APMONIA THERAPEUTICS

APMONIA THERAPEUTICS

About the company

Apmonia Therapeutics is a biotechnology company dedicated to developing therapeutic strategies towards cancer. They are developing a first-in-class pipeline of next-generation peptide-based therapies targeting the tumor microenvironment to improve the lives of patients with cancer.

Using molecular modeling (i.e., ligand:protein and protein:protein docking simulations, as well as molecular dynamics simulations) and their vast knowledge of matrix biology and oncology, they are developing a portfolio of proprietary first-in-class peptide-based therapies targeting the tumour extracellular matrix (ECM) molecules. After years of research on cancer-stroma interactions, they identified several proteins which are overexpressed in different types of solid tumours, converting them into potential targets for anticancer treatments. By producing peptides that selectively target ECM components, they can regulate the interplay between cancer and stromal cells within the TME, disrupting tumoural activity.

About the solution

Their lead program, AP-01 (or TAX2), is a peptide-based technology targeting tumor-overexpressed thrombospondin-1 (TSP-1) to prevent CD47 receptor activation. AP-01 acts as a modulator of the tumor-tolerant microenvironment, reprogramming highly vascularized tumors into poorly angiogenic ones while concomitantly activating the tumor-inhibiting immune system. Thanks to its unique mode of action, AP-01 does not recapitulate the hematologic toxicities related to CD47 blockade, hence realizing the full potential of targeting this axis for cancer therapy.

A large body of in vivo efficacy data supports the proof-of-concept for AP-01 use as an anti-cancer therapy. TAX2 activates the adaptive (tumor-specific) immune response, as demonstrated by activation of T-cells, production of interferon gamma, and significant tumor reduction. The T cell stimulatory activities of AP-01 also position it as an excellent candidate for combination therapies in the context of a broad immune-oncology approach.

Their current focus for clinical development is ovarian cancer, an orphan indication. They plan to target other indications including glioblastoma, colorectal cancer, and pancreatic cancer.

Key information

–  Therapeutic areas: Oncology

–  Based in: Reims (FRANCE)

–  Employees: 1 – 10

–  Created in: 2019

VECT-HORUS

VECT-HORUS

About the company

Vect-Horus is a privately held biotechnology company that designs and develops molecular vectors that facilitate targeting and delivery of therapeutic or imaging agents to organs, including the brain and tumors. Founded in 2005, Vect-Horus is a spin-off of the Institute for Neurophysiopathology (INP, UMR7051, CNRS and Aix Marseille University), formerly headed by Dr Michel Khrestchatisky, co-founder of the company. Vect-Horus has 40 employees (most in R&D).

By combining pharmaceutical agents to its vectors, VECT-HORUS enables their transport across the BBB, which significantly impedes brain delivery of most drugs. Proof of concept of the technology was demonstrated in animal models for different vectorized molecules (Oligonucleotides, Antibodies, NPs…).

Based on its potential to target specific receptors, notably those that are found at high levels in some pathological tissues, the Company is also targeting cancers (pancreatic, adrenal cancer, glioblastoma, etc.), where there is a high unmet medical need.

About the solution

VECT-HORUS discovered, validated, and optimized different families of molecular vector that target the LDL Receptor, Transferrin Receptor and undisclosed ones that allow drug targeted delivery to different organs.

The vectors are protected by several families of patents and ongoing patent applications. They have different properties (structure, affinity, stability, organ specificity) allowing adaptation of the vectorization process on a case-to-case basis.

Vect-Horus seeks to develop the broad potential of its proprietary VECTrans® technology platform through partnerships and licensing agreements with pharmaceutical and biotechnology companies in multiple therapeutic applications.

Key information

–  Therapeutic areas: Central Nervous System, Neuromuscular, Cardiovascular, Ophtalmological, Oncology, Pulmonary

–  Based in: Marseille (FRANCE)

–  Employees: 11 – 50

–  Created in: 2005

ORAKL ONCOLOGY

ORAKL ONCOLOGY

About the company

The current drug development process does not capture cancer complexity or heterogeneity. This is a main reason why 96% of drugs fail when they meet patients in clinical trials, lacking efficacy in the patient population.

Orakl Oncology stands at the forefront of the techbio landscape, pioneering the use of patient tumor avatars to meticulously accelerate and de-risk drug development in collaboration with oncology players.


As a spin-out from Gustave Roussy (2023), the 4th cancer center in the world, Orakl’s boasts unique access to a vast repository of patient tissue samples and associated data. This strategic foundation positions them to scale quickly across a vast number of cancer subtypes starting with colorectal and pancreatic cancers.

