ODDIFACT


Oddifact SAS develops and licenses orphan drug designations (ODDs) and applies an internal AI platform to identify repurposing opportunities for rare diseases. The company integrates regulatory, market-access and commercialization activities to collaborate with manufacturers and laboratories on bringing biotherapy-based solutions and research outputs to patients. It also offers purchasable research products and consumer supplements through an online store.

Industries

N/A

Nr. of Employees

small (1-50)

ODDIFACT

3 Villa Poirier, 75015 Paris, France


Products

Clinical Trial Data Analysis Report

Comprehensive report on clinical trial data analysis offered as a purchasable product.

Drug Interaction Research Paper

In-depth research paper on drug interactions offered for purchase.

Digestive Health Probiotics

Probiotic supplement marketed for digestive health.

Allergy Relief Tablets

Non-drowsy allergy relief tablets sold via the online store.

Omega-3 Fish Oil Softgels

Omega-3 supplement marketed for general health.

Protein Powder Blend

Protein supplement offered via the online storefront.

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Services

Development and licensing of orphan drug designations and support to obtain ODD status.

Application of an AI platform to search academic research and prioritize biologics for repurposing to rare-disease indications.

Support integrating regulatory specifics and accelerating dossier development steps ahead of submission.

Preparation and sale of comprehensive clinical trial data analysis reports.

In-depth drug–drug interaction research papers available for purchase.

Services to connect identified candidates with manufacturers and laboratories, and to structure supply agreements.

Expertise Areas

  • AI-driven drug repurposing
  • Orphan drug designation development
  • Regulatory dossier preparation and submission support
  • Clinical data analysis and reporting
  • Show More (2)

Key Technologies

  • Artificial intelligence for biomedical literature search
  • Machine learning model iteration and continuous improvement
  • Clinical trial data analysis tools
  • Regulatory dossier generation workflows
  • Show More (1)

News & Updates

Video discussion linked from the company news section referencing a Davos 2025 appearance.

FDA granted an orphan drug designation for infliximab for the indication of Kawasaki disease in children.

FDA granted an orphan drug designation for rituximab for ITP.

FDA granted an orphan drug designation for adalimumab for Takayasu arteritis.

FDA granted an orphan drug designation for rituximab for IIM.

FDA granted an orphan drug designation for rituximab for AHA.

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