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MEDICAL RECORDCONSENT TO PARTICIPATE IN AN NIH CLINICAL RESEARCH STUDYPRINCIPAL INVESTIGATOR: Tim Green, MD STUDY TITLE:Phase II Study of Combination of Trametinib (ME inhibitor) and Hydroxychloroquine
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01
Consult with a healthcare provider to determine if trametinib MEK combination therapy is appropriate for your condition.
02
Follow the dosage instructions provided by your healthcare provider or pharmacist.
03
Take trametinib MEK combination therapy as directed and at the same time every day.
04
Report any side effects or concerns to your healthcare provider immediately.
05
Do not adjust the dosage or stop taking trametinib MEK without consulting your healthcare provider.

Who needs combination of trametinib mek?

01
Patients with unresectable or metastatic melanoma with a BRAF V600E or V600K mutation may benefit from combination trametinib MEK therapy.
02
Individuals with non-small cell lung cancer with a BRAF V600E mutation may also be candidates for trametinib MEK combination treatment.
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The combination of trametinib and MEK refers to the use of trametinib, a MEK inhibitor, in conjunction with other treatments for specific types of cancer, particularly melanoma and certain other solid tumors.
Oncology clinicians and healthcare providers involved in administering trametinib and MEK inhibitor therapies are required to file combinations, along with pharmaceutical companies developing or studying these drugs.
Filling out the combination of trametinib and MEK typically involves documenting patient information, treatment regimens, dosages, and any adverse effects in clinical trial or treatment records.
The purpose of the trametinib and MEK combination is to enhance the therapeutic efficacy against cancer by targeting specific molecular pathways involved in tumor growth and survival.
Information that must be reported includes patient demographics, treatment details, response rates, side effects, and any relevant clinical outcomes.
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