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Coherus Oncology Announces Publication in Molecular Cancer Therapeutics Highlighting the Strong Pharmacology of Investigational CCR8 Antibody Tagmokitug (CHS-114)

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Coherus Oncology (NASDAQ: CHRS) announced publication in Molecular Cancer Therapeutics describing preclinical and first-in-human biomarker data for investigational anti-CCR8 antibody tagmokitug (CHS-114).

Key findings: picomolar binding affinity, no off-target binding, selective depletion of CCR8+ regulatory T cells, high prevalence and density of CCR8 across many solid tumors, tumor regression in mouse models with enhanced activity when combined with anti-PD-1, and translational proof-of-mechanism showing selective CCR8+ Treg reductions in patients.

The publication supports ongoing clinical development of tagmokitug in combination with toripalimab across multiple solid tumor settings.

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Positive

  • Picomolar binding affinity to CCR8
  • No off-target binding detected
  • Selective depletion of CCR8+ Tregs in patients
  • Mouse tumor regression; enhanced with anti-PD-1 combo
  • High CCR8 prevalence across many solid tumors

Negative

  • No clinical tumor response or survival data reported
  • Efficacy shown in mice, not yet demonstrated in humans

News Market Reaction – CHRS

+5.11% 2.3x vol
1 alert
+5.11% News Effect
-5.3% Trough Tracked
+$9M Valuation Impact
$184M Market Cap
2.3x Rel. Volume

On the day this news was published, CHRS gained 5.11%, reflecting a notable positive market reaction. Argus tracked a trough of -5.3% from its starting point during tracking. This price movement added approximately $9M to the company's valuation, bringing the market cap to $184M at that time. Trading volume was elevated at 2.3x the daily average, suggesting notable buying interest.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Median OS (combo): 64.8 months Median OS (chemo): 33.7 months Hazard ratio: HR 0.62 (95% CI 0.45–0.85) +5 more
8 metrics
Median OS (combo) 64.8 months LOQTORZI plus chemotherapy in JUPITER-02 Phase 3
Median OS (chemo) 33.7 months Chemotherapy alone arm in JUPITER-02 Phase 3
Hazard ratio HR 0.62 (95% CI 0.45–0.85) Overall survival benefit for LOQTORZI combo vs chemotherapy
Shelf capacity $150.0 million Maximum aggregate offering under Form S-3 shelf filed Nov 13, 2025
UDENYCA sale proceeds $483.4 million Upfront all-cash consideration from divestiture completed Apr 11, 2025
ESPP shares registered 1,500,000 shares Additional common shares for 2014 Employee Stock Purchase Plan on Form S-8
Net loss (Q3 2025) $(35,531) Quarterly net loss including discontinued operations in Q3 2025 10-Q
Shares outstanding 116,236,018 Common shares outstanding as of Sept 30, 2025

Market Reality Check

Price: $1.67 Vol: Volume 645,430 is about 0...
normal vol
$1.67 Last Close
Volume Volume 645,430 is about 0.74x the 20-day average 877,809, indicating no pre-news accumulation surge. normal
Technical Shares at $1.37 are trading above the $1.14 200-day moving average, despite being 27.51% below the 52-week high.

Peers on Argus

CHRS was down 3.52% while peers were mixed: AGEN up 1.57%, THTX up 0.89%, TIL up...

CHRS was down 3.52% while peers were mixed: AGEN up 1.57%, THTX up 0.89%, TIL up 0.99%, MCRB up 0.26%, and GLSI down 8.51%, suggesting stock-specific dynamics rather than a coordinated sector move.

Historical Context

5 past events · Latest: Dec 08 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Dec 08 Clinical survival data Positive +6.7% Phase 3 JUPITER-02 showed LOQTORZI nearly doubled median overall survival.
Nov 07 Clinical biomarker data Positive -10.1% SITC data showed strong CHS-114 Treg depletion and CD8+ increases in HNSCC.
Nov 06 Earnings and update Negative -4.8% Q3 2025 showed modest LOQTORZI revenue growth but sizeable net loss.
Nov 06 Leadership appointment Positive -4.8% New Chief Strategy and Corporate Affairs Officer joined to support oncology focus.
Oct 30 Earnings scheduling Neutral -1.7% Announcement of timing for Q3 2025 results and investor call.
Pattern Detected

Recent history shows mixed alignment: strong positive clinical data sometimes led to gains but also sharp selloffs, while financial and corporate updates more often aligned with modest declines.

