SciTransfer
MYCureX · Project

First-in-class cancer therapy targeting the previously undruggable MYC protein

healthTestedTRL 6

Imagine a cancer cell has a master engine called MYC that keeps it growing and resisting medicine, but this engine is shaped like a slippery knot that normal drugs can't grab. This project created a special 'mini-protein' that can actually grip and shut down that engine. It also uses AI to find a biological fingerprint that tells doctors exactly which patients will respond best to the treatment.

By the numbers
49%
tumor volume reduction in a metastatic PDAC patient
70%
cancers where MYC is dysregulated
10%
PDAC patients surviving beyond 5 years
8 of 12
evaluable patients with stabilized disease
The business problem

What needed solving

Pancreatic cancer has a survival rate of less than 10% over 5 years because the MYC protein, which drives tumor growth, has been considered 'undruggable' due to its structure and location.

The solution

What was built

A patented cell-penetrating mini-protein (OMO-103) and AI-driven companion diagnostic tests for patient stratification and response monitoring.

Audience

Who needs this

Large Pharmaceutical CompaniesOncology Research InstitutesBiotech Venture Capital FirmsPrecision Medicine Diagnostic Labs
Business applications

Who can put this to work

Pharmaceuticals
enterprise
Target: Large oncology drug developer

If you are a pharmaceutical company dealing with the lack of effective treatments for pancreatic cancer — this project developed OMO-103 that showed a 49% tumor volume reduction in a metastatic PDAC patient. This provides a first-in-class asset to fill a critical gap in the oncology pipeline.

Biotechnology
mid-size
Target: Companion diagnostics developer

If you are a biotech company dealing with poor patient stratification in clinical trials — this project developed machine learning-enabled biomarker signatures that allow for real-time response monitoring. This ensures the right patients receive the therapy, increasing trial success rates.

Contract Manufacturing (CDMO)
any
Target: Specialized protein manufacturer

If you are a CDMO dealing with the need for high-scale mini-protein production — this project is developing a commercial-ready manufacturing process to sustain the scale-up phase. This creates a blueprint for producing complex cell-penetrating proteins at scale.

Frequently asked

Quick answers

What is the current IP and licensing status?

The drug OMO-103 is patented. Peptomyc's explicit business goal is to reach a licensing agreement with a pharmaceutical company for its further development and commercialization.

How is the project addressing industrial scale-up?

The project aims to develop a commercial-scale compatible manufacturing process to sustain the scale-up phase of the product.

What is the cost or pricing of the therapy?

Based on available project data, specific pricing or cost-per-dose information is not provided.

What is the clinical timeline for the next phase?

The next step is to perform a Phase 1b clinical trial in 1st-line pancreatic ductal adenocarcinoma (PDAC) patients to assess safety and efficacy in combination with the standard of care.

How is the drug integrated with existing treatments?

OMO-103 is designed to foster synergy with personalized therapies and will be tested in combination with the standard of care for PDAC.

Consortium

Who built it

The project is led by a single Spanish SME, Peptomyc SL, with a 100% industry ratio. This lean structure indicates a highly focused, agile development approach typical of specialized biotech startups aiming for a licensing exit rather than a large academic consortium.

How to reach the team

Contact Peptomyc SL in Spain regarding OMO-103 licensing

Next steps

Talk to the team behind this work.

Contact us to explore licensing opportunities for MYC-inhibitor technology.

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