The addition of Brentuximab vedotin (Bv) to combination chemotherapy will be safe, well tolerated and effective in children, adolescents and young adults with all stages of newly diagnosed Hodgkin lymphoma (HL).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Day 1 and 15 Dose: 1.2 mg/kg/dose. (Maximum dose is 120 mg)
Days: 1 and 15 Dose: 25 mg/m2/dose.
Days: 1 and 15 Dose: 1.5 mg/m2/dose (max: 2 mg/dose).
New York Medical College
Valhalla, New York, United States
To determine if this combination of chemoimmunotherapy is safe to administer. (Adverse events)
Adverse events will be monitored each cycle to determine if there are any events related possibly, probably or definitely related to study therapy
Time frame: 1 year
To determine the response rate
disease evaluations will be performed after the 2nd, 4th and 6th cycles.
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Days: 2 and 16 Dose: 375 mg/m2/dose.