MorphoSys BLA For Cancer Drug Gets Priority Review From FDA

 | Mar 02, 2020 02:55AM ET

Germany-based MorphoSys AG (NASDAQ:MOR) announced today that the FDA has accepted its Biologics License Application (BLA) and granted Priority Review to lead pipeline candidate, tafasitamab.

Tafasitamab is the company’s experimental anti-CD19 antibody, which is being evaluated in combination with Revlimid for the treatment of relapsed or refractory diffuse large B cell lymphoma (r/r DLBCL).

The BLA was submitted at the end of last year. The FDA has set a Prescription Drug User Fee Act (PDUFA) goal date of Aug 30, 2020.

The FDA has informed the company that they are not currently planning to hold an advisory committee meeting to discuss the application.

The BLA was submitted based on the primary analysis data from the L-MIND trial of tafasitamab in combination with Bristol Myers’ (NYSE:BMY) Revlimid in patients with r/r DLBCL and the retrospective observational matched control cohort of Re-MIND, evaluating efficacy outcomes of r/r DLBCL patients who received lenalidomide monotherapy.

We note that Priority Review is granted to therapies that the FDA determines to have the potential to provide significant improvements in the treatment, diagnosis or prevention of serious conditions. This designation shortens the review period to six months compared to 10 months of standard review.

The above-mentioned combination was granted Breakthrough Therapy designation by the FDA in r/r DLBCL in 2017.

In 2010, MorphoSys licensed exclusive worldwide rights to develop and commercialize tafasitamab from Xencor, Inc. (NASDAQ:XNCR) . Per the terms of the collaboration and licensing agreement, the FDA acceptance of the BLA of tafasitamab triggers an undisclosed milestone payment to be received by Xencor from MorphoSys.

A potential approval will boost growth prospects of this clinical-stage biopharmaceutical company, which primarily focuses on cancer treatments.

The company’s shares have gained 0.8% in the past year against the industry ’s decline of 11.5%.