Syntara (SNT) Investor update summary
Event summary combining transcript, slides, and related documents.
Investor update summary
30 Apr, 2026FDA 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.
Latest events from Syntara
- FDA-backed late-stage trials and strong cash position set up major clinical catalysts in H2 2026.SNT
Q4 2026 TU28 Jul 2026 - Lead asset amsulostat shows strong Phase 2 efficacy and safety, with multiple pipeline catalysts ahead.SNT
Investor presentation26 Jul 2026 - 73% achieved TSS50 and 44% SVR25 with strong tolerability and ongoing development plans.SNT
Study Update9 Jul 2026 - Phase 2 myelofibrosis trial fully recruited; A$5m raised; interim data due December 2024.SNT
Q1 2025 TU8 Jul 2026 - Shareholders voted on two share placement resolutions, with results to be announced later today.SNT
EGM 202623 Jun 2026 - Phase II/2a trial of SNT-4728 targets neuroinflammation in iRBD, results due by June or 2026.SNT
Status update2 Jun 2026 - FDA supports Phase 2b for amsulostat; cash runway extended after A$8m placement.SNT
Q3 2026 TU30 Apr 2026 - Amsulostat shows promising efficacy in myelofibrosis, with funding secured for pivotal trials.SNT
Investor presentation29 Apr 2026 - Net loss widened to $15.1M as revenue fell and cost reductions followed the MBU sale.SNT
H2 20247 Apr 2026