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Sionna Therapeutics to Present at the 44th Annual J.P. Morgan Healthcare Conference

Key Takeaway: Sionna Therapeutics will present at the 44th Annual J.P. Morgan Healthcare Conference on January 13, 2026. The company focuses on developing novel medicines to enhance the function of the CFTR protein for cystic fibrosis treatment. A live webcast of the presentation will be available on their Investor Relations website.
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POSITIVE FACTORS

  • Sionna Therapeutics is advancing innovative treatments for cystic fibrosis.
  • The company is presenting at a prestigious healthcare conference.
  • Management aims to improve clinical outcomes and quality of life for CF patients.

Full Press Release Details

WALTHAM, Mass., Jan. 05, 2026 (GLOBE NEWSWIRE) -- Sionna Therapeutics, Inc. (Nasdaq: SION), a clinical-stage biopharmaceutical company on a mission to revolutionize the current treatment paradigm for cystic fibrosis (CF) by developing novel medicines that normalize the function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, today announced that management will present at the 44thAnnual J.P. Morgan Healthcare Conference on Tuesday, January 13th, 2026 at 9:45 a.m. PT/12:45 p.m. ET.
A live webcast of the presentation will be available under the “Events” page within the Investors section of Sionna’s website athttps://investors.sionnatx.com/. A replay will also be available following the event.
About Sionna TherapeuticsSionna Therapeutics is a clinical-stage biopharmaceutical company on a mission to revolutionize the current treatment paradigm for cystic fibrosis (CF) by developing novel medicines that normalize the function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Sionna’s goal is to deliver differentiated medicines for people living with CF that can restore their CFTR function to as close to normal as possible by directly stabilizing CFTR’s nucleotide binding domain 1 (NBD1), which Sionna believes is central to potentially unlocking dramatic improvements in clinical outcomes and quality of life for people with CF. Leveraging more than a decade of the co-founders’ research on NBD1, Sionna is advancing a pipeline of small molecules engineered to correct the defects caused by the F508del genetic mutation, which resides in NBD1. Sionna is also developing a portfolio of complementary CFTR modulators that are designed to work synergistically with its NBD1 stabilizers to improve CFTR function. For more information about Sionna, visitwww.sionnatx.com.
Sionna intends to use its Investor Relations website as a means of disclosing material nonpublic information and for complying with its disclosure obligations under Regulation FD. Accordingly, investors should monitor Sionna’s Investor Relations website, in addition to following Sionna’s press releases, SEC filings, public conference calls, presentations, and webcasts.

Media ContactAdam DaleyCG Life212.253.8881adaley@cglife.com

Investor ContactJuliet Labadorfir@sionnatx.com

Frequently Asked Questions

When will Sionna Therapeutics present at the conference?

Sionna Therapeutics will present on January 13, 2026, at 9:45 a.m. PT.

What is the focus of Sionna Therapeutics?

Sionna Therapeutics aims to develop treatments that normalize CFTR protein function for cystic fibrosis.

Where can I watch the presentation?

The presentation will be available via live webcast on Sionna's Investor Relations website.

What is the goal of Sionna's research?

Sionna seeks to improve clinical outcomes for cystic fibrosis patients by stabilizing CFTR's NBD1.

Last updated: Jan 5, 2026