An Australian stem cell and regenerative medicine company

July 14, 2022

Notice of Allowance from the United States Patent and Trademark Office

In July, Cynata received a Notice of Allowance from the United States Patent and Trademark Office (USPTO) for a patent application covering the use of its Cymerus™ MSCs in treating asthma and allergic airways disease. The patent adds yet another string to the Company’s bow which now has multiple applications under investigation for its off-the-shelf stem cell product. 

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June 21, 2022

Cymerus MSCs as a potential stem cell therapy for IPF

A study conducted by Professor Chrishan Samuel, a Monash Biomedicine Discovery Fellow and Head of the Fibrosis Laboratory, Department of Pharmacology at Monash University, found that in an animal model of idiopathic pulmonary fibrosis (IPF), Cynata’s stem cells ameliorated the mediators of lung inflammation while at the same time promoting anti-inflammatory effects. Why is this exciting? 

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June 11, 2022

Riding the wave with Dr Ross Macdonald

An avid surfer of over 50 years, Ross has a vested interest in helping us live better for longer, especially protecting our joints. In early June he spoke with the Australian Financial Review about his love of surfing, and how he finds peace of mind and strategic clarity while riding waves 

https://www.afr.com/life-and-luxury/health-and-wellness/why-this-ceo-brainstorms-while-sitting-on-a-surfboard-20220705-p5az9z

June 01, 2022

Ross sits down with Bulls n Bears following FDA Phase 2 trial clearance

Managing Director Dr Ross Macdonald spoke to Matt Birney on the Bulls N’ Bears Report about the FDA clearing Cynata’sInvestigational New Drug (IND) application for a Phase 2 acute graft versus host disease (aGvHD) trial adding yet another indication to Cynata's broad and robust clinical pipeline. 

Listen to the interview here

May 26, 2022

Cynata gets the green light for Phase 2 aGVHD trial

In exciting news, the US FDA cleared Cynata’s Investigational New Drug (IND) application for a Phase 2 clinical trial of CYP-001 in patients with acute graft versus host disease (aGvHD). The planned Phase 2 clinical trial will seek to recruit approximately 60 patients with high risk aGvHD, at clinical centres in several countries, including the US and Australia. FDA clearance is a major achievement and valuation milestone for the Company.

The stock was up 10 per cent following the announcement, read the full details on The Australian: