News
Events
2020/08/22
On Demand Video Available: COLLABORATIONS THAT TRANSFORM | Rare Disease: Spinal Muscular Atrophy
Online Forum
Throughout our "Collaborations That Transform" rare disease series, we have seen countless examples of rare disease R&D breakthroughs resulting from great partnerships and global collaboration. Spinal Muscular Atrophy is a rare disease community, which holds no exception to this trend.
Read more2020/08/13
Announcing Full Program for "Collaborations That Transform" Webinar Series: Progress in Halting Spinal Muscular Atrophy (SMA)
Online Forum
August is the month each year when special efforts are made to raise awareness of patients suffering from Spinal Muscular Atrophy (SMA), a crippling, degenerative neuromuscular disease. In its most severe form, SMA is the leading genetic cause of infant death. WuXi AppTec welcomes the opportunity to contribute to SMA Awareness Month this year through our next webinar, "Progress in Halting Spinal Muscular Atrophy", on August 20.
Read more2020/07/22
On Demand Video Available: COLLABORATIONS THAT TRANSFORM | Rare Disease: Hemophilia
Online Forum
More than 600 colleagues and friends signed up for the promising developments in the treatment of the rare bleeding disorder hemophilia during the second WuXi AppTec webinar series "Collaborations That Transform".
Read more2020/07/13
Join us July 16 for a Special Webinar on Collaborations that Transform | Advances in Rare Diseases: Hemophilia
Online Forum
WuXi AppTec is pleased to invite you to join us for the second session of our webinar series “Collaborations That Transform,” highlighting the impact of partnerships in bringing effective therapies to patients.
Read more2020/05/19
Collaborations That Transform: Rare Disease Neurofibromatosis
Online Forum
In honor of World Neurofibromatosis (NF) Awareness Month, the WuXi AppTec community is proud to join the millions around the world working to enhance our understanding of this rare disease. To this end, on May 15 WuXi AppTec – in close collaboration with the Children’s Tumor Foundation and other vital partners – convened a multi-track webinar series on neurofibromatosis, rare disease research awareness, industry collaborations and innovations.
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