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.
Developing a Disease-Modifying Drug for Pulmonary Arterial Hypertension and Cardiopulmonary Diseases
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.
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.
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.
Who needs this
Who can put this to work
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.
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.
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.
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.
Contact ATXA Therapeutics Ltd in Ireland regarding NTP42 licensing
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