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RESPIRE · Project

Oral Disease-Modifying Treatment to Stop COPD Progression

healthTestedTRL 6

Imagine COPD as a fire in the lungs that current inhalers only blow air on to keep the smoke away. This project developed a pill that acts like a fire extinguisher, targeting the root cause of the inflammation. It blocks a specific receptor to stop the disease from getting worse, rather than just treating the symptoms.

By the numbers
65 million
people suffering from COPD
30M
funding target for phase 3 trial
2032
target year for market entry
The business problem

What needed solving

COPD is the third leading cause of death worldwide, yet current treatments only relieve symptoms and do not stop the disease from progressing.

The solution

What was built

A first-in-class oral A1R antagonist (PBF-680) and the clinical evidence from a phase 2 trial showing reduced inflammation in COPD patients.

Audience

Who needs this

Pharmaceutical companiesBiotech investorsRespiratory health clinicsPublic health insurance providers
Business applications

Who can put this to work

Pharmaceuticals
enterprise
Target: Drug developers specializing in respiratory medicine

If you are a drug developer dealing with the lack of disease-modifying COPD therapies — this project developed PBF-680 that targets A1R signaling to reduce inflammation. It aims to move beyond symptom relief to actually slow disease progression.

Healthcare Providers
enterprise
Target: Hospital networks and pulmonary clinics

If you are a clinic dealing with high hospitalization rates for 65 million COPD sufferers — this project developed an oral therapy that reduces circulating eosinophil levels. This could significantly lower healthcare costs and patient readmissions.

Biotechnology
mid-size
Target: Venture capital and biotech investment firms

If you are an investor dealing with high-risk early-stage assets — this project developed a compound that has already passed phase 1 and phase 2 trials. It provides a clear path toward a phase 3 trial and market entry by 2032.

Frequently asked

Quick answers

What is the estimated cost or pricing for the treatment?

Based on available project data, specific pricing for the drug is not provided, though the project aims to lower overall healthcare costs related to hospitalizations.

Is the production ready for industrial scale?

The project has reached phase 2 clinical trial success; however, industrial scale manufacturing details are not specified in the provided data.

What is the IP or licensing status of PBF-680?

Based on available project data, PBF-680 is being developed by Palo Biofarma SL, but specific patent or licensing terms are not listed.

What is the regulatory timeline for market entry?

The company targets regulatory approval and market entry by 2032, following a planned phase 3 trial.

How does this integrate into current COPD treatment plans?

It is an oral medication designed to complement or replace current inhalers by modifying the disease course rather than just providing bronchodilation.

Consortium

Who built it

The project is led by a single partner, Palo Biofarma SL, a Spanish SME. This 100% industry-led structure indicates a highly focused commercial drive, with the company managing the entire clinical development pipeline from preclinical to phase 2 trials internally.

How to reach the team

Contact Palo Biofarma SL in Spain regarding PBF-680 clinical partnerships.

Next steps

Talk to the team behind this work.

Contact us to explore licensing opportunities for A1R antagonists.

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