DelveInsight’s “Non-Small-Cell Lung Cancer Pipeline Insight 2025” report delivers in-depth analysis of the NSCLC pipeline, highlighting more than 10 companies and 10+ emerging therapies. It encompasses detailed profiles of NSCLC pipeline drugs across clinical and preclinical stages, along with assessments based on product type, development stage, administration route, and molecule type. The report also covers inactive pipeline products in this therapeutic area.
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DelveInsight’s NSCLC pipeline report reveals a dynamic field with over 10 active players advancing more than 10 therapies for NSCLC management.
Leading NSCLC developers include major pharmaceutical firms like GlaxoSmithKline, Novartis, AstraZeneca, Eli Lilly and Company, Pfizer Inc., F. Hoffmann-La Roche Ltd., Merck, Millennium Pharmaceuticals, Inc., Boehringer Ingelheim Pharmaceuticals, Inc., Bristol Myers Squibb, and Sanofi. Innovative biotech companies such as IO Biotech, Transgene, Immutep S.A., Daiichi Sankyo, Inc., Regeneron Pharmaceuticals, Hanmi Pharmaceutical Company Limited, TYK Medicines, Inc.,OBI Pharma , Yuhan Corporation ,Chugai Pharmaceutical , and others are also key contributors.
Yuhan Corporation is advancing Lazertinib (YH25448), a third-generation EGFR tyrosine kinase inhibitor selective for activating EGFR mutations and T790M, currently in Phase 1, 2, and 3 trials. The Phase 1/2 trial is identified as NCT03046992, while the Phase 3 LASER301 trial (NCT04248829) met its primary endpoint compared to gefitinib in EGFR-mutated NSCLC. Lazertinib is approved in Korea and partnered globally. Additionally, Yuhan Corporation, in collaboration with Janssen, is developing the combination of Amivantamab and Lazertinib. Amivantamab is an EGFR/MET bispecific antibody with immune effector function, and Lazertinib is an EGFR TKI; this combination is in Phase 3 under the MARIPOSA trial (NCT04487080), which demonstrated statistically significant overall survival and progression-free survival benefits versus standard EGFR TKIs. The combination is approved or under regulatory review in multiple regions, including Asia.
Chugai Pharmaceutical is involved with Alectinib, an ALK tyrosine kinase inhibitor, in Phase 3 post-approval lifecycle studies. Multiple global trials, such as those in the ALEX lineage, support its use, and recent Japanese label updates include adjuvant and early-line settings based on accumulated global data. Japanese industry-sponsored platform trials, involving various pharmaceutical companies, are evaluating multiple investigational agents and combinations in Phase 1b and 2, with a mixed mechanism of action including immunotherapy combinations and targeted agents. The trial ID is jRCT2031250529, and it focuses on novel drug combinations in advanced NSCLC, with Japanese companies as formal sponsors or co-sponsors.
OBI Pharma does not have any directly sponsored NSCLC trials, focusing instead on ADC and cancer vaccine platforms targeting Globo-H, TROP2, and Nectin-4, with an emphasis on earlier-stage and non-lung indications. Other Taiwanese biotech sponsors primarily participate as trial sites rather than primary sponsors, with no confirmed Phase 1–3 NSCLC trials led by Taiwanese companies in public registries.
Notable NSCLC pipeline therapies include Brigatinib, Tyrosine kinase inhibitors, sintilimab in combination with anlotinib, Osimertinib, Gefitinib, SSGJ-707, Vandetanib, Atezolizumab, Tiragolumab, and more.
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AMG 510: Amgen Developed by Amgen, AMG 510 completed Phase 1 trials in late 2020. Targeting the G12C KRAS mutation—present in about 14% of NSCLC adenocarcinoma cases and 5% of colorectal cancers—AMG 510 is the pioneering drug for this mutation, generating significant anticipation. It has received Fast Track designation from the FDA for metastatic NSCLC with the G12C KRAS mutation and is now in the preregistration phase for NSCLC treatment.
CMP 001: Cytos Biotechnology CMP 001 is a short DNA oligonucleotide mimicking bacterial DNA, encapsulated in noninfectious virus-like particles (VLPs). Designed for direct tumor administration, it triggers the immune system to recognize VLPs as foreign, activating antigen-presenting cells to release the DNA. CMP 001 is currently in Phase 1 trials for NSCLC.
The report offers comprehensive details on companies developing NSCLC therapies, including the total number of therapies per company. It segments therapeutic candidates into early, mid, and late development stages for NSCLC. It also examines targeted therapeutics, including active and inactive (dormant or discontinued) projects. Drugs are analyzed by development stage, administration route, target receptor, monotherapy or combination approach, mechanism of action, and molecular type. Additionally, it provides an in-depth look at collaborations (company-to-company and company-academia), licensing deals, and funding for advancing the NSCLC market. Discover more about NSCLC drug opportunities in our innovative research and development initiatives @ NSCLC Unmet Needs- https://www.delveinsight.com/sample-request/non-small-cell-lung-cancer-nsclc-pipeline-insight?utm_source=apac&utm_medium=promotion&utm_campaign=kkpr
Prominent players include GlaxoSmithKline, Novartis, AstraZeneca, Eli Lilly and Company, Pfizer Inc., F. Hoffmann-La Roche Ltd., Merck, Millennium Pharmaceuticals, Inc., Boehringer Ingelheim Pharmaceuticals, Inc., Bristol Myers Squibb, and Sanofi. Innovative biotech companies such as IO Biotech, Transgene, Immutep S.A., Daiichi Sankyo, Inc., Regeneron Pharmaceuticals, Hanmi Pharmaceutical Company Limited, TYK Medicines, Inc.,OBI Pharma , Yuhan Corporation ,Chugai Pharmaceutical , and others are also actively engaged.
The Non-Small-Cell Lung Cancer (NSCLC) pipeline report evaluates therapies by route of administration, categorizing products as:
By molecule type, NSCLC products are classified as:
By product type, explore the newest developments in NSCLC treatment on our site. Stay updated on our contributions to neurology's future @ NSCLC Market Drivers and Barriers, and Future Perspectives- https://www.delveinsight.com/sample-request/non-small-cell-lung-cancer-nsclc-pipeline-insight?utm_source=apac&utm_medium=promotion&utm_campaign=kkpr
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Non-Small Cell Lung Cancer (NSCLC) Market Insight, Epidemiology and Market Forecast -2034
DelveInsight's “Non-small Cell Lung Cancer Market Insights, Epidemiology, and Market Forecast – 2034” report delivers an in-depth understanding of top oncogenic drivers/biomarkers in NSCLC (such as EGFR, c-MET, ROS1, KRAS, ALK, HER2, BRAF, RET fusion, NRG1 Fusion, NTRK1/2/3 gene fusion, PD-L1, etc.), historical and forecasted epidemiology as well as the NSCLC market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. The NSCLC therapeutics market is driven by advancements in targeted therapies, immunotherapy, and personalized medicine, improving patient outcomes globally.The leading NSCLC Companies developing therapies include - AstraZeneca, Boehringer Ingelheim, Pfizer, Takeda, Johnson & Johnson Innovative Medicine, Eli Lilly and Company, Merck, Bristol-Myers Squibb, Roche, Shanghai Henlius Biotech, AbbVie, Daiichi Sankyo, Nuvation Bio, PDC*line Pharma, Moderna Therapeutics, Pfizer, GSK, Gilead Sciences, BieGene, Nuvalent, and others.
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