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The first effective and safe reversal agent to stop or prevent life-threatening bleeding in patients taking the emerging generation of anticoagulants.

VarmX aims to develop VMX-C001, the first safe reversal agent for FXa-DOACs, to reduce life-threatening bleeding risks in anticoagulant patients, seeking €2.5M grant and €15M equity for scaling production.

Subsidie
€ 2.500.000
2022

Projectdetails

Introduction

50 Million patients worldwide use oral anticoagulants to prevent venous thrombosis and stroke. Since the last decade, unpredictable and risky indirect anticoagulant treatments are being replaced by the latest generation of blood-thinning medication: Factor Xa Direct Oral Anticoagulants (FXa-DOACs, used by >10 million patients in EU+US).

Efficacy and Risks

With superior predictability, efficacy, and safety profiles, these life-saving medications remain associated with a risk of uncontrolled and severe bleeding. Alarmingly, there is no safe reversal agent that restores blood clotting in patients who take FXa-DOACs, resulting in life-threatening bleeding episodes and >400k hospital admissions.

Solution Development

To address the urgent unmet need, VarmX has developed VMX-C001, the first effective and safe reversal agent to FXa-DOACs.

Funding Request

VarmX requests a €2.5M grant and €15M in equity from EIC to accelerate upscaling and improve the cost-effectiveness of the complex manufacturing process required to produce VMX-C001.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 2.500.000
Totale projectbegroting€ 4.842.087

Tijdlijn

Startdatum1-9-2022
Einddatum31-3-2025
Subsidiejaar2022

Partners & Locaties

Projectpartners

  • VARMX BVpenvoerder

Land(en)

Netherlands

Inhoudsopgave

EIC Accelerator

EU-subsidieprogramma voor mkb en start-ups met grants tot €2,5 mln en equity-investeringen tot €15 mln voor baanbrekende innovaties.

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