The founders and team collectively bring unparalleled expertise in cancer cell biology and engineering. With over 30 years of combined academic experience across France, the UK, and the US, they are dedicated to improving cancer treatment. The company has already been funded 5M€ in equity and grants for their first developments.

About the solution

Orakl Oncology is a techbio platform that is building a unique collection of patient tumor avatars, each of them combining the best biology and patient clinical and molecular data. As a spin-out from Gustave Roussy, the 4th cancer center in the world, they are positionned to scale quickly across a vast number of cancer subtypes starting with colorectal and pancreatic cancers. This combination of biology and data, scalable and supported by proprietary know-how, is an extraordinary differenciating factor.


Their cutting-edge approach involves the integration of functional testing and AI-powered analysis to predict patient response to treatments and stratify populations. They already obtained excellent predictive values, at the patient and population levels.


Orakl discovers and develops new drugs that will succeed in the clinic, for their own pipeline or in co-development with oncology companies.

Key information

–  Therapeutic areas: Oncology

–  Based in: Paris (FRANCE)

–  Employees: 1-10

–  Created in: 2023

MABSILICO

MABSILICO

About the company

MAbSilico is the TechBio pionner company specializing in computational solutions for discovering and designing therapeutic antibodies. Their solutions leverages artificial intelligence (AI) and machine learning to characterize, optimize and design therapeutic antibodies.

MAbSilico’s platform aims to accelerate the antibody discovery process by structural design with epitope-driven and multiparametric approaches. This allows to design highly effective antibodies, saving time and resources compared to traditional methods. We provide fully characterized antibodies against a target within 21 days that are internally validated with wet lab assays, leading to faster development of life-saving antibody therapies.

About the solution

MAbSilico uses a combination of 3D modeling, interaction simulation, and sequence analysis to identify promising antibody candidates after assessing for various factors, including their binding target (epitope), affinity, potential off-target effects, and developability.

While the solutions can be applied to antibody characterization, optimization and design, MAbSilico does not need to generate biological data to apply their solutions.

Integrating multi-parameters for the antibody design and validating the newly sequence with state of the art biological assays, MAbSilico is pioneering a game-changing approach to antibody discovery with internal discovery pipeline.

Key information

–  Therapeutic areas: Computational antibody design & discovery applied in oncology, Immuno-oncology, Infectious diseases, Rare diseases

–  Based in: Tours & Paris (FRANCE)

–  Employees: 11 – 50

–  Created in: 2017

BRENUS PHARMA

BRENUS PHARMA

About the company

Despite therapeutic advancements, fighting cancer requires new allies. Cancer cells can adapt themselves under therapeutic pressure and express tumor antigens that hide from our immune system’s surveillance. This mechanism leads to treatment failure of 90% of patients with solid tumors (16 million in 2022).

Brenus Pharma is a French clinical-stage biotech developing a pioneering discovery platform Stimulated-Tumor-Cell (STC) leading the path of a new generation of immunotherapies. STC doesn’t just fight cancer as it is today; it anticipates how cancer will evolve tomorrow, training the patient’s immune system to recognize and destroy tumors, even as they change.

Brenus Pharma is on the brink of a breakthrough and will start its First in Human study in 2024 in colorectal cancer, killing 9.7 million of patient per year.
They are building a strong portfolio in solid tumors, leveraging our patented STC platform, and surpassing other approaches to change a paradigm in oncology.

About the solution

The STC Platform mimics patient’s relapsing conditions in vitro to produce next-generation immunotherapies educating patient’s immune system against tumor evolution and mechanisms of relapse.

Thanks to their unique mode of production, the STCs will educate the immune system to the largest number of specific targets of interest, validated with multi-omics analysis and patient’s biopsies databases. Thanks to the standardization of the platform, access to the drug will not be limited by production or price, and they can also anticipate synergies with other innovations (ADC, ICP).

Their first candidate, STC-1010, is focused on metastatic colorectal cancer (mCRC) an urgent unmet need.

Key information

–  Therapeutic areas: Primary TA: Metastatic Colo Rectal Cancer (mCRC)
Secondary TA : Pancreas Cancer, Liver cancer, Ovarian Cancer, Solid Tumors

–  Based in: Lyon & Clermont-Ferrand (FRANCE)

–  Employees: 11 – 50

–  Created in: 2020

PHOST’IN THERAPEUTICS

PHOST’IN THERAPEUTICS

About the company

Phost’in develops First-in-Class N-glycosylation inhibitors for the treatment of cancers and fibrosis (First-in-Human currently on-going in Europe for the first program).

