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PAH-Advance · Project

Developing a Disease-Modifying Drug for Pulmonary Arterial Hypertension and Cardiopulmonary Diseases

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Imagine your lungs have a plumbing problem where the pipes are blocked, making the heart work too hard to push blood through. Current medicines only mask the symptoms, like putting a bandage on a leak. This project created a drug that targets the actual root cause of the blockage to fix the system in both the heart and lungs.

By the numbers
1,000,000,000
expected sales 5 years post-launch (USD)
100
target FTE growth
The business problem

What needed solving

Current standard-of-care drugs for pulmonary arterial hypertension only treat symptoms rather than the root cause and cause serious side-effects. This leaves a massive gap in the market for a disease-modifying treatment.

The solution

What was built

A capsule formulation of the drug NTP42 for home use and the necessary safety and manufacturing data required for Phase II clinical trials.

Audience

Who needs this

Pharmaceutical companiesCardiopulmonary drug developersClinical research organizationsVenture capital firms specializing in biotech
Business applications

Who can put this to work

Pharmaceuticals
enterprise
Target: Big Pharma Company

If you are a pharmaceutical enterprise dealing with a lack of curative treatments for PAH — this project developed NTP42 that blocks the thromboxane receptor. This allows for a licensing deal to bring a disease-modifying drug to market.

Biotechnology
SME
Target: Drug Development SME

If you are a biotech firm dealing with the challenge of moving from liquid formulas to patient-friendly dosing — this project developed a capsule form of NTP42. This enables patients to take the medication at home in non-clinical settings.

Healthcare Providers
mid-size
Target: Specialized Pulmonary Clinic

If you are a clinic dealing with patients who suffer from severe side-effects of standard-of-care drugs — this project developed a drug that treats clinical hallmarks in both lungs and heart. This offers a more effective option for devastating cardiopulmonary diseases.

Frequently asked

Quick answers

What is the expected revenue potential after launch?

The objective states that sales are expected to exceed $1B at 5 years post-launch.

How will the technology be commercialized?

ATXA intends to secure a licensing deal with a pharmaceutical company to accelerate the drug to market and receive royalty returns.

What is the scale of the current clinical development?

The project has moved past Phase I trials in healthy men and is preparing for a Phase II clinical trial in PAH patients.

What regulatory steps were addressed in this phase?

The project focused on pre-trial work for regulatory approval, including drug manufacture, safety studies, and a bridging clinical trial for the capsule form.

What is the timeline for the grant-funded portion?

The project period was from 2023-01-01 to 2023-12-31.

Consortium

Who built it

The project is led by a single SME, ATXA Therapeutics Ltd, based in Ireland. With a 100% industry ratio and no university or research partners, the consortium is lean and focused entirely on commercial translation and clinical acceleration.

How to reach the team

Contact ATXA Therapeutics Ltd in Ireland regarding NTP42 licensing

Next steps

Talk to the team behind this work.

Contact us to identify potential pharma partners for NTP42 licensing.

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