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Reneo Pharmaceuticals Announces Poster Presentation at Upcoming Scientific Meetings

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Reneo Pharmaceuticals will present a poster on their selective PPARδ agonist, mavodelpar, at upcoming scientific meetings. The drug shows potential as a therapeutic option for mitochondrial myopathies.
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  • Reneo Pharmaceuticals will present findings on mavodelpar, a selective PPARδ agonist that improves cellular bioenergetics in fibroblasts from patients with mitochondrial complex I deficiency. The drug has potential as a therapeutic option for primary mitochondrial myopathies.
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IRVINE, Calif., Oct. 25, 2023 (GLOBE NEWSWIRE) -- Reneo Pharmaceuticals, Inc. (NASDAQ: RPHM), a clinical stage pharmaceutical company focused on the development and commercialization of therapies for patients with rare genetic mitochondrial diseases, today announced the company will present a poster titled “Selective peroxisome proliferator-activated receptor (PPAR) delta (δ) agonist, mavodelpar, improves cellular bioenergetics in fibroblasts from patients with mitochondrial complex I deficiency” at the following upcoming scientific meetings.

PittGene Meeting
Date: Wednesday, October 25, 2023, at 2:00-2:45pm ET
Location: University Club at University of Pittsburgh, Pittsburgh, PA
Presenter: Bianca Seminotti, PhD

Translational Research in Mitochondria, Metabolism, Aging and Disease (TRiMAD) Meeting 2023
Date: Monday, November 6, 2023, at 5:30-7:00pm ET
Location: University Club at University of Pittsburgh, Pittsburgh, PA
Presenter: Bianca Seminotti, PhD

In this presentation, Reneo and collaborators will report findings which demonstrate that the bioenergetic deficiencies and mitochondrial dysfunction observed in CI-deficient patient fibroblasts can potentially be alleviated by treatment with mavodelpar, a potent and selective PPARδ agonist. Furthermore, because mavodelpar activation results in increased transcription of genes involved in mitochondrial biogenesis, fatty acid oxidation and energy production in the form of ATP, these results provide mechanistic evidence for the potential of mavodelpar as a therapeutic option in this and similar types of primary mitochondrial myopathies (PMM).

Mavodelpar is an investigational drug product candidate that is under clinical investigation, and which has not yet been approved for marketing by the U.S. Food and Drug Administration, European Medicines Agency, or any other regulatory agency.

About Reneo Pharmaceuticals
Reneo is a clinical-stage pharmaceutical company focused on the development and commercialization of therapies for patients with rare genetic mitochondrial diseases, which are often associated with the inability of mitochondria to produce adenosine triphosphate (ATP). Our lead product candidate, mavodelpar (REN001), is a potent and selective agonist of the peroxisome proliferator-activated receptor delta (PPARδ). Mavodelpar has been shown to increase transcription of genes involved in mitochondrial function, increase fatty acid oxidation, and may increase production of new mitochondria. For additional information, please see reneopharma.com.

Contacts:

Danielle Spangler 
Investor Relations 
Reneo Pharmaceuticals, Inc. 
dspangler@reneopharma.com

Matthew Purcell, Pharm.D.
Media Inquiries 
Russo Partners, LLC 
matthew.purcell@russopartnersllc.com


Reneo Pharmaceuticals is presenting a poster on mavodelpar, a selective PPARδ agonist.

Mavodelpar has shown potential in improving cellular bioenergetics in patients with mitochondrial complex I deficiency, making it a possible therapeutic option for primary mitochondrial myopathies.

No, mavodelpar is still under clinical investigation and has not yet been approved for marketing by regulatory agencies.
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About RPHM

reneo is a clinical stage pharmaceutical company focused on the development of therapies for patients with genetic mitochondrial diseases. many of these diseases are associated with deficits in cellular metabolism and energy production. our goal is to improve daily function and quality of life of patients suffering from these diseases, most specifically, by improving how their mitochondria work, preserving muscle function and preventing muscle injury, weakness and wasting. we are currently advancing a novel molecule into several diseases. our experienced team of drug development experts, who have collaborated in many successful programs, are dedicated and passionate about finding effective therapies for these complex rare diseases.