Investor update
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Syntara (SNT) Investor update summary

Event summary combining transcript, slides, and related documents.

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Investor update summary

30 Apr, 2026

FDA Feedback and Clinical Development Pathway

  • Achieved formal FDA alignment on the Phase 2b trial protocol for amsulostat/imsulostat in myelofibrosis, de-risking the regulatory path and validating the clinical strategy.

  • FDA supports TSS50 (50% reduction in Total Symptom Score) as the primary endpoint after 9 months, with secondary endpoints including spleen volume, overall survival, and safety.

  • The Phase 2b study will enroll about 100 patients in a double-blind, placebo-controlled format, targeting those with inadequate response to standard care.

  • Trial preparation is underway, with commencement targeted for Q4 2026 and recruitment over 18 months.

  • FDA alignment enhances the asset's attractiveness for potential partners and supports ongoing licensing and commercial partnership discussions.

Clinical Data and Competitive Positioning

  • Phase 2a data showed rapid and sustained symptom improvement, with 73% of patients achieving TSS50 at 24 weeks or beyond.

  • Meaningful spleen volume reductions were observed, and several patients continued treatment beyond 52 weeks.

  • Amsulostat/imsulostat offers a distinct mode of action, improved tolerability, and potential for disease modification compared to current JAK inhibitor standard of care.

  • Fast Track and Orphan Drug Designations have been secured, reinforcing its differentiated position.

  • Strong differentiation from competitors due to significant symptom improvement, a key factor for both regulators and partners.

Capital Raising and Financial Position

  • Raised AUD 8 million via institutional placement and targeting an additional AUD 2 million through a Share Purchase Plan, extending cash runway to Q3 2027.

  • The raise was timed to leverage the de-risked FDA pathway, providing funding for five key clinical trial readouts in 2026.

  • Strong support from existing and new specialist healthcare investors, maintaining a robust investor base.

  • Phase 2b trial estimated to cost $20–25 million; company is exploring both partnerships and non-dilutive funding options.

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