What will study participants be asked to do?

If you decide to participate in the FAR-131 clinical research study, you will be asked to:

• Provide informed consent
  Informed consent is the process of learning key facts about a clinical trial before deciding whether to participate. This process also continues throughout the trial to provide you with additional information that may become available during the trial. You will be given an informed consent document. This document includes clinical trial details, risks and benefits, and an explanation of your rights as a clinical trial participant.
  
  
• Speak with the study staff about your current health and medical history
  
  
• Attend study visits
  
  
• Receive the study drugs by infusion
  
  
• Undergo study-related assessments and laboratory tests
  
  
• Have periodic CT scans, MRIs, or x-rays
  
  

Trial participation is voluntary and you may stop at any time. Please ask your doctor or nurse for more information about your rights as a clinical trial participant.

 

Thank you for your interest in the FAR-131 study. At this time we are no longer recruiting patients for this study.