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Prescient Therapeutics’ PTX-100 Gains FDA Fast Track Status

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The latest announcement is out from Prescient Therapeutics Limited ( (AU:PTX) ).

Prescient Therapeutics Limited has received the U.S. FDA Fast Track designation for its PTX-100 drug, aimed at treating relapsed or refractory mycosis fungoides, a subtype of Cutaneous T Cell Lymphoma (CTCL). This designation is a significant milestone, facilitating accelerated approval processes and potentially expediting the drug’s availability to patients. The Fast Track status underscores the FDA’s recognition of PTX-100’s promise in addressing unmet medical needs, enhancing Prescient’s strategic positioning in the oncology market.

More about Prescient Therapeutics Limited

Prescient Therapeutics Limited is a clinical stage oncology company focused on developing personalized medicine approaches for cancer treatment, including targeted and cellular therapies. Their primary product, PTX-100, is a first-in-class compound that inhibits the cancer growth enzyme GGT-1, disrupting oncogenic pathways in cancer cells. The company is also developing innovative cell therapy platforms such as CellPryme-M, CellPryme-A, and OmniCAR, which enhance the efficacy and adaptability of cellular immunotherapies.

YTD Price Performance: -16.00%

Average Trading Volume: 503,898

Technical Sentiment Signal: Buy

Current Market Cap: A$33.82M

Learn more about PTX stock on TipRanks’ Stock Analysis page.

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