Saol Therapeutics (pronounced "Sail") is a privately held, clinical-stage, pharmaceutical company with operations in Roswell, GA, Dublin, Ireland and Hamilton, Bermuda. The company is focused on development activity in CNS disorders such as pain management and spasticity and orphan diseases. Saol is committed to providing and advancing therapeutic options for patients and the physicians treating these populations and currently has two Phase 2 trials and one Phase 3 trail underway in the United States.
External link for Saol Therapeutics
1000 Holcomb Woods Parkway
Suite 270
Roswell, GA 30076, US
First Floor, 9 Windsor Place
Dublin, Dublin 2 D02 YF30, IE
H.P. House 21 Laffan Street
Hamilton, HM 09, BM
Saol Therapeutics reposted this
Introducing our Leigh syndrome symposium speaker, David Penake. Dave will provide an update on Saol Therapeutics current activities and completed clinical trial in Pyruvate Dehydrogenase Complex Deficiency (PDCD). Approximately 5-10% of people with Leigh’s Syndrome also have PDCD and 25-30% of people with PDCD have Leigh syndrome. Please register at: https://lnkd.in/eMmX6ryB #leighsyndrome #mitochondrialdisease
Saol Therapeutics reposted this
Color and win prizes: https://lnkd.in/eG9YEdu9 Dedicated to the Mitochondrial Disease Awareness 2024! Prize 1: iPad Mini Prize 2: AirPods Prize 3: Amazon $50 gift card First 10 participants to enter will get a kid's book "Zara shares her stripes: a story about accepting your rare condition" (1 book per family). #WorldMitoWeek #colorformito #mitochondrialdisease #leighsyndrome
EY Announces David Penake of Saol Therapeutics as an Entrepreneur Of The Year® 2024 Southeast Award Finalist
More great work by parents and #hopeforpdcd to make national newborn screening a reality
Marketing Operations | Genetic Sciences, Thermo Fisher Scientific | Hope for PDCD Board Member | Rare Disease Mom 🧬 | Proud Military Wife
Fellow Hope for PDCD Foundation parent board member Layna O'Connor leading the charge for newborn screening efforts for #pdcd. Hear their story and why #newbornscreening is critical for this disease. Just another example of how the Hope for PDCD Foundation is dividing and conquering the path to a cure. We will not stop. #raredisease
On this Rare Disease Day, join Saol in honoring the strength and resilience of individuals facing the challenges of a rare disease, including those bravely navigating Pyruvate Dehydrogenase Complex Deficiency (PDCD). In solidarity with the rare disease community, we proudly display our stripes. Just as zebras stand out in their beauty and uniqueness, so do those living with rare diseases. We would like to extend our gratitude to organizations like National Organization for Rare Disorders, United Mitochondrial Disease Foundation, Cure Mito Foundation, MitoAction, and Hope for PDCD Foundation, whose unwavering advocacy provides crucial support to patients and families with a rare disease. PDCD, a rare genetic disorder impacting energy metabolism, presents formidable obstacles. Saol is proud to sponsor an ongoing trial for PDCD, and looks forward to the day when there are more treatments for rare diseases. As we #ShowYourStripes today let's raise awareness and advocate for the needs of the rare disease community. #RareDiseaseDay #Saolrx #PDCD🦓
Saol Therapeutics reposted this
I am thrilled to announce that SL-1009 has been granted Fast Track status by the FDA for the treatment of PDCD! This is a significant milestone for us at #saolrx as we work toward bringing the first approved treatment to patients. We are grateful to the FDA for their continued partnership and look forward to working closely with them to make this a reality. #PDCD https://lnkd.in/ek8eSkVn
Saol Therapeutics reposted this
Join us on Monday, Dec 11 at 12:00pm ET for a Bench-to-Bedside Clinical Trials Update with Abliva AB, Baylor College of Medicine, GenSight Biologics, Khondrion, Minovia Therapeutics , OMEICOS Therapeutics GmbH, Saol Therapeutics, Stealth BioTherapeutics, Tisento Therapeutics, and UCB. Register and find more info: https://lnkd.in/dS35SHF4
As we reach the end of World Mitochondrial Disease Awareness Week we want to thank the many Advocacy Groups, Physicians, Community Members, and Companies that are "warriors" in the continuing fight against mitochondrial diseases. Cure Mito Foundation United Mitochondrial Disease Foundation Hope for PDCD Foundation MitoAction #WorldMitoWeek #PDCD
We are excited to share our "Color for Mito" winners! Payton, a sister to an LS warrior, won the first prize - iPad Mini! Kinsley, a friend to an LS warrior won second prize - Airpods! Sabrina, won 3rd prize - Amazon gift card! We have received almost 50 entries, ALL were beautiful, the winners were chosen RANDOMLY. Thank you again to all for participating, we will be sharing all pictures in the coming weeks! Thank you to our wonderful sponsors Saol Therapeutics Reneo Pharmaceuticals Minovia Therapeutics Standigm #worldmitoweek #leighsyndrome #mitochondrialdisease
Today as part of World Mitochondrial Disease Week we would like recognize Hope for PDCD Foundation - they are working tirelessly to improve diagnosis and treatment of PDCD.
💚🧬💚 September 18 - 24 is World Mitochondrial Disease Week. Pyruvate Dehydrogenase Complex Deficiency is one of the most common types of mitochondrial disease. It is the second most common genetically resolved mitochondrial disorder in the NAMDC [1] and some experts believe it is the most common type of mitochondrial disease. An estimated 1 in 4,300 children will be born with a devastating mitochondrial disease yet children are not routinely tested for mitochondrial disease. [2] Mitochondrial disease is not a single disorder, but an umbrella term for dozens of individual disorders in which the body’s cells have problems producing energy. Treatments need to be individualized to the specific disease, there is no umbrella cure or treatment. Together, mitochondrial diseases are about as common as childhood cancer, yet they do not have the same level of awareness or understanding. [3] Sources: 1. Barca et al. (2020) Neurol Genet 6:402 2. Facts about Mitochondria. The Children's Hospital of Philadelphia. https://lnkd.in/gjr6yg8i... 3. Mitochondrial Disease | Boston Children's Hospital. #worldmitochondrialweek #mitochondrialdisease #mito #mitowarrior #mightymito #raredisease #lightupformito #weargreenformito #rarediseaseresearch #rarediseasewareness Saol Therapeutics United Mitochondrial Disease Foundation
Saol Therapeutics Announces Completion of Enrollment in Both the Phase II COMPASS Osteoarthritis Knee Pain Trial and the Phase II RAISE Limb Spasticity Trial https://lnkd.in/ghm8FJgi