Recent Company History

Over the past few months, Coherus reported several key developments. Phase 3 JUPITER-02 data showed LOQTORZI plus chemotherapy improved median overall survival to 64.8 months vs 33.7 months, with a price gain of 6.67%. Earlier, detailed multiomic biomarker data for CHS-114 at SITC 2025 coincided with a -10.07% move, indicating volatility around early oncology data. Q3 2025 results highlighted LOQTORZI net revenue of $11.2M and a net loss of $(44.5)M, with the stock down modestly. A new strategy executive hire and the Q3 results pre-announcement also saw small negative reactions. Today’s tagmokitug pharmacology publication extends this oncology-focused trajectory.

Regulatory & Risk Context

Active S-3 Shelf · $150.0 million
Shelf Active
Active S-3 Shelf Registration 2025-11-13
$150.0 million registered capacity

The company has an active Form S-3 shelf filed on Nov 13, 2025, allowing up to $150.0 million of mixed securities to be offered over time, which provides capital-raising flexibility but also represents potential future equity or debt issuance for shareholders.

Market Pulse Summary

The stock moved +5.1% in the session following this news. A strong positive reaction aligns with the...
Analysis

The stock moved +5.1% in the session following this news. A strong positive reaction aligns with the article’s emphasis on robust pharmacology and proof-of-mechanism for tagmokitug, reinforcing Coherus’ oncology pipeline narrative alongside prior LOQTORZI survival data of 64.8 months vs 33.7 months. However, history shows that favorable early CHS-114 data previously coincided with a -10.07% move, underscoring volatility. The existing $150.0 million shelf also allowed flexibility for future financing, which could influence how durable any price strength became.

Key Terms

pharmacology, picomolar, monoclonal antibody, t regulatory cells, +4 more
8 terms
pharmacology medical
"This publication presents the robust pharmacology of tagmokitug in preclinical and clinical studies"
Pharmacology is the science of how drugs affect the body and how the body affects drugs — including what a drug does, how much is needed, how long it lasts, and possible side effects. For investors, pharmacology matters because it determines whether a medicine is likely to work safely, how it will be dosed, what risks regulators and doctors will see, and therefore how big its market and approval chances might be — like testing a recipe to see if it will reliably satisfy customers.
picomolar medical
"high selectivity, picomolar binding affinity and significant effector mediated killing"
Picomolar is a measure of concentration equal to one trillionth (10⁻¹²) of a mole per liter, roughly a few hundred billion individual molecules in a liter of fluid. In biotech and pharma, picomolar levels indicate very low amounts of a substance needed to have an effect or be detected—like needing a single drop of dye to color a large pool—so reporting picomolar activity speaks to drug potency or diagnostic sensitivity that can affect commercial value.
monoclonal antibody medical
"its investigational anti-CCR8 monoclonal antibody"
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
t regulatory cells medical
"selectively eliminates CCR8+ T regulatory cells and not other T cells"
T regulatory cells are a specialized type of immune cell that act like the body’s brake or thermostat, keeping immune responses from becoming too aggressive and preventing damage to healthy tissues. Investors watch them because therapies that boost, suppress, or mimic these cells can treat autoimmune disease, control inflammation, or affect cancer immunotherapy outcomes, so changes in Treg-related science, trial results, or regulation can strongly influence a drug’s safety, effectiveness and market potential.
biomarker medical
"publication of preclinical and clinical biomarker research in Molecular Cancer Therapeutics"
A biomarker is a measurable indicator found in the body, such as in blood or tissues, that provides information about health, disease, or how the body responds to treatment. For investors, biomarkers can signal the potential success or risk of medical products or therapies, influencing the value of related companies and industry trends. They act like signals or clues that help assess the progress of medical advancements and their market impact.
anti-pd-1 antibody medical
"activity was enhanced with anti-PD-1 antibody combination treatment"
An anti-PD-1 antibody is a lab-made protein drug that blocks a safety switch on certain immune cells, allowing them to recognize and attack cancer cells. Investors watch these drugs because trial results, approvals, or safety issues can rapidly change a biotech’s sales prospects and valuation — like cutting a car’s brake cable to free the engine, with big potential reward but also safety and regulatory risks.
first-in-human clinical study medical
"In the first-in-human clinical study, proof of mechanism is established"
A first-in-human clinical study is the initial test of a new drug, vaccine, or medical device in human volunteers after laboratory and animal work; it checks basic safety, dose ranges, and how the body responds. Investors watch these studies like a company’s first product demo — positive safety and clear biological effects reduce risk and can unlock larger, more expensive trials or partner deals, while setbacks often lower a program’s commercial value.
preclinical medical
"robust pharmacology of tagmokitug in preclinical and clinical studies"
Preclinical describes the stage of drug or medical-product development when researchers test a candidate in the lab and in animals to see if it is safe, reaches intended targets, and shows basic effectiveness before any human trials begin. For investors, preclinical status signals an early, higher‑risk opportunity where positive lab results can increase value but significant work, time, and regulatory hurdles remain — like proofing a prototype in a workshop before road testing.

