drugs: Tti-0102: Cysteamine-Pantetheine Disulfide, D-Mannitol, Tti-0102. These drug candidates are in various stages of clinical development as the company works toward FDA approval.