Koru Life Science
UK drug repurposing company

New purpose for proven medicines.

Koru Life Science is a UK company that finds new uses for existing medicines and matches them to the patients most likely to benefit. We focus on rare and hard-to-treat diseases, where patients cannot wait for a decade of new-molecule discovery.

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What defines Koru

One UK company. Two disciplines that make each other stronger.

01

A UK company

Koru Life Science is a UK research-led company. We draw on the UK's strengths in genomics, translational research and rare-disease communities, and partner internationally.

About us →
02

Drug repurposing

We start from compounds that already have human safety data — approved, clinical-stage or shelved — and test them against new disease biology, shortening the road to patients.

Our repurposing approach →
03

Stratified & personalised medicine

From the first experiment, we define who a treatment is for — using genetic and molecular markers to select the patients most likely to respond.

How we stratify →
Pipeline

Three programmes in rare and hard-to-treat disease

View full pipeline →
KLS-101 Diffuse intrinsic pontine glioma (DIPG) Paediatric brain tumour Lead validation KLS-201 Frontotemporal dementia with GRN mutations (FTD-GRN) Genetic neurodegeneration Discovery KLS-301 Chondrosarcoma (advanced / metastatic) Rare bone cancer Discovery
Why repurposing

Why start from an existing medicine?

Known safety

Human safety and pharmacology data already exist, removing much of the early risk that ends new-molecule programmes.

A shorter path

Programmes can move to patient studies sooner, which matters most for diseases that progress quickly.

Capital efficiency

Lower development cost makes small patient populations viable to serve.

Value in shelved assets

Compounds discontinued for commercial or strategic reasons can find a second life in a new indication.

Rare disease initiative

Rare diseases are not rare in aggregate.

More than 7,000 rare diseases have been described, and most still have no approved treatment. Repurposing and patient stratification are among the most practical ways to change that.

Read about the Koru Rare Disease Initiative →
1 in 17

people in the UK will be affected by a rare disease at some point in their lives.

Source: UK Rare Diseases Framework, DHSC (2021)

Holding a shelved asset, a patient cohort or a biomarker?

We'd like to hear from pharmaceutical companies, researchers, clinicians and patient organisations.

Talk to us