Ifebemtinib
Ifebemtinib (also known as IN10018, ifebe, BI853520) is an orally administered, highly potent and selective small molecular inhibitor of the focal adhesion kinase (FAK). InxMed translational research has advanced FAK targeting as an essential mean to fight against cancer.
Anchor Targeting Tumor Defense with POC achieved over different indications
Ifebemtinib has a significant synergy with a broad spectrum of therapeutic modalities. Clinically, ifebemtinib has demonstrated therapeutic synergy with chemotherapy agents, targeted therapies, antibody-drug conjugates, and immunotherapies. InxMed is currently pursuing a registrational trial in platinum-resistant ovarian cancer in China, and multiple proof-of-concept trials are ongoing in lung, colorectal, melanoma, and pancreatic cancers, with selected tumor types to progress into pivotal clinical trials.

Good Safety Profile
Ifebemtinib demonstrated good safety profile demonstrated in more than 600 patients. Single agent or in combination with PLD, docetaxel, paclitaxel-carboplatin, cobimetinib, and anti-PD(L)-1 in multiple solid tumors. Most common AEs include reversible proteinuria, Gl related side effects. The majority of ifebemtinib-related AEs are CTCAE grade 1 or 2. Safety profile for combo is consistent to AE profile of single agent, nooverlapping toxicity reported.
Registrational Stage with Breakthrough Potential
Ifebemtinib received fast track designation from the U.S. Food and Drug Administration (FDA) in August 2021, and breakthrough designation from China National Medical Products Administration (NMPA) in April 2022. A placebo-controlled, randomized, double-blind pivotal trial is ongoing in platinum-resistant ovarian cancer (PROC). The company plans to submit a New Drug Application to the NMPA in early 2025.
Ifebemtinib would have the biggest impacts via synergy with two unprecedent opportunities for cancer treatment: RASi and ADC, potentially powering toward IO therapy. Further expansions of ifebemtinib to pivotal trials in combination with RAS inhibitors and POC trials in combination with ADC are already in preparation.


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