Evaluation of the absolute oral bioavailability of the anaplastic lymphoma kinase/c-ROS oncogene 1 kinase inhibitor lorlatinib in healthy participants
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Cancer Research,Pharmacology,Toxicology,Oncology
Link
https://link.springer.com/content/pdf/10.1007/s00280-021-04368-1.pdf
Reference13 articles.
1. Zou HY, Friboulet L, Kodack DP, Engstrom LD, Li Q, West M et al (2015) PF-06463922, an ALK/ROS1 inhibitor, overcomes resistance to first and second generation ALK inhibitors in preclinical models. Cancer Cell 28:70–81. https://doi.org/10.1016/j.ccell.2015.05.010
2. Shaw AT, Solomon BJ, Chiari R, Riely GJ, Besse B, Soo RA et al (2019) Lorlatinib in advanced ROS1-positive non-small-cell lung cancer: a multicentre, open-label, single-arm, phase 1–2 trial. Lancet Oncol 20:1691–1701. https://doi.org/10.1016/s1470-2045(19)30655-2
3. Solomon BJ, Besse B, Bauer TM, Felip E, Soo RA, Camidge DR et al (2018) Lorlatinib in patients with ALK-positive non-small-cell lung cancer: results from a global phase 2 study. Lancet Oncol 19:1654–1667. https://doi.org/10.1016/s1470-2045(18)30649-1
4. Syed YY (2019) Lorlatinib: first global approval. Drugs 79:93–98. https://doi.org/10.1007/s40265-018-1041-0
5. Shaw AT, Bauer TM, de Marinis F, Felip E, Goto Y, Liu G, Mazieres J, Kim DW, Mok T, Polli A, Thurm H, Calella AM, Peltz G, Solomon BJ, CROWN Trial Investigators (2020) First-line Lorlatinib or Crizotinib in advanced ALK-positive lung cancer. N Engl J Med 383(21):2018–2029. https://doi.org/10.1056/nejmoa2027187
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