본 보고서에서는 미국, EU4(독일, 프랑스, 이탈리아, 스페인), 영국, 일본에서 FAP 억제제 시장 배경, 경쟁 구도, 시장 동향을 상세하게 조사·분석했습니다.
또한 본 보고서는 현재 치료의 실태, 신규 치료제의 동향, 각 치료제 시장 점유율, 2021년부터 2034년까지의 7MM(주요 7개 시장 : 미국, EU4, 영국, 일본)에 있어서 시장 규모의 현황 및 예측을 제공합니다. 또한 미충족 의료 수요에 대해서도 다루어 시장의 잠재성을 평가하고 최적의 사업 기회를 파악하기 위한 내용이 되고 있습니다.
조사 기간 : 2021-2034년
DelveInsight's "FAP Inhibitor - Target Population, Competitive Landscape, and Market Forecast - 2040" report delivers an in-depth understanding of the FAP, Historical and Competitive Landscape as well as the FAP Inhibitor market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.
The FAP market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted 7MM FAP market size from 2020 to 2040. The report also covers current FAP treatment practices/algorithms and unmet medical needs to curate the best opportunities and assess the market's potential.
Study Period: 2020-2040
FAP Understanding
FAP Overview
FAP is a type II transmembrane serine protease selectively expressed on activated fibroblasts, particularly within the tumor microenvironment and sites of tissue remodeling. While largely absent in normal adult tissues, FAP is significantly upregulated in over 90% of epithelial cancers, where it contributes to tumor progression through extracellular matrix remodeling, angiogenesis, immune suppression, and facilitating tumor cell invasion. It is also elevated in fibrotic and inflammatory conditions such as liver cirrhosis, pulmonary fibrosis, rheumatoid arthritis, and wound healing, highlighting its broader role in pathological tissue remodeling. Due to its restricted expression in disease states and functional relevance, FAP has emerged as a valuable target for both diagnostic imaging and therapeutic intervention. Radiolabeled FAP inhibitors (FAPIs) have shown remarkable success in positron emission tomography (PET) imaging, providing high-contrast visualization of tumors and fibrotic lesions with minimal background activity.
These advances have prompted the exploration of FAP-targeted radioligand therapies, antibody-drug conjugates, and CAR T-cell strategies to modulate the tumor stroma and enhance anti-tumor responses. However, challenges remain, including the need for selective inhibition over related proteases and managing off-target effects in fibrotic diseases. Ongoing research aims to improve FAPI pharmacokinetics, enhance therapeutic efficacy, and explore synergistic combinations with immunotherapies. Importantly, the application of FAP-targeted imaging and treatment is expanding beyond oncology into cardiology, pulmonology, and autoimmune disorders. As a result, FAP is increasingly recognized as a promising biomarker and therapeutic target with the potential to revolutionize precision medicine in both cancer and fibrotic disease management.
The FAP epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented as total cases of selected indication for FAP inhibitor, total eligible patient pool for FAP inhibitor in selected indication, total treated cases in selected indication for FAP inhibitor 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 FAP inhibitors reports encloses a detailed analysis of mid and early-stage (Phase II and Phase I) pipeline drugs. It also helps understand the FAP's clinical trial details, 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 Drugs
[18F]FAPI-74: SOFIE
A radioconjugate composed of FAPI-74, a quinoline-based fibroblast activation protein (FAP)-targeted tracer belonging to the group of FAP inhibitors (FAPi) conjugated to the bifunctional, macrocyclic chelating agent 1,4,7-triazacyclononane-N,N',N''-triacetic acid (NOTA) and labeled with the positron-emitting radioisotope fluorine F 18, with potential use as a tracer for FAP-expressing tumors and cancer-associated fibroblasts (CAFs) during PET. Upon administration of fluorine 18F FAPI-74, the FAPI-74 moiety targets and binds to FAP-expressing tumor cells and FAP-expressing CAFs. Upon binding and internalization, FAP-expressing tumor cells and CAFs can be detected during PET imaging. FAP, a cell surface protein, is overexpressed in a variety of human cancer cell types and on CAFs in the tumor microenvironment (TME). NCT05641896 is a clinical trial, specifically a Phase II, multicenter, single-arm, open-label, non-randomized study, evaluating the use of [18F] FAPI-74 PET in patients with gastrointestinal cancers
In October 2023, SOFIE and GE Healthcare (GEHC) entered a licensing agreement to develop, manufacture, and commercialize [68Ga] FAPI-46 and [18F] FAPI-74 for diagnostic and companion diagnostic use. In this agreement, GE HealthCare took on global rights for [68Ga] FAPI-46 and outside-US rights for [18F] FAPI-74. Although SOFIE maintained clinical development and commercialization rights for [18F] FAPI-74 in the US.
