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Allogenica’s bioproduction process consists in:

Transferring therapeutic transgene to these immature cells (called pre-T cells)

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Transferring therapeutic transgene to these immature cells
Harvesting stem cell from healthy donors

Harvesting stem cell from healthy donors

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Our commitment

Inna MENKOVA

We are committed to making T-cell therapies universally accessible by delivering treatments that are safer, more readily available to patients, and up to ten times less expensive to manufacture.

While cancer remains our primary focus, we also aim to address rare diseases and autoimmune disorders.

Inna MENKOVA, PhD

CEO and Co-founder of ALLOGENICA

Cell therapy

WHY Allogenica

Our unique approach

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After production, engineered pre-T cells are stored and ready to be delivered "off-the-shelf" when a patient needs them

engineered pre-T cells are stored and ready to be delivered "off-the-shelf" when a patient needs them
Differentiate and expand the engineered pre-T cells at large scale in a bioreactor

Differentiate and expand the engineered pre-T cells at large scale in a bioreactor

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Allogenica's unique expertise enables the differentiation of stem cells into immature precursor T cells. Allogenica's innovative vector allows these cells to be modified to produce a new generation of allogeneic T-cell therapies.

Allogenica’s most advanced drug candidate is expected to enter clinical trials in 2026.

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Allogenica’s solution

Allogenica has developed unique worldwide expertise:

Latest news

COLLABORATIONS

They support Allogenica

Allogenica’s pre-T advantages:

Our Management Team

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Inna Menkova, PhD

Chief Executive Officer

and co-founder

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Tobias Abel, PhD

Chief Scientific Officer

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Aymeric Bordet

Chief Financial ​Officer

VISION

Future-ready Cell Therapy

Future-ready Cell Therapy

At Allogenica we are transforming cell therapies for a healthier tomorrow.

Our mission is to disrupt the treatment landscape for cancer, rare diseases, and autoimmune disorders. We're developing a breakthrough cell therapy platform with the potential to:

  • Replace transplants: Providing less invasive, accessible alternatives for thousands of patients who currently have limited treatment options.

  • Expand access for all: With predictable safety and efficacy, we aim to make cell therapies available to a a broader patient population.

  • Dramatically reduce costs: By streamlining production, we aim to significantly lower the cost of cell therapies, making transformative treatments more accessible globally.

Here is an example of an application of the Allogenica platform that could revolutionize, for example, CAR-T therapy. Watch the video below to learn more.

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A revolution in the field of cell therapy

Engineered T-cell therapies are one of the key therapies revolutionizing the healthcare landscape. The approach involves reprogramming immune cells to recognize and kill cancer cells.

 

But traditional T-cell therapies, even when truly effective, are long and complex to manufacture, leading to delays that are often too long for patients battling life-threatening diseases.

Board of directors

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Jean-Guillaume Lafay

Chairman of the BOD and co-founder

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Jean-Marie Grumel, MD

Board member and co-founder

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Stephane Legastelois, PhD

President at 33 Californie

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Eglantine Rollet, PhD

Investment Manager Pulsalys

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Jean Pascal Tranie

Partner, Aloe Private Equity

Scientific Advisory Board

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Prof. Charles Dumontet,
MD, PhD

Chairman of the SAB

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Prof. Olivier Adotevi,
MD, PhD

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Prof. Jean Daniel Lelièvre, MD, PhD

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Julien Marie,
PhD

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Join our team

  • High quality of start material

  • Biobanking

  • Great expansion capacity

  • No exhaustion markers

  • Potency assay available

Advantages for bioproduction

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patiente
  • No Graft vs Host disease (no TCR expression)

  • Long-term persistence (over 10 years)

  • Efficient thymic maturation

  • Potent anti-cancer activity

Therapeutic advantages

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