Press Releases April 6, 2026 08:00 PM

Sionna Therapeutics to Participate in the Raymond James 2026 Biotech Innovation Symposium

Sionna Therapeutics to engage investors at 2026 Biotech Innovation Symposium showcasing its novel treatments for cystic fibrosis.

By Caleb Monroe SION
Sionna Therapeutics to Participate in the Raymond James 2026 Biotech Innovation Symposium
SION

Sionna Therapeutics, a clinical-stage biotech focused on cystic fibrosis therapies, announced participation in the Raymond James 2026 Biotech Innovation Symposium with one-on-one investor meetings. The company aims to revolutionize treatment by developing small molecules targeting the CFTR protein's nucleotide binding domain to correct defects caused by the F508del mutation.

Key Points

  • Sionna is advancing small molecule drugs to stabilize CFTR's nucleotide binding domain 1, addressing a key cystic fibrosis mutation.
  • The company is developing complementary CFTR modulators to potentially synergize with their NBD1 stabilizers.
  • Participation in a major biotech symposium could enhance investor visibility and confidence in their pipeline.

WALTHAM, Mass., April 07, 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 participate in one-on-one investor meetings at the Raymond James 2026 Biotech Innovation Symposium on Tuesday, April 14th, 2026.

About Sionna Therapeutics 
Sionna 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 occurs 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, visit www.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 Contact
Sarah Spencer
[email protected]

Investor Contact
Juliet Labadorf
[email protected]


Risks

  • As a clinical-stage company, Sionna faces uncertainties related to clinical trial outcomes and regulatory approvals.
  • The success of their novel NBD1 stabilizers in improving clinical outcomes for CF patients remains to be fully demonstrated.
  • Market acceptance and competition in the cystic fibrosis therapy sector may impact commercial prospects.

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