AVA6000: Avacta
AVA6000 is very similar to a standard chemotherapy drug called doxorubicin. Like doxorubicin, AVA6000 works to slow or stop the growth of cancer cells by blocking an enzyme. Unlike doxorubicin, however, AVA6000 is a "prodrug," meaning it remains inactive until it reaches the site of the cancer. Because of the way AVA6000 works, it may be useful for treating cancer with fewer side effects than doxorubicin. AVA6000 is given intravenously (by vein).
On 16 January 2025, Avacta announced positive new data from the AVA6000 Phase I trial, demonstrating clinically meaningful tumor shrinkage in patients with salivary gland cancers. Meaningful tumor shrinkage was observed in five out of ten patients, with partial and minor responses, and a 90% disease control rate in this patient group.
FAPI represents a new class of tracers that have applications in the assessment and treatment of various cancers. Ongoing clinical trials are exploring the safety and effectiveness of FAP inhibitors in both cancer and fibrotic diseases, with several compounds progressing to mid-phase clinical trials. Currently there are no approved therapies of FAP inhibitors in the market and despite challenges such as optimizing drug delivery and minimizing toxicity, the development of FAP inhibitors marks a significant advancement in targeted cancer and fibrosis therapy. With further research and clinical validation, FAP inhibitors show promise as a novel therapeutic approach to improve outcomes for patients facing these complex diseases. FAP has garnered attention as a specific marker of carcinoma-associated fibroblasts (CAFs) and activated fibroblasts in tissues undergoing extracellular matrix (ECM) remodeling due to chronic inflammation, fibrosis, or wound healing. Numerous studies have evaluated FAPI across various tumor types, both in diagnostic and therapeutic contexts. The tumor microenvironment (TME) is crucial in understanding cancer biology, primarily located in the ECM comprising blood vessels, growth factors, cytokines, and fibroblasts. Fibroblasts play a key role in collagen production and regulating the homeostasis and inflammation of surrounding cells. A distinct subset, myofibroblasts, possess contractile properties akin to smooth muscle cells. Overexpression of FAP in colorectal cancer (CRC) fibroblasts is linked to adverse clinical outcomes such as increased lymph node metastasis, tumor recurrence, angiogenesis, and reduced overall survival.
Key players, including AstraZeneca, SOFIE/GE Healthcare, BioXcel/OnkosXcel, Boehringer Ingelheim, Avacta, Lantheus and Others, are involved in developing drugs for FAP inhibitors for various indications such as prostate cancer, NSCLC, pancreas cancer, and other malignancies.
This section focuses on the uptake rate of potential emerging FAP expected to be launched in the market during 2025-2040.
FAP Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase 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 FAP market growth over the forecasted period.
Pipeline Development Activities
The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for FAP 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 FAP' evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, drug uptake, along challenges related to accessibility.
DelveInsight's analysts connected with 15+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Centers such as Johns Hopkins Sidney Kimmel Cancer Center, UCSF Health, Memorial Sloan Kettering Cancer Center, Department of Biomedical Science in Penn's School of Veterinary Medicine, Division of Hematology & Oncology, University of Illinois Health, Oncology Department at San Luigi Hospital Center for Thoracic Cancers at the Massachusetts General Hospital, Dana-Farber Brigham Cancer Center, and others.
Their opinion helps understand and validate current and emerging therapy treatment patterns or FAP 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, Medicaid, 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.
Key Updates on FAP