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BeiGene Announces Clinical Data on Zanubrutinib to Be Presented at the 15th International Conference on Malignant Lymphoma (ICML)

CAMBRIDGE, Mass. and BEIJING, China, June 12, 2019 (GLOBE NEWSWIRE) -- BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160), a commercial-stage biopharmaceutical company focused on developing and commercializing innovative molecularly-targeted and immuno-oncology drugs for the treatment of cancer, today announced upcoming data in three oral presentations and one poster presentation on its investigational BTK inhibitor zanubrutinib at the 15th International Conference on Malignant Lymphoma (ICML), taking place June 18-22, 2019 in Lugano, Switzerland. The company will also host an investor conference call and webcast of mid-2019 clinical data updates on Thursday, June 20 at 8:00 a.m. EDT.
Oral Presentations:

Title:



Zanubrutinib in Patients with Relapsed/Refractory Mantle Cell Lymphoma



Session:



Focus on Mantle Cell Lymphoma



Date:



Wednesday, June 19



Time:



17:45 CEST



Lead Author:



Yuqin Song, M.D., Ph.D.




Title:



Zanubrutinib for Patients with Relapsed or Refractory Chronic Lymphocytic Leukemia



Session:



Session 3 a?? CLL



Date:



Thursday, June 20



Time:



14:45 CEST



Lead Author:



Wei Xu, M.D.




Title:



Zanubrutinib Plus Obinutuzumab in Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) or Relapsed/Refractory (R/R) Follicular Lymphoma (FL)



Session:



Focus on Non-Clinical and Early Clinical Data with New Combinations



Date:



Thursday, June 20



Time:



17:25 CEST



Lead Author:



Constantine S. Tam, M.D.

Poster Presentation:

Title:



Updated Safety and Efficacy Data in the Phase 1 Trial of Patients with Mantle Cell Lymphoma (MCL) Treated with Bruton Tyrosine Kinase (BTK) Inhibitor Zanubrutinib (BGB-3111)



Abstract Code:



191



Session:



Mantle Cell Lymphomas section



Dates and Times:



Wednesday, June 19 (12:00-17:00), Thursday, June 20 (9:00-17:00) and Friday, June 21 (9:00-18:30) CEST



Lead Author:



Constantine S. Tam, M.D.


Mid-2019 Clinical Data Update Conference Call and Webcast Information:BeiGene will host a conference call and webcast on Thursday, June 20 at 8:00 a.m. EDT. Investors and analysts are invited to join the conference call using the following dial-in information:U.S. Toll-Free: +1 (844) 461-9930
U.S. Toll: +1 (478) 219-0535
Hong Kong Toll-Free: +852 800 279 19250
China Toll-Free: +86 800 914 686
Conference ID: 1790069A live webcast of the conference call can be accessed from the investors section of BeiGenea??s website atAhttps://ir.beigene.com/ or https://hkexir.beigene.com. An archived replay will be available two hours after the event for 90 days.About ZanubrutinibZanubrutinib (BGB-3111) is an investigational small molecule inhibitor of Brutona??s tyrosine kinase (BTK) discovered by BeiGene scientists that is currently being evaluated in a broad pivotal clinical program globally as a monotherapy and in combination with other therapies to treat various B-cell malignancies.Clinical trials of zanubrutinib include a fully-enrolled, global Phase 3 clinical trial in patients with WaldenstrAm macroglobulinemia (WM) comparing zanubrutinib to ibrutinib, currently the only approved BTK inhibitor for WM; a global Phase 3 clinical trial in patients with previously untreated chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL); a pivotal Phase 2 trial in patients with relapsed/refractory (R/R) follicular lymphoma in combination with GAZYVAA (obinutuzumab); a pivotal Phase 2 trial in patients with R/R marginal zone lymphoma (MZL); a Phase 3 trial comparing zanubrutinib to ibrutinib in patients with R/R CLL/SLL; and a global Phase 1 trial. In China, BeiGene has completed two pivotal Phase 2 clinical trials of zanubrutinib in patients with MCL and CLL/SLL and the enrollment in the pivotal Phase 2 clinical trials in patients with WM.Zanubrutinib has been granted by the U.S. Food and Drug Administration (FDA) Fast Track designation for the treatment of patients with WM, and Breakthrough Therapy designation for the treatment of adult patients with MCL who have received at least one prior therapy. The NDAs in China for R/R MCL and R/R CLL/SLL have been accepted by the China National Medical Products Administration (NMPA) and granted priority review.About BeiGeneBeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly-targeted and immuno-oncology cancer therapeutics. With a team of approximately 2,400 employees in China, the United States, Australia and Europe, BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for cancer. BeiGene is also working to create combination solutions aimed to have both a meaningful and lasting impact on cancer patients. BeiGene markets ABRAXANEA (nanoparticle albumina??bound paclitaxel), REVLIMIDA (lenalidomide), and VIDAZAA (azacitidine) in China under a license from Celgene Corporation.1Investor ContactAAAA AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA Media Contact
Craig WestAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA Liza Heapes
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ir@beigene.com AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA media@beigene.com1 ABRAXANEA, REVLIMIDA and VIDAZAA are registered trademarks of Celgene Corporation.
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