PUBLISHER: DelveInsight | PRODUCT CODE: 2167057
PUBLISHER: DelveInsight | PRODUCT CODE: 2167057
DelveInsight's, "AXL Inhibitors - Pipeline Insight, 2026" report provides comprehensive insights about 16+ companies and 20+ pipeline drugs in AXL Inhibitors pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.
AXL Inhibitors: Understanding
AXL Inhibitors: Overview
AXL (anexelekto) is a Receptor Tyrosine Kinase (RTK) belonging to the TAM family. It is a cell-surface transmembrane receptor that exerts regulated kinase activity through its cytoplasmic domain. Other members of the TAM family are Mer and Tyro3. AXL is widely expressed in many organs, such as macrophages, endothelial cells, the heart, liver and skeletal muscle, where it plays a variety of roles, including clearing apoptotic material, regulating cell survival, maintaining vascular integrity, and hematopoiesis.
AXL kinase is a cell membrane receptor and an essential mediator of the biological mechanisms underlying life-threatening diseases. In malignant cells, AXL plays important roles in migration, invasion, cell cycle, and drug sensitivity. AXL therefore plays a role in cancer progression, and has been implicated in a wide variety of malignancies, from solid tumors to hematopoietic cancers, where it is often associated with a poor prognosis.
The kinase structure comprises an extracellular part with two immunoglobulin (Ig)-like domains responsible for ligand binding, a transmembrane region, and an intracellular domain. The growth arrest-specific 6 (Gas6) protein precursor and protein S are primarily responsible for kinase activation as their ligands. Both ligands share a similar domain composition.
AXL inhibitors have been shown to potentiate tumor cell apoptosis and suppress migration and invasion. Targeting AXL enhances the therapeutic efficacy of chemotherapy and other small-molecule inhibitors, such as VEGF, EGFR, PI3K, PARP, and HER2 inhibitors. AXL inhibitors, therefore, have potential high value at the centre of cancer combination therapy, addressing significant unmet medical needs and multiple high-value market opportunities.
"AXL Inhibitors - Pipeline Insight, 2026" report by DelveInsight outlays comprehensive insights of present scenario and growth prospects across the mechanism of action. A detailed picture of the AXL Inhibitors pipeline landscape is provided which includes the disease overview and AXL Inhibitors treatment guidelines. The assessment part of the report embraces, in depth AXL Inhibitors commercial assessment and clinical assessment of the pipeline products under development. In the report, detailed description of the drug is given which includes mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, AXL Inhibitors collaborations, licensing, mergers and acquisition, funding, designations and other product related details.
AXL Inhibitors Emerging Drugs Chapters
This segment of the AXL Inhibitors report encloses its detailed analysis of various drugs in different stages of clinical development, including phase II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.
AXL Inhibitors Emerging Drugs
KC1036 is an investigational, orally administered, small-molecule multi-kinase inhibitor developed by Beijing Konruns Pharmaceutical for the treatment of advanced solid tumors. It targets AXL, FLT3, and vascular endothelial growth factor receptor 2 (VEGFR2), inhibiting tumor-cell proliferation, angiogenesis, metastasis, and mechanisms associated with drug resistance. The drug is being investigated across several cancer indications, including advanced digestive system tumors, esophageal squamous cell carcinoma (ESCC), thymic tumors, and pediatric Ewing sarcoma. In a Phase I study (NCT04387916) involving patients with advanced or metastatic solid tumors, KC1036 demonstrated preliminary antitumor activity, with an objective response rate (ORR) of 13.9% and a disease control rate (DCR) of 80.6% among 36 evaluable patients. In 2026, the drug also demonstrated encouraging Phase II results in advanced or recurrent thymic carcinoma, with an ORR of 20.0% and a DCR of 80.0% in the thymic carcinoma cohort. Currently, the drug is in the Phase III stage of its development for the treatment of Squamous cell cancer.
BA3011 (CAB-AXL-ADC) is a CAB antibody drug conjugate that targets the receptor tyrosine kinase AXL. AXL is an important target as they are expressed in many solid tumors with higher frequency of expression observed in tumors previously treated with anti-PD-1 therapy. This, coupled with the therapeutic index advantages provided by BioAtla's proprietary CAB technology, lends strong rationale for investigating BA3011 and BA3021 in combination with Opdivo. The drug is in the Phase II stage of development for the treatment of ovarian cancer and Non-Small-Cell Lung Cancer.
Denfivontinib (SKI-G-801) is an investigational, orally administered small-molecule dual AXL/FLT3 inhibitor developed by Oscotec, Inc. for the treatment of acute myeloid leukemia (AML). It targets AXL and FLT3 signaling pathways, which are implicated in leukemia-cell survival, proliferation, and treatment resistance. The candidate has undergone clinical evaluation in patients with relapsed or refractory AML. In March 2026, Oscotec entered into an exclusive global option-to-license agreement with Yatiri Bio for the development and commercialization of denfivontinib in AML. It is currently in Phase I for AML and Solid Tumors.
AXL Inhibitors: Therapeutic Assessment
This segment of the report provides insights about the different AXL Inhibitors drugs segregated based on following parameters that define the scope of the report, such as:
There are approx. 16+ key companies which are developing the therapies for AXL Inhibitors. The companies which have their AXL Inhibitors drug candidates in the most advanced stage, i.e. Phase III include, Beijing Konruns Pharmaceutical.
Phases
DelveInsight's report covers around 20+ products under different phases of clinical development like
AXL Inhibitors pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
Products have been categorized under various Molecule types such as
Drugs have been categorized under various product types like Mono, Combination and Mono/Combination.
AXL Inhibitors: Pipeline Development Activities
The report provides insights into different therapeutic candidates in phase II, I, preclinical and discovery stage. It also analyses AXL Inhibitors therapeutic drugs key players involved in developing key drugs.
Pipeline Development Activities
The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging AXL Inhibitors drugs.
Current Treatment Scenario and Emerging Therapies:
Key Players
Key Products
Introduction
Executive Summary
AXL Inhibitors : Overview
Pipeline Therapeutics
Therapeutic Assessment
AXL Inhibitors - DelveInsight's Analytical Perspective
Late Stage Products (Phase III)
KC1036: Beijing Konruns Pharmaceutical
Mid Stage Products (Phase II)
BA 3011: BioAtla
Early Stage Products (Phase I)
Denfivontinib: Oscotec
Preclinical Stage Products
Drug Name: Company Name
Inactive Products
AXL Inhibitors - Collaborations Assessment- Licensing / Partnering / Funding
AXL Inhibitors - Unmet Needs
AXL Inhibitors - Market Drivers and Barriers