OUR STORY
Our Story
In June 2017, the International Clinical Council (ICC) on Fibrodysplasia Ossificans Progressiva FOP was established to help consolidate a global voice for the best practices for clinical care and clinical research for people who suffer from FOP. The ICC is an autonomous and independent group of 21 internationally-recognized clinician experts in FOP from 14 nations (Argentina, Australia, Brazil, Canada, China, France, Germany, Italy, Japan, Netherlands, South Africa, South Korea, United Kingdom, and United States) and six continents (Africa, Asia, Australia, Europe, North America and South America).
“During the past 25 years, the Fibrodysplasia Ossificans Progressiva (FOP) community has moved from the wastelands of a rare disease to the watershed of clinical trials. Together, we identified the genetic cause of FOP and used that knowledge to spearhead worldwide research efforts to develop therapies that will transform the care of individuals with FOP. We have expanded the frontiers of discovery and drug development, dismantled the physical and perceptual barriers that have impeded progress, and inspired global research in small molecules, antibodies, and gene therapy for FOP. We have formulated best practices and assembled teams of experts to optimize ambulatory and in-patient care of the FOP patient.”
ICC Members
First row: Fred Kaplan, Robert Pignolo, Ed Hsiao, Mona Al Mukaddam, Patricia Delai, Richard Keen, Chris Scott
Second row: Elisabeth Marelise Eekhoff, Zvi Grunwald, Genevieve Baujat, Robert J. Diecidue, Vrisha Madhuri, Clive Friedman, Carmen De Cunto,
Third row: Alberto Hidalgo-Bravo, Jung Min Ko, Raphaella Stander, Clemens Stockklausner, Staffan Berglund
Associate Members
Xiaobing Yu, Javier Bachiller Corral, Angela Cheung, Lisa Friedlander, Johannes Roth
Advisory Members
Tae-Joon Cho, Michael Zasloff, Keqin Zhang, Rolf Morhart, J. Coen Netelenbos
The ICC & FOP
Presentation
by Frederick S. Kaplan, M.D.
