PUBLISHER: DelveInsight | PRODUCT CODE: 1809571
PUBLISHER: DelveInsight | PRODUCT CODE: 1809571
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DelveInsight's "Bispecifics in Oncology Market Size, Target Population, Competitive Landscape and Market Forecast - 2040" report delivers an in-depth understanding of Bispecifics in Oncology, addressable patient pool, competitive landscape, and future market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the UK, and Japan.
The Bispecifics in Oncology market report provides insights around existing treatment practices in patients with Bispecifics in Oncology, approved (if any) and emerging Bispecifics in Oncology market size & market share of individual therapies, patient pool eligible for treatment with Bispecifics in Oncology, along with current and forecasted 7MM Bispecifics in Oncology market size from 2020-2040 by therapies and by indication. The report also covers current unmet needs and challenges while incorporating new classes in treatment paradigm, variations in accessibility and acceptability of new Bispecifics in Oncology in different geographies, along with insights on Bispecifics in Oncology pricing reimbursements to curate the best opportunities and assess the market's potential.
Key Factors Driving the Growth of the Bispecifics in Oncology Market
Rising Cancer Incidence
The increasing global prevalence of cancer is a significant driver for the bispecific antibodies market. As cancer rates climb, there is a heightened demand for innovative therapies that can offer more effective and targeted treatment options. Bispecific antibodies, which can simultaneously target two different antigens, provide a promising solution to this challenge.
BLINCYTO's Evolving Role in Hematologic Oncology
BLINCYTO has been around for almost a decade. This therapy is the current market leader in the ALL sector, and Amgen is expanding its use to earlier stages of illness, as it was first licensed for relapsed/refractory ALL. It is also FDA authorized for Minimal residual disease-positive patients. Amgen is now attempting to enter niche markets with BLINCYTO.
Rising M&A Activity in Dual-Targeted Oncology Therapies
Amid rising industry interest in PD-(L)1 X VEGF bispecifics, Pfizer made a landmark move by acquiring 3SBio's SSGJ-707 for USD 1.25 billion upfront, with potential milestones reaching USD 4.8 billion, marking the largest deal in this emerging field. This follows BioNTech's USD 800 million acquisition of Biotheus, including BNT327, and Merck & Co.'s USD 588 million upfront payment for LaNova Medicines' LM-299, underscoring the growing momentum behind dual-targeted therapies.
Robust Bispecifics in Oncology Clinical Trial Activity
The bispecifics in oncology clinical trials include several promising therapies such as Givastomig (I-MAB Biopharma and BMS), Volrustomig (AstraZeneca), BNT327 (BioNTech and Bristol Myers Squibb), Acasunlimab (Genmab), Rilvegostomig (AstraZeneca), CTX-009 (Compass Therapeutics), IBI363 (Innovent), REGN5459 (Regeneron Pharmaceuticals), CA-170 (Aurigene Oncology and Curis), and others.
Bispecifics in Oncology Drugs Market Overview
This segment will provide detailed information beginning with the inhibitor journey from discovery of the mutation or protein expression to its entry into clinical development followed by its upcoming commercial potential in the Bispecifics in Oncology Drugs Market. This segment will dive into the different indications in Bispecifics in Oncology Market Size for which the inhibitor is being developed for, which would further give insights on the potential addressable patient population. Moreover, this segment will also give a brief overview around the existing treatment paradigm of the target indications.
Bispecifics in Oncology Clinical Trials
This section will give in depth information about the existing local and systemic options in the current treatment paradigm of all the potential indications, in which most of the pharmaceutical companies are actively evaluating their inhibitors. Potential of the emerging Bispecifics in Oncology Market Size in changing the current clinical practice guidelines is crucial to analyze especially when it comes to real world scenario.
It will also include the relevance and importance of incorporation of biomarker testing at varying stages of the disease. It is also important to understand that implementing such tests in routine clinical practice is not uniform in different countries due to issues such as cost, accessibility, reimbursement and non-recommendation in guidelines.
Bispecifics In Oncology Target Patient Pool Analysis:
Bispecifics in Oncology Recent Developments
The Bispecifics in Oncology Drugs Market segment encloses a detailed analysis of marketed therapies and late-stage (Phase III and Phase II) therapies. It also helps understand the Bispecifics in Oncology Clinical Trial details, pharmacological action, agreements and collaborations related to Bispecifics in Oncology, their approval timelines, patent details, advantages and disadvantages, latest news and press releases.
Bispecifics in Oncology Marketed Drugs
The Bispecifics in Oncology marketed drug section will provide detailed drug profiles of already approved therapies. Information around clinical development activities, launch timing, regulatory milestones along with safety and efficacy data of the therapy will be included.
Bispecifics in Oncology Emerging Drugs
Apart from a comprehensive Bispecifics in Oncology Market Forecast competitive landscape in tabular form, the emerging drug chapters provides the product details and other development activities of the emerging Bispecifics in Oncology Market Size under the late and mid-stage of clinical development for various indications.
