Algenscribe

Algenscribe

Biotech

$1.8M raised

Created in 2022

1-5 employees

Reach the full potential of genome editing

Algenscribe is a pre-clinical stage biotechnology company developing a first-in-class Gene Replacement platform. The flexible platform aims to improve the efficiency and quality of Gene Editing from single bases to multi-kilobase replacements.

Algenscribe’s platform tackles technological challenges in gene editing:
1°) Boosts Efficiency: Dramatically increases gene replacement rates
2°) Enhances Precision: Minimizes nuclease-induced mutations
3°) Full-Scale Flexibility: Edits from single bases to multi-kilobase insertions
4°) Versatile Utility: Spans therapeutics and bioproduction
5°) Non-viral: Bypasses AAV-related delivery constraints.

CONTACT INFORMATION

Frédéric Zampatti

CEO

Nice, France

fredericzampatti@algenscribe.com

LinkedIn

MAbSilico

MAbSilico

Tech Bio, Biotech

$5M raised

Created in 2017

11-20 employees including 1-5 in the USA

20 days to design the best antibody candidates

MAbSilico is a premier TechBio company dedicated to developing and providing cutting-edge AI-based solutions for antibody drug design and discovery. They empower biotech and pharmaceutical companies to significantly leverage antibody discovery risks by providing high-potential computational candidates in just a matter of days. These candidates are meticulously designed and characterized in silico and subsequently validated with state-of-the-art biological technologies, ensuring a seamless transition from digital modeling to laboratory success. By combining sophisticated 3D modeling, complex interaction simulations, and advanced linear sequence analysis, MAbSilico defines antibody drug candidates through a rigorous assessment of their epitope, affinity, off-target risk, cross-species reactivity, and developability, ensuring they are fully prepared for biological activity evaluation.

Beyond their services, MAbSilico is advancing its own innovative discovery pipeline available for out-licensing, featuring high-quality leads in monoclonal, bispecific, and antibody-drug conjugate modalities. Their commitment to global innovation is reflected in an aggressive US development strategy, where they are actively seeking strategic partners to extend the deployment of their antibody design platform across the North American ecosystem. This international reach is further strengthened by their exclusive partnership with Yntoab to serve the Korean market and a landmark collaboration with Sartorius. The Sartorius partnership offers a comprehensive end-to-end solution that bridges the gap between lead candidate design and lead candidate production, including integrated cell line development to accelerate the path to clinical trials.

Furthermore, MAbSilico utilizes advanced NLP technologies to gather exhaustive information about antibodies and their targets from global databases, ensuring robust competitive landscape analysis and the freedom to operate for all computationally designed candidates. Through these integrated technologies and global alliances, MAbSilico transforms the traditional discovery process into a predictive, high-velocity engine for the next generation of immunotherapy.

CONTACT INFORMATION

Vincent Puard

CEO

Tours, France

vincent.puard@mabsilico.com

LinkedIn

Établissement Français du Sang

Établissement Français du Sang

Institution & Others

Created in 2000

500+ employees

Let’s Give Blood the Power to Heal

With 25 years of expertise in cell therapy, immunology and virology across fundamental, translational and clinical stages, Etablissement Français du Sang (EFS) combines strong capabilities in translational research, GMP-grade bioproduction and access to high-quality biological samples.

EFS operates four ATMP bioproduction platforms across France as a CDMO, supporting clinical manufacturing for a broad range of cell types including MSC, CAR-T, iPSC, hESC and HSC. EFS also performs the GMP manufacturing of cell banks (Master & Working) for its partners.

In addition, EFS has strenghten its offer, through its PIBT (Pôle d’Innovation en Biothérapies), a dedicated development platform, focused on the maturation of advanced therapy projects. This includes the evaluation and integration of innovative bioproduction technologies, process and analytical development, and scalability, with early consideration of manufacturing and GMP constraints.

Together, these capabilities provide a continuum from early-stage development to clinical production, enabling a smoother and more reliable transition toward industrialisation.

