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  • AML treatment Mylotarg stalled at the DREC review
  • by Lee, Tak-Sun | translator Hong, Ji Yeon | Jan 9, 2025 05:56am
HIRA disclosed reports from the DREC review held in November last year
Priced higher than that of alternative drugs¡¦does not meet the criteria for an economic assessment
 ¡ã Product photo of Mylotarg
The high price was found to be the reason Pfizer Korea's new drug Mylotarg (gemtuzumab ozogamicin), a treatment for acute myeloid leukemia (AML), did not pass the Health Insurance Review and Assessment Service (HIRA) stage.

HIRA acknowledged the drug's improvement in clinical utility but did not approve its cost-effectiveness.

According to industry sources on January 7, HIRA recently disclosed a report from the Drug Reimbursement Evaluation Committee (DREC) held in November 2024 on the non-reimbursement assessment review for Mylotarg inj 4.5mg.

Mylotarg is an antibody-drug conjugate (ADC) that can be used for the first-line treatment of newly diagnosed adult patients with CD33-positive AML. It binds to cells
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