Sionna Therapeutics

Sionna Therapeutics

Dedicated to delivering therapies that could be transformational for people living with cystic fibrosis.

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DateInvestorsAmountRound
investor investor investor investor investor investor investor

€0.0

round
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€0.0

round
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N/A

$191m

IPO
Total Funding000k

Financials

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Revenues, earnings & profits over time
USD202220232024202520262027
Revenues000000000000000000000000
EBITDA000000000000000000000000
Profit000000000000000000000000
EV000000000000000000000000
EV / revenue00.0x00.0x00.0x00.0x00.0x00.0x
EV / EBITDA00.0x00.0x00.0x00.0x00.0x00.0x
R&D budget000000000000000000000000

Source: Company filings or news article, Equity research estimates

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More about Sionna Therapeutics
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Sionna Therapeutics is a biotechnology startup that is focused on revolutionizing the treatment of cystic fibrosis (CF). The company is developing innovative small molecule therapies that target the most common genetic mutation in CF patients, known as ΔF508. Their ultimate goal is to normalize CFTR function, which is a protein that helps control the balance of salt and water in the body. When this protein is not functioning properly, it leads to the symptoms of CF.

Sionna operates in the healthcare market, specifically within the realm of genetic diseases. Their clients are primarily patients suffering from cystic fibrosis, a life-threatening genetic disorder that severely damages the lungs and digestive system.

The business model of Sionna Therapeutics is centered around the research, development, and eventual commercialization of their novel therapies. They generate revenue through the successful development and sale of these therapies to healthcare providers who then administer them to CF patients.

The company prides itself on its collaborative approach to drug discovery, with a team that is dedicated to making a positive impact on patients' lives. They are currently in the DC / IND-Enabling stage, which means they are conducting necessary studies and preparing to submit an Investigational New Drug (IND) application to the FDA. This is a crucial step in the process of getting a new drug approved for use in patients.

Keywords: Biotechnology, Cystic Fibrosis, Small Molecule Therapies, Genetic Mutation, CFTR Function, Healthcare Market, Drug Discovery, Research and Development, Commercialization, IND-Enabling.

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