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TOPFIBRO · Project

Developing a First-in-Class Curative Drug Treatment for Idiopathic Pulmonary Fibrosis

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Imagine your lungs are like sponges that become stiff and scarred, making it hard to breathe. Current medicines only slow this down, but often make patients feel sick. This project is creating a new drug that stops the scarring process at the very start, potentially allowing the lungs to heal themselves.

By the numbers
3-5
Average survival years after IPF diagnosis
40%
Patients stopping current treatment within first year due to side-effects
The business problem

What needed solving

Current IPF treatments do not cure the disease and are often discontinued by over 40% of patients due to severe side effects. There is a massive unmet need for a well-tolerated, potentially curative therapy.

The solution

What was built

A drug candidate, OXC-201, and the associated preclinical safety and efficacy data required for human clinical trials.

Audience

Who needs this

Large Pharmaceutical CompaniesBiotech Venture CapitalistsPulmonary Research InstitutesDrug Licensing Agencies
Business applications

Who can put this to work

Pharmaceuticals
enterprise
Target: Large pharmaceutical company

If you are a large pharmaceutical company dealing with a lack of curative IPF treatments — this project developed OXC-201 that targets inflammation and fibrosis to potentially halt disease progression.

Biotechnology
mid-size
Target: Drug development firm

If you are a drug development firm dealing with high patient dropout rates in lung therapy — this project developed a candidate with improved safety and tolerability in preclinical models.

Healthcare Providers
any
Target: Specialized pulmonary clinics

If you are a pulmonary clinic dealing with patients who stop treatment within the first year due to side-effects — this project developed a therapy aimed at being better tolerated than current standards.

Frequently asked

Quick answers

What is the cost or price of the treatment?

Based on available project data, the specific cost of OXC-201 is not mentioned, though it is noted that current market therapies are very costly.

Is the drug ready for industrial scale production?

Based on available project data, the project is currently moving toward first-in-human clinical studies and is not yet at industrial scale.

What is the IP and licensing strategy?

The end goal is to bring OXC-201 to market via a licensing deal with a large pharmaceutical company.

What regulatory hurdles are being addressed?

The project is preparing the Investigational Medicinal Product Dossier (IMPD), Clinical Trial Application (CTA), and ethical applications to initiate human studies.

What is the timeline for clinical results?

The project period runs from 2023-05-01 to 2026-08-31, during which first-in-human clinical studies will be performed.

Consortium

Who built it

The project is led by a single Swedish SME, OXCIA AB, representing a 100% industry ratio. This lean structure suggests a focused, agile approach to drug development, aiming for a high-value exit via licensing to a larger pharmaceutical entity.

How to reach the team

Contact OXCIA AB in Sweden regarding OXC-201 licensing

Next steps

Talk to the team behind this work.

Connect with OXCIA AB to explore early-stage licensing opportunities for OXC-201.

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