Why Did Rapport Therapeutics, Inc Shares Skyrocket in Premarket?
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Why Did Rapport Therapeutics, Inc Shares Skyrocket in Premarket?

Rapport Therapeutics shares surged in premarket trading after announcing positive Phase 2a trial results for RAP-219, showing 77.8% reduction in clinical seizures.
Neither the author, Tim Fries, nor this website, The Tokenist, provide financial advice. Please consult our website policy prior to making financial decisions.

Rapport Therapeutics, Inc. (NASDAQ: RAPP) experienced a dramatic surge in premarket trading on September 8, 2025, with shares jumping over 143% to $34.99 from the previous close of $14.36. This explosive movement came after the clinical-stage biotechnology company announced overwhelmingly positive results from its Phase 2a clinical trial of RAP-219, an investigational treatment for drug-resistant focal onset seizures.

The trial results exceeded expectations across multiple key metrics, positioning the company to advance into Phase 3 registrational trials and potentially bringing hope to patients suffering from epilepsy who haven’t responded to existing treatments.

Rapport Announces Groundbreaking Phase 2a Results

The Phase 2a clinical trial of RAP-219 delivered impressive efficacy results that far exceeded typical outcomes in epilepsy research. In the 8-week treatment period, patients achieved a remarkable 77.8% median reduction in clinical seizures compared to baseline, with statistical significance (p=0.01). Perhaps most importantly for patients and their families, 24% of participants achieved complete seizure freedom during the treatment period, a outcome that occurred with high statistical significance (p<0.0001).

The trial also met its primary endpoint with flying colors, as 85.2% of patients achieved at least a 30% reduction in long episodes (LEs) – an objective electrographic biomarker for seizure activity – compared to baseline (p<0.0001). Additionally, 72% of patients experienced at least a 50% reduction in clinical seizures, demonstrating the drug’s potential to meaningfully improve quality of life for people with drug-resistant epilepsy. These results are particularly significant because up to 40% of patients with focal epilepsy continue to experience seizures despite available therapies, representing a substantial unmet medical need.

RAP-219 was generally well-tolerated throughout the trial, with no serious adverse events reported during the treatment period. The most common side effects were mild, including dizziness (26.7%), headache (16.7%), and fatigue (13.3%), with only 10% of patients discontinuing treatment due to adverse events. This safety profile, combined with the strong efficacy results, supports the drug’s potential as a new treatment option for patients who have exhausted other therapeutic alternatives.

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RAPP Stock Up 143% in Premarket Trading

The premarket surge to $34.99 represents a stunning 143.66% increase from Friday’s closing price of $14.36, demonstrating investors’ enthusiasm for the trial results. This dramatic movement occurred at 7:50:55 AM EDT on September 8, 2025, shortly after the company released its positive topline results. The stock had been trading in a 52-week range of $6.43 to $29.74, making the premarket price a new high for the company and reflecting the market’s assessment of RAP-219’s commercial potential.

Prior to this announcement, RAPP had been struggling with negative returns, showing a year-to-date decline of 19.05% and a one-year return of -32.33% as of September 5, 2025. The company’s market capitalization stood at approximately $524 million before the surge, and analyst price targets averaged $34.20 with a high of $42.00, suggesting the premarket movement aligns closely with professional expectations. The dramatic price appreciation reflects investors’ recognition that successful Phase 2a results significantly de-risk the development pathway and increase the probability of eventual commercial success.

Looking ahead, Rapport plans to meet with the FDA in Q4 2025 for an end-of-Phase 2 meeting and expects to initiate two Phase 3 pivotal trials in Q3 2026. The company will also present additional efficacy analyses and 8-week follow-up results in 2026, which could provide further catalysts for the stock. Beyond epilepsy, Rapport is evaluating RAP-219 in bipolar mania (Phase 2 results expected in H1 2027) and diabetic peripheral neuropathic pain, potentially expanding the drug’s addressable market significantly and creating multiple value inflection points for investors.

Disclaimer: The author does not hold or have a position in any securities discussed in the article. All stock prices were quoted at the time of writing.

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