PUBLISHER: DelveInsight | PRODUCT CODE: 1745764
PUBLISHER: DelveInsight | PRODUCT CODE: 1745764
DelveInsight's "Anti- C-C Motif Chemokine Receptor 8 (CCR8) Antibodies - Target Population, Competitive Landscape, and Market Forecast - 2040" report delivers an in-depth understanding of the anti-CCR8 antibodies, historical and competitive landscape as well as its market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
The anti-CCR8's market report provides current treatment practices, emerging therapies, market share of individual therapies, and current and forecasted 7MM anti-CCR8's market size from 2020 to 2040. The report also covers current anti-CCR8's treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market's potential.
Study Period: 2020-2040
Anti- C-C Motif Chemokine Receptor 8 (CCR8) Antibodies Overview
C-C motif chemokine receptor 8 (CCR8) is a class A GPCR that is predominantly and selectively expressed on Treg cells within tumors. These Treg cells suppress anti-tumor immune responses by inhibiting effector T cell activity. Elevated levels of intratumoral Tregs are associated with worse clinical outcomes and poorer prognoses across various cancer types. This has led to the hypothesis that targeting and selectively depleting these Treg cells could restore anti-tumor immunity and enhance the effectiveness of cancer immunotherapy. Supporting this, recent preclinical studies in mice have shown that using an anti-CCR8 antibody to eliminate Treg cells can elicit potent anti-tumor effects. CCR8 belongs to the ten-member CCR) subfamily. It is activated by its natural ligand, CCL1 (C-C motif chemokine ligand 1), and signals through the inhibitory G protein Gi. However, the detailed molecular structure of CCR8 and the precise mechanisms underlying its activation are still not fully understood. Antibodies targeting GPCRs hold great promise for therapeutic use, in particular for protein ligand GPCRs such as chemokine receptors that may be more challenging to drug with small molecules.
The epidemiology chapter anti-CCR8 antibodies in the report provides historical as well as forecasted epidemiology segmented as total cases in selected indications for anti-CCR8 antibodies, total eligible patient pool in selected indications for anti-CCR8 antibodies, and total treated cases in selected indications for anti-CCR8 antibodies in the 7MM covering the United States, EU4 (Germany, France, Italy, and Spain), and the United Kingdom, and Japan from 2020 to 2040.
The drug chapter segment of the anti-CCR8 antibodies report encloses a detailed analysis of early and mid-stage anti-CCR8 antibodies. It also helps understand the clinical trial details of anti-CCR8 antibodies, expressive pharmacological action, agreements and collaborations, approval, and patent details, advantages and disadvantages of each included drug, and the latest news and press releases.
Emerging Therapies
BMS-986340 (ONO-7427) + OPDIVO: BMS/Ono Pharma
BMS-986340 is an anti-CCR8 IgG1 biologic with an enhanced non-fucosylated (NF) Fc region that binds to CCR8 and effectively depletes regulatory T cells while sparing effector CD8 T cells. The drug is currently being investigated in a Phase I/II (NCT04895709) clinical trial for solid tumors in the US, EU, and Japan.
In its April 2025 annual presentation, the company reported that ONO-7427, an anti-CCR8 antibody, is undergoing clinical evaluation in trial NCT04895709 for solid tumors, with the study being conducted in Japan, the US, and the EU. The trial's primary completion is anticipated within fiscal year 2025.
GS-1811 +- Zimberelimab: Gilead Sciences
GS-1811, a potentially first-in-class immunotherapy, is designed to selectively deplete immunosuppressive tumor-infiltrating T regulatory cells in the tumor microenvironment and is currently in Phase I (NCT05007782) clinical development as a possible treatment for patients with solid tumors.
In December 2023, Gilead Sciences and Jounce Therapeutics amended their existing license agreement for GS-1811 (formerly JTX-1811), enabling Gilead to buy out remaining contingent payments potentially due under the license agreement executed in August 2020. As part of the transaction, certain operational obligations of the parties related to GS-1811, an anti-CCR8 antibody, set forth in the license agreement have also been terminated. Gilead will acquire certain related intellectual property, including all outstanding rights of Jounce to GS-1811, pursuant to the transaction agreement.
