Ascentage reports Phase I safety data for IAP inhibitor in solid tumors
Ascentage Pharma Group Corp. Ltd. (Hong Kong, China) said IV APG-1387 once every week for three out of four weeks in each 28-day cycle was well tolerated with manageable adverse events in 28 evaluable patients with advanced solid tumors in a Phase I trial. The data were released in an abstract ahead of the American Society of Clinical Oncology (ASCO) meeting in Chicago.
The most common treatment-emergent adverse events reported were vomiting, abdominal pain, anemia, cough, headache, elevated aspartate aminotransferase (AST) levels and ventricular arrhythmia. The maximum tolerated dose (MTD) has not yet been reached...
BCIQ Target Profiles