




Mobocertinib, also known as Mobosertib, Exkivity, or TAK-788, is a targeted therapy drug for treating non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations. The drug is available in various versions, each with its own price point. This article will provide a detailed overview of the different versions of Mobocertinib and their respective prices.
Understanding the different versions of Mobocertinib and their prices can help patients make informed decisions about their treatment options. Here is a breakdown of the available versions and their costs:
The original research version of Mobocertinib is produced by Takeda Pharmaceutical Company Limited, a Japanese company. This version is available in two main forms:
These prices reflect the high cost of research and development for new drugs. Patients should consider these costs when deciding on treatment options.
Several companies produce generic versions of Mobocertinib, which are more affordable alternatives to the original research drug. Here are the details:
These generic versions offer a more accessible option for patients who may not be able to afford the original research drug. However, it is essential to purchase from reputable sources to ensure the quality and safety of the medication.
There are additional generic versions of Mobocertinib available, including:
Patients should consult with their healthcare provider to determine the best version of Mobocertinib for their specific needs and budget. It is also important to verify the authenticity and quality of the medication before use.
While Mobocertinib is an effective treatment for NSCLC with EGFR exon 20 insertion mutations, it is crucial to be aware of potential side effects and precautions. Here are some important considerations for using Mobocertinib:
Mobocertinib can cause life-threatening prolongation of the corrected QT interval (QTc), including potentially fatal torsades de pointes. Before starting treatment, assess the QTc and baseline electrolyte levels. Correct any abnormalities in sodium, potassium, calcium, and magnesium. Regularly monitor QTc and electrolyte levels during treatment. Increase monitoring frequency for patients with risk factors for QTc prolongation, such as congenital long QT syndrome, heart disease, or electrolyte imbalances. Avoid concurrent use of drugs known to prolong the QTc interval and strong or moderate CYP3A inhibitors, which can further prolong the QTc. Adjust the dosage or discontinue Mobocertinib based on the severity of QTc prolongation.
Mobocertinib can cause fatal interstitial lung disease (ILD)/pneumonia. Monitor patients for new or worsening pulmonary symptoms that may indicate ILD/pneumonia. Immediately discontinue Mobocertinib if ILD/pneumonia is suspected, and permanently discontinue the drug if ILD/pneumonia is confirmed.
Mobocertinib can lead to cardiac toxicity, including reduced ejection fraction, cardiomyopathy, and congestive heart failure, which can result in fatal heart failure. Monitor heart function, including baseline and periodic assessments of left ventricular ejection fraction. Adjust the dosage or discontinue Mobocertinib based on the severity of cardiac toxicity.
By being aware of these potential risks and taking appropriate precautions, patients can maximize the benefits of Mobocertinib while minimizing the risks. Always follow the guidance of your healthcare provider and report any unusual symptoms promptly.
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