# ReviR Therapeutics Receives FDA Rare Pediatric Disease Designation for RTX-117 in Charcot-Marie-Tooth Disease

- Link: https://www.thailand-business-news.com/pr-news/revir-therapeutics-receives-fda-rare-pediatric-disease-designation-for-rtx-117-in-charcot-marie-tooth-disease
- Published: 2026-08-26T20:00:00+07:00
- Author: PR Newswire

_Designation supports the global development of RTX-117 and may provide potential
future access to a transferable Priority Review Voucher, subject to approval and
applicable requirements_

BRISBANE, Calif., Aug. 26, 2026 /PRNewswire/ — ReviR Therapeutics, a clinical-stage
biotechnology company advancing small-molecule therapies through the integration
of artificial intelligence and RNA biology, today announced that the U.S. Food and
Drug Administration (FDA) has granted Rare Pediatric Disease Designation (RPDD) 
to RTX-117, the company’s investigational oral small-molecule candidate, for its
development in Charcot-Marie-Tooth disease (CMT). The designation applies to CMT
broadly and is not limited to a specific subtype.

The FDA’s RPDD program is intended to encourage the development of therapies for
serious or life-threatening rare diseases that predominantly affect children. If
RTX-117 is ultimately approved and meets applicable statutory requirements and program
criteria, ReviR may be eligible to receive a Rare Pediatric Disease Priority Review
Voucher (PRV). The voucher may be transferred to another sponsor or redeemed to 
obtain priority review for a future marketing application and may hold potential
commercial value for ReviR.

CMT comprises a group of progressive inherited neuromuscular disorders that often
emerge during childhood or adolescence. Patients may experience leg weakness and
muscle wasting, skeletal deformities, pain, sensory impairment and delayed motor
development. Despite the longstanding need for new treatment options, there are 
currently no approved disease-modifying therapies for CMT.

RTX-117 is ReviR’s investigational therapy developed through ReviR’s proprietary
VoyageR AI platform and is designed to modulate the integrated stress response (
ISR) pathway. By activating eIF2B, RTX-117 is intended to restore normal mRNA translation
and protein-expression homeostasis. ReviR is advancing the program in CMT while 
expanding its translational research in ISR-related diseases, including fibrotic
conditions.

Previously, RTX-117 has received FDA Orphan Drug Designation(ODD) for CMT and clinical
trial authorizations in both the United States and China. The program is currently
in Phase 1 clinical development, with completion of the Phase 1 study anticipated
by the end of this year.

"People living with CMT, particularly children, urgently need more effective disease-
modifying treatment options," said Paul R. August, Ph.D., Chief Scientific Officer
of ReviR Therapeutics. "This designation provides additional support for the continued
development of RTX-117. As the CMT program progresses, we will continue to build
clinical and translational evidence that may inform our work in additional ISR-related
diseases."

"RPDD adds another important strategic dimension to the global development of RTX-
117," said Peng Yue, Ph.D., Co-founder and CEO of ReviR Therapeutics. "The experience
and capabilities we build through RTX-117 will help inform the expansion of our 
small-molecule RNA platform into a broader range of serious diseases, including 
genetic diseases, immunology and inflammation, and oncology. We look forward to 
working with partners worldwide to advance new therapeutic options for patients."

**About ReviR Therapeutics**

ReviR Therapeutics is a clinical-stage global biotechnology company developing innovative
therapies for patients with serious and difficult-to-treat diseases across neurology,
immunology and inflammation, and oncology. Founded in 2021 by leaders in computational
biology, RNA biology, genomics and drug discovery, ReviR integrates artificial intelligence
with RNA biology to create disease-modifying therapies designed to be highly specific,
effective and safe. ReviR’s lead clinical-stage program, RTX-117, is advancing across
multiple ISR-related disease areas, including CMT and VWM, with fibrotic diseases
among the additional indications under exploration. ReviR’s broader pipeline includes
orally administered small molecules designed to modulate RNA function by splicing.
For more information, visit [www.revirtx.com](https://www.revirtx.com/home).

**About RTX-117**

RTX-117 is a potential first-in-class, orally administered small-molecule therapy
developed by ReviR Therapeutics, with discovery and molecular design supported by
XtalPi’s AI and robotics-enabled drug discovery platform. RTX-117 is designed to
modulate the integrated stress response (ISR) pathway through activation of eIF2B,
a key regulator of protein translation. By restoring mRNA translation and protein-
expression homeostasis, the program aims to address molecular mechanisms implicated
in ISR-related diseases.

RTX-117 is currently in a Phase 1 clinical trial, with Investigational New Drug (
IND) clearance secured for CMT and VWM in the United States and China. In parallel,
ReviR is expanding development of RTX-117 into additional ISR-related indications,
including fibrotic diseases.

**Forward-Looking Statements**

This press release contains forward-looking statements, including statements regarding
the clinical development, potential therapeutic applications, regulatory pathway
and future development of RTX-117, as well as ReviR’s potential eligibility for 
a Rare Pediatric Disease Priority Review Voucher. These statements are based on 
current expectations and are subject to risks and uncertainties that could cause
actual results to differ materially, including risks related to clinical development,
preclinical findings, regulatory review, program timing and other factors. Preclinical
findings may not be replicated in clinical trials, and RTX-117 has not been approved
by the FDA or any other regulatory authority. ReviR undertakes no obligation to 
update these forward-looking statements except as required by applicable law.

 

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