Some of the potential therapies in the pipeline include -
Volrustomig: AstraZeneca
Volrustomig (MEDI5752) is a monovalent, PD-1/CTLA-4 bispecific, humanized IgG1 monoclonal antibody engineered to inhibit PD-1, with increased CTLA-4 blockade on PD-1+ specifically activated T cells compared to PD-1- resting peripheral T cells. This mode of action may facilitate enhanced CTLA-4 inhibition at tolerable doses beyond those achievable with current PD-1/CTLA-4 combinations. Volrustomig in multiple Phase III trials across various cancer types, including the eVOLVE-cervical study for locally advanced cervical cancer, eVOLVE-HNSCC for unresected locally advanced head and neck squamous cell carcinoma (HNSCC), eVOLVELung02 for first-line metastatic NSCLC, and eVOLVE-Meso for first-line unresectable malignant pleural mesothelioma.
As per the Q1 2025 presentation, anticipated results for the Phase IIb eVOLVE-01 (NCT06448754) trial of volrustomig in NSCLC are expected in H2 2025.
Givastomig: I-MAB Biopharma and BMS
Givastomig, also known as TJ-CD4B/ABL111 or TJ033721, is a bispecific antibody designed to bind to Claudin 18.2 (CLDN18.2) as a tumor engager and 4-1BB as a conditional T-Cell activator. Givastomig uniquely binds to tumor cells expressing various levels of CLDN18.2, including gastric cancer and pancreatic cancer cells, and conditionally activates intra-tumoral T-cells at the tumor site through 4-1BB. The US FDA granted Orphan Drug Designation to givastomig for the treatment of gastric cancer, including cancer of the gastroesophageal junction.
BNT327: BioNTech and Bristol Myers Squibb
BNT327 is a novel investigational bispecific antibody combining two complementary, validated mechanisms in oncology into one single molecule. BNT327 combines PD L1 checkpoint inhibition aimed at restoring T cells' ability to recognize and destroy tumor cells with the neutralization of VEGF-A. Multiple global trials are ongoing or planned to start in 2025, including three global clinical trials with registrational potential in firstline small cell lung cancer (SCLC), first-line NSCLC and first-line triple-negative breast cancer (TNBC).
Bispecifics in Oncology Drug Class Insights
The Bispecifics in Oncology Drugs Market Insights section will provide comprehensive information on Bispecifics in Oncology as a class. This will include a broad overview of the class and its role in treating specific conditions. Insights may cover the historical clinical development of Bispecifics in Oncology, their mechanism of action, their subtypes and future commercial prospects. Additionally, the section will provide detailed information about current trends, challenges, and future prospects for this class of drugs.
This section will include details on changing Bispecifics in Oncology market dynamics post initiation of clinical development activities of the inhibitor. It will also provide a detailed summary and comparison of all the therapies being developed by leading players in this space. This section will highlight the advantages of one therapy over the other after assessment based on parameters such as data availability in the form of safety and efficacy, number of patients enrolled in each trial, and trial's inclusion criteria. There will be a Key focus on the importance of development and need for the commercial success of these targeted therapies to achieve treatment goals that physicians and patients are looking for. It will also sum up all the early stage players active in this space.
Bispecifics in Oncology Drugs Market Uptake
This section focuses on the Bispecifics in Oncology Drugs Market Uptake rate of potential Bispecifics in Oncology already launched and expected to be launched in the market during 2020-2040, which depends on the competitive landscape, safety, efficacy data, and order of entry. It is important to understand that the key players evaluating their novel therapies in the pivotal and confirmatory trials should remain vigilant when selecting appropriate comparators to stand the greatest chance of a positive opinion from regulatory bodies, leading to approval, smooth launch, and rapid uptake.
Bispecifics in Oncology Pipeline Development Activities
The Bispecifics in Oncology Market report provides insights into different Bispecifics in Oncology clinical trials within Phase III and Phase II stages. It also analyzes key players involved in developing targeted therapeutics.
Bispecifics in Oncology Pipeline Development Activities
The Bispecifics in Oncology Market report covers information on collaborations, acquisitions and mergers, licensing, and patent details for Bispecifics in Oncology.
KOL Views
To keep up with current and future market trends, we incorporate Key physicians, Therapy Area Researcher's, and other Industry Experts' opinions working in the domain through primary research to fill in the data gaps and validate our secondary research. 25+ Key Opinion Leaders (KOLs) were contacted for insights on Bispecifics in Oncology' incorporation in the evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, drug uptake, along with challenges related to accessibility.
Bispecifics in Oncology Qualitative Analysis
We perform qualitative and market Intelligence analysis using various approaches, such as SWOT analysis and Analyst views. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided. These pointers are based on the analyst's discretion and assessment of the cost analysis and existing and evolving treatment landscape.
Bispecifics in Oncology Market Access and Reimbursement
This section will include Bispecifics in Oncology market insights around the standard HTA pricing, recent reformations in 2024 and modifications in reimbursement process in the 7MM. For example, In the United States, a multi payer model exists when it comes to drug pricing regime, which is currently undergoing significant changes, with recent federal legislation, such as the Prescription Drug Pricing Reform provisions of the Inflation Reduction Act, significantly altering the pricing regime under certain federal programs. Whereas in Germany, the market access differs from the systems followed in many other countries as no pricing and reimbursement approval is required during launch of a new therapy.
Moreover, this section will also provide details on reimbursement of approved therapy, if any.
Scope of the Bispecifics in Oncology Market Report
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