Goldman Sachs 47th Annual Global Healthcare Conference 2026
Logotype for Rapport Therapeutics Inc

Rapport Therapeutics (RAPP) Goldman Sachs 47th Annual Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Rapport Therapeutics Inc

Goldman Sachs 47th Annual Global Healthcare Conference 2026 summary

8 Jun, 2026

Key clinical program updates

  • Phase III studies in focal-onset seizures are actively enrolling globally, with rolling site activation and a partnership in China to aid recruitment and efficiency.

  • Phase II data for RAP-219 in focal-onset seizures showed a 78% median reduction in seizure frequency and a 24% seizure freedom rate, supporting confidence in phase III trial design.

  • Phase II study in bipolar mania is nearing completion, with top-line data expected in Q4 this year, ahead of previous guidance.

  • Open label extension study for RAP-219 is enrolling, with initial safety and efficacy data expected in Q4, focusing on long-term safety exposure.

  • Primary generalized tonic-clonic seizure trial and long-acting injectable PK study are planned to start in 2027.

Trial design, regulatory, and operational strategy

  • Conservative powering of phase III trials aims to ensure high probability of success and sufficient safety exposure for registration.

  • Placebo response in phase III is managed through rigorous patient selection, eDiary training, and collaboration with The Epilepsy Study Consortium.

  • FDA is receptive to global data accumulation, including from China, with no anticipated regulatory issues.

  • Regulatory strategy for the long-acting injectable will be determined after PK data in 2027, with potential for either bridging or full efficacy studies.

Commercial and strategic outlook

  • RAP-219 is positioned as a best-in-class anti-seizure medication with a novel mechanism, strong efficacy, and favorable tolerability, supporting broad use by both epileptologists and general neurologists.

  • Market research indicates potential for second-line utilization, which could significantly boost sales trajectory.

  • Long-acting injectable formulation could extend IP runway into the late 2040s and transform patient adherence and asset value.

  • Partnership with Tenacia in China is expected to accelerate global trial recruitment and future commercialization.

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