Arbor Vita

Arbor Vita

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Private Company

Total funding raised: $93.0M

Overview

Arbor Vita is a private, commercial-stage diagnostics company founded in 1999. It has built a unique technology foundation around PDZ domain biology and monoclonal antibodies to develop rapid, actionable diagnostic tests for global health challenges, with a focus on infectious disease pandemics and cervical cancer screening. The company has successfully brought FDA-cleared products to market, operates a CLIA-certified testing lab for COVID-19, and collaborates with entities like the U.S. Navy and Yale University. Its strategy targets both advanced and low-resource healthcare settings to improve early detection and health outcomes.

Infectious DiseasesOncology

Technology Platform

Proprietary PDZ proteomics platform for target discovery, combined with a proprietary monoclonal antibody (mAb) library for development of rapid diagnostic tests. This enables the creation of sensitive, point-of-care tests for specific protein markers in infectious diseases and cancers.

Funding History

23
Total raised:$93.0M
Grant$961K
Grant$95K
Grant$198K
Grant$339K

Opportunities

Significant opportunity in global cervical cancer screening, targeting over 2 billion at-risk women, especially in low-resource settings underserved by current infrastructure-heavy methods.
The persistent threat of influenza pandemics and emerging infectious diseases creates a recurring need for rapid, deployable diagnostic tests for public health containment at points of entry like airports.

Risk Factors

Commercial success relies on adoption of niche products in competitive markets and is vulnerable to episodic demand for pandemic flu tests.
The company faces ongoing regulatory and reimbursement challenges for market expansion and must continuously innovate to avoid technological disruption from advanced molecular diagnostics.

Competitive Landscape

In rapid influenza diagnostics, Arbor Vita competes with other FDA-cleared test manufacturers and broader PCR-based lab services. In cervical cancer screening, it competes directly with established Pap smear cytology, HPV DNA tests (like Roche Cobas, Qiagen), and newer molecular assays, differentiating itself through a protein-based, point-of-care format designed for low-resource settings.