ALITRAMETINIB

COMPOSITION
Trametinib dimethyl sulfoxide………………………………2mg
INDICATION
• Trametinib is a kinase inhibitor indicated as a single agent for the treatment of BRAF-inhibitor treatment-naive patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations.
Or in combination with dabrafenib:
• To treat unresectable or metastatic melanoma patients with BRAF V600E or V600K mutation positivity.
• For postoperative adjuvant treatment of BRAF V600E or V600K mutation positive melanoma.
• Used to treat metastatic non-small cell lung cancer caused by BRAF V600E mutation.
PACKAGING: 30 tablets/bottle.
Reg No: 11 L 1256/24
Download ALITRAMETINIB Drug Registration Certificate

Brand name: ALITRAMETINIB


Composition:
Each tablet contains:
Trametinib dimethyl sulfoxide………………………………2mg


Indications:
• Trametinib is a kinase inhibitor indicated as a single agent for the treatment of BRAF-inhibitor treatment-naive patients with unresectable or metastatic melanoma with BRAF V600E or V600K mutations.
Or in combination with dabrafenib:
• To treat unresectable or metastatic melanoma patients with BRAF V600E or V600K mutation positivity.
• For postoperative adjuvant treatment of BRAF V600E or V600K mutation positive melanoma.
• Used to treat metastatic non-small cell lung cancer caused by BRAF V600E mutation.


Dosage:
• Adult patients:2mg orally once daily.
• Pediatric patients:
Body weight 26-37kg:1mg orally once a day.
Body weight 38-50kg:1.5mg orally once a day.
Body weight 51kg and above:2mg orally once daily.
• Take this product at least 1 hour before meals or 2 hours after meals.
• Continue medication, until disease progression or unacceptable toxicity.


Contraindications: None.


Warnings:
• New Primary Malignancies, Cutaneous and Non-Cutaneous.
• Be alert to bleeding events when combined with Dabrafenib and stop taking this product if the situation is serious.
• It may cause venous thromboembolism.
• Cardiomyopathy should be monitored during treatment.
• Embryo-Fetal Toxicity: Can cause fetal harm. Advise females of reproductive potential of potential risk to a fetus and to use effective contraception.


Adverse Effects: Fever, nausea, rash, chills, diarrhea, vomiting, etc.


Dosage form: Yellow tablets.


Expiry date: 24 months from the date of manufacture.


Packaging: 30 tablets/bottle.


Storage:
• Protected from light, sealed in original packaging, and stored at 20℃- 25℃.
• Keep out of reach of children.


DISCLAIMER

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