PAIGE

Overview
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AI Drug Discovery?
Product stageSegments
Go-to-Market
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AI SaaS | Biomarker Development
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Paige offers an AI-powered pathology computational platform for detecting cancer subtypes, enabling pathologists to make accurate digital diagnoses. The company claims its deep-learning algorithms have detected prostate cancer, skin cancer, and breast cancer accurately. 

Paige's platform can be used to access proprietary data to generate and test digital biomarker hypotheses and also for SaaS-based deployment of digital biomarkers to identify patients for therapies and clinical trials, as well as cancer detection. Paige is the first company to receive FDA’s breakthrough designation in 2019 for one of its pathology products, a prostate module. In October 2023 , it received another breakthrough device designation from the FDA for its breast cancer detection tool, Paige Lymph Node.

Key customers and partnerships

The company started commercializing its Paige Prostate from 2019, which is a first-to-market prostate cancer detection solution. Its AI solutions are vendor-agnostic, which allows Paige to cater to a broad range of customers. 

The company collaborated with several companies, including Invicro LLC (January 2020), Janssen (June 2022), OptraSCAN (September 2022), Leica Biosystem s (March 2023), Ohio State University’s Wexner Medical Center (August 2023), and Microsoft (September 2023). Funding and financials

The company closed a USD 220 million Series C funding in March  2021, co-led by Casdin Capital, Johnson and Johnson Innovation (JJDC) and Kolberg KravisRoberts, with plans to expand geographically and grow further develop clinical applications, biomarkers, and AI-based diagnostics.

HQ location:
11 Times Square Floor 37 New York NY USA
Founded year:
2018
Employees:
101-250
IPO status:
Private
Total funding:
USD 220.0 mn
Last Funding:
USD 125.0 mn (Series C; Jan 2021)
Last valuation:
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