The mpn Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the mpn Hub cannot guarantee the accuracy of translated content. The mpn and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The MPN Hub is an independent medical education platform, sponsored by AOP Health and GSK, and supported through an educational grant from Bristol Myers Squibb. The funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Now you can support HCPs in making informed decisions for their patients
Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.
Find out more
Create an account and access these new features:
Bookmark content to read later
Select your specific areas of interest
View mpn content recommended for you
New agents in the MF therapeutic landscape
Jean-Jacques Kiladjian
Tiziano Barbui
Laura Michaelis
Haifa Kathrin Al-Ali
Steffen KoschmiederDuring the MPN Hub Steering Committee meeting, we invited Steffen Koschmieder, Uniklinikum RWTH Aachen, Aachen, DE, to give a presentation and chair a discussion on new agents in the myelofibrosis (MF) therapeutic landscape. MPN Hub Steering Committee members Jean-Jacques Kiladjian, Haifa Kathrin Al-Ali, Tiziano Barbui, and Laura Michaelis joined the discussion.
New agents in the MF therapeutic landscape
In this video, Steffen Koschmieder discusses recent clinical trials in MF, including MOMENTUM, BOREAS, IMpactMF, MANIFEST-2, TRANSFORM-1, LIMBER-313, and INDEPENDENCE. Koschmieder details the study designs and endpoints, as well as results data available to date. The committee members discuss data from each trial and the potential implications for the management of MF.