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3077

Dr. Margot Karlikow

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Dr. Margot Karlikow
CEO & Co-Founder of
En Carta Diagnostics (2022)
About

Dr. Margot Karlikow is Co-Founder and CTO of En Carta Diagnostics, a Paris-based deeptech startup pioneering rapid, PCR-precision molecular diagnostics operable without lab infrastructure.

Before founding

Margot earned her PhD as a researcher at Institut Pasteur and conducted postdoctoral research at the University of Toronto, where she specialized in cell-free synthetic biology and developed foundational diagnostic sensing technologies.

Founder Insights

She co-invented patented cell-free synthetic biological circuit technology for pathogen detection and spearheaded landmark field trials for Zika virus testing, demonstrating the real-world robustness of the platform.

Experience

Under her technical leadership, En Carta secured FDA Breakthrough Device Designation in January 2026 for its EC Pocket Lyme test and raised over €6.5M in cumulative funding from investors including Blue Forest Ventures, Ring Capital, and CentraleSupelec Venture.

Scale & Impact

En Carta's platform has been validated across pathogens including Zika, Ebola, chikungunya, and Lyme disease, with 10 peer-reviewed publications, two active clinical trials, and a EUR 13M commercial partnership with diagnostics leader AAZ.

3077

Dr. Margot Karlikow

En Carta Diagnostics
Co-Founder
Logo
Dr. Margot Karlikow

Company(s)

En Carta Diagnostics

Industry

Healthtech & Biotech

Year Founded

2022

Stage/Funding

Seed • $6.5M

Company Location

fr

Connect

About

Dr. Margot Karlikow is Co-Founder and CTO of En Carta Diagnostics, a Paris-based deeptech startup pioneering rapid, PCR-precision molecular diagnostics operable without lab infrastructure.

Before founding

Margot earned her PhD as a researcher at Institut Pasteur and conducted postdoctoral research at the University of Toronto, where she specialized in cell-free synthetic biology and developed foundational diagnostic sensing technologies.

Founder Insights

She co-invented patented cell-free synthetic biological circuit technology for pathogen detection and spearheaded landmark field trials for Zika virus testing, demonstrating the real-world robustness of the platform.

Experience

Under her technical leadership, En Carta secured FDA Breakthrough Device Designation in January 2026 for its EC Pocket Lyme test and raised over €6.5M in cumulative funding from investors including Blue Forest Ventures, Ring Capital, and CentraleSupelec Venture.

Scale & Impact

En Carta's platform has been validated across pathogens including Zika, Ebola, chikungunya, and Lyme disease, with 10 peer-reviewed publications, two active clinical trials, and a EUR 13M commercial partnership with diagnostics leader AAZ.

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