One of the most exciting advantages of the TREAT-NMD trial site and patient registries is the way they enable companies to conduct market analyses and feasibility assessments with far less effort and at an earlier stage than before. Questions ranging from the number of patients per country fulfilling certain inclusion criteria to the number of trial sites with experience in a particular technique or study type can be answered with a targeted feasibility enquiry to our registries, resulting in valuable information that can help companies establish how many sites would be required to fulfil their recruitment goals or how many countries they would need to run their study in.
All of the TREAT-NMD registries keep the same mandatory dataset. Details of the data set for each disease is shown below.
Since this information is so readily available through our registries, we encourage companies to complete one of the forms below or contact us at email@example.com to express your interest at an early stage in their trial planning, as an early enquiry based on preliminary data can help focus and refine trial plans.