It's sure that a successful drug should be dosing-dependent in efficacy. While, is the dosing-dependent in safety study strictly required? When the dosing-independent occured in safety, how to explain this phenomenon. In my study (repeated 3 times), a compound for cancer exhibited dosing-independent. In different dose groups (1 mpk, 10 mpk, 25 mpk and 50 mpk), the body weight of mice decrease ~15% compared with placebo group. Someone can give me a answer or articles?