Coherus Oncology Showcases Multiomic Biomarker Data for CHS-114, a Selective Anti-CCR8 Cytolytic Antibody, at SITC Conference
CHS-114 Clinical Trial Results: Coherus Oncology's CHS-114, an anti-CCR8 antibody, showed effective depletion of CCR8+ Tregs and increased CD8 T cells in head and neck squamous cell carcinoma (HNSCC) patients, indicating promising immune remodeling and antitumor activity.
Combination Therapy with Toripalimab: The combination of CHS-114 with toripalimab resulted in enhanced immune activation and a significant increase in CD8+ T cell proliferation, supporting further development of this treatment strategy in advanced solid tumors.
Safety Profile and Efficacy: The ongoing Phase 1b trial demonstrated a manageable safety profile for CHS-114, with early signs of antitumor activity, including a partial response in a refractory HNSCC patient.
Future Development Plans: Coherus aims to optimize dosing for CHS-114 in combination with toripalimab, addressing FDA's Project Optimus and advancing to Phase 2 trials based on the promising results from the current study.
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- Funding Size: Coherus Oncology has priced an underwritten public offering of 28.6 million shares at $1.75 each, raising a total of $50.1 million, with the transaction expected to close on February 17, 2026, aimed at supporting the commercialization of LOQTORIZ and ongoing clinical development.
- Revenue Growth: The company reported Q3 2025 net revenue of $11.6 million, a significant increase from $6.05 million in the previous quarter, reflecting strong market demand for LOQTORIZ and a recovery in overall business performance.
- Clinical Trial Results: LOQTORIZ demonstrated a median overall survival of 64.8 months in the JUPITER-02 trial, nearly double that of chemotherapy alone, reinforcing its position as the standard-of-care first-line treatment for recurrent or metastatic nasopharyngeal carcinoma.
- Future Milestones: Coherus plans to release initial data from the CHS-114 and LOQTORIZ combination therapy in HNSCC in H1 2026, which is expected to drive further development of its immuno-oncology programs and enhance its competitive edge in the market.
- Strong Financial Results: Applied Materials reported first-quarter revenue of $7.01 billion, exceeding analyst expectations of $6.87 billion, indicating robust demand in the semiconductor equipment market and reinforcing its market leadership.
- Earnings Beat: The company posted adjusted earnings of $2.38 per share for the first quarter, surpassing the $2.20 estimate, reflecting improved cost control and operational efficiency, which is likely to attract more investor interest.
- Stock Surge: Following the earnings report, Applied Materials shares jumped 11.9% to $367.50 in pre-market trading, indicating a positive market sentiment towards the company's growth prospects, potentially boosting investor confidence further.
- Positive Q2 Guidance: The company issued second-quarter guidance above market expectations, demonstrating management's confidence in future performance, which is expected to drive more capital inflows and enhance its competitive position in the industry.
- Offering Size: Coherus Oncology has priced an underwritten public offering of 28.6 million shares at $1.75 per share, expecting to raise approximately $50.1 million in gross proceeds before fees and expenses, indicating the company's strong capital market capabilities.
- Underwriter Option: The company is also granting underwriters a 30-day option to purchase an additional 4.29 million shares at the same price, a strategy that may enhance market demand and liquidity for its stock.
- Use of Proceeds: The net proceeds will support the commercialization of LOQTORZI (toripalimab-tpzi), continue clinical development of its pipeline, and fund working capital and other general corporate purposes, demonstrating the company's strategic planning for future growth.
- Expected Closing Date: The offering is expected to close around February 17, 2026, subject to standard closing conditions, reflecting the company's cautious and forward-looking approach to capital operations.
- Offering Size: Coherus Oncology has announced a public offering of 28,600,000 shares at a price of $1.75 per share, with expected gross proceeds of approximately $50.1 million, which will support ongoing commercialization and clinical development efforts.
- Underwriter Selection: The offering is being managed by TD Cowen, Guggenheim Securities, and Oppenheimer & Co., reflecting market confidence in Coherus' stock and potentially enhancing investor expectations for the company's future growth.
- Use of Proceeds: The proceeds from the offering will be utilized to support the commercialization of LOQTORZI®, continue clinical development, and for general corporate purposes, indicating strategic decisions aimed at expanding the company's product line and market share.
- Additional Share Option: The underwriters have a 30-day option to purchase an additional 4,290,000 shares at the same offering price, which further enhances the flexibility and potential revenue of the offering.
- Clinical Trial Collaboration: Johnson & Johnson (JNJ) has agreed to supply Coherus Oncology (CHRS) with its bispecific antibody pasritamig to evaluate its combination with Coherus' monoclonal antibody tagmokitug for a phase 1b trial in metastatic castration-resistant prostate cancer, highlighting the synergistic potential in cancer treatment between the two companies.
- Trial Funding Arrangement: Coherus will sponsor the phase 1b clinical trial, which not only provides a crucial clinical validation opportunity for its product tagmokitug but also has the potential to enhance its market competitiveness through successful trial outcomes.
- Retention of Commercial Rights: Both companies will retain commercial rights to each other's compounds, whether as monotherapies or combination therapies, which helps facilitate independent brand development while laying the groundwork for future collaborations.
- Antibody Characteristics: Pasritamig is considered a T-cell engaging bispecific antibody, while tagmokitug is an anti-CCR8 cytolytic monoclonal antibody, and this technological combination may offer new treatment options for prostate cancer patients, further driving innovation in the biopharmaceutical sector for both companies.
- Market Potential: The global oncology therapy market is projected to reach $668 billion by 2034, and Oncolytics Biotech is seizing investment opportunities through execution-focused registration study designs in this rapidly growing sector.
- Leadership Enhancement: Oncolytics Biotech appointed John McAdory as Executive Vice President of Strategy and Operations and Yujun Wu as Vice President, Head of Biostatistics, both bringing extensive experience in late-stage oncology trial execution and regulatory strategy to advance the company's registration-directed programs in gastrointestinal cancers.
- Breakthrough Efficacy Data: The company reported that pelareorep achieved a 33% objective response rate in second-line KRAS-mutant microsatellite stable metastatic colorectal cancer patients, significantly surpassing the historical 6-11% response rate for chemotherapy alone, indicating its potential in difficult-to-treat populations.
- FDA Study Design Approval: Oncolytics Biotech has secured FDA alignment on its Phase 3 study design for pelareorep in first-line metastatic pancreatic cancer, marking the imminent launch of the only immunotherapy registration trial currently planned for this disease, further solidifying its market position.









