Continuing our mission to advance therapies for patients who have limited treatment options: our promising early clinical results continue as we report on our third patient from our Deltacel-01 Phase 1 clinical trial treating stage 4 metastatic non-small cell lung cancer (NSCLC) at Beverly Hills Cancer Center. #cartcelltherapy #celltherapy #patientsfirst https://lnkd.in/eEcfirVu
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R&D, Drug Development & Medical Affairs, Market Access Global Clinical Studies and Product Marketing Lifecycle Management across the Globe
Results of Tropion lung study
#BreakingNews: Today we announced topline results from the TROPION-Lung01 phase 3 trial evaluating our investigational #ADC in certain adult patients with previously treated locally advanced or metastatic #NSCLC (non-small cell lung cancer). Click the image for more information about these top line results and what it may mean for patients.
Press Releases - Daiichi Sankyo US
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Did you know? A week ago The FDA has approved #Alecensa (alectinib) for adjuvant treatment in early-stage ALK-positive non-small cell lung cancer following tumor resection #FDAApproval #Lungcancer #Genentech #Alecensa #Oncology #Innovation #Lungcancer #NSCLC #RASLifescienceSolutions
The FDA has given the green light to #Alecensa (alectinib) for adjuvant treatment in early-stage ALK-positive non-small cell lung cancer post-tumor resection. This approval makes #Alecensa the first and only #ALKinhibitor authorized for this use. The decision follows impressive Phase III ALINA trial results, showing a remarkable 76% reduction in disease recurrence or death versus platinum-based chemotherapy. This milestone further solidifies #Genentech's position as a leader in #oncology innovation. #FDAApproval #LungCancer #Genentech #Alecensa #Oncology #Innovation #Lungcancer #NSCLC #RASLifescienceSolutions Detailed News: https://lnkd.in/dvqmbpp2 Follow our page for more industry updates: https://lnkd.in/dGRWp6FD
Genentech Wins FDA Approval for First Adjuvant Therapy for ALK-Positive, Early NSCLC | BioSpace
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Unlocking New Horizons in HER2-Negative Breast Cancer Treatment Pipeline: In-Depth Analysis of Clinical Trials, Therapies, and FDA Approvals – Deep dive into recent developments #Business #HealthMedicine #MarketingSales #PharmaceuticalsBiotech
Unlocking New Horizons in HER2-Negative Breast Cancer Treatment Pipeline: In-Depth Analysis of Clinical Trials, Therapies, and FDA Approvals – Deep dive into recent developments | ABNewswire
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The FDA has given the green light to #Alecensa (alectinib) for adjuvant treatment in early-stage ALK-positive non-small cell lung cancer post-tumor resection. This approval makes #Alecensa the first and only #ALKinhibitor authorized for this use. The decision follows impressive Phase III ALINA trial results, showing a remarkable 76% reduction in disease recurrence or death versus platinum-based chemotherapy. This milestone further solidifies #Genentech's position as a leader in #oncology innovation. #FDAApproval #LungCancer #Genentech #Alecensa #Oncology #Innovation #Lungcancer #NSCLC #RASLifescienceSolutions Detailed News: https://lnkd.in/dvqmbpp2 Follow our page for more industry updates: https://lnkd.in/dGRWp6FD
Genentech Wins FDA Approval for First Adjuvant Therapy for ALK-Positive, Early NSCLC | BioSpace
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Research Analyst @ RAS LifeScience Solutions | Competitive Intelligence | Market Intelligence | Strategic Consulting | Pharma, Life Sciences, Medtech, Healthcare
The FDA approved #Alecensa (alectinib) for early-stage ALK-positive non-small cell lung cancer after tumor removal, making it the first ALK inhibitor for this use. Based on the Phase III ALINA trial, it showed a 76% reduction in disease recurrence or death compared to chemotherapy. This approval reinforces #Genentech's leadership in oncology innovation. ##FDAApproval #LungCancer #Genentech #Alecensa #Oncology #Innovation #Lungcancer #NSCLC #RASLifescienceSolutions Detailed News: https://lnkd.in/dvqmbpp2 Follow our page for more industry updates: https://lnkd.in/dGRWp6FD
