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Asset Modality / Target Regimen Indication Discovery Pre-Clinical FIH POC Pivotal
IN10018         Small molecular FAK inhibitor + PLD  PROC (double-blind, placebo controlled, randomized study)
 
+ MEKi ± IO IO-failed NRAS melanoma Uveal melanoma
 
+ PLD ± IO PROC, TNBC, HNSCC
 
+ chemotherapy + IO IO-failed NSCLC (randomized study)
 
+ chemotherapy + IO bispecific Pancreatic cancer
 
+ KRASG12C inhibitor KRASG12CCRC and NSCLC
 
+3rd EGFR inhibitor EGFR mutant NSCLC
 
OMTX705 ADC Targeting FAP Mono / Combo Solid Tumor
 
INES103 Antibody Target undisclosed Combo Solid Tumor
 
IN30718 ADC Target undisclosed Mono Solid Tumor
 
IN30728 ADC Target undisclosed Mono Solid Tumor
 
IN20019 Small molecular Target undisclosed Mono Solid Tumor
 

IN10018

IN10018 is a highly potent and selective inhibitor of the focal adhesion kinase (FAK). Anti-tumor activities of IN10018 have been demonstrated in multiple animal models for human cancers. More than 250 patients have been dosed and IN10018 has showed its safety and promising efficacy signal in platinum ovarian cancer and NRAS melanoma.

OMTX705

IN30705 is an ADC formed by a new humanized anti-FAP mAb that has been conjugated to a novel cytolysin, TAM470, a synthetic microtubule inhibitor from the tubulysin family. IN30705 is designed to target FAP-expressing Cancer Associated Fibroblasts (CAFs) in tumor microenvironment. 

INES103

INES103 is an injectable recombinant humanized VHH (single variable domain of heavy chain, VHH)-Fc fusion protein against tumor associate macrophage(TAM)related target, to be administered for treatment of advanced or metastatic solid tumor and hematological malignancies. INES103 is designed to improve tissue penetration against solid tumors.

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