News

Hollywood celebrities Kaley Cuoco, Mandy Moore and Elizabeth Olsen have designed the latest Charity by Design collection by eco-conscious jewelry brand Alex and Ani to benefit the Epidermolysis Bullosa Medical Research Foundation (EBMRF). To support the epidermolysis bullosa (EB) community, Cuoco, Moore and Olsen were each responsible for the design…

Researchers found two mutations in a gene that carries the instructions for the protein plectin in a patient with epidermolysis bullosa simplex (EBS). Plectin helps maintain the integrity of the skin, and the research team believes the mutations they found might be the cause of the disease in this patient. The…

Orphan Drug Designation was recently granted to ProQR Therapeutics’ investigational therapy QR-313 for the treatment of dystrophic epidermolysis bullosa (DEB) by the European Medicines Agency (EMA). Orphan Drug Designation (ODD) in Europe is granted to drug candidates intended for the treatment, prevention or diagnosis of diseases that…

Moin Younis, the ambassador for Acorns Children’s Hospice, won a Pride of Britain award as a “Teenager of Courage” for his character as a leader and for inspiring other children around him to stay strong despite life-limiting conditions. As the ambassador for Acorns, a center for children with life-limiting or life-threatening…

A group of physicians and researchers in Germany and Italy were quietly making history in 2015, aware they were doing something extraordinary but refraining from going public. They needed time to ensure their feat — giving a dying boy with epidermolysis bullosa (EB) genetically engineered new skin — would be a…

The National Organization for Rare Disorders (NORD) says it’s “disappointed and dismayed” after the House of Representatives voted 227-205 last week to repeal the Orphan Drug Tax Credit as part of a U.S. tax reform package. A similar package before the Senate Finance Committee does not repeal the credit…

Krystal Biotech recently announced that its leading investigational therapy for epidermolysis bullosa, KB103, has received clearance from the Recombinant DNA Advisory Committee. Krystal Biotech is a gene therapy company developing new therapeutics for dermatological diseases including epidermolysis bullosa. Its lead candidate KB103 is being studied as a potential treatment for dystrophic epidermolysis…

A 7-year-old boy with life-threatening epidermolysis bullosa has German and Italian researchers to thank for acquiring a new skin — and with it, the potential for a normal life. The team used genetically modified skin stem cells to grow new skin, which was successfully transplanted on 80 percent of the boy’s…

A potential gene therapy for dystrophic epidermolysis bullosa (DEB), KB103 by Krystal Biotech, has been designed an Orphan Drug by the U.S. Food & Drug Administration (FDA) to help it move along in preclinical testing. KB103 is the company’s lead candidate, and is intended to treat…

The gene therapy company Krystal Biotech has received a $700,000 equity-based award from the Epidermolysis Bullosa Research Partnership (EBRP) and the Epidermolysis Bullosa Medical Research Foundation (EBMRF) to continue developing a treatment for dystrophic epidermolysis bullosa (DEB). EBRP and EBMRF are nonprofit organizations dedicated to funding medical research in…

The biopharmaceutical company BERG was honored with a Partners in Progress Award from the Dystrophic Epidermolysis Bullosa Research Association of America (debra of America). The award recognized BERG’s efforts in developing new therapeutic strategies for epidermolysis bullosa (EB). “We’re honored to be recognized by debra…

Children’s National Health System no longer treats just kids. Its Rare Disease Institute, launched in April 2017, has partnered with the National Organization for Rare Disorders (NORD) to become the first of many U.S. “centers of excellence” to look after patients with rare diseases, regardless of age. The effort…