NS Pharma @NSPharmaInc
Dedicated to improving patient outcomes in #Duchenne muscular dystrophy, eosinophilic granulomatosis with polyangiitis (#EGPA) and other #rarediseases. nspharma.com Paramus, NJ Joined April 2020-
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JFK once said, “Children are the world’s most valuable resource and its best hope for the future.” We were overjoyed to host our employees’ kids on Bring Your Kid to Work Day. Twenty amazing children visited our office for learning, crafts, pizza and a little bit of Mad Science.
We are grateful to be joining leading healthcare practitioners and pharmaceutical professionals this weekend at the 20th Asembia Specialty Pharmacy Summit. We look forward to connecting with everyone over the next few days. #Asembia24
Over the course of the next two days, we'll be at the 17th Annual Pediatric Neurology Symposium with @LeBonheurChild. We look forward to engaging in meaningful discussions on how to improve diagnoses and enhance treatment plans in #Duchenne and other nervous system disorders.
Visit We Speak Duchenne to learn more about exon-skipping therapies for #Duchenne. We Speak Duchenne Is Here to Help fb.watch/rEMIyXoDBA/ via @FacebookWatch
Happy #OTMonth! #OccupationalTherapy can help maximize independence and increase mobility for individuals living with #neuromuscular diseases. We want to thank all occupational therapists who work to improve the #qualityoflife for patients.
This weekend, we’re attending the @ParentProjectMD Together meeting to celebrate the 30th anniversary of this incredible organization. Visit us on Saturday at the Industry Vendor Fair to learn more about how we provide support to individuals living with #Duchenne.
#WeAreHiring: We’re looking for innovators who are passionate about challenging the status quo of treatments and resources available for individuals living with #RareDiseases. Check out our open positions to learn more: bit.ly/nspcareers.
We’re traveling to Colorado this week for the @AANmember Annual Meeting and looking forward to sharing new data on our #ExonSkipping candidate for #Duchenne. If you’re attending, visit us at booth 1665! #raredisease
A #ClinicalTrial is now enrolling participants over 18 years of age with eosinophilic granulomatosis with polyangiitis (#EGPA). Learn more about the study: bit.ly/42PhdBs.
#DYK NS Support provides patient care coordination and resources? Whether navigating the initial stages of a #Duchenne diagnosis or seeking treatment information, NS Support is here to assist families every step of the way. Contact us: bit.ly/3xplkIO.
Our team is heading to Long Island this weekend for the @CureDuchenne Family Workshop. We look forward to discussing ways to pave a positive path forward for the #Duchenne community. #raredisease
This weekend, we’re joining healthcare professionals, advocates, and families at the @JettFoundation Family Workshop to learn more about the latest research and developments in the #Duchenne space. We hope to see you there! #raredisease
Congratulations to our Innovation Research Partnering (IRP) team (pictured) on advancing our latest partnership! Our nucleic acid drug tech will meet @MiNA_Tx's #RNAa therapeutics. Read more: bit.ly/NSPnews. #neurology #RNA #raredisease
Yuki Kawabata works with our U.S.-based team and Japanese parent company, Nippon Shinyaku, to foster collaboration and help recognize our shared commitment of providing healthier futures through product innovation. Learn more about our mission: bit.ly/49zVQGz
We’re growing and looking for innovative thinkers to #JoinUs in our pursuit of delivering new treatment options to individuals living with #RareDiseases. View our open positions by visiting: bit.ly/48FxUjQ
Our pipeline is growing! We’re committed to developing advanced therapies to provide more treatment options for families impacted by #RareDiseases. Explore our pipeline here: bit.ly/49Vrn5U
#ICYMI we shared new data from the phase 2 trial assessing our FDA-approved treatment for #Duchenne. Read more about the findings presented at the #MDAConference: bit.ly/3Ve5xpT
#ICYMI we shared new data from the phase 2 trial assessing our FDA-approved treatment for #Duchenne. Read more about the findings presented at the #MDAConference: bit.ly/3Ve5xpT
#ICYMI: At the 2024 @MDAorg Clinical and Scientific Conference, we shared our new clinical trial data on pulmonary and motor function in ambulatory and non-ambulatory individuals living with #Duchenne. Read our press release to learn more: bit.ly/4319MHu #MDAconference
We are in awe of the drive and tenacity of our colleagues at NS Pharma. Thank you to all members of our team for working to provide healthier futures for individuals living with #RareDiseases. To learn more about who we are, visit: bit.ly/3wz2COv #EmployeeAppreciationDay
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#MDA families – Do you have a boy with #Duchenne #MuscularDystrophy (#DMD) who might benefit from exon 44 skipping therapy? @NSPharmaInc is looking for participants for a phase 2 clinical trial. Interested? Learn more in this Quest blog: mdaquest.org/clinical-study…
A hot new collab between the UK 🇬🇧 and Japan 🇯🇵 to advance small activating #RNA therapeutics for #CNS disorders leads our neuro news to end the week. More from @MiNA_Tx & @NSPharmaInc ⤵️ bit.ly/3TOushl
. @NSPharmaInc Announces Research Alliance with @MiNA_Tx to Develop Therapies for #RareDiseases of the Central Nervous System brnw.ch/21wIvvp
@NSPharmaInc recently joined PPMD for a community webinar to share an overview of two of the company’s new exon skipping trials: Brogidirsen (exon 44) and NS-050/NCNP-03 (exon 50). Watch the recording now: parentprojectmd.org/watch-ns-pharm…
Today, #MDA VP of Public Policy, @PMelmeyer, testified at the #ACHDNC meeting, covering the ongoing review of #Duchenne #MuscularDystrophy by the RUSP. Thanks to Dr. Kemper, the TEP, & the Committee for their diligence. @MDAorg is honored to contribute to the #DMD evaluation.
PPMD is excited to announce another significant milestone: Minnesota has officially approved the addition of Duchenne to the state’s newborn screening panel! Learn more: parentprojectmd.org/duchenne-added…
@NSPharmaInc Many thanks.
#Duchenne muscular dystrophy is a genetic #raredisease caused by a missing protein called dystrophin. We’re working to address this underlying cause and change the way families with Duchenne live, now and in the future.
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