CONTACT INFORMATION

Célia Mercier

Business Development Manager

La Plaine Saint-Denis, France

Celia.Mercier@efs.sante.fr

LinkedIn

Caisse d’épargne

Caisse d’épargne

Services

Created in 1818

10 000+ employees

Caisse d’Epargne supports you in your projects

A major player in regional economic financing, supporting 1 in 5 SME and 1 in 3 mid-sized companies through its 110 Business Centers located across all regions of France and its overseas territories (over $15 billion in financing by 2024). Caisse d’Epargne, a local cooperative banking network, supports businesses in their growth and transition projects. More than 38,000 businesses (SMEs, startups, mid-sized companies, and large corporate clients) are supported by our local experts, regardless of their size or industry.

Discover their dedicated sales teams: 400 relationship managers working closely with regional ecosystems to support your projects with responsiveness and expertise. A local support system reinforced by experts in cash management, international business, or innovation, for example. Being of service to you also means supporting you on your transformation journey and fully understanding your transition challenges, whether environmental, social, or governance-related.

With concrete solutions to meet your needs and support your development projects:

Day-to-day management of your cash flows and online payment solutions;
Financing for capital expenditures and working capital;
Financing for land and real estate in the broadest sense (establishment, relocation, capacity expansion, headquarters, etc.);
Financing of investments in production assets (machinery, equipment, IT, etc.) and mobility solutions;
Strategic risk management for operations (energy, raw materials, etc.);
Support for transformative transactions (external growth, IPOs, etc.);
Implementation of insurance, employee savings, and retirement solutions for your employees;
Investment of your excess cash;
Wealth optimization;
Support for your import-export operations and international expansion projects.

CONTACT INFORMATION

Audrey Dubois

Head of Healthcare Sector

Paris, France

audrey.dubois@bpce.fr

LinkedIn

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Ceres Brain Therpeutics

Ceres Brain Therpeutics

Biotech, Pharma

Series A – $18M raised

Created in 2019

6-10 employees

Rescuing neurons to treat brain diseases

Ceres Brain Therapeutics is a biotechnology company advancing CBT101, a novel central nervous system (CNS) therapeutic candidate that has recently progressed into Phase 2 clinical development. CBT101 is positioned to address major unmet needs in severe neurological diseases through a differentiated, indication specific approach to neuronal energy dysfunction.

CBT101 is being developed in amyotrophic lateral sclerosis (ALS), a rapidly progressive and fatal neurodegenerative disease with limited treatment options, as well as in creatine transporter deficiency (CTD), a rare paediatric neurological disorder with no effective disease modifying therapies. While based on a single molecular entity, CBT101 applies distinct mechanistic rationales aligned with each indication: targeting neuronal and mitochondrial energy dysfunction in ALS, and restoring intracellular creatine availability in neurons in CTD.

The program is supported by robust non clinical data and early clinical evidence demonstrating central nervous system activity and target engagement in humans. CBT101 is delivered as a non invasive nasal spray, offering a clear advantage in terms of patient convenience and treatment burden compared with injectable or hospital based therapies.

To support ongoing Phase 2 development and pipeline expansion, Ceres Brain Therapeutics is currently seeking to raise USD 20 million and is actively exploring strategic partnership opportunities, including co‑development, licensing, and regional collaborations, to accelerate development and maximize the value of CBT101 across its neurological indications.

CONTACT INFORMATION

Thomas Joudinaud

CEO

Paris, France

thomas.joudinaud@ceres-brain.com

LinkedIn

Diva Expertise

Diva Expertise

CRO/CDMO

Created in 2015

6-10 employees

The expert of studies and supply in human adipose tissue

DIVA Expertise is the leading global scientific partner for companies in the health, nutraceuticals and cosmetics industries seeking to evaluate the efficacy of an active ingredient or product directly on human adipose and skin tissue, ex vivo and in vitro. DIVA Expertise offers turnkey R&D projects – using unique, scientifically validated predictive human biological models – to provide industrial players with robust mechanistic evidence that accelerates and ensures the safe market launch of their innovations in cosmetics, nutraceuticals, and pharma metabolism/obesity.

