Epizyme To File NDA For Tazemetostat In Follicular Lymphoma

 | Jan 07, 2019 06:14AM ET

Epizyme, Inc. (NASDAQ:EPZM) announced that it has identified a path to submission for accelerated approval of its lead candidate, tazemetostat for patients with relapsed and/or refractory follicular lymphoma (FL), both with and without EZH2 activating mutations, where patients’ disease has progressed following two or more lines of therapy.

The company held a meeting with the FDA to discuss the same based on the current patient population in its ongoing phase II study. The company expects to submit a new drug application (NDA) for the stated indication in the fourth quarter of 2019. The NDA submission for FL will be the company’s second NDA, following its first submission for epithelioid sarcoma (ES). Epizyme will further advance the phase II study, with updated data to be reported at a medical meeting in mid-2019.

As part of an accelerated approval strategy, Epizyme plans to conduct a confirmatory program to support full approval of tazemetostat in FL, while also supporting its potential expansion into the second-line treatment of FL.

Epizyme is also advancing preparations for its first NDA submission for tazemetostat, using the accelerated approval pathway, for the treatment of patients with ES. This NDA is expected to be submitted in the second quarter of 2019.

Share price of Epizyme decreased 39.2% in the past year compared with the industry ’s decline of 20.6%.