14th edition

Format
HYBRID

December 2nd & 3rd, 2025

IN-PERSON | STRASBOURG

December 8th ,2025

ONLINE MEETINGS

14th edition

Format
HYBRID

December 2nd & 3rd, 2025

IN-PERSON | STRASBOURG

December 8th ,2025

ONLINE MEETINGS

Cancéropôle Est : fostering innovation in oncology

Cancéropôle Est : Fostering innovation in oncology

Wednesday, December 3rd, 2025
9.00 am – 11.15 am
Room 3

ABOUT CANCÉROPÔLE EST

Cancéropôle Est brings together over 1,000 scientists and clinicians who join efforts to bring the latest innovations in terms of prevention, screening, diagnostic and therapeutic options in oncology to the 8.4 million inhabitants of the area that Cancéropôle covers (the Grand Est and Burgundy Franche-Comté regions). 

Organising, coordinating, and strengthening cancer research by partnering with academic and clinical institutions and bringing together researchers, healthcare professionals, economic partners, and patients is a top priority for the Cancéropôle Est. 

PROGRAMME

9.00 – 9.05 am – Dr Guillaume VETTER-GENOUD (Director of Quest for health Startup Incubator), Pr Pierre FUMOLEAU (Scientific Director of Cancéropôle Est), Dr Marie-Julie TILLY (Project manager at Cancéropôle Est)
Opening

9.05 – 9.30 am – Pr Pierre FUMOLEAU – Scientific Director of Cancéropôle Est
Major developments and progress in oncology made over the past decade

9.30 – 9.45 am – Msc Mehdi CHELBI – CEO of BiPER Therapeutics
Translational approach for First-in-class therapeutics : Internal data –  real-world data and AI – which strategy to adopt?
BiPER Therapeutics opens a new therapeutic pathway in the treatment of cancers and life-threatening diseases. Our first clinical candidate BPR001-615 is a first-in-class small molecule to treat gastro-intestinal tumors by pushing cancer cells to burn out. BPR001 is a selective inhibitor of BiP/GRP78, a key protein involved in cancer cells survival and associated with very poor prognosis of patients when overexpressed in tumors and in plasma of patients. BPR001-615 has been developed to treat the 50% of BIP+ patients through a precision medicine approach based on a simple blood test. BPR001-615 has been developed as an oral drug in monotherapy or in combination with standards of care to improve patient outcomes. In preclinical studies, patent-protected data demonstrate that BPR001-615 administered orally in monotherapy outperforms 1st line chemotherapy 5FU (Folfox) in gastro-intestinal cancer models

9.45 – 10.00 am – Msc Sébastien VACHENC – CEO of Sagacity Health
Intratumoral strenghts, new players… Toward a paradigm shift in oncology
Sagacity Health is a cutting-edge AI-Biotech company at the forefront of the convergence between AI and Biotechnology, specializing in the exploration of intratumoral microbiota, a key but unknown driver of treatment resistance in oncology. Founded in 2025 by a multidisciplinary European team with deep expertise in pharmaceutical and biotech industries, we are developing a unique agentic AI platform to decipher the dynamic interactions between microbes, tumors, and therapies, thereby reinventing drug discovery. With a strong European ambition, Sagacity Health is emerging as a leading player in pharmacomicrobiomics in oncology, turning therapeutic failures into opportunities and paving the way for precision medicine that integrates the microbial dimension.

10.00 – 10.15 am – Dr Meddy EL ALAOUI  – CEO of AbTx
Smaller ADC formats based on Therano Stick ™ technology could make the difference for solid tumors!
AbTx is a next-generation pure-play biotech company deploying a novel ADC platform (Therano Stick™) to develop differentiated antibody-drug conjugates (ADCs) and improve their therapeutic index (efficacy/safety). Although ADCs have evolved over the past 40 years, poor solid tumor penetration and long half-life still limit their clinical impact, particularly in pancreatic cancer. Using AbTx’s Therano Stick™ technology, smaller ADCs such as antibody fragment conjugates (FDCs) are generated, offering improved tumor access, faster clearance, and enhanced cytotoxic activity. The Therano Stick™ platform employs enzymatic conjugation via bacterial transglutaminase (mTG), combined with a patented Q-Tag system, to enable site-specific conjugation across multiple antibody formats (full-length, Fab, scFv, VHH). Additionally, AbTx aims to expand its technology to develop dual cytotoxic payload ADCs through enzymatic conjugation, further enhancing therapeutic potential.

 10.15- 10.30 am – Dr Albin JEANNE – CEO of Apmonia Therapeutics
Apmonia Tx – Breaking boundaries in cancer by targeting its microenvironment 
Apmonia Tx is a leading French company offering a breakthrough technology by attacking extracellular matrix proteins as a new oncology class. At the convergence of several scientific and technological advances, Apmonia Tx is developing both a unique in silico discovery platform [powered by virtual screening and AI], and a portfolio of drug candidates. Flagship product is a tumor microenvironment modulator that blocks the interaction between thrombospondin-1 (TSP-1) and CD47 receptors. It is ready to enter Phase 1/2a trial in several advanced solid tumors (CTA/IND-ready).

10.30 – 10.45 am – Dr Jean-Marc LIMACHER – Co-Founder, Chairman, CMO of Odimma Therapeutics
ODI-2001: A new platform for personalized cancer immunotherapy
Odimma Therapeutics is an Alsatian start-up working in the field of personalized cancer immunotherapy. The company is developing a next-generation immunization platform based on artificial intelligence and the use of synthetic DNA.

10.45 – 11.00 am – Florent GROS – CEO, Co-Founder of Priothera
Priothera is redefining the standard of care in hemato-oncology by unlocking the full potential of cell therapies.
While cell therapies have transformed cancer treatment, major challenges remain, especially for patients with AML, a disease still responsible for 50,000 deaths every year worldwide.
Priothera’s lead candidate, mocravimod, is a breakthrough immunomodulator designed to both boost the anti-cancer power of cell therapies (including stem cell transplantation and CAR-T) and significantly reduce the severe side effects that limit their use and compromise patient survival.
Backed by impressive preliminary clinical results, mocravimod is now advancing into the Phase 3 MO-TRANS trial marking a major step toward changing the future of AML treatment. 

To access Cancéropôle Est session, you must be registered for BioFIT 

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