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Bispecific Antibody

CD33*CD3 BsAb for Acute Myeloid Leukemia

Phase 1
Waitlist Available
Led By Jessica Pollard, MD
Research Sponsored by Y-mAbs Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 52 weeks
Awards & highlights

Study Summary

This trial is testing a new antibody drug to treat relapsed or refractory acute myeloid leukemia in pediatric patients.

Eligible Conditions
  • Acute Myeloid Leukemia, Childhood

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~52 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 52 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Occurrence of Adverse Events
Occurrence of dose limiting toxicities (DLTs)

Trial Design

1Treatment groups
Experimental Treatment
Group I: Subcutaneous administration of CD33*CD3 BsAb up to 12 cyclesExperimental Treatment1 Intervention
Subcutaneous administration of CD33*CD3 BsAb up to 12 cycles

Find a Location

Who is running the clinical trial?

Children's Oncology GroupNETWORK
456 Previous Clinical Trials
239,783 Total Patients Enrolled
Y-mAbs TherapeuticsLead Sponsor
25 Previous Clinical Trials
1,554 Total Patients Enrolled
Jessica Pollard, MDPrincipal InvestigatorDana-Farber Cancer Institute
~1 spots leftby May 2025