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Allysta Pharmaceuticals

Leveraging Orphan Drug Status To Launch A Drug Pipeline

About this Event

Allysta Pharmaceuticals has developed a first-in-class therapeutic that has the potential to treat liver disease, lung fibrosis, and even heart disease. this drug has also achieved a rare disease designation for Duchenne Muscular Dystrophy allows for accelerated approvals and extended patent protections.

Preclinical tests have produced substantial data showing the treatment reduced muscle cell death, enhanced muscle regeneration, and reduced inflammation and fibrosis. They have observed improvement in muscle function, including strength and endurance. This suggests the ability of ALY688ER to alter the trajectory of the disease, potentially allowing boys to maintain muscle function and quality of life.

Join this Fireside Chat with:
  • Jason Dinges: Family Office VC, Morningside Technology Advisory
  • Dr. Henry Hsu: CEO, Allysta Pharmaceuticals

To hear how the company is leveraging Rare Disease Designation to help launch this pipeline as a product.

ALY688 has received Orphan Drug Designation for DMD from the FDA and is ready to begin Phase 1 clinical trials.

Register now to watch this webinar with Allysta Pharmaceutical CEO, Dr. Henry Hsu to learn how their first-in-class therapy improves in muscle function allowing boys to maintain muscle function and improve quality of life.

Hosted by Steven Saltzstein. CEO, Force Family Office

Video On Demand

– Recorded

June 19

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