Abeona Therapeutics

Living with Epidermolysis Bullosa (EB) comes with unique challenges including silent stares from strangers, bouts of anxiety and so much more. Listen to their voices and let's learn from their experiences. #patientvoices #nowyouknow #geneandcelltherapy #rdeb #abeonatherapeutics #patientinspiration #wefightEB

We were honored to participate in this year’s debra of America Care Conference. Thank you to everyone who stopped by our booth, attended our session, and shared their stories with us. Our team is still energized from meeting and connecting with the brave people living with Epidermolysis Bullosa. Abeona Therapeutics remains committed to making a difference in the lives of those affected by RDEB. Your strength and resilience continue to drive our mission. #patientcare #cellandgenetherapy #connectingwithEB #RDEB #abeonatherapeutics #innovation #wefightEB #patientinspiration

🌟Watch and see just how cool scientists are. At Abeona Therapeutics, our mission is driven by the incredible strength and resilience of the patients we aim to help. Every member of our team is fueled by the bravery of those living with Recessive Dystrophic Epidermolysis Bullosa (RDEB) 💪💙 #Geneandcelltherapy #RDEB #Abeonatherapeutics #Innovation #Scienceinaction #WeFightEB #Behindthescenes #Patientinspiration

🇺🇸 From Cleveland, Ohio, to the nation, Happy 4th of July. At Abeona Therapeutics, we're advancing cutting-edge gene and cell therapy to help those living with recessive dystrophic epidermolysis bullosa. This Independence Day, we celebrate the innovation and determination that drive us toward a brighter future for all. #IndependenceDay #cellandgenetherapy #RareDiseases #Innovation #AbeonaTherapeutics #RDEB #WeFightEB #PatrioticScience

Understanding leads to compassion and support. That is why knowledge is power. Swipe to learn 5 things about people living with Epidermolysis Bullosa. #wefightEB #whenyouknowyouknow #raredisease #EBLife #Abeonatherapeutics #Cellandgenetherapy

When you live with Recessive Dystrophic Epidermolysis Bullosa (RDEB), hope and life, like skin, are fragile. Watch and see how one RDEB dad is helping his daughter live with strength and pride. Happy Father's Day from Abeona Therapeutics.   #UnbreakableBonds #FathersDay #EBWarrior #WeFightEB #FamilyStrength #RDEB #Raredisease #Abeonatherapeutics

This week, Abeona Therapeutics is proudly attending the American Academy of Dermatology (AAD) Annual Meeting and the 36th Annual Society for Pediatric Dermatology Pre-AAD Meeting in San Diego. We are excited to be here and committed to supporting advancements in treatments for people living with severe dystrophic epidermolysis bullosa (DEB). Stay up to date on the latest advances in severe DEB by visiting bit.ly/3IpLygx #PreAAD2024 #AAD2024 #SevereDEB #RDEB #AbeonaTherapeutics #WeFightEB

This Rare Disease Day, listen to Dr. Karen Wiss talk about the possibilities and changing landscape of treatment for severe dystrophic epidermolysis bullosa (DEB) as we all work together to make a difference. At Abeona, we are dedicated to advancing therapies for severe DEB. Our commitment to innovation is steadfast, and every story of patient courage fuels our pursuit of new advancements. #WeFightEB #EpidermolysisBullosa #RDEB #SevereDEB #RareDiseaseDay

This morning, we provided an update on our progress on the FDA review for the pz-cel (prademagene zamikeracel) BLA for recessive dystrophic epidermolysis bullosa #RDEB, including completion by the FDA of both a Bioresearch Monitoring (BIMO) inspection of Abeona and the BLA mid-cycle review meeting. We are on track for the PDUFA date of May 25, 2024. Read our press release here bit.ly/3vZNGsm

Skincare routine for anyone living with RDEB hurts! Their skin is tender and raw. Cleaning it is described as one of the most painful parts of this disease. Click here bit.ly/46G4uky to learn more about people who live this rare skin condition called Recessive Dystrophic Epidermolysis Bullosa (RDEB). Abeona’s BLA submission for pz-cel for RDEB, has been accepted by the FDA for formal review with a PDUFA target action date of May 25, 2024. Read the press release here bit.ly/47SH5NZ #RDEB #raredisease #EBLife #Abeonatherapeutics #FightEB #Ebawareness