Immitra Bio logoImmitra Bio
A new class of genetic medicine

Unlock Hidden Biology

7000+ rare genetic diseases affect 400 million people worldwide. 95% lack therapy, 50% are children. We seek solutions within the vast redundancy already present in the human genome.

Our mission

In-vivo
Scalable
Gene
Editing
Platform

Today's approved stem cell therapies for genetic disorders are toxic, unscalable, slow, and expensive, all rooted in ex-vivo approaches. We're developing an in-vivo alternative, a single, off-the-shelf injection that cures patients without chemotherapy or cell transplantation. Accessible to all patients worldwide and independent of their genetic mutations, no patient will be left behind.

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30 Apr 2026 - Gebert Rüf Stiftung

Immitra Bio wins 150'000 CHF Innobooster funding supported by Gebert Rüf Stiftung

Gebert Rüf Stiftung supports high-potential businesses from the Venture Kick program with the aim of substantially accelerating their market entry. The funding line is calling for top talents with convincing applications of how a research & development or design boost can speed up a successful market penetration of their deeptech business.
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18 Mar 2026 - Venturelab

Immitra Bio Among Ten Swiss biotech startups selected for Venture Leaders Boston Roadshow 2026

Ten startups have been selected for the 2026 Venture Leaders Biotech program, which will take them to Boston from May 31st to June 5th as part of the Swiss National Startup Team. During their roadshow, Immitra Bio will connect with international investors and industry leaders, acquiring expertise to help scale their ventures internationally.
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29 Jan 2026 - Venture Kick

Immitra Bio awarded Venture Kick Stage-II to Advance Scalable In-vivo Gene Edtiting Therapies

Immitra Bio has received Venture Kick support to advance an in-vivo gene editing platform for blood disorders. The approach enables gene correction directly in the body, without chemotherapy, making curative therapies faster, safer, and more scalable.
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08 Dec 2025 - Forbes

Our CEO, Jan Nelis, Recognized Among Forbes 30Under30 Swiss Innovators

Forbes 30Under30, the annual premier list that presents influential personalities in Switzerland, Germany, and Austria who positively impact business and society. Selected from startups offering solutions in various sectors and prominent figures supporting the ecosystem.
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Rethinking the given

Utilize inherent potential

Our biological blueprint is layered with echoes and redundancies, an untapped pool of information waiting to be exploited.

Redundancy is not noise, it is a reserve
Life is written in repetitions and shadows of itself , an unused reserve of code waiting to be called upon when systems fail. Beneath the visible layer, parallel possibilities remain intact, hinting that repair may come not from outside, but from what has always been there.
Meet the team

Leadership and scientific team

We are building at the frontier of biology and engineering, turning fundamental discoveries into new therapeutic possibilities.

Translational Top-tier academic and industry expertise combined to translate ideas into once-and-done genomic medicine.
Founder-Led Combining deep scientific expertise with disciplined execution to translate breakthrough research into real-world impact.

Jan Nelis

Co-founder and Chief Executive Officer

Driving vision and strategy at Immitra Bio, translating a bold scientific thesis into a scalable company.

Amir Taheri

Co-founder and Chief Scientific Officer

Seasoned gene editing expert with extensive experience in the pharmaceutical industry.

Jacob Corn

Co-founder and Scientific Advisor

Key Opinion Leader in cutting-edge CRISPR-Cas9 technologies, Genome Biology Professor at ETH Zurich.

Veera Vainio

R&D Scientist

Cell and Molecular Biologist, experienced with characterization of proteins and their function, ETH Zurich alumni.

Gülkiz Baytek Barbini

R&D Scientist

Cell and Molecular Biologist, experienced in primary and stem cell biology as well as mass spec proteomics, ETH Zurich alumni.

We are a multidisciplinary team spanning gene editing, computational biology, and translational medicine, united by a shared goal to make genetic therapies more precise, scalable, and accessible.
Institutional backing

Backed by leading institutions

Supported by a growing network of leading investors and research partners.