Celgene (CELG) Submits NDA For MS Drug To FDA For Review

 | Mar 26, 2019 05:15AM ET

Celgene Corporation (NASDAQ:CELG) announced that it has submitted a New Drug Application (NDA) to the FDA for multiple sclerosis (MS) candidate, ozanimod.

Ozanimod, an oral, sphingosine 1-phosphate (S1P) receptor modulator, is currently being evaluated for the treatment of relapsing forms of multiple sclerosis (RMS).

The NDA contains efficacy and safety data from the SUNBEAM and RADIANCE part B phase III, multicenter, randomized, double-blind, double-dummy, active-controlled studies.

We remind investors that the company suffered a setback early 2018, when it received Refusal to File letter from the FDA regarding its NDA for ozanimod. The FDA stated that the nonclinical and clinical pharmacology sections in the NDA were inadequate to allow a complete review.

Celgene has also submitted its application for review in Europe for the same.

Ozanimod is also being evaluated for ulcerative colitis and Crohn's disease.

Celgene’s stock has lost 0.4% in the past six months compared with the industry ’s decline of 18.4%.