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    Capmatinib Rahika 200mg Tablets

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    🩺Medically reviewed by Dr. Elena Vasquez, MD, PhD, FASCO · Last reviewed: May 2025
    Generic:CapmatinibFormat:Box of 12 tabletsStrength:200mgManufacturer:NovartisCategory:Anti CancerAvailability:Limited Stock

    What is Capmatinib (Rahika) Used For?

    • Capmatinib (Rahika) is used for:
    • MET Exon 14 Skipping NSCLC – Treatment of metastatic non-small cell lung cancer with MET exon 14 skipping mutations
    • Treatment-NaΓ―ve Patients – First-line therapy for MET-altered NSCLC
    • Previously Treated NSCLC – For patients who progressed on prior therapies

    How Does Capmatinib Work?

    • Capmatinib contains a selective MET inhibitor, which:
    • Blocks the MET receptor tyrosine kinase signaling pathway
    • Inhibits MET phosphorylation and downstream signaling
    • Stops cancer cell proliferation driven by MET pathway abnormalities

    How to Use Capmatinib

    Dosage: 400mg (two 200mg tablets) twice daily, totaling 800mg per day

    Administration: Take orally with or without food; swallow tablets whole

    Precaution: Requires confirmation of MET exon 14 skipping mutation via FDA-approved test; monitor for interstitial lung disease; oncologist supervision mandatory

    Side Effects of Capmatinib

    Common Side Effects: Peripheral edema, nausea, fatigue, vomiting, dyspnea, decreased appetite

    Serious Side Effects (seek medical help): Interstitial lung disease/pneumonitis, hepatotoxicity, photosensitivity reactions

    Benefits

    • Selective MET kinase inhibitor β€” first FDA-approved targeted therapy for MET exon 14 skipping NSCLC
    • Oral twice-daily dosing provides convenient outpatient treatment
    • Effective in both treatment-naΓ―ve and previously treated patients
    • High response rate in MET exon 14 skipping mutation-positive disease (GEOMETRY mono-1 trial)
    • Biomarker-driven precision therapy β€” only appropriate when MET exon 14 mutation is confirmed

    Warnings and Precautions

    • ILD/pneumonitis: monitor for new or worsening respiratory symptoms; withhold and investigate promptly
    • Hepatotoxicity: liver function tests required before starting, every 2 weeks for 3 months, then monthly
    • Photosensitivity: use broad-spectrum sunscreen SPF 30+; limit direct sun exposure during treatment
    • Embryo-fetal toxicity: effective contraception required during treatment and 1 week after last dose
    • Peripheral edema is common β€” grade severity and manage with dose modification or diuretics if needed
    • Confirm MET exon 14 skipping mutation via FDA-approved diagnostic test before initiating

    Drug Interactions

    • CYP1A2 substrates (theophylline, certain antidepressants): Capmatinib inhibits CYP1A2 β€” monitor and consider dose reduction of these substrates
    • P-glycoprotein substrates (digoxin): Capmatinib may increase plasma concentrations
    • Strong CYP3A4 inducers (rifampicin, carbamazepine): may reduce Capmatinib efficacy β€” avoid concurrent use

    Storage Information

    • Store at room temperature 20Β°C–25Β°C in original packaging; protect from moisture
    • Keep tablets in original blister until time of use
    • Do not use after expiry date

    Frequently Asked Questions

    Q1: What is Capmatinib (Rahika) used for?

    Capmatinib is a targeted therapy for metastatic non-small cell lung cancer (NSCLC) specifically with MET exon 14 skipping mutations, identified through FDA-approved molecular testing.

    Q2: How does Capmatinib work?

    Capmatinib is a selective MET kinase inhibitor. It blocks the MET receptor tyrosine kinase signaling pathway, preventing MET-driven tumor cell proliferation, survival, and migration.

    Q3: What test is needed before starting Capmatinib?

    An FDA-approved test to confirm MET exon 14 skipping mutation in tumor tissue or blood (liquid biopsy) is required before starting Capmatinib. Without this mutation, the drug is not indicated.

    Q4: How is Capmatinib administered?

    Take 400mg (two 200mg tablets) orally twice daily, totaling 800mg/day, with or without food. Swallow tablets whole β€” do not crush or split.

    Q5: How long is Capmatinib treatment continued?

    Treatment continues until disease progression or unacceptable toxicity, as determined by your oncologist. Response is monitored by imaging and clinical assessment.

    Q6: What are the most common side effects?

    Common side effects include peripheral edema (hand/foot swelling), nausea, fatigue, vomiting, dyspnea, and decreased appetite. These are generally manageable.

    Q7: What serious side effects require emergency care?

    Seek immediate care for: new or worsening respiratory symptoms (possible interstitial lung disease/pneumonitis), signs of liver damage (jaundice, dark urine), or severe skin reactions to sunlight (photosensitivity).

    Q8: Does Capmatinib interact with other drugs?

    Capmatinib interacts with CYP1A2 substrates (certain antidepressants, theophylline) and P-gp substrates. Strong CYP3A4 inducers may reduce efficacy. Always disclose all medications to your oncologist.

    Q9: Can Capmatinib be taken with food?

    Yes, Capmatinib can be taken with or without food. Consistent timing twice daily is more important than meal timing.

    Q10: Is Capmatinib safe during pregnancy?

    No. Capmatinib can cause fetal harm. Women of reproductive potential must use effective contraception during treatment and for 1 week after the last dose. Male patients should use contraception for 1 week after treatment.

    Q11: What monitoring is required during Capmatinib treatment?

    Regular monitoring includes liver function tests (before starting, every 2 weeks for 3 months, then monthly), renal function, and imaging to assess tumor response. Report any new respiratory symptoms promptly.

    Q12: Is Capmatinib available without a prescription?

    No. Capmatinib is a prescription-only targeted oncology drug requiring oncologist supervision, molecular testing, and regular monitoring.

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