From disease modification to disease resolution

Disease resolution is possible.

While conventional disease-modifying medicines can slow pathologic, symptomatic and functional decline, they cannot reverse disease and may suppress repair. Our approach has the potential to go beyond conventional disease modification by rebuilding damaged tissue to restore normal architecture. This could enable patients to not only reduce symptoms but also reverse their decline, resolving disease and regaining lost function.

Our groundbreaking products program disease resolution and offer novel treatments for a wide range of disorders. Our lead asset is in development for autoimmunity and fibrosis.

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Pipeline

Our pipeline consists of programmed disease-resolving drugs, offering novel treatments for a wide range of disorders.

Leramistat

Rheumatoid arthritis
Discovery Pre-clinical Phase 1 Phase 2 Phase 3

Leramistat

Idiopathic pulmonary fibrosis (IPF)
Discovery Pre-clinical Phase 1 Phase 2 Phase 3

MBS2687

Autoimmune, neuroprotection/fibrosis
Discovery Pre-clinical Phase 1 Phase 2 Phase 3

IST004

Neuroprotection/autoimmunity
Discovery Pre-clinical Phase 1 Phase 2 Phase 3
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"It’s hard to imagine anything more rewarding than translating exciting science into treatments with the potential to benefit patients."

Lisa Patel

Chief Executive Officer

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