Previous name for @SyntaraTX - biotech leaders in drug discovery for diseases linked to fibrosis and inflammation.

Australia
Joined November 2023
Syntara (#ASX: $SNT) was featured this week at Twilight Briefings where Gary Phillips provided updates on clinical trials targeting #myelofibrosis, IRBD and #ParkinsonsDisease, skin scarring and Myelodysplastic Syndrome. View the investor presentation: cdn-api.markitdigital.com/ap…
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Following news of Syntara's (#ASX: $SNT) new Phase 2 clinical study targeting #MyelodysplasticSyndrome, CEO Gary Phillips was featured on @proactive_au to discuss the trials that will aim to reduce dependence on transfusions among #bloodcancer patients: youtu.be/PoG380EMVlo?si=RGgP…
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In partnership with @Uni_Newcastle and @ALLGtrials, Syntara (#ASX: $SNT) has announced a Phase 2 trial evaluating SNT-5505 in combination with chemotherapy in patients with risk of myelodysplastic syndrome. It follows a $0.83m grant by the MRFF. More: cdn-api.markitdigital.com/ap…
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Syntara (#ASX: $SNT) is pleased to release its first quarterly report since divesting the mannitol business unit, providing a robust financial foundation to focus on the 3 Phase 1c/2 clinical studies targeting unmet needs. View the full report: cdn-api.markitdigital.com/ap…
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Syntara (#ASX: $SNT) is delighted to welcome new and existing investors that have committed $10m towards SNT drug development, including the attractive commercial opportunity for SNT-5505 as a #myelofibrosis treatment. CEO Gary Phillips discusses more: youtu.be/CpA9Amph-3E?si=9wJp…
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The first patients in the final cohort of Syntara (#ASX: $SNT)'s Phase 2 trials to treat #myelofibrosis, have commenced dosing. This cohort is undergoing a combination treatment of SNT-5505 with the market leading JAK inhibitor, #ruxolitinib. Read more: cdn-api.markitdigital.com/ap…
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Pharmaxis retweeted
At today’s AGM, @Syntara's Board and management set out the value opportunities as the newly named company completes a restructure and advances its new drug assets in blood cancer, skin scarring and neurodegeneration.
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At today’s AGM, @Syntara's Board and management set out the value opportunities as the newly named company completes a restructure and advances its new drug assets in blood cancer, skin scarring and neurodegeneration.
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The first patient has been dosed in our Phase 2 study for isolated Rapid Eye Movement Sleep Behavior Disorder (#iRBD), a precursor of #Parkinsonsdisease. The trial is primarily funded by a program founded by @ParkinsonsUK. View more: pharmaxis.com.au/assets/Docu…
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As Pharmaxis prepares for its transformation to Syntara, a #biotech focused on clinical stage drug development, CEO Gary Phillips updated investors on the potential for 5 phase 1c/2 studies to deliver clinical data in a 9 month window. View more: pharmaxis.com.au/investor-ce…
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$PXS Pharmaxis finalises sale of MBU to Arna Pharma; shifts focus to blood-related cancer treatments tinyurl.com/ytturzvn @Pharmaxis $PMXSF #PXS #PMXSF
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We are pleased to release a new Investor Presentation, the first on our Syntara branding, subject to shareholder approval. The presentation outlines Syntara as a specialist drug development company prioritising haematological malignancies. View here: pharmaxis.com.au/assets/Docu…
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