Rapport Therapeutics Inc

Rapport Therapeutics Inc (RAPP) News & Events

$29.570

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RAPP News

RAPP Events

9/23 15:00

Rapport Therapeutics Shares Drop 17.3%

Shares of Rapport Therapeutics (RAPP) were dropping after the company presented at TD Cowen's 6th Annual Novel Mechanisms in Neuropsychiatry Summit. Of note, CEO Abe Cassey said that he would "not be surprised" if some portion of patients in a trial of a bipolar mania treatment had "worsening mania symptoms," adding that bipolar mania could be a blockbuster plus "without a doubt." Shares of Rapport are down 17.3% in afternoon trading.

5/7 07:40

Rapport Reports Q1 Revenue of $20 Million

Reports Q1 revenue $20,000, consensus $6M. "We entered 2026 with strong momentum across the RAP-219 development program, highlighted by compelling new follow-up Phase 2a data recently presented at AAN that further reinforces RAP-219's treatment effect in focal onset seizures and builds confidence as we enter our Phase 3 trials," said Abraham N. Ceesay, chief executive officer of Rapport. "With multiple important development milestones ahead, including continued advancement of our epilepsy franchise, progress in bipolar mania, and development of our long-acting injectable formulation, we believe we are well positioned to continue building value across our pipeline."

4/21 16:40

Rapport Therapeutics Announces RAP-219 Trial Results

Rapport Therapeutics announced results from the follow-up period of its Phase 2a trial of RAP-219 in focal onset seizures, FOS, in a late-breaker podium presentation at the 2026 American Academy of Neurology, AAN, Annual Meeting, taking place April 18-22, 2026 in Chicago. In the Phase 2a trial, patients received RAP-219 for 8 weeks and then entered an 8-week follow-up period after treatment ended to evaluate the effect of RAP-219 on long episodes and clinical seizures. Therapeutic levels of RAP-219 were sustained, resulting in continued biomarker and clinical responses in the 8-week follow-up period. In the first four weeks of follow-up, RAP-219 showed greater reductions in LEs and clinical seizures than were observed during the 8-week treatment period. Clinically meaningful improvements over baseline continued through the second four weeks of follow-up.

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