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Thiogenesis Therapeutics Advances LSS Treatment with New TTI-0102 Study

Thiogenesis Therapeutics Advances LSS Treatment with New TTI-0102 Study

Thiogenesis Therapeutics Corp ((TSE:TTI)) announced an update on their ongoing clinical study.

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Thiogenesis Therapeutics Corp is advancing its research on TTI-0102 with a new clinical trial aimed at treating Leigh Syndrome Spectrum (LSS). Officially titled ‘A Phase 2a Partially Randomized, Placebo-controlled, Sequential Dose-ranging Study of TTI-0102 in Adults and Children With Leigh Syndrome Spectrum,’ the study seeks to evaluate the pharmacokinetics, safety, and preliminary efficacy of TTI-0102. This research is significant as it could pave the way for more effective treatments for LSS, a rare and severe neurological disorder.

The intervention being tested is TTI-0102, a cysteamine-pantetheine disulfide, designed to improve treatment outcomes for LSS patients by optimizing drug levels and efficacy measures. The study also includes a placebo comparator using D-Mannitol.

The study design is interventional, with a partially randomized, placebo-controlled, sequential dose-ranging model. It involves masking all parties during the placebo-controlled sequence to ensure unbiased results. The primary purpose is treatment-focused, aiming to establish a suitable dose level for future studies.

Key dates for this study include a start date of May 6, 2025, with the last update submitted on July 8, 2025. These dates are crucial as they mark the timeline for recruitment and subsequent phases of the study.

The market implications of this study update could be significant for Thiogenesis Therapeutics Corp, potentially boosting investor confidence and stock performance if the results are positive. In the competitive landscape of rare disease treatment, advancements in LSS therapies could position Thiogenesis as a leader in this niche market.

The study is currently ongoing, with further details available on the ClinicalTrials portal.

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