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Logo - Restore Vision

Restore Vision

Contact
Susanne Vorhagen (Dr. rer. nat.) Project Coordinator/ Data Steward
Kick-off Date
April 30, 2027

Description

Restore Vision is a collaborative European research project dedicated to developing and testing new treatments for seven rare eye diseases (REDs) that affect the cornea and ocular surface. These diseases are a significant cause of visual impairment and blindness across all ages, yet current treatments are often expensive, ineffective, and come with serious side effects. By bringing together leading scientists, clinicians, small and medium-sized enterprises (SMEs), and patient representatives from across Europe, Restore Vision aims to deliver real hope to over 500,000 patients who currently have limited therapeutic options.

Approach & Methods

  • Repurposing and Innovation: The consortium is evaluating six existing drugs already approved for other conditions and developing three new compounds, leveraging their potential for vision restoration in rare ocular surface diseases.
  • Disease Models: Advanced laboratory and preclinical models are used to validate therapeutic targets, test drug efficacy, and understand disease mechanisms in detail.
  • Formulation Science: The team is optimizing safe and effective drug formulations for use as eye drops or subconjunctival injections.
  • Clinical Translation: Promising candidates will move into phase 1b and compassionate clinical trials to assess safety and initial effectiveness in patients.
  • Data Management: The MeDIC team at University Hospital Cologne is responsible for preparing and updating the Data Management Plan, ensuring compliance with data protection and open science standards.

Project Steps & Milestones

  • Project Management & Coordination: Ensuring smooth execution and timely reporting across all work packages.
  • Validation of Drug Targets: Testing the effects of candidate drugs on human tissues and fluids to understand their mechanisms of action.
  • Formulation Development: Creating eye drop and injectable versions of promising compounds.
  • Preclinical Studies: Using disease models to evaluate safety and efficacy.
  • Clinical Trials: Conducting first-in-human studies for the most promising therapies.
  • Data Management: Delivering and updating the Data Management Plan and reporting on data collection strategies.

Consortium Partners

Restore Vision unites 10 partners from 9 EU countries, including leading research institutions, SMEs, and a European patient organisation. The combined expertise covers basic science, clinical research, pharmaceutical development, project management, and patient advocacy.

Collaboration Partner

National University of Ireland Galway Learn More
Linköping University Learn More
San Raffaele Hospital Learn More
Miguel Hernández University of Elche Learn More
Centre de Recherche des Cordeliers Learn More
Cell2Cure Learn More
Aniridia Europe Learn More
Laboratoires KÔL Learn More
Catalyze Learn More

This project is supported by

Flag - European Union

Achievements & Results

Development of Innovative Treatments: Restore Vision will create and test both novel and repurposed drugs for seven rare eye diseases, including aniridia-associated keratopathy, neurotrophic keratopathy, limbal stem cell deficiency, ocular cicatricial pemphigoid, EEC syndrome, ocular graft versus host disease, and corneal neovascularisation.

New Drug Formulations: The project will develop optimal eye drop and injectable formulations for several pharmaceutical compounds, ensuring safety and effectiveness for patients.

Mechanistic Insights: By investigating the underlying mechanisms of these diseases, the project will identify how new and repurposed drugs interact with specific genes, proteins, and pathways, enabling tailored therapies.

Clinical Readiness: Restore Vision will advance promising compounds from preclinical validation to first-in-human clinical trials, accelerating the path to real-world patient benefit.

Data Management Excellence: The project will deliver a robust Data Management Plan to ensure all research outputs are managed according to GDPR and FAIR principles.