A clinical trial has potential benefits and risks. The study drug has already undergone a lot of testing and investigation to understand the drug safety and side effects. Your study doctor will inform you of the known risks and side effects of the study drug and trial related test procedures. You will be informed in a timely manner whenever new information becomes available that may be relevant to your safety and your willingness to continue participation in a trial. Throughout the clinical trial, you will be assessed carefully for any side effects and you will be treated accordingly. You will be closely monitored by your study doctor and his/her study team, with extra follow-up care provided to ensure your safety and well-being. Your participation in the clinical trial may be terminated at any time if it is determined by your study doctor to be in your best interest, safety and well-being. Patient rights, safety and well-being are primary emphasis in a clinical trial.