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Epizyme, a commercial-stage biopharmaceutical company, will host a conference call on November 9, 2021, at 8:30 a.m. ET to discuss its third quarter 2021 financial results and provide a business update. The call can be accessed at (877) 844-6886 for domestic callers and (970) 315-0315 for international participants. A live webcast will also be available on their website. Epizyme focuses on developing epigenetic therapies, currently offering one FDA-approved product, TAZVERIK®, for specific cancer indications.
Positive
Epizyme has one FDA-approved product, TAZVERIK®, enhancing its market position.
Potential expansion in treatment indications for TAZVERIK® through ongoing clinical trials.
Negative
Continued approval of TAZVERIK® is contingent upon verification of clinical benefits in confirmatory trials.
CAMBRIDGE, Mass.--(BUSINESS WIRE)--
Epizyme, (Nasdaq: EPZM), a fully integrated, commercial-stage biopharmaceutical company developing and delivering novel epigenetic therapies, today announced that management will host a conference call to discuss its third quarter 2021 financial results and provide a business update on Tuesday, November 9, 2021 at 8:30 a.m. ET.
To participate in the conference call, please dial (877) 844-6886 (domestic) or (970) 315-0315 (international) and refer to conference ID 8536979. A live webcast will be available in the investor section of the company's website at www.epizyme.com, and will be archived for 60 days following the call.
About Epizyme, Inc.
Epizyme, Inc. is a fully integrated, commercial-stage biopharmaceutical company committed to its mission of rewriting treatment for cancer and other serious diseases through novel epigenetic medicines. In addition to an active research and discovery pipeline, Epizyme has one U.S. FDA approved product, TAZVERIK® (tazemetostat), for the treatment of adults and pediatric patients aged 16 years and older with metastatic or locally advanced epithelioid sarcoma (ES) who are not eligible for complete resection; adult patients with relapsed or refractory follicular lymphoma (FL) whose tumors are positive for an EZH2 mutation as detected by an FDA-approved test and who have received at least two prior systemic therapies; and adult patients with relapsed or refractory follicular lymphoma who have no satisfactory alternative treatment options. These indications are approved under accelerated approval based on overall response rate and duration of response. Continued approval for these indications may be contingent upon verification and description of clinical benefit in a confirmatory trial(s). The company is also exploring the treatment potential of tazemetostat in investigational clinical trials in other solid tumors and hematological malignancies, as a monotherapy and combination therapy in both relapsed and front-line disease settings. By focusing on the genetic drivers of disease, Epizyme seeks to match medicines with the patients who need them. For more information, visit www.epizyme.com.
TAZVERIK® is a registered trademark of Epizyme, Inc.
