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HomeAboutAboutMOANewly Diagnosed Adult AML (Combination Regimen)Newly Diagnosed Pediatric AML (Combination Regimen)Newly Diagnosed Adult AML (Single-Agent-Regimen)Relapsed or Refractory AML (Single-Agent-Regimen)DosingNewly Diagnosed Adult AML (Combination Regimen)Dosing and Dose ModificationsPreparation and AdministrationNewly Diagnosed Pediatric AML (Combination Regimen)Dosing and Dose ModificationsPreparation and AdministrationNewly Diagnosed Adult AML (Single-Agent-Regimen)Dosing and Dose ModificationsPreparation and AdministrationRelapsed or Refractory AML (Single-Agent-Regimen)Dosing and Dose ModificationsPreparation and AdministrationEfficacy and SafetyNewly Diagnosed Adult AML (Combination Regimen)EfficacyStudy DesignSafety ProfileNewly Diagnosed Pediatric AML (Combination Regimen)EfficacyStudy DesignSafety ProfileNewly Diagnosed Adult AML (Single-Agent Regimen)EfficacyStudy DesignSafety ProfileRelapsed or Refractory AML (Single-Agent Regimen)EfficacyStudy DesignSafety ProfileSupport Your PatientsSupport Your PatientsAccess and Patient SupportOrdering MYLOTARG
Full Prescribing Information, Including BOXED WARNINGIndications
Preparation & AdministrationNewly Diagnosed Adult AML (Single-Agent Regimen)RECONSTITUTIONDILUTIONADMINISTRATIONDilution1

Calculate the required volume of the reconstituted solution needed to obtain the appropriate dose according to patient BSA.1

Withdraw this amount from the vial(s) using a syringe. PROTECT FROM LIGHT.1

Discard any unused reconstituted solution left in the vial.1

Doses must be mixed to a concentration between 0.075 mg/mL to 0.234 mg/mL. For additional dilution information, see below. PROTECT FROM LIGHT.1

Calculate the required volume of the reconstituted solution needed to obtain the appropriate dose according to patient BSA.1

Withdraw this amount from the vial(s) using a syringe. PROTECT FROM LIGHT.1

Discard any unused reconstituted solution left in the vial.1

Doses must be mixed to a concentration between 0.075 mg/mL to 0.234 mg/mL. For additional dilution information, see below. PROTECT FROM LIGHT.1

Additional Dilution Information1,2

Doses must be mixed to a concentration between 0.075 mg/mL to 0.234 mg/mL according to the following instructions:

  • Doses less than 3.9 mg must be prepared for administration by syringe. Add the reconstituted MYLOTARG solution to a syringe with 0.9% Sodium Chloride Injection to a final concentration between 0.075 mg/mL to 0.234 mg/mL. PROTECT FROM LIGHT.
  • Doses greater than or equal to 3.9 mg are to be diluted in a syringe or a polyvinyl chloride (PVC) with di(2-ethylhexyl)phthalate (DEHP), non-PVC polyolefin, or ethylene vinyl acetate intravenous infusion bag in an appropriate volume of 0.9% Sodium Chloride Injection to ensure a final concentration between 0.075 mg/mL to 0.234 mg/mL. PROTECT FROM LIGHT.

Examples of appropriate infusion containers based on dose are summarized in the table below:


Gently invert the infusion container to mix the diluted solution. DO NOT SHAKE.1


Following dilution with 0.9% Sodium Chloride Injection, MYLOTARG solution should be infused immediately. If not used immediately, the diluted solution may be stored up to 18 hours in a refrigerator (2°C to 8°C; 36°F to 46°F) and for up to 6 hours at room temperature (up to 30°C). The allowed time at room temperature (up to 30°C) includes the time required for preparation of the diluted solution, equilibration, if needed, and the 2 hours needed to administer to the patient. PROTECT FROM LIGHT and DO NOT FREEZE.1

Gently invert the infusion container to mix the diluted solution. DO NOT SHAKE.1

Following dilution with 0.9% Sodium Chloride Injection, MYLOTARG solution should be infused immediately. If not used immediately, the diluted solution may be stored up to 18 hours in a refrigerator (2°C to 8°C; 36°F to 46°F) and for up to 6 hours at room temperature (up to 30°C). The allowed time at room temperature (up to 30°C) includes the time required for preparation of the diluted solution, equilibration, if needed, and the 2 hours needed to administer to the patient. PROTECT FROM LIGHT and DO NOT FREEZE.1

BSA=body surface area.References:MYLOTARG Prescribing Information. New York, NY: Pfizer Inc.Data on file. Pfizer Inc., New York, NY.
Newly Diagnosed Adult AML 
(Single-Agent Regimen)

To report an adverse event, please call 1-800-438-1985

Pfizer for Professionals 1-800-505-4426

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INDICATIONS

MYLOTARG™ (gemtuzumab ozogamicin) is indicated for the treatment of:

  • Newly diagnosed CD33-positive acute myeloid leukemia (AML) in adults and pediatric patients 1 month and older
  • Relapsed or refractory CD33-positive AML in adults and pediatric patients 2 years and older
Important Safety Information

WARNING: Hepatotoxicity, including severe or fatal hepatic veno-occlusive disease (VOD), also known as sinusoidal obstruction syndrome (SOS), has been reported in association with the use of MYLOTARG as a single agent, and as part of a combination chemotherapy regimen. Monitor frequently for signs and symptoms of VOD after treatment with MYLOTARG.

Contraindications: Hypersensitivity to MYLOTARG or any of its components. Reactions have included anaphylaxis.

