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NASDAQ:RAPP

Rapport Therapeutics Q3 2026 Earnings Results & Report

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$25.47 +0.03 (+0.12%)
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Rapport Therapeutics beat analyst earnings expectations in its Q3 2026 results, released November 4, 2026. The company reported EPS of -$0.84 versus the -$1.20 consensus estimate.

Earnings Announcement Details

Quarter
Q3 2026
Report Date
Time
Before Market Opens
Conference Call
7:00 AM ET

Rapport Therapeutics EPS Results

Actual EPS
-$0.84
Consensus EPS
-$1.20
Beat/Miss
Beat by +$0.36
One Year Ago EPS
N/A
EPS Beat Rate
6 of last 8 quarters

Rapport Therapeutics Revenue Results

Actual Revenue
N/A
Expected Revenue
N/A
Beat/Miss
N/A
YoY Revenue Growth
N/A

Rapport Therapeutics Q3 2026 Earnings FAQ

Rapport Therapeutics (NASDAQ:RAPP) reported earnings of -$0.84 per share for Q3 2026, beating the consensus estimate of -$1.20. The report was announced on Wednesday, November 4, 2026.

Rapport Therapeutics Earnings Headlines

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About Rapport Therapeutics

Rapport Therapeutics (NASDAQ:RAPP) is a clinical-stage biopharmaceutical company focused on developing precision medicines for central nervous system disorders. The company’s approach is designed to selectively target receptor-associated proteins that regulate synaptic receptors, with the goal of improving therapeutic selectivity and reducing the side effects associated with broader-acting neurological medicines.

Rapport’s lead product candidate, RAP-219, is an orally administered small molecule being developed for neurological conditions, including focal epilepsy. The candidate is designed to selectively modulate AMPA receptor complexes through their associated proteins. The company is also advancing a broader pipeline of discovery and development programs intended to address additional disorders involving abnormal neuronal signaling, such as pain and psychiatric conditions.

Rapport Therapeutics was established in 2018 and is headquartered in Boston, Massachusetts. Its research and development activities are focused on creating medicines for patients with central nervous system diseases, with clinical and commercial opportunities expected to span international markets. The company’s programs remain in development and are subject to the results of clinical trials and regulatory review.

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