Emmaus Life Sciences submits NDA to FDA for sickle cell disease treatment

The NDA represents the first potential treatment for pediatric patients with sickle cell disease, and the first potential new treatment in nearly 20 years for adult patients. Emmaus is requesting Priority Review of the application.

Emmaus chairman and CEO Yutaka Niihara said: “We would like to thank the NIH, FDA and Ajinomoto Corporation for the funding of our early work at LA BioMed.

“We are also thankful to our clinicians, employees, and partners for their efforts and to our investors for funding the work.”

“We are pleased to submit our NDA during National Sickle Cell Disease Awareness Month, and following the formation of the Sickle Cell Disease Coalition spearheaded by the American Society of Hematology,” Dr. Niihara added.  “We hope our NDA submission will result in a change of the status quo of Sickle Cell Disease treatment.”

Data from the Company’s Phase 3 sickle cell disease trial demonstrated a reduction in the frequency of sickle cell crises and hospitalizations, as well as a reduction in cumulative days hospitalized, and a lower incidence of the life-threatening acute chest syndrome. 

The clinical trial enrolled 230 adult and pediatric patients as young as five years old, across 31 experienced sickle cell disease treatment centers in the United States.  No major adverse events were attributable to the treatment.

Emmaus’ sickle cell disease therapy has Orphan Drug designation in the U.S. and Europe and Fast Track designation from the FDA.  Emmaus also plans to submit a marketing authorization application to the European Medicines Agency.

About Sickle Cell Disease

Sickle Cell Disease is an inherited blood disorder characterized by the production of an altered form of hemoglobin which polymerizes and becomes fibrous, causing red blood cells to become rigid and change form so that they appear sickle shaped instead of soft and rounded. Patients with Sickle Cell Disease suffer from debilitating episodes of sickle cell crisis, which occur when the rigid, adhesive and inflexible red blood cells occlude blood vessels. 

Sickle cell crisis causes excruciating pain as a result of insufficient oxygen being delivered to tissue, referred to as tissue ischemia, and inflammation. These events may lead to organ damage, stroke, pulmonary complications, skin ulceration, infection and a variety of other adverse outcomes.

Sickle Cell Disease is an orphan disease in the U.S affecting approximately 100,000 patients in the U.S and millions worldwide with significant unmet medical needs.