
In the pursuit of health and recovery, rational use of drugs is a crucial part. Patients should be fully aware of the information about the drug, including but not limited to efficacy, dosage, and contraindications, before using any drug. Be sure to follow the doctor's guidance and do not increase or decrease the dose or change the drug at will, so as not to affect the efficacy or cause adverse reactions; Be aware of drug-drug interactions and avoid self-medication.
Lorlatinib is a third-generation anaplastic lymphoma kinase (ALK)/c-ros oncogene 1 (ROS1) tyrosine kinase inhibitor, primarily indicated for the treatment of ALK-positive locally a···【more】
Article source:Captain MedicineRelease date:2026-01-23Recommended:207
Lorlatinib is a third-generation dual-target inhibitor of ALK/ROS1, primarily indicated for the treatment of ALK-positive advanced non-small cell lung cancer (NSCLC). It is particu···【more】
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The price of lorlatinib varies significantly, mainly depending on the drug source (innovator or generic), availability of medical insurance reimbursement, and purchase channel.Late···【more】
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This drug is a prescription medicine. Its use must strictly follow the doctor’s instructions, and it shall not be purchased or dosed without authorization.What is the price of one ···【more】
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The price of Lorlatinib is subject to significant fluctuations due to the impacts of regions, purchase channels, dosage specifications, and medical insurance policies.What is the P···【more】
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The monthly treatment cost of lorlatinib currently available in China fluctuates according to specifications and regional differences, and may change in the future with the adjustm···【more】
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Pfizer recently announced that the U.S. Food and Drug Administration (FDA) has approved a supplemental New Drug Application (sNDA) for the targeted anticancer therapy Lorbrena (lor···【more】
Article source:Captain MedicineRelease date:2026-01-23Recommended:208
On March 3, 2021, Pfizer announced that the U.S. Food and Drug Administration (FDA) had approved the supplemental New Drug Application (sNDA) for Lorbrena (lorlatinib), expanding i···【more】
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At the Presidential Symposium of the 2020 ESMO Annual Congress, results of a head-to-head study comparing lorlatinib versus crizotinib as first-line therapy for advanced ALK-positi···【more】
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In December 2020, the U.S. Food and Drug Administration (FDA) accepted a supplemental New Drug Application (sNDA) for Lorbrena (lorlatinib) for the first-line treatment of patients···【more】
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Pfizer recently announced that the Phase III CROWN study, which evaluates Lorbrena (lorlatinib) as a first-line treatment for patients with advanced anaplastic lymphoma kinase (ALK···【more】
Article source:Captain MedicineRelease date:2026-01-23Recommended:182
Lorbrena (generic name: Lorlatinib) is a next-generation tyrosine kinase inhibitor specifically developed to combat tumors that have developed resistance to other ALK inhibitors, w···【more】
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On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
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Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
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Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address: No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com

Name: Lucius

Telegram name: Vira
No.:0085253923643
Telegram name: Vira
No.:0085253923643