AI-generated analysis. Not financial advice.

-Coherus Oncology formally introduces non-proprietary name: tagmokitug-

-Publication shows picomolar affinity for CCR8 with no off-target binding and proof-of- mechanism in preclinical and clinical studies-

-Data show CCR8 target is present with high prevalence and density in many solid tumors-

REDWOOD CITY, Calif., Jan. 05, 2026 (GLOBE NEWSWIRE) -- Coherus Oncology, Inc. (NASDAQ: CHRS) today announced the publication of preclinical and clinical biomarker research in Molecular Cancer Therapeutics describing the high selectivity, picomolar binding affinity and significant effector mediated killing of CCR8+ cells of its investigational anti-CCR8 monoclonal antibody. The findings show that the antibody, now named tagmokitug, demonstrated no off-target binding, and selectively eliminates CCR8+ T regulatory cells and not other T cells, supporting its potential as an anticancer treatment. The full article may be accessed in the December 2025 issue of Molecular Cancer Therapeutics.

The publication provides important scientific evidence for the program and supports the ongoing advancement of tagmokitug in clinical studies evaluating its antitumor activity across multiple solid tumor settings in combination with toripalimab.

“This publication presents the robust pharmacology of tagmokitug in preclinical and clinical studies, and with a selectivity profile and potent binding and killing of CCR8+ T regulatory cells and not other immune cells. These data provide evidence that tagmokitug has the potential for a differentiated profile,” said Theresa LaVallee, PhD, Chief Scientific and Development Officer at Coherus. “The data show a high abundance of CCR8 target expression in a broad range of solid tumors suggesting the promise of the tagmokitug program. We look forward to advancing the development as we continue to explore tagmokitug in patients with solid tumors.”

Key highlights from this publication include:

CCR8 is highly abundant and preferentially over expressed in Treg cells in solid tumors and that most solid tumors have a high level of CCR8.

Anti-tumor and tumor immune remodeling activity of anti-CCR8 antibody treatment was observed in mouse tumor models and activity was enhanced with anti-PD-1 antibody combination treatment.

Tagmokitug has robust characteristics with picomolar binding affinity, exquisite selectivity for CCR8 with no off target binding and potent target cell killing by a bind and kill mechanism that induces tumor regression in mice.

In the first-in-human clinical study, proof of mechanism is established with translational data showing tagmokitug administration leads to selective reductions in CCR8+ Tregs and not other T cell subsets in cancer patients.

About Tagmokitug

Tagmokitug is an investigational monoclonal antibody that selectively targets CCR8, a receptor highly enriched on regulatory T cells within the tumor microenvironment. Tagmokitug is currently being evaluated in Phase 1b/2a clinical trials in patients with solid tumors in combination with the PD-1 inhibitor toripalimab and chemotherapy. It is part of Coherus Oncology’s next-generation immunotherapy pipeline being evaluated across multiple solid tumor settings.

