Larotrectinib 100 mg (Vitrakvi)

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Larotrectinib, marketed possibly as “Lotenib,” is a targeted cancer therapy primarily indicated for solid tumors in both adults and children harboring neurotrophic receptor tyrosine kinase (NTRK) gene fusion. It is recommended when tumors are metastatic or when surgery poses significant risks, and when alternative treatments are not effective or the disease has progressed. The typical dosage is 100 mg orally twice daily, with or without food, until disease progression or unacceptable side effects occur. Larotrectinib capsules should be swallowed whole and not chewed or crushed. Caution is advised during pregnancy due to potential fetal harm, and breastfeeding is not recommended during treatment and for one week after the final dose.

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    Lalotrectinib (brand name Vitrakvi) is a groundbreaking drug that attacks rare genetic defects in certain types of cancer. It is also one of the most selective tropomyosin receptor-kinase (TRK) inhibitors (TRKs), approved for adults and pediatric patients with diagnosed cancer tumors containing NTRK gene fusions, regardless of where the tumor develops within the body. Lalotrectinib is usually administered in liquid or capsule form, with 100 mg being one of the most common strengths in clinical practice.


    Mechanism of action

    Larotrectinib acts by inhibiting TRK fusion proteins by abnormal fusions of Ntrk Genes (Ntrk1, Ntrk2, or Ntrk3). By binding and blocking this TRK protein, lalotrectinib inhibits downstream signaling, which promotes cancer cell proliferation and survival. This particular mechanism makes the drug highly selective, with minimal damage to normal cells and fewer side effects than traditional chemotherapy.


    Indication

    Patients with solid tumors can utilize 100 mg of lalotrectinib.

     

    It has an NTRK gene fusion without acquiring resistance mutations.

     

    If metastatic or surgical resection probably leads to greater morbidity,

     

    There is no adequate alternative therapy, and it will resume after treatment.

     

    It is unique in the fact that it was approved by the US Food and Drug Administration (FDA) based on tumor indications.

    Dosage and administration

    In adults, the dose of lalotrectinib should be 100 mg up to twice daily (200 mg total per day) until disease progression or unacceptable toxicity. In pediatric patients, doses are calculated based on body surface area (BSA).

     

    The individual taking the medicine ought to avoid chewing or grinding the capsules; rather than they should be consumed whole. Patients who are unable to swallow pills have a liquid form.


    Side Effects

    Clinical studies have shown a high response rate in patients with NTRK fusion-positive tumors when treated with Larotrectinib. Most patients have a persistent response, with some tumors significantly diminishing or disappearing completely. General response rates (ORRs) were unanimously high for tumor types, with clinical studies having an average response period of over 12 months.


    Side effects and security profiles

    In contrast to typical chemotherapeutic materials, lalotrectinib is generally well tolerated. However, it may have adverse effects, just like any other medication. Side effects include:

    Fatigue

    Dizziness

    Nausea and vomiting

    anemia

    Increased liver enzymes

    constipation

    cough

    Less common but serious side effects are neurotoxicity, hepatotoxicity, and allergic reactions. Liver function and neurological symptoms should be closely monitored during treatment.


    Drug interactions and preventive measures

    Lalotrectinib is metabolized primarily by the liver enzyme CYP3A4. Therefore, concurrent use with potent CYP3A4 inhibitors (such as ketoconazole) or inductors (such as rifampin) has a significant effect on drug levels. This dosage adjustment must be made. It may also need to be split to give it to patients with existing liver dysfunction, and dosage adjustments may be required based on the results of liver function tests.


    Conclusion

    Larotrectinib 100 mg is a major leap in cancer treatment and provides a powerful and targeted treatment for patients with NTRK fusion-positive cancer. The ability to treat different types of tumors based on genetic variation is a major milestone in personalized medicine. With its impressive security profile and effectiveness, lalotrectinib is the beacon of hope for those who otherwise have limited treatment options.


    Order Now At Mdx Pharma bd….

    To order from MDX Pharma BD, visit their website at https://mdxpharmabd.com, where you can browse products and place orders online. For inquiries or orders via email, contact emedicarepharma@gmail.com. Alternatively, call (+88) 01929123476. Their address is 29, Abdullahpur, Uttara, Dhaka-1230, Bangladesh.

     

    1. How is my reaction to Larotrectinib being monitored over time?

    Doctors monitor tumor size, symptoms, and side effects through imaging scans, clinical tests and regular clinical reviews.

     

    2. Do I need to undergo a genetic test before taking lalotrectinib?

    Yes, genetic testing is necessary to confirm the presence of NTRK gene fusions specifically targeting larotrectinib in tumors.

     

    3. How does larotrectinib function in the body?

    Larotrectinib blocks TRK proteins from NTRK gene fusions, stops cancer cells from growing and helps to shrink or stabilize tumors.

     

    4. What should I do if I missed my lalotrectinib dose?

    Take the missed dose as quickly as possible, unless it is near the next dose. There is absolutely no dosage. Please contact your doctor.

     

    5. What are the frequent side effects of lalotrectinib?

    Frequent side effects include fatigue, dizziness, nausea, vomiting, constipation, cough, and an increase in liver enzymes observed in blood tests.

     

    6. Can I use lalotrectinib during pregnancy or breastfeeding?

    Lactoferrin can be harmful to babies. We do not recommend this during pregnancy or breastfeeding without consultation or risk assessment from a doctor.

    Product Name

    Lotenib

    Generic Name

    Larotrectinib

    Formulation:

    Each capsule contains 100 mg of Larotrectinib.

    Available Pack Size

    Each container includes 30 capsules in a box.

    Available Strength

    100 mg