The FDA has given the green light to #Alecensa (alectinib) for adjuvant treatment in early-stage ALK-positive non-small cell lung cancer post-tumor resection. This approval makes #Alecensa the first and only #ALKinhibitor authorized for this use. The decision follows impressive Phase III ALINA trial results, showing a remarkable 76% reduction in disease recurrence or death versus platinum-based chemotherapy. This milestone further solidifies #Genentech's position as a leader in #oncology innovation. #FDAApproval #LungCancer #Genentech #Alecensa #Oncology #Innovation #Lungcancer #NSCLC #RASLifescienceSolutions Detailed News: https://lnkd.in/dvqmbpp2 Follow our page for more industry updates: https://lnkd.in/dGRWp6FD
Genentech Wins FDA Approval for First Adjuvant Therapy for ALK-Positive, Early NSCLC | BioSpace
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In case you missed it... 🎉 Big news in the world of oncology! The FDA has approved Genentech's Alecensa as the first ALK inhibitor for early-stage, ALK-positive non-small cell lung cancer post-surgery. 🚀 This follows impressive results from the Phase III ALINA trial where Alecensa reduced the risk of disease recurrence or death by a whopping 76% compared to traditional chemotherapy. It's not just about extending lives; it's about improving the quality of those years, with significant gains in central nervous system-disease-free survival. Genentech is on a roll, also showcasing strong data for Ocrevus and Columvi this week! #HealthcareInnovation #Oncology #FDAApproval #Genentech
Genentech Wins FDA Approval for First Adjuvant Therapy for ALK-Positive, Early NSCLC | BioSpace
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The hottest cancer technology from the turn of the century is finally getting its glow-up moment: antibody-drug conjugates (ADCs) have been outperforming other available drugs across a range of indications, overturning decades of standards of care, and spurring pharma companies to spend $50 billion to snap up their share of the market. Read my latest article in AJMC - The American Journal of Managed Care to learn what this might mean for patients and the broader healthcare industry: https://bit.ly/4c4tUf3 #cancer #oncology #ADCs #pharma #biotech #cancerresearch
Wave of Antibody-Drug Conjugates Poised to Change Treatment Paradigms Across Multiple Cancers
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Innovating HSC-derived NK Immunotherapies | Enthusiast of Biotech Stocks Investing | RTs =/= Endorsements | CCO (Chief Cleaning Officer) of Family
Exciting news from Eli Lilly and Company, announced (08/04/2023) Retevmo® (selpercatinib, a highly selective and potent RET kinase inhibitor) met its primary endpoint from a phase 3 #clinicaltrial (https://lnkd.in/gp7bByze) that demonstrated a statistically significant and clinically meaningful improvement progression-free survival (PFS) compared to a PD-1 inhibitor plus chemotherapy for adults with newly-diagnosed advanced or metastatic RET fusion-positive non-small cell lung cancer. 👍👍👍 Looking forward very much to seeing more results of secondary endpoints.
Lilly's Retevmo® (selpercatinib) is the First Targeted Therapy to Demonstrate Superior Progression-Free Survival Compared to a PD-1 Inhibitor Plus Chemotherapy for Adults with Newly-Diagnosed Advanced or Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer | Eli Lilly and Company
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Co-Director, Center for Applied Proteomics and Molecular Medicine University Professor, George Mason University
Paolo- this is so true! we now have technologies that can quantify the protein expression of all of the current repertoire of ADCs in the same tumor all at once: HER2, HER3, MET, TROP2, CLAUDIN18.2, TF, NECTIN4, FRalpha, MESOTHELIN, CEACAM, PSMA, LIV1, and many others. What are the ADC co-expression dynamics within the same tumor? how do these change after exposure to each ADC? does it even matter what the protein expression levels are? The sequencing will be incredibly interesting as will the resistance mechanisms that ultimately are likely to occur...
With three Antibody-Drug Conjugates approved for treating metastatic breast cancer and several more in phase 3 testing, how are we going to sequence these agents in the clinic? And how can we mitigate their side effects? Thanks to Medscape for this interview. https://t.co/9p4kXvLgHV
How Groundbreaking ADCs Are Helping More Patients With MBC
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Datopotamab Deruxtecan Met Dual Primary Endpoint of Progression-Free Survival in Patients with Advanced Non Small Cell Lung Cancer in TROPION-Lung01 Phase 3 Trial
Positive results from the TROPION-Lung01 Phase III trial of datopotamab deruxtecan demonstrated a statistically significant improvement in PFS compared to chemotherapy
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