Praxis Precision Medicines Reports Q2 2026 Results and Regulatory Progress

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Praxis Precision Medicines, Inc. (NASDAQ:PRAX) reported second quarter 2026 financial results and provided updates on its two lead drug candidates under FDA review. The company ended the quarter with $1.4 billion in cash and marketable securities, up from $926.1 million at the end of 2025, and said its cash runway extends into 2028. Net loss for the quarter was $83.7 million, with research and development expenses of $69.4 million and general and administrative expenses of $27.5 million. The FDA completed mid-cycle reviews for both ulixacaltamide, for essential tremor, and relutrigine, for SCN2A and SCN8A developmental and epileptic encephalopathies, and indicated no advisory committee meetings are planned for either asset. Ulixacaltamide has a PDUFA date of January 29, 2027, and relutrigine has a PDUFA date of December 27, 2026. The company also announced a collaboration with Remagine Labs to develop a transdermal formulation of ulixacaltamide and said it plans to restart the POWER2 and POWER3 studies for vormatrigine in the fourth quarter of 2026.

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Collaboration to develop transdermal formulation of ulixacaltamide.

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