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Pembrolizumab is a modern immuno-oncology drug used to treat patients with unresectable or metastatic melanoma — advanced stages of an aggressive malignant tumor that arises from melanocytes, the pigment-producing cells of the skin.
The drug is widely known under the trade name Keytruda and is manufactured by Merck & Co.
Pembrolizumab is prescribed according to criteria approved by the Ministry of Health of Ukraine. These include:
Criteria for discontinuing therapy have also been defined:
Criteria for prescribing and discontinuing the drug (PDF)
Important. The drug can be obtained exclusively at the National Cancer Institute (Kyiv) — the state enterprise Medical Procurement of Ukraine does not distribute it to the regions.
Further treatment and monitoring will take place under the supervision of oncologists at the National Cancer Institute.
| Course duration | 1 to 2 years depending on the stage (17–35 infusions) |
| Frequency | once every 21 days |
| Infusion duration | 30 minutes |
| Monitoring | before each course, within three days prior to the next infusion |
| National Cancer Institute call center | +38 (044) 334-64-18 |
| Online | Health24 app or website |

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