USP: 1. Orally active, monovalent IAP antagonist exhibits anti-tumor efficacy as a single agent 2. nM level target binding with nM level in vitro efficacy Colony formation Assay against chemotherapy resistant colon cancer cells 3. Oral Bioavailability 55 4. Better preclinical efficacy and bioavailability than existing Phase-II clinical trial comparators 5. Detailed molecular mechanisms deciphered for its mode of action 6. IAP antagonism is the major reason for its cytotoxic phenotype
Central Drug Research Institute Lucknow CDRI