CHS-114 +- LOQTORZI: Coherus Biosciences and Vaccinex
CHS-114, is an investigational IgG1 antibody targeting CCR8, a chemokine receptor highly expressed on Treg cells" in the tumor microenvironment. CHS-114 is designed as a cytolytic antibody to cause depletion of intra-tumoral Treg cells, important regulators of immune suppression and tolerance, through ADCC, or ADCP or both. CHS-114 has shown anti-tumor activity as monotherapy or in combination with anti-PD-1 antibodies in preclinical models. W
The Company is enrolling patients with advanced solid tumors and HNSCC in the US in a clinical trial evaluating safety and pharmacokinetics of CHS-114 with and without LOQTORZI (toripalimab) (NCT05635643). The Company is currently evaluating CHS-114 in combination with toripalimab in a Phase Ib clinical study in second-line HNSCC (NCT05635643). The Company also has an ongoing Phase Ib clinical study of CHS114 in combination with LOQTORZI and/or other treatments in participants with advanced solid tumors with the first cohort evaluating gastric cancer (NCT06657144).
In April 2025, Coherus BioSciences announced that the data from its ongoing Phase I clinical trial evaluating CHS-114 in patients with recurrent/metastatic HNSCC was presented at the 2025 American Association for Cancer Research (AACR) Annual Meeting, taking place April 25-30, 2025.
The global anti- CCR8 inhibitor market is expected to witness substantial growth in the coming years, driven by the increasing prevalence of autoimmune diseases, robust clinical pipeline activity, and expanding regulatory approvals.
In recent years, there has been increasing interest in the development of CCR8-targeted therapies for the treatment of solid tumors. Several promising candidates are currently under investigation, including BMS-986340 (ONO-7427) in combination with OPDIVO by Bristol Myers Squibb and Ono Pharma, CHS-114 in combination with LOQTORZI by Coherus Biosciences and Vaccinex-targeting various solid tumors including head and neck cancer and gastric cancer-and GS-1811 combined with Zimberelimab by Gilead Sciences for advanced solid tumors. Additional investigational therapies include BAY3375968 with Pembrolizumab from Bayer and BGB-A3055 alongside Tislelizumab or chemotherapy from BeOne Medicines, formerly BeiGene, both focused on advanced or metastatic solid tumors. Parallel to this, there has also been growing exploration of anti-CCR8 antibodies for a wide range of conditions, including several cancer types such as gastric cancer, CRC, TNBC, NSCLC, melanoma, HNSCC, pancreatic adenocarcinoma, and ovarian cancer, as well as autoimmune and inflammatory diseases.
Overall, this is an exciting new class with great potential for development. The maturation of current studies over the next few years will lead to a better understanding of anti-CCR8 antibodies and define their role in autoimmune indications.
Anti- C-C Motif Chemokine Receptor 8 (CCR8) Antibodies Market Overview
In recent years, there has been a growing interest in the exploration of anti-CCR8 antibodies for a variety disorders, encompassing cancer indications (gastric cancer, CRC, TNBC, NSCLC, HNSCC, melanoma, ovarian cancer, and others), and others, autoimmune and inflammatory diseases, and other indications.
This section focuses on the uptake rate of potential approved and emerging anti-CCR8 antibodies expected to be launched in the market during 2025-2040.
Anti- C-C Motif Chemokine Receptor 8 (CCR8) Antibodies Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase I/II and Phase I. It also analyzes key players involved in developing targeted therapeutics.
The presence of numerous drugs under different stages is expected to generate immense opportunity for anti-CCR8 antibodies market growth over the forecast period.
Pipeline Development Activities
The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for anti-CCR8 antibodies therapies.
KOL Views
To keep up with current and future market trends, we take Industry Experts' opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Industry experts were contacted for insights on anti-CCR8 antibodies' evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, drug uptake, along challenges related to accessibility.
DelveInsight's analysts connected with 10+ KOLs to gather insights; however, interviews were conducted with 5+ KOLs in the 7MM. Centers such as Duke University School of Medicine, and others.
Their opinion helps understand and validate current and emerging therapy treatment patterns or anti-CCR8 antibodies' market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
Qualitative Analysis
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, patient burden, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided. These pointers are based on the analyst's discretion and assessment of the patient burden, cost analysis, and existing and evolving treatment landscape.
Market Access and Reimbursement
Reimbursement may be referred to as the negotiation of a price between a manufacturer and payer that allows the manufacturer access to the market. It is provided to reduce the high costs and make the essential drugs affordable. Health Technology Assessment (HTA) plays an important role in reimbursement decision-making and recommending the use of a drug. These recommendations vary widely throughout the seven major markets, even for the same drug.
In the US healthcare system, both Public and Private health insurance coverage are included. Also, Medicare and Medicaid are the largest government-funded programs in the US. The major healthcare programs including Medicare, Continuing Medical Education (CME) program, the Children's Health Insurance Program (CHIP), and the state and federal health insurance marketplaces are overseen by the Centers for Medicare & Medicaid Services (CMS). Other than these, Pharmacy Benefit Managers (PBMs), and third-party organizations that provide services, and educational programs to aid patients are also present.
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of approved therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.
The abstract list is not exhaustive, will be provided in the final report