How Vincristine Works in Babies

Phase: Recruiting

Condition(s): Cancer

NCT Number: NCT05359237 Other Study ID Number(s): PEPN22P1

What Is the Purpose of This Study?

This pilot trial compares drug exposure levels using a new method for dosing vincristine in infants and young children compared to the standard dosing method based on body surface area (BSA) in older children.

Who Can Take Part in This Study?

  • Patients must be =< 12 years of age at the time of study enrollment.
  • Newly diagnosed and relapsed cancer diagnosis that is being treated with vincristine at the 1.5 mg/m^2 dose level.
For a full list of eligibility requirements, visit https://clinicaltrials.gov/study/NCT05359237

 

What Will Happen During This Study?

  • Patients will receive vincristine IV per the standard of care (SOC).
  • Patients will undergo collection of blood samples at baseline (before first vincristine dose), and 2, 6-8, and 18-24 hours after a dose of vincristine.
  • Patients may also undergo collection of blood samples with a second SOC vincristine dose at the same time points.

Principal Investigator

Bhuvana A. Setty
MD

Hematology & Oncology

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