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ASX: SNTSyntara LimitedHealth Care

Syntara SNT-4728 Shows Motor Signal in iRBD Phase 2 Data

Syntara reports a statistically significant MDS-UPDRS Part III motor difference for SNT-4728 versus placebo at Week 24 in its Phase 2 iRBD study of 41 people.

By Digifin Pty Ltd · About this coverage

Key Points

  • Statistically significant MDS-UPDRS Part III motor difference versus placebo at Week 24 (p=0.021)
  • Week 24 was 12 weeks after treatment ceased; 41 participants randomised 3:1
  • Smartphone motor composite directionally consistent but not statistically significant
  • No treatment-related serious adverse events reported
  • No marked changes in other MDS-UPDRS, cognitive or quality-of-life measures
Syntara Limited (ASX:SNT)

About Syntara (ASX:SNT)

Syntara Limited is an ASX-listed clinical-stage drug development company headquartered in Sydney. It develops small-molecule drugs targeting inflammation and fibrosis, with programs in neurodegenerative disease and blood cancers.

Syntara (ASX:SNT) released secondary endpoint results from its Phase 2 study of SNT-4728 in isolated REM Sleep Behaviour Disorder (iRBD), which it says support further clinical development of the drug as a potential disease-modifying therapy in prodromal and early Parkinson's Disease.

The randomised, double-blind, placebo-controlled study enrolled 41 participants, randomised 3:1 to SNT-4728 or placebo. Clinician-assessed motor signs measured by MDS-UPDRS Part III showed a statistically significant difference for SNT-4728 versus placebo at Week 24, 12 weeks after treatment ceased (p=0.021). Treated participants showed slightly improved motor scores after the 12 week treatment period and further improvement at week 24, while placebo participants' scores worsened. A smartphone-based motor composite score was directionally consistent, with no statistically significant difference between groups. These results add to the primary imaging endpoint reported 6 July 2026, a statistically significant reduction in brain inflammation unilaterally in the putamen (p-value 0.0145), with 20 out of 30 patients on active treatment recording a reduction from baseline. No treatment-related serious adverse events were reported.

No marked changes were observed in other MDS-UPDRS measures or in cognitive, quality-of-life and iRBD questionnaire measures. The study was small and exploratory, and further analysis of digital, clinical and biomarker data remains outstanding.

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Source: Syntara Limited (ASX:SNT), 7 October 2026. Summary content supplied by Digifin Pty Ltd.

News summary only, not financial advice. It does not consider your objectives, financial situation or needs.

Wednesday, 7 October 2026

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