Welcome to our dedicated page for Coherus news (Ticker: CHRS), a resource for investors and traders seeking the latest updates and insights on Coherus stock.
Coherus Oncology, Inc. (NASDAQ: CHRS) is a commercial-stage oncology company whose news flow is centered on its PD-1 inhibitor LOQTORZI (toripalimab-tpzi) and a proprietary immuno-oncology pipeline. Company announcements frequently highlight clinical data, regulatory developments, financial results and strategic updates related to its antibody-based cancer therapies.
News about Coherus Oncology often covers LOQTORZI in nasopharyngeal carcinoma (NPC), including long-term survival data from the JUPITER-02 Phase 3 trial evaluating LOQTORZI plus chemotherapy in recurrent or metastatic NPC. Releases also describe LOQTORZI’s approved indications in the United States and its role as the only FDA-approved and available treatment for recurrent, locally advanced or metastatic NPC across all patient subsets and lines of therapy.
Investors and clinicians following CHRS can expect regular updates on pipeline programs such as CHS-114 and casdozokitug. Coherus reports biomarker and proof-of-mechanism data for CHS-114, a highly selective cytolytic anti-CCR8 antibody, in head and neck squamous cell carcinoma and other solid tumors, as well as clinical and translational findings for casdozokitug, a novel IL-27 antagonist in advanced solid tumors including hepatocellular carcinoma and non-small cell lung cancer.
The company’s news stream also includes quarterly financial results, business updates, participation in major healthcare and oncology conferences, and investor-focused events. These items provide context on revenue trends for LOQTORZI, research and development spending on its immuno-oncology programs, and corporate strategy.
For market participants tracking CHRS, the Coherus Oncology news page on Stock Titan aggregates these press releases and related coverage, offering a centralized view of clinical milestones, regulatory disclosures and financial communications that can influence perceptions of the company’s oncology franchise and pipeline progress.
Coherus BioSciences (CHRS) announced that the FDA has accepted its 351(k) Biologics License Application (BLA) for CHS-201, a biosimilar of Lucentis. The FDA's target action date is set for August 2, 2022. If approved, Coherus plans to launch CHS-201 in the U.S. in the second half of 2022. The BLA was submitted by Coherus’ partner Bioeq AG, from whom they acquired U.S. commercial rights in 2019. Coherus also anticipates future launches of additional biosimilars, building on their successful biosimilar commercialization track record.
Coherus BioSciences (Nasdaq: CHRS) has announced the passing of board member Dr. Samuel Nussbaum, who served since May 2018. Dr. Nussbaum was a prominent healthcare executive and physician with significant contributions to the industry. His leadership was valued by Coherus, and CEO Denny Lanfear expressed deep gratitude for his service. Dr. Nussbaum previously held executive roles at Anthem and had a distinguished career in medicine and research, including a tenure at Harvard Medical School. His absence will be felt across the organization.
Coherus BioSciences, Inc. (Nasdaq: CHRS) announced on Sept. 24, 2021, that it granted options to purchase 229,500 shares of common stock to newly hired employees, effective Sept. 22, 2021. The options have an exercise price of $17.06, matching the closing trading price on the grant date. Among the recipients, a new Senior Vice President received options for 100,000 shares. These grants were made under the Coherus BioSciences 2016 Employment Commencement Incentive Plan, approved to attract new talent.
Coherus BioSciences (CHRS) and Junshi Biosciences announced positive interim results from the Phase 3 JUPITER-06 trial on toripalimab combined with chemotherapy for advanced esophageal squamous cell carcinoma (ESCC). The study demonstrated statistically significant improvements in both progression-free survival (PFS) and overall survival (OS) compared to chemotherapy alone, meeting co-primary endpoints. The companies plan to submit a Biologics License Application (BLA) supplement in 2022 to expedite toripalimab's availability for ESCC patients in the U.S. Full data will be presented at the ESMO Congress on September 17, 2021.
Coherus BioSciences (Nasdaq: CHRS) and Shanghai Junshi Biosciences announced significant findings from the JUPITER-02 clinical trial, published in Nature Medicine. The Phase 3 trial demonstrated that toripalimab combined with standard chemotherapy improved progression-free survival (PFS) in patients with advanced nasopharyngeal carcinoma (NPC), showing a median PFS of 11.7 months versus 8.0 months with chemotherapy alone. While overall survival data is not yet mature, a 40% reduction in death risk was noted. A biologics license application has been submitted to the FDA for approval.
Coherus Biosciences (CHRS) and Junshi Biosciences have announced positive interim results from the Phase 3 clinical trial CHOICE-01, assessing toripalimab plus chemotherapy for advanced non-small cell lung cancer (NSCLC). The interim analysis showed significant improvement in progression-free survival (PFS) compared to chemotherapy alone. The data was presented at the World Conference on Lung Cancer. Further analyses are anticipated later this year, with plans for FDA discussions for a biologics license application for toripalimab in the U.S.
Coherus BioSciences, Nasdaq: CHRS, has announced that its senior management will present at the 23rd Annual H.C. Wainwright Global Investment Conference on September 14, 2021, at 7 a.m. ET. The presentation will be accessible via the investors’ page on Coherus’ website. The company focuses on providing cost-effective medicines and aims to enhance its immuno-oncology franchise, leveraging revenue from its commercial biosimilars. For more details, visit www.coherus.com.
Coherus BioSciences (Nasdaq: CHRS) announced key presentations at upcoming medical conferences. Toripalimab clinical data will be shared on September 13 at the IASLC 2021 World Conference on Lung Cancer and on September 17 at the ESMO Congress 2021. Additionally, a study on pegfilgrastim will be presented at the ASCO Quality Care Symposium on September 25, and clinical data from the CHS-201 program will be highlighted on October 1 at the Retina Society's Annual Meeting. These events showcase Coherus’ commitment to advancing cancer treatment options.
Coherus (Nasdaq: CHRS) and Junshi Biosciences have completed the rolling submission of a Biologics License Application (BLA) to the FDA for toripalimab in combination with chemotherapy and as a monotherapy for nasopharyngeal carcinoma (NPC). The FDA granted Breakthrough Therapy Designation for both treatment options, intended to expedite drug development for severe diseases. Toripalimab has shown significant efficacy in clinical studies and received early approval in China. Coherus plans to file additional BLAs for toripalimab over the next three years.
On August 27, 2021, Coherus BioSciences (Nasdaq: CHRS) announced the grant of stock options totaling 278,000 shares to newly hired employees, effective as of August 26, 2021. The options have an exercise price of $15.82 per share, matching the closing price on the grant date. Among the recipients, two Vice Presidents received options for 45,000 shares each, while an additional 188,000 shares were granted to fifteen non-officer employees. This grant is part of the 2016 Employment Commencement Incentive Plan approved by the board to attract new talent.