Hepatotoxicity, Including Veno-occlusive Liver Disease (VOD): Hepatotoxicity, including life-threatening and sometimes fatal hepatic VOD events, have been reported in patients receiving MYLOTARG as a single agent or as part of a combination chemotherapy regimen. Based on an analysis across trials, the risk of VOD was higher in adult patients who received higher doses of MYLOTARG as monotherapy, in patients with moderate or severe hepatic impairment prior to receiving MYLOTARG, in patients treated with MYLOTARG after HSCT, and in patients who underwent HSCT after treatment with MYLOTARG. Although no relationship was found between VOD and time of HSCT relative to higher MYLOTARG monotherapy doses, the ALFA-0701 study recommended an interval of 2 months between the last dose of MYLOTARG and HSCT. Assess ALT, AST, total bilirubin, and alkaline phosphatase prior to each dose of MYLOTARG. After treatment with MYLOTARG, monitor frequently for signs and symptoms of VOD; these may include elevations in ALT, AST, and total bilirubin, hepatomegaly, rapid weight gain, and ascites. Monitoring only total bilirubin may not identify all patients at risk of VOD. For patients who develop abnormal liver tests, more frequent monitoring of liver tests and clinical signs and symptoms of hepatotoxicity is recommended. For patients who proceed to HSCT, monitor liver tests frequently during the post-HSCT period, as appropriate. Manage signs or symptoms of hepatic toxicity by dose interruption or discontinuation of MYLOTARG. In patients who experience VOD, discontinue MYLOTARG and treat according to standard medical practice.

Infusion-Related Reactions (Including Anaphylaxis): Life-threatening or fatal infusion-related reactions can occur during or within 24 hours following infusion of MYLOTARG. Signs and symptoms of infusion-related reactions may include fever, chills, hypotension, tachycardia, hypoxia, and respiratory failure. Premedicate prior to MYLOTARG infusion. Monitor vital signs frequently during infusion. Interrupt infusion immediately for patients who develop evidence of infusion reaction, especially dyspnea, bronchospasm, or hypotension. Monitor patients during and for at least 1 hour after the end of the infusion or until signs and symptoms completely resolve. Discontinue use of MYLOTARG in patients who develop signs or symptoms of anaphylaxis, including severe respiratory symptoms or clinically significant hypotension.

Hemorrhage: MYLOTARG is myelosuppressive and can cause fatal or life-threatening hemorrhage due to prolonged thrombocytopenia. In ALFA-0701, (MYLOTARG in combination with chemotherapy), all grades and Grade 3-4 bleeding events were reported in 118/131 (90%) and 27/131 (21%) patients, respectively. Fatal bleeding events (including cerebral hematoma, intracranial hematoma, and subdural hematoma) occurred in 4/131 (3%) patients. The proportion of patients with persistent thrombocytopenia increased with progressive treatment phases and was higher in patients treated with MYLOTARG plus chemotherapy than with chemotherapy alone. In AAML0531, the addition of MYLOTARG to chemotherapy in pediatric patients was associated with a higher incidence of prolonged thrombocytopenia and neutropenia particularly when used in Intensification 2. Assess blood counts prior to each dose of MYLOTARG and monitor blood counts frequently after treatment with MYLOTARG until resolution of cytopenias. Monitor patients for signs and symptoms of bleeding during treatment with MYLOTARG. Manage severe bleeding, hemorrhage, or persistent thrombocytopenia using dose delay or permanent discontinuation of MYLOTARG, and provide supportive care per standard practice.

QT Interval Prolongation: QT interval prolongation has been observed in patients treated with other drugs containing calicheamicin. When administering MYLOTARG to patients who have a history of or predisposition for QTc prolongation, who are taking medicinal products that are known to prolong QT interval, and in patients with electrolyte disturbances, obtain electrocardiograms and electrolytes prior to the start of treatment and as needed during administration.

Adverse Cytogenetics: In a subgroup analysis in ALFA-0701, the addition of MYLOTARG to standard combination chemotherapy did not improve event-free survival in the subgroup of patients having adverse-risk cytogenetics. For patients being treated with MYLOTARG in combination with daunorubicin and cytarabine for newly diagnosed de novo AML, when cytogenetics testing results become available consider whether the potential benefit of continuing treatment with MYLOTARG outweighs the risks for the individual patient.

Embryo-Fetal Toxicity: MYLOTARG can cause embryo-fetal harm when administered to a pregnant woman. Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with MYLOTARG and for at least 6 months after the final dose. Advise males with female partners of reproductive potential to use effective contraception during treatment with MYLOTARG and for at least 3 months after the last dose.

Adverse Reactions: All grade treatment-emergent adverse events (>15%) in adult patients exposed to MYLOTARG 3 mg/m2 on Days 1, 4, and 7 as monotherapy included fever (79%), infection (42%), increased AST (40%), bleeding (23%), nausea and vomiting (21%), constipation (21%), mucositis (21%), headache (19%), increased ALT (16%), and rash (16%). In a study of newly diagnosed pediatric patients 1 month and older (AAML0531), in the MYLOTARG + chemotherapy arm, grade 3 or 4 adverse reactions (≥15%) during induction 1 included infection (36%), febrile neutropenia (32%), and decreased appetite (15%); grade 3 or 4 adverse reactions (≥15%) during intensification 2 included infection (67%), febrile neutropenia (24%), and decreased appetite (19%).

IndicationSMYLOTARG is indicated for the treatment of
  • Newly diagnosed CD33-positive acute myeloid leukemia (AML) in adults and pediatric patients 1 month and older
  • Relapsed or refractory CD33-positive AML in adults and pediatric patients 2 years and older
Please see full Prescribing Information, including BOXED WARNING.