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  • DOSING, RECONSTITUTION, AND ADMINISTRATION GUIDE
    Calculate the required dose (mg) of TRODELVY based on the patient’s body weight at the beginning of each treatment cycle (or more frequently if the patient's body weight changed by more than 10% since previous administration)
  • TRODELVY Reconstitution, Dilution, and Administration Guide
    Determine the final volume of the infusion solution to deliver the appropriate dose at a TRODELVY concentration range of 1 1 mg mL to 3 4 mg mL For the infusion solution, only use 0 9% Sodium Chloride Injection, USP, since the stability of the reconstituted TRODELVY solution has not been determined with other infusion-based solutions
  • Dosing Information | TRODELVY® (sacituzumab govitecan-hziy)
    Your first infusion will take approximately 3 hours Your healthcare team will observe you during the infusion After that, if prior treatment was well tolerated, your infusions with TRODELVY may take 1 to 2 hours
  • HIGHLIGHTS OF PRESCRIBING INFORMATION See Full Prescribing Information . . .
    First infusion: Administer infusion over 3 hours Observe patients during the infusion and for at least 30 minutes following the initial dose, for signs or symptoms of infusion-related reactions [see Warning and Precautions (5 3)]
  • label - Food and Drug Administration
    TRODELVY was administered as an intravenous infusion once weekly on Days 1 and 8 of 21-day treatment cycles at doses of 10 mg kg until disease progression or unacceptable toxicity
  • TRODELVY® POWDER FOR SOLUTION FOR INFUSION 180 MG VIAL
    Recommended Dose and Schedule The recommended dose of TRODELVY is 10 mg kg administered as an intravenous infusion once weekly on Days 1 and 8 of 21-day treatment cycles Continue treatment until disease progression or unacceptable toxicity Do not administer TRODELVY at doses greater than 10 mg kg Administer TRODELVY as an intravenous
  • HIGHLIGHTS OF PRESCRIBING INFORMATION See Full Prescribing Information . . .
    Prior to each dose of TRODELVY, premedication for prevention of infusion reactions and prevention of chemotherapy-induced nausea and vomiting (CINV) is recommended
  • label - Food and Drug Administration
    TRODELVY was administered as an intravenous infusion once weekly on Days 1 and 8 of 21-day treatment cycles at doses up to 10 mg kg until disease progression or unacceptable toxicity
  • Dosing and Administration | GileadPro
    The recommended dose of Trodelvy® is 10 mg kg administered as an intravenous infusion once weekly on Days 1 and 8 of 21-day treatment cycles1 Watch this short video to learn more about how to appropriately dose and administer Trodelvy®
  • SACITUZUMAB GOVITECAN (Trodelvy) - Thames Valley Cancer Alliance
    **First infusion is to be given over 3 hours, followed by observation period of at least 30 minutes after completion of the infusion to monitor for signs of infusion related reactions





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