Ochre Bio

Ochre Bio

Is this your company? Claim your profile to update info and connect with investors.
Claim profile

Private Company

Total funding raised: $63.2M

Overview

Ochre Bio is a private, preclinical-stage biotech pioneering a data-driven approach to liver disease. The company has built a unique 'Human Discovery Platform' combining extensive human liver datasets, AI-driven causal prediction, and validation in sophisticated human ex vivo models like perfused livers. This integrated strategy, coupled with an in-house RNA therapeutic manufacturing capability, aims to rapidly translate novel targets into clinical candidates, as evidenced by a significant partnership with GSK and a pipeline targeting fibrosis and cirrhosis.

Chronic Liver DiseaseLiver FibrosisCirrhosisMASH/MASLD

Technology Platform

Integrated platform combining: 1) Human Discovery Platform (AI analysis of proprietary human liver genomic and gene perturbation data), 2) Human Validation Platform (ex vivo validation using perfused human livers, tissue slices), and 3) an in-house RNA therapeutic manufacturing platform.

Funding History

3
Total raised:$63.2M
Series A$30M
Venture$30M
Seed$3.2M

Opportunities

The massive unmet need in advanced chronic liver disease, driven by the global MASLD epidemic, presents a multi-billion dollar market with few effective therapies.
Ochre's platform and partnership strategy position it to rapidly generate a pipeline of novel, human-validated targets, creating multiple shots on goal for a breakthrough therapy.

Risk Factors

Key risks include the unproven clinical translatability of its human-ex-vivo-centric discovery platform, the high failure rate inherent in novel drug development, and intense competition in the liver disease space from large pharma and other well-funded biotechs.

Competitive Landscape

Ochre operates in the highly competitive chronic liver disease space, competing with large pharma (e.g., Novo Nordisk, Madrigal, Boehringer Ingelheim) and other biotechs pursuing small molecules, FXR agonists, and other modalities for MASH/MASLD and fibrosis. Its differentiation lies in its human-data-first AI platform and use of sophisticated human ex vivo validation models, aiming to de-risk target selection.