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Current projections suggest the following timeline: Phase 3 trials complete around 2026 Regulatory submissions occur shortly after Potential approval may occur between 2027 and 2028 if results remain favorable (GLP3 Planner) These timelines depend heavily on: Final safety data Regulatory review Post-trial analyses Drug development is inherently uncertain, and unexpected findings can delay approval

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This observed cytotoxicity may be attributed to the elevated uptake of GSH and/or -EC, potentially disturbing GSH homeostasis

These algorithms provide structured approaches to clinical decision-making and reduce provider uncertainty about when to suspect endometriosis