
Orchard Therapeutics - U.S.
@orchard_tx
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Dedicated to transforming the lives of patients with inherited diseases through innovative gene therapy.
Joined January 2017
At Orchard, diversity is key to our strength and vibrancy, which is why inclusion and allyship are not confined to one day, week or month. #OrchardProud
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Tomorrow is International Neonatal Screening Day. We stand with like-minded organizations dedicated to advancing #NewbornScreening for treatable genetic diseases. Learn more:
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Today is #MPSAwarenessDay. We join with the community to shine a light on this group of rare, life-limiting, inherited genetic diseases. Learn more at:
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We are honored to recognize and celebrate #RareDiseaseDay with the more than 300 million people worldwide living with a rare disease. Learn more about how to get involved: #RareDiseaseDay #ShowYourRare #EndTheDiagnosticOdyssey #SupportRareDiseases
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We look forward to participating in the @RSTMH event “Unveiling Gene Therapy: Transforming medical practice through ATMPs.” Learn more:
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We are excited to join the leukodystrophy community in taking strides to support @ELAOfficielle ‘Met tes baskets’ (wear your trainers) at work international challenge! Learn more at:
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Today is #MPSAwarenessDay. We join with the community to shine a light on this group of rare, life-limiting, inherited genetic diseases. Learn more at:
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We are incredibly proud our fearless leader, Dr. @bobby_gaspar, has been named to the inaugural 2024 #TIME100HEALTH list. Please read our press release for more information: and see the full list of honorees here:
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We are thrilled to announce that the @US_FDA has approved Lenmeldy™ (atidarsagene autotemcel), the only therapy for eligible children with early-onset metachromatic leukodystrophy in the U.S. Read more in our press release:
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On #RareDiseaseDay please join us in helping raise awareness and #ShowYourColours in support of the millions of people living with rare diseases. Learn more at
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We look forward to participating in @WORLDSymposia 2024 and hosting a symposia featuring expert speakers sharing their knowledge and experience to establish new standards and advance #newbornscreening through interdisciplinary collaboration. Learn more:
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Today is World Sanfilippo Awareness Day. Join us in spreading awareness about this rare and life-limiting neurometabolic disease. Visit @CureSanfilippoF for more information: #WorldSanfilippoDay
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We look forward to joining @RareDiseases at this week’s #NORDSummit where our Chief Medical Officer Leslie Meltzer, Ph.D., will participate in a panel on opportunities in cell and gene therapy. Learn more:
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