Advancing therapies
for rare disease patients

SHRARE transforms unexploited research into ready-to-license rare disease therapies, connecting the world of science with the world of patients.

For Researchers

We back your science. We help bring it to life.

  • IP protection & regulatory strategy
  • Financial models & R&D roadmaps
  • Global pharma connections
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AI-Powered PlatformHow we transform research into therapies

For Life Science Players

License faster. Execute better. Increase ROI.

  • De-risked, clinical-stage assets
  • Streamlined due diligence
  • Exclusive early access pipeline
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The Rare Disease Reality

The scale of rarity, the promise of speed: breakthroughs to patients.

0+

rare diseases worldwide

Nature • Haendel et al. 2020

0%

of global population affected

Nature • Nguengang et al. 2020

USA
0M

patients in USA

NIH • 2023

EU
0M

The Hidden Scale of Rare Cancer

Rare Cancer Research Can't Wait!
SHRARE researchers will strive to contribute
to accelerate the development of rare cancer therapies

0M

New rare-cancer cases per year in Europe

• EORTC 2024

0%

of pediatric cancers are classified as rare

• National Cancer Institute 2024

0%

of all cancers are rare

National Cancer Institute (MyPART)

The SHRARE Solution

Process flow illustration

RESEARCH

TRANSFORM

LICENSE

SHRARE transforms unexploited research into ready-to-license rare disease therapies through augmented intelligence, connecting researchers and Life Science players to get treatments to patients faster

Ready to accelerate rare disease research?

Involved in Research?

Turn your research into real-world impact

Looking for licencing in?

License faster, execute better, increase ROI

How SHRARE Transform and Share