About Coherus Oncology

Coherus Oncology is a fully integrated commercial-stage innovative oncology company with an approved next-generation PD-1 inhibitor, LOQTORZI® (toripalimab-tpzi), growing revenues and a promising proprietary pipeline that includes two mid-stage clinical candidates targeting liver, lung, head & neck, colorectal and other cancers. The Company’s strategy is to grow sales of LOQTORZI in nasopharyngeal carcinoma and advance the development of new indications for LOQTORZI in combination with both its pipeline candidates as well as its partners, driving sales multiples and synergies from proprietary combinations.

Coherus’ immuno-oncology pipeline includes multiple antibody immunotherapy candidates focused on enhancing the innate and adaptive immune responses to enable a robust antitumor response and enhance outcomes for patients with cancer. Casdozokitug is a novel IL-27 antagonistic antibody currently being evaluated in a randomized Phase 2 study in patients with HCC. Tagmokitug (CHS-114) is a highly selective cytolytic anti-CCR8 antibody currently in Phase 1b/2a studies in patients with advanced solid tumors, including head and neck cancer, colorectal cancer, gastric cancer, and esophageal cancer.

Forward-Looking Statements

The statements in this press release include express or implied forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended about Coherus that involve risks and uncertainties relating to future events and the future performance of Coherus. Forward-looking statements relate to expectations, beliefs, projections, future plans and strategies, anticipated events or trends and similar expressions concerning matters that are not historical facts. Words such as “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “future,” “opportunity,” “likely,” “target,” variations of such words, and similar expressions or negatives of these words are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. You can also identify forward-looking statements by discussions of strategy, plans or intentions.

Examples of such forward-looking statements include, but are not limited to, express or implied statements regarding: the ability of Coherus’ pipeline to enhance outcomes for cancer patients; expectations about future synergies; projections about growth in sales; expectations for future enrollment in clinical trials; projections about the expansion of indications for LOQTORZI; and the assumptions underlying or relating to such statements.

These forward-looking statements are based on Coherus’ current plans, estimates and projections. Such forward-looking statements involve substantial risks and uncertainties that could cause actual results to differ materially from those contemplated in any forward-looking statements. Such risks and uncertainties include, without limitation: uncertainties about the potential impact of unforeseen liabilities, future capital expenditures, revenues, costs, expenses, earnings, economic performance, indebtedness, financial condition and losses on Coherus’ prospects, business and operations in the future; risks and uncertainties in executing collaboration agreements and other joint ventures; risks and uncertainties of conducting clinical trials; the risks of Coherus’ dependence on an ability to raise funds, which may not be available on acceptable terms or at all; and risks and uncertainties of any litigation, regulatory actions and other legal proceedings.

All forward-looking statements contained in this press release speak only as of the date of this press release. Coherus undertakes no obligation to update or revise any forward-looking statements. For a further discussion of these and other factors that could cause Coherus’ future results to differ materially from any forward-looking statements see the section entitled “Risk Factors” in Coherus’ Quarterly Report on Form 10-Q for the period ended September30, 2025, filed with the Securities and Exchange Commission (SEC) on November 6, 2025, as updated by Coherus’ subsequent reports filed with the SEC.

LOQTORZI® is a registered trademark of Coherus Oncology, Inc.

©2026 Coherus Oncology, Inc. All rights reserved.

Coherus Oncology Contact Information:

For Investors:
Carrie Graham
VP, Investor Relations & Advocacy
IR@coherus.com


FAQ

What did Coherus announce about tagmokitug (CHRS) on January 5, 2026?

Coherus announced a publication reporting tagmokitug's picomolar CCR8 affinity, selectivity, and translational proof-of-mechanism.

How does tagmokitug (CHRS) work against tumors according to the publication?

Tagmokitug selectively binds CCR8 and mediates killing of CCR8+ regulatory T cells, remodeling tumor immunity.

Did the CHRS publication report clinical efficacy for tagmokitug?

The paper reports translational biomarker proof-of-mechanism in patients but does not report clinical tumor response or survival outcomes.

Is tagmokitug being studied with other therapies for CHRS trials?

Yes; the publication notes ongoing evaluation of tagmokitug in combination with toripalimab (anti-PD-1).

What evidence supports CCR8 as a target for CHRS tagmokitug?

Data show high prevalence and density of CCR8 in many solid tumors and preferential expression on tumor Tregs.
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242.14M
95.04M
Biotechnology
Biological Products, (no Diagnostic Substances)
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United States
REDWOOD CITY