What sets DIVA apart: DIVA biobank offering and innovative in vitro and ex vivo models enable preclinical expertise that closely aligns with the physiology of human adipose tissue, by working with real human biological materials from donors and adhering to the 3Rs principle (reduction of animal testing).

CONTACT INFORMATION

Susan Benjamin

Business Developer

Toulouse, France

susan.benjamin@diva-expertise.com

LinkedIn

DeepLife

DeepLife

Tech Bio

Series A – $19M raised

Created in 2019

21-50 employees

Digital Twin of Cells for Drug Discovery

DeepLife is a techbio company advancing drug positioning through artificial intelligence and digital twins of human cell types.

Its platform, TwinCell, simulates cell-type-specific behaviour by integrating over 1 billion harmonized single-cell omics data points with causal AI, enabling more precise target identification, drug repositioning and disease understanding.

DeepLife applies this technology across autoimmune, neurodegenerative and cardio metabolic diseases among others. It partners with pharmaceutical and biotech companies on asset de-risking, indication expansion and disease relevant assessment. The company has established strategic collaborations including with Biersdorf in skin disease and aging.

DeepLife leverages cell-type-specific digital twin models to pinpoint the most relevant disease indications for any therapeutic compound. At the core is TwinCell – a large-scale causal model of cell biology that identifies the molecular drivers of disease and how to reverse them. TwinCell combines this insight with large scale single cell multi omics data to build precise models of human cell types and their regulatory networks.

These digital twins replicate real cellular behaviour, predicting preclinical outcomes and enabling researchers to explore disease mechanisms in silico. This approach uncovers how compounds act at the cell-type level, enhancing target validation, biomarker discovery and indication selection.

Applied across the drug development lifecycle, TwinCell accelerates decision making, reduces risk and improves translational relevance. It supports novel target discovery, asset de-risking, indication expansion and pipeline prioritization through strategic collaborations with pharmaceutical and biotech partners.

CONTACT INFORMATION

Jonathan Baptista

CEO & Co-founder

Paris, France

jonathan.baptista@deeplife.co

LinkedIn

INPART

INPART

Services

$71.3M raised

Created in 2010

51-200 employees including 6-10 in North America

One platform to help bring science to life

Inpart, the platform purpose-built for biopharma partnering and external innovation.

Trusted by 500+ organizations across the life sciences ecosystem, including 70% of the world’s top 50 pharmaceutical companies. Inpart helps life science teams discover and evaluate external innovation more effectively.

Through a global scientific discovery network spanning 3,000+ research institutions and 6,000+ emerging biotech companies, they proactively surface new partnering opportunities aligned with our clients’ scientific priorities.

Inpart’s AI-enabled platform then supports the full partnering lifecycle; helping BD, R&D, Alliance Management and leadership teams structure evaluation workflows, collaborate across teams, and capture critical decision insights. By transforming fragmented evaluation data into structured intelligence, organizations gain better visibility across their external pipeline and unlock the foundation for AI-driven insight.

Deal is Inpart’s industry-leading partnering intelligence platform that helps BD, R&D, Alliance Management and leadership teams structure the evaluation and management of external opportunities across the partnering life-cycle. The platform captures scientific and commercial evaluation data, enables efficient collaboration across teams, and creates a clear history of partnering evaluations and decisions.

By transforming fragmented opportunity data into structured intelligence, Deal unlocks AI-driven insights that help organizations surface patterns across evaluations, identify strategic gaps, and generate portfolio-level visibility, enabling leadership teams to answer critical partnering questions in minutes and make faster, more reliable decisions.

