Finding studies
Finding studies
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Medical College of Wisconsin Cancer Center Clinical Trials Office
CONTACT
Medical College of Wisconsin Cancer Center Clinical Trials Office
CONTACT
Lead
Medical College of Wisconsin
This trial combines two novel agents, mosunetuzumab subcutatneous and polatuzumab vedotin (Mosun-Pola), with cytotoxic chemotherapy while allowing de-escalation in rapidly responding patients. After completing the first two cycles of Mosun-Pola-SD-CHP therapy, subjects will undergo an interim response assessment with positron emission tomography (PET) / computed tomography (CT) and minimal residual disease (MRD) testing (ClonoSEQ; Adaptive Biotechnology) prior to Cycle 3A. Patients who are interim PET-negative and MRD-negative will be placed on an abbreviated treatment regimen, where they will receive Mosun-Pola-SD-CHP therapy for only four cycles.
Age
70–any
Sex
ALL
Healthy volunteers
Not accepted
