Rapport Therapeutics to Present Data for TARPγ8 AMPAR Negative Modulator at IASP 2024 World Congress on Pain
July 29 2024 - 7:00AM
Rapport Therapeutics, Inc. (Nasdaq: RAPP), a clinical-stage
biotechnology company focused on discovery and development of
transformational small molecule medicines for patients suffering
from central nervous system disorders, today announced that
the Company will present preclinical data on RTX-1738, an analog to
Rapport’s lead product candidate RAP-219, across a variety of acute
and chronic pain models at the upcoming International Association
for the Study of Pain (IASP) 2024 World Congress on Pain taking
place August 5-9, 2024, in Amsterdam, Netherlands. RTX-1738
demonstrated analgesic activity across a broad range of preclinical
pain models.
Details of the poster presentation are as follows:
Poster Title: RTX-1738
Exhibits Analgesic Activity Across a Broad Range of Preclinical
Pain Models (#TU377)Date: Tuesday, Aug.
06, 2024, 3:15 - 4:45 p.m. CESTPresenter: Jose
Matta, Ph.D., Senior Director of Biology Discovery, Rapport
Therapeutics
For more information on IASP, please visit the event website.
Following the conference, Rapport’s presentation will be available
within the Publications section of the company’s website.
Similar to Rapport’s lead product candidate RAP-219, RTX-1738 is
an AMPAR (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
receptor) negative allosteric modulator (“NAM”) designed to achieve
neuroanatomical specificity through its selective targeting of a
receptor associated protein (RAP) known as TARPγ8, which is
associated with the neuronal AMPAR
(α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor).
RTX-1738 was used in established preclinical pain models to explore
the potential of the mechanism to treat chronic pain, including
peripheral neuropathic pain. RAP-219 is being studied in a Phase 2a
trial in patients with drug-resistant focal epilepsy. Rapport
intends to initiate Phase 2a trials evaluating RAP-219 in patients
with peripheral neuropathic pain and bipolar disorder in the second
half of 2024 and in 2025, respectively.
About Rapport TherapeuticsRapport Therapeutics
is a clinical-stage biotechnology company dedicated to discovering
and developing transformational precision neuromedicines for
patients suffering from central nervous system (CNS) disorders. The
Company’s founders have made pioneering discoveries related to the
function of RAPs in the brain. Their findings form the basis of
Rapport’s RAP technology platform, which enables a differentiated
approach to generate precision small molecule product candidates
with the potential to overcome many limitations of conventional
neurology drug discovery. Rapport’s precision neuroscience pipeline
includes the Company’s lead clinical program, RAP-219, designed to
achieve neuroanatomical specificity through its selective targeting
of a RAP expressed in only discrete regions of the brain. The
Company is currently advancing RAP-219 in clinical trials in focal
epilepsy, peripheral neuropathic pain, and bipolar disorder.
Additional preclinical and late-stage discovery stage programs are
also underway, targeting CNS disorders including chronic pain and
hearing disorders.
Forward-Looking StatementsThis press release
contains “forward-looking statements” within the meaning of
Section 27A of the Securities Act of 1933 and Section 21E of the
Securities Exchange Act of 1934, each as amended. The words
“anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,”
“intend,” “may,” “plan,” “potential,” “predict,” “project,”
“should,” “target,” “would” and similar expressions are intended to
identify forward-looking statements, although not all
forward-looking statements contain these identifying words. These
forward-looking statements include, but are not limited to, express
or implied statements regarding: the ongoing and planned clinical
development of RAP-219 for the treatment of drug-resistant focal
epilepsy, peripheral neuropathic pain and bipolar disorder; the
potential activity and tolerability of RAP-219; and the potential
of Rapport’s RAP technology platform.
Forward looking statements are based on management’s current
expectations and are subject to risks and uncertainties that could
negatively affect Rapport’s business, operating results, financial
condition and stock value. Factors that could cause actual results
to differ materially from those currently anticipated include:
risks relating to the company’s research and development
activities; Rapport’s ability to execute on its strategy including
obtaining the requisite regulatory approvals on the expected
timeline, if at all; uncertainties relating to preclinical and
clinical development activities; the company’s dependence on third
parties to conduct clinical trials, manufacture its product
candidates and develop and commercialize its product candidates, if
approved; Rapport’s ability to attract, integrate and retain key
personnel; risks related to the company’s financial condition and
need for substantial additional funds in order to complete
development activities and commercialize a product candidate, if
approved; risks related to regulatory developments and approval
processes of the U.S. Food and Drug Administration and comparable
foreign regulatory authorities; risks related to establishing and
maintaining Rapport’s intellectual property protections; and risks
related to the competitive landscape for Rapport’s product
candidates; as well as other risks described in “Risk Factors,” in
the company’s Registration Statement on Form S-1 filed with the
Securities and Exchange Commission (the SEC), as well as subsequent
filings with the SEC. Rapport expressly disclaims any obligation or
undertaking to release publicly any updates or revisions to any
forward-looking statements contained herein to reflect any change
in its expectations or any changes in events, conditions or
circumstances on which any such statement is based, except as
required by law, and claims the protection of the safe harbor for
forward-looking statements contained in the Private Securities
Litigation Reform Act of 1995.
ContactJulie DiCarloHead of
Communications & IRRapport
Therapeuticsjdicarlo@rapportrx.com
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