CONTACT INFORMATION

Alex Barker

President, Pharma & Na

Toronto, ON, Canada

alex.barker@inpart.io

LinkedIn

AgenT

AgenT

TechBio, Medtech

Series A – $8M raised

Created in 2018

6-10 employees

Detect Alzheimer’s early, when it could be prevented

AgenT is a precision diagnostics company dedicated to transforming the prediction and monitoring of neurodegenerative diseases, with an initial focus on Alzheimer’s disease. Built on more than a decade of research, AgenT has developed a strong scientific and technological foundation combining patented biomarkers, proprietary targeted mass spectrometry methods, and AI-based software. This approach enables the company to generate highly specific, clinically relevant insights from blood samples and to address a major unmet need in brain health: earlier, more scalable, and less invasive detection.

AgenT’s proprietary platform is designed to monitor key biological pathways involved in age-related diseases and to support multiple applications ranging from diagnostics and companion diagnostics to therapeutic target discovery. The company also benefits from a unique proprietary database built from more than 5,000 retrospective plasma samples collected across the US, Europe, and Australia, enriched with longitudinal clinical follow-up data. Through this integrated platform and data strategy, AgenT is positioning itself as a next-generation player in precision medicine for neurodegenerative diseases, with a clear path toward clinical validation, commercial deployment, and strategic partnerships in both healthcare and life sciences.

AgenT’s innovative solutions are built around HORIZON™, a proprietary multiomic platform designed to predict and monitor neurodegenerative diseases through a simple blood sample. HORIZON™ combines patented biomarkers, targeted mass spectrometry, and AI-based software, and can monitor 8 key biological pathways through 85 biomarkers. Its first applications, B-HEALED™ and B-AHEAD™, are blood-based tests designed to predict progression to Alzheimer’s dementia symptoms in cognitively unimpaired and impaired individuals. These products have already shown strong performance in a first multicenter retrospective study involving 632 individuals across the US, Europe, and Australia, with 3x fewer false positives than current tests on the market. AgenT is now advancing these solutions through an ongoing 4,200-participant pivotal clinical validation study.

CONTACT INFORMATION

Baptiste Billoir

Co-founder

Paris, France

baptiste.billoir@agent-biotech.com

LinkedIn

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HEPHAISTOS

HEPHAISTOS

Biotech

Seed/Series A – $5M raised

Created in 2018

11-20 employees

Turn up the heat on cold tumors

HEPHAISTOS is a preclinical-stage biopharmaceutical company focused on designing and developing a third-generation innate immune activator. Its mission is to address a major challenge in oncology: improving patient responses to existing immunotherapies by overcoming myeloid-driven tumor immunosuppression.

The company’s lead candidate, HEPHA-440, enhances antitumor activity through multiple mechanisms. It promotes the recruitment of immune effector cells into the tumor microenvironment (TME), reverses macrophage polarization, activates dendritic cells and antigen presentation, and triggers CD8 T-cell–mediated cytotoxicity.

HEPHA-440 is an engineered small-molecule TLR4 agonist of the third generation. Compared to earlier clinical-stage compounds such as GLA and GSK1795091, it is 30 to 400 times safer, and it is twice as effective as first-generation molecules like GLA and MPL. It is also suitable for intravenous administration.

Preclinical studies have shown that HEPHA-440 achieves a balanced MyD88–TRIF signaling profile that favors antitumor cytokine production while maintaining low pyrogenicity. It has demonstrated strong single-agent efficacy, including complete tumor regressions and systemic effects against metastases. In combination therapies, it shows synergy with anti-PD-1 and anti-CD20 antibodies, achieving up to 100% complete tumor regression in some models. Additionally, it significantly increases PD-1 and PD-L1 expression within the tumor microenvironment.

HEPHAISTOS has been awarded funding from the EIC Accelerator ($3 million) and the France 2030 RHU program ($11.5 million), and has also received recognition from Sanofi and Amgen through their Golden Ticket programs.

CONTACT INFORMATION

Frédéric Caroff

CEO

Orsay, France

fc@hephaistos-pharma.com

LinkedIn

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