About the solution

PhOx430, First-In-Class selective GnT-V inhibitor, now evaluated in Ph.I in patients with Advance Solid Tumors.

Key information

–  Therapeutic areas: Oncology, Fibrosis

–  Based in: Montpellier (FRANCE)

–  Employees: 1-10

–  Created in: 2014

CEVIDRA

CEVIDRA

About the company

Founded 17 years ago, Cevidra is an independent pharmaceutical company with a strong expertise in hospital affairs, particularly in tenders, and a vast network of experts. As a rapidly growing entity in the early access domain, Cevidra acts as a gateway to the French market for foreign companies. Rooted in innovation, agility, and commitment, Cevidra offers comprehensive services from its headquarters in Grasse, with additional offices in Paris and Lyon.

Holding GDP/GMP certifications, it excels as an « Exploitant » for pharmaceutical products, specializing in distribution through its logistical platform. Cevidra provides services ranging from regulatory affairs to market access and real-world data collection. It has a strong track record in managed access programs across various areas, including ATMPs.

About the solution

As an Exploitant with an in-house GDP platform, Cevidra offers flexible support to foreign companies launching medicines in France. They handle compassionate/early access programs, market approval, and distribution, including market access and promotional activities in hospitals and pharmacies. Their tailored approach ensures a seamless entry into the French market.

Key information

–  Therapeutic areas: All therapeutic areas including Oncology, Rare diseases and Addictive medicine.

–  Based in: Grasse, Lyon and Paris (FRANCE)

–  Employees: 11 – 50

–  Created in: 2007

ALGENSCRIBE

ALGENSCRIBE

About the company

Algenscribe operates in the field of Gene Editing: the company is developing a new platform for Gene Replacement with its first applications in Gene Therapy and Oncology.

About the solution

The aim is to achieve the full potential of Gene Editing for Gene Replacement. Algenscribe’s technologies address two major constraints of the field: the number of cells edited is significantly increased, while certain undesirable effects are reduced.

Key information

–  Therapeutic areas: Gene Editing, Gene Therapy, Oncology

–  Based in: Gif sur Yvette & Nice (FRANCE)

–  Employees: 1 – 10

–  Created in: 2022

SYNDIVIA

SYNDIVIA

About the company

Syndivia is dedicated to enhancing treatment options for patients with solid tumors. They specialize in utilizing their proprietary and unique GeminiMab™ technology — the first and only hinge-region Cys229 site-specific ADC technology applicable to native monoclonal antibodies. Specifically, they take advantage of the distinctive GeminiMab™-DAR1 ADCs, which offer improved antitumor efficacy and reduced toxicity.

About the solution

The key technology behind Syndivia’s unique site-specific approach is GeminiMab™, the first and only technology for hinge-region site-specific conjugation (2xCys229), enabling unprecedented efficiency and scope in creating site-specific DAR1 ADCs.

Their proprietary candidates include:

1. SDV2102: GeminiMab anti-PSMA ADC (mCRPC, GBM, HCC)

2. SDV2103: GeminiMab anti-Trop2 ADC (NSCLC)

Key information

–  Therapeutic areas: Antibody-drug-conjgutes, Oncology

–  Based in: Strasbourg (FRANCE)

–  Employees: 1 – 10

–  Created in: 2014

FIRALIS MOLECULAR PRECISION

FIRALIS MOLECULAR PRECISION

About the company

Firalis Molecular Precision (FMP), established in 2019 and rooted in the Firalis Group, operates as a leading Contract Research Organization (CRO) from Huningue, France.

Specialized in biomarker discovery and multi-omic analysis (genomics, proteomics, metabolomics), FMP accelerates precision medicine by improving diagnostics, understanding disease mechanisms, and evaluating drug efficacy. With advanced laboratories and a dedicated team of over 55 experts, FMP supports biotech and pharma companies globally, offering a suite of services that span pre-clinical to clinical trials, thus playing a pivotal role in advancing healthcare innovations.

About the solution

Firalis Molecular Precision (FMP) is at the forefront of the multi-omics revolution bringing progress and innovation to the biopharmaceutical industry. By harnessing advanced -omics technologies and bioinformatics, they excel in identifying promising therapeutic targets and enhancing the drug development process for greater speed and reliability. Their state-of-the-art multi-omics solutions facilitate precise, high-throughput genomics, transcriptomics, and proteomics, leading to pioneering healthcare breakthroughs.

Key information

–  Therapeutic areas: Neurology, Oncology, Immunology  

–  Based in: Huningue (FRANCE) & Cambridge (USA)

–  Employees: 51 – 200

–  Created in: 2016