LET THE FDA KNOW ABOUT YOUR EXPERIENCE LIVING WITH PV, ET OR MF!
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MICHELLE WOEHRLE | JULY 08, 2019
You may have heard that MPNRF, along with fellow MPN advocates, is holding an externally-led Patient Focused Drug Development meeting with the FDA this September. If you are living with PV, ET or MF we are making sure your voice counts and is heard by the FDA. One of the means of doing this is collecting feedback via a quick phone survey with two questions:
- What has been the most difficult part of living with this disease for you?
- How has your diagnosis impacted the fulfillment of your life goals?
It will only be open for the month of July so please don’t hesitate to dial in and participate at your earliest convenience! Responses to this survey will be used in an audio montage of patient testimony during the meeting as well as in the follow-up Voice of the Patient report.
The number to dial is (877) 851-5399
There will also be the opportunity to attend in person or via the webinar as this meeting is open to the public. Our goal is to represent all perspectives from the MPN community so that FDA is as well informed as possible about YOUR experience living PV, ET, and MF as they look at clinical trial designs, data, outcome measures, etc.