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NTX1088 · Project

Next-Generation Cancer Therapy Targeting PVR to Unlock Immune System Response

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Imagine cancer cells have a 'do not disturb' sign that stops the body's immune system from attacking them. This drug removes that sign and simultaneously wakes up the immune cells to start fighting the tumor. It acts like a triple-action key that unlocks the body's natural ability to destroy advanced tumors.

By the numbers
80 billion
Immuno-oncology market size in Euros
85
Patients treated in Phase 1 study
86
Weeks of longest ongoing response
The business problem

What needed solving

Many cancer patients are refractory to current PD1 therapies, leaving a massive unmet need in the 80 billion euro immuno-oncology market for treatments that can overcome tumor-driven immune suppression.

The solution

What was built

A first-in-class monoclonal antibody (NTX1088) and a clinical trial infrastructure across the US, Israel, and Poland.

Audience

Who needs this

Oncology drug developersImmuno-oncology research institutesCancer treatment centersBiopharmaceutical investors
Business applications

Who can put this to work

Pharmaceuticals
enterprise
Target: Biotech drug developer

If you are a drug developer dealing with patients who no longer respond to standard PD1 therapies — this project developed NTX1088 that showed activity in heavily pretreated patients, including 1 complete response and 5 partial responses in a combination group.

Healthcare Providers
mid-size
Target: Specialized Oncology Clinic

If you are a clinic dealing with advanced solid malignancies that are hard to treat — this project developed a first-in-class antibody that can be used as a monotherapy or combined with pembrolizumab to improve patient outcomes.

Clinical Research
SME
Target: Contract Research Organization (CRO)

If you are a CRO dealing with the need for new EU-based clinical trial sites — this project developed a regulatory pathway via CTIS and established an active enrollment site at the Maria Sklodowska Curie National Research Institute of Oncology.

Frequently asked

Quick answers

What is the estimated cost or price of the therapy?

Based on available project data, the specific cost or pricing for NTX1088 is not disclosed.

Is the production ready for industrial scale?

The project is currently in Phase 1 clinical trials with dose escalation up to 1750 mg, but industrial manufacturing scale details are not provided.

What is the IP or licensing status?

Based on available project data, the drug is developed by Nectin Therapeutics Ltd, a venture-backed company, though specific patent numbers are not listed.

What is the regulatory timeline for EU entry?

The company has already engaged with the European Medicines Agency via CTIS and has an active site in Poland for patient enrollment.

How does the drug integrate with existing treatments?

NTX1088 is designed to work as a monotherapy or in combination with pembrolizumab, showing potential for combined antitumor responses.

Consortium

Who built it

The project is led by a single partner, Nectin Therapeutics Ltd, an Israeli SME. This 100% industry-led structure indicates a high level of commercial drive and streamlined decision-making, typical of venture-backed biotech firms moving rapidly through clinical trial phases.

How to reach the team

Contact Nectin Therapeutics Ltd in Israel

Next steps

Talk to the team behind this work.

Contact us to explore licensing or partnership opportunities for PVR-targeting therapies.

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