Welcome to our dedicated page for Zymeworks news (Ticker: ZYME), a resource for investors and traders seeking the latest updates and insights on Zymeworks stock.
Zymeworks Inc. (Nasdaq: ZYME) generates frequent news flow as a biotechnology and clinical-stage biopharmaceutical company managing licensed healthcare assets while developing a diverse pipeline of novel, multifunctional biotherapeutics. Company announcements highlight its focus on difficult-to-treat diseases, including cancer, inflammation, and autoimmune disease, and its integrated model that combines internal R&D with an asset and royalty aggregation strategy.
News about Zymeworks often centers on clinical trial progress and key data readouts. A major theme is the development of Ziihera ® (zanidatamab-hrii), a HER2-targeted bispecific antibody engineered using the company’s Azymetric™ technology. Press releases have detailed positive Phase 3 HERIZON-GEA-01 results in first-line HER2-positive gastroesophageal adenocarcinoma, as well as regulatory approvals for previously treated HER2-positive biliary tract cancer in the U.S., Europe, and China. Updates also cover the advancement of partnered programs like pasritamig with Johnson & Johnson Innovative Medicine and early-stage data from wholly owned ADC candidates such as ZW191 and ZW251.
Investors following ZYME news can also expect regular coverage of strategic and corporate developments. The company reports on its evolving royalty- and asset-focused strategy, share repurchase authorizations, milestone and royalty revenues from partners, and leadership and board appointments designed to support capital allocation and partnership execution. Participation in major medical and investor conferences, such as ASCO GI and the J.P. Morgan Healthcare Conference, is another recurring topic in its news releases.
This news feed provides a centralized view of Zymeworks’ clinical milestones, partnership updates, financial and strategic announcements, and governance changes, offering context for how the company is executing its stated goal of building a diversified portfolio of revenue-generating healthcare assets alongside an active R&D engine.
Zymeworks Inc. (NYSE: ZYME) has initiated a Phase 1 trial, dosing the first patient with zanidatamab, combined with Tukysa® (tucatinib) and capecitabine, targeting HER2-positive breast cancer. This follows positive results from previous trials combining tucatinib with trastuzumab and chemotherapy. Zanidatamab employs a bispecific design to enhance anti-tumor activity and is viewed as a promising treatment for patients with advanced HER2-positive breast cancer. The FDA has granted Breakthrough Therapy designation for zanidatamab in specific cancer types, indicating potential accelerated approval for its use.
Zymeworks Inc. (NYSE: ZYME), a clinical-stage biopharmaceutical company, will present at the Ladenburg Thalmann Healthcare Conference on July 14, 2021, at 4:00 p.m. ET. The presentation can be viewed live or later via Zymeworks’ website. The company focuses on developing next-gen multifunctional biotherapeutics, with its lead candidate, zanidatamab (ZW25), granted Breakthrough Therapy designation by the FDA. It is currently enrolling patients in pivotal and Phase 2 trials for cancers like HER2-amplified biliary tract cancer. ZW49, another candidate, is in Phase 1 development.
Zymeworks Inc. (NYSE: ZYME) will present at the Jefferies Virtual Healthcare Conference from June 1-4, 2021. The Company’s presentation is scheduled for June 3, 2021, at 10:00 a.m. ET. Interested individuals can access the live webcast through Zymeworks’ website, with a recorded replay available later.
Zymeworks focuses on developing multifunctional biotherapeutics, including zanidatamab (ZW25), a bispecific antibody with FDA Breakthrough Therapy designation, currently undergoing pivotal clinical trials for biliary tract cancer and Phase 2 trials for other cancers.
Zymeworks Inc. (NYSE: ZYME) held its Annual General Meeting of Shareholders on May 5, 2021, where key proposals were voted on. Proposal 1 re-elected directors, with votes for each nominee exceeding 71%. Proposal 2 regarding executive compensation was also approved with 89.30% support. Proposal 3 confirmed the appointment of KPMG LLP as auditors, receiving 98.99% approval. The detailed voting results are accessible through SEDAR and EDGAR. The company continues to advance its innovative therapies, including zanidatamab, which has received Breakthrough Therapy designation from the FDA.
Zymeworks Inc. (NYSE: ZYME) reported Q1 2021 financial results, highlighting a significant corporate milestone with FDA clearance for zanidatamab's first Phase 3 trial in HER2-positive gastric cancer. Revenue decreased to $0.6 million from $8.3 million in Q1 2020, attributed to fewer milestone payments. Research and development expenses rose to $44.3 million, leading to a net loss of $44.6 million. Despite these challenges, Zymeworks maintains $411.5 million in cash resources, forecasting continued investment in clinical trials and strategic partnerships.
Zymeworks Inc. (NYSE: ZYME) announced the transition of Diana Hausman, M.D., from Chief Medical Officer to an executive advisory role effective until November 15, 2021. Neil Josephson, M.D., currently Senior Vice President, will serve as interim CMO. Dr. Hausman played a pivotal role in advancing zanidatamab through significant clinical milestones. Under Josephson's leadership, Zymeworks aims to continue progressing towards the commercialization of zanidatamab, which has received Breakthrough Therapy designation by the FDA.
Zymeworks Inc. (NYSE:ZYME) will present at the 2021 Bloom Burton Healthcare Investor Conference on April 20-21, 2021. The presentation is scheduled for April 20 at 11:30 a.m. ET and can be accessed via a live webcast on Zymeworks’ website. The company focuses on developing multifunctional biotherapeutics, with its lead candidate, zanidatamab (ZW25), currently in pivotal trials for HER2-amplified biliary tract cancer. Zymeworks is also advancing ZW49, a bispecific HER2-targeting antibody-drug conjugate, along with a robust preclinical pipeline.
Zymeworks Inc. (NYSE: ZYME) announced five presentations at the AACR Annual Meeting, focusing on new insights into zanidatamab's mechanisms of action, the introduction of its ProTECT™ therapy platform, and two preclinical assets targeting IL-12 and 4-1BB. Presentations highlighted zanidatamab's promising activity in HER2-expressing cancers and its current pivotal trial for biliary tract cancer. The ProTECT™ platform aims to enhance safety and efficacy by selectively activating therapies in the tumor microenvironment. These insights support Zymeworks’ clinical strategies and development of diverse cancer treatments.
Zymeworks Inc. (NYSE: ZYME) announced five abstracts for poster presentations at the AACR Annual Meeting 2021, taking place virtually from April 10-15, 2021. Highlights include presentations on the PROTECT™ antibody platform, tumor-specific IL-12 engineering, insights into bispecific antibodies, and the bispecific antibody zanidatamab's mechanisms and anti-tumor activity in HER2 cancers. Zymeworks is advancing its lead candidate, zanidatamab, in pivotal clinical trials for refractory HER2-amplified biliary tract cancer and other HER2-expressing cancers.
Zymeworks Inc. (NYSE: ZYME) reported a 32% revenue increase in 2020, reaching $39.0 million, up from $29.5 million in 2019. The growth was driven by milestone payments from partnerships. Research and development expenses rose significantly to $168.5 million, reflecting expanded clinical trials for zanidatamab and ZW49. The company received a Breakthrough Therapy designation for zanidatamab, paving the way for pivotal trials in 2021. Additionally, Zymeworks strengthened its balance sheet with a $320.8 million public financing.