Catalyst @CatalystForRare
We are committed to improving the lives of patients with rare diseases. catalystpharma.com Coral Gables, FL Joined October 2013-
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🎙️: Prioritizing Access “Who’s improving access to care—and what do they need?” “We owe it to the community to keep them in the forefront of our minds.” Darby Garvin, from @RareDiseases, & Carrie Ostrea break down our shared responsibility to rural rare disease communities and…
Our team was honored to attend @ParentProjectMD Together in Charlotte and meet some incredible families who shared their stories with us. We learned so much about the resources available to the Duchenne community and what really matters to families on this journey. Thank you to…
Catalyst Pharmaceuticals is honored to join forces with the Myasthenia Gravis Foundation of America, Inc. for the 2025 Chicago Community Health Fair. This vital partnership highlights our shared commitment to supporting and empowering those living with myasthenia gravis (MG),…
We're thrilled to announce that we're at PPMD Together once again! This incredible event brings together families of individuals with Duchenne muscular dystrophy (DMD), leading researchers, and a community all eager to connect, share, and learn from one another. We invite you…
Team Catalyst recently went to the @GreatDebatesCME in Solid Tumors Conference in Miami, FL. Our team appreciated the insights shared by Dr. Langer during his lunchtime symposium on the impact of Lambert-Eaton myasthenic syndrome (LEMS) on patients with small cell lung cancer…
If you're at @GreatDebatesCME's Great Debates in Solid Tumors conference #GDST, stop by the Catalyst Innovation Theater in Salon B at 12:45PM to listen to Corey J. Langer, MD, FACP, discuss Neurologic Paraneoplastic Syndromes and the Impact of Lambert-Eaton Myasthenic Syndrome…
Are you attending @GreatDebatesCME's Great Debates in Solid Tumors conference #GDST in Miami? Visit Catalyst's booth to learn more about Lambert-Eaton myasthenic syndrome (LEMS), a rare neuromuscular disorder often associated with small cell lung cancer (SCLC). We look forward to…
"What was once new, unfamiliar, and uncomfortable to me is now my new normal." You are never alone when it comes to having Lambert-Eaton myasthenic syndrome (LEMS). In our blog post, read more about how a patient has been living her life for the past six years. From deciding…
Here at Catalyst, we don't take for granted the opportunity to collaborate with global leaders in Duchenne research, patient care, and innovation dedicated to improving and extending the lives of those affected by the disease. That's why we're proud to once again sponsor an event…
Catalyst is pleased to share that our President and CEO, Richard Daly, is attending the @HCWCO's 27th Annual Global Investment Conference in New York. We invite you to tune in for insights into the latest developments in the biotech investment space from Rich and others with…
Catalyst is pleased to share that our President and CEO, Richard Daly, is attending the @HCWCO's 27th Annual Global Investment Conference in New York. We invite you to tune in for insights into the latest developments in the biotech investment space from Rich and others with…
Today is World Duchenne Awareness Day (#WDAD). This date, 7/9, recognizes the 79 exons of the dystrophin gene that are linked to Duchenne muscular dystrophy (DMD). DMD is a rare and progressive genetic disorder that causes muscle weakness. It's estimated to affect up to 1 in…
Get ready for World Duchenne Awareness Day on September 7th! Catalyst is thrilled to be involved, and we're inviting you to join the @JettFoundation's in-person and virtual events, with t-shirts and more. Tomorrow, we're coming together to honor, raise awareness for Duchenne…
Attending the Academia Puertorriqueña de Neurología's 2025 Jornadas Neurológicas #APNMeeting2025? Join Alexandra Montalvo Acevedo, MD on September 6 at 11:45 AM in Ballroom B for a session discussing Insights in Action: The AGAMREE® Clinical Profile.
Team Catalyst is at @ASBMR's 2025 Annual Meeting #ASBMR2025 in Seattle! Visit booth #100 to learn more about our work in Duchenne muscular dystrophy (DMD), a rare neuromuscular disease. We look forward to engaging with healthcare professionals on current approaches to care and…
Team Catalyst is at Academia Puertorriqueña de Neurología's 2025 Jornadas Neurológicas #APNMeeting2025 in Puerto Rico, supporting education and awareness in rare neuromuscular disease. Visit booth #39 to explore our latest initiatives and connect with peers in the field.
Catalyst Pharmaceuticals is excited to partner with the @MyastheniaOrg for the 2025 Boston Community Health Fair. We look forward to meeting families, hearing your stories, and discussing your experiences with myasthenia gravis (MG). Because symptoms of MG can overlap with other…
🎙️: Care Knows No Map Before outreach begins, ask: How far is care—really? Can emergency help arrive in time? Terri Klein, President & CEO of the MPS Society, explains why defining rural through patient experience must come first to give the access that they deserve.…
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