Development and full validation of an LC–MS/MS methodology to quantify capmatinib (INC280) following intragastric administration to rats
Author:
Affiliation:
1. Intensive Care UnitShengli Oilfield Central Hospital Dongying China
Publisher
Wiley
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/bmc.4768
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2. Preliminary activity of capmatinib with gefitinib in NSCLC
3. Phase I dose‐escalation study of capmatinib ( INC 280) in Japanese patients with advanced solid tumors
4. Food and Drug Administration. (2018).Guidance for industry: bioanalytical method validation. US Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research and Center for Veterinary Medicine
5. Acquired Resistance of MET-Amplified Non-small Cell Lung Cancer Cells to the MET Inhibitor Capmatinib
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