
Santhera
@Santhera
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#Santhera is passionate about improving the lives of patients suffering from a rare disease. #Duchenne #DMD #neuromuscular #theirfutureourfocus #raredisease
Pratteln, Switzerland
Joined July 2009
At #Santhera, we recognize the vital significance of #InternationalWomensDay in celebrating the achievements and contributions of women worldwide. Together, let's continue to champion for opportunities for women in our organization and beyond. #IWD2024 #EmpowerWomen #WomenLeaders
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At #Santhera, we are dedicated to developing medicines to meet the needs of patients living with #raredisease. Please join us in recognizing #RareDiseaseDay on February 29, 2024, when we come together to raise awareness for rare disease! #theirfutureourfocus #Duchenne #DMD
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With rare disease day coming up on February 29, Dr. Kerry Nip, our Head Medical Affairs EU & ROW, shares what it means to her in her role at Santhera. #Santhera #theirfutureourfocus #Duchenne #DMD #rarediseaseday #raredisease #showyourcolours
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We are thrilled to announce that the U.S. FDA has approved our novel corticosteroid drug for the treatment of #Duchenne muscular dystrophy (#DMD) in children and adults aged 2 years and older. Read more here #Santhera #theirfutureourfocus
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#Santhera and Catalyst are proud to partner in the development of an innovative therapy to address unmet needs in the #Duchenne muscular dystrophy community! Our med reps are welcoming HCPs at #WMS2023 booth #19. #theirfutureourfocus #musculardystrophy #DMD
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We are participating in the 2023 WMS World Muscle Society conference! Our medical representatives are looking forward to meeting health care professionals at our scientific exhibit (booth #19). #Santhera #theirfutureourfocus #Duchenne #musculardystrophy #DMD #WMS2023
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We're at the H.C. Wainwright & Co, LLC 25th Annual Global Investment Conference in NYC! Our CEO Dario Eklund will share updates and future goals of #Santhera. Join him on Sep 12, 2023, at 10:00 AM EDT, room Kennedy II, Lotte NY Palace Hotel. #HCWainright #investorconference #DMD
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Excited to be at the #CureDuchenne Futures Conference in San Diego/CA which is focused on bringing education, connection, and hope to the #Duchenne community. Visit our booth to learn about our mission to improve the lives of those living with #DMD. #Santhera #theirfutureourfocus
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Next week, #CureDuchenne will bring patients, caregivers & HCPs together for the CureDuchenne Futures Conference. We are proud to have Rob Halter, Field Medical Director, speaking as part of a panel on preserving muscle during Friday’s (April 21) agenda. #santhera #Duchenne #DMD
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Congratulations @WHO on your 75th anniversary. HEALTH FOR ALL All envisions that all people have good health for a fulfilling life in a peaceful, prosperous, and sustainable world. #HealthForAll #WHO75 #santhera #theirfutureourfocus #Duchenne #DMD
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Proud to be a partner of @mdaorg’s 2023 MDA Clinical & Scientific Conference in Dallas, March 19-22. The conference will explore the latest research advancements & clinical achievements in #neuromuscular disease. Learn more: #MDAconference #MDA #Santhera
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#Duchenne muscular dystrophy is a rare muscle disorder affecting approx. 1 in 3,500–5,000 male births worldwide, mostly diagnosed between the ages of 2-6. On Feb 28, #Santhera will recognize #RareDiseaseDay to raise awareness of those living with #DMD and other rare diseases.
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