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Rapport Therapeutics, Inc./$RAPP

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About Rapport Therapeutics, Inc.

Rapport Therapeutics Inc is a clinical-stage biotechnology company dedicated to the discovery and development of small-molecule precision medicines for patients with neurological or psychiatric disorders. The company's portfolio of programs from its RAP technology platform includes RAP-219, an investigational small molecule being developed as a therapy for focal onset seizures, primary generalized tonic-clonic seizures, and bipolar mania. Additionally, it has two discovery-stage nicotinic acetylcholine receptor (nAChR) programs stemming from its RAP technology platform: one being developed for the treatment of chronic pain, and the second, being developed for the treatment of hearing disorders. Geographically, the company operates in the United States.
Ticker
$RAPP
Sector
Health
Primary listing
NASDAQ
Employees
84

RAPP Metrics

BasicAdvanced
$1.4B
-
-$3.05
1.03
-

What the Analysts think about RAPP

Analyst ratings (Buy, Hold, Sell) for Rapport Therapeutics, Inc. stock.
Analyst projections of the future price of Rapport Therapeutics, Inc. stock.

Bulls say / Bears say

RAP-219 showed sustained activity after treatment stopped in a 30-patient Phase 2a focal-seizure study, with median clinical-seizure reductions of 90% in weeks 9–12 and 59% in weeks 13–16. Rapport has now moved the programme into the pivotal FOCUS 1 and FOCUS 2 Phase 3 trials. (Rapport Therapeutics, Rapport Therapeutics)
RAP-219 offers several potential value drivers beyond focal seizures: bipolar-mania Phase 2 results are due in October, a primary generalised tonic-clonic seizure Phase 3 trial is planned for the first half of 2027, and a long-acting injectable is being developed. This gives investors more than one route to clinical and commercial validation. (Rapport Therapeutics, EarningsCalls)
Rapport ended the second quarter with $436.1 million in cash, cash equivalents and short-term investments, which management expects to fund operations into the second half of 2029. That should let it run the pivotal seizure programme and pursue upcoming catalysts without an immediate funding requirement. (Rapport Therapeutics, SEC filing)
The strongest seizure evidence still comes from a small Phase 2a dataset of 30 patients, while the pivotal FOCUS 2 study is only recruiting and is not scheduled for primary completion until July 2029. The key efficacy claim therefore remains unconfirmed by a controlled Phase 3 outcome. (Rapport Therapeutics, ClinicalTrials.gov)
The company is still loss-making and its latest filing says it will need additional financing over time, even though current cash is expected to last into the second half of 2029. If trials take longer, costs rise or results disappoint, a future equity raise could dilute existing shareholders. (SEC filing, Rapport Therapeutics)
Long-term safety is not yet established at scale: the focal-seizure Phase 2a study enrolled only 30 patients, and initial data from the open-label long-term safety trial are not expected until the fourth quarter. The drug’s prolonged exposure makes that safety readout particularly important before investors can treat the early efficacy signal as durable and broadly usable. (Rapport Therapeutics, Rapport Therapeutics)
Data summarised monthly by Lightyear AI. Last updated on 23 Sept 2026.

RAPP Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

RAPP Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing RAPP

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