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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
453 Previous Clinical Trials
237,697 Total Patients Enrolled
Y-mAbs TherapeuticsLead Sponsor
25 Previous Clinical Trials
1,554 Total Patients Enrolled
Jessica Pollard, MDPrincipal InvestigatorDana-Farber Cancer Institute

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there an ongoing recruitment process for this medical research?

"Affirmative, the clinical trial in question is open to participants. The initial posting date was May 25th 2022 with a most recent update taking place on November 18th of that same year. As many as 36 patients are needed between 13 various medical centres."

Answered by AI

To whom is this experiment open to apply?

"Up to 36 minors between the ages of two and twenty-one suffering from acute myeloid leukemia may be admitted into this clinical trial. To qualify, they must present with a pathology confirming their relapsed or refractory AML (excluding APML), have ≥5% disease burden in their marrow, give informed consent as well as assent if required by local regulations, display adequate body weight (>11kg) and performance status scores according to age group (Karnofsky >50/ Lansky >50), WBC count ≤25 x 109/L, no signs or symptoms of cranial palsy nor any radiographic"

Answered by AI

To what degree is CD33*CD3 BsAb a hazard to human health?

"Due to its Phase 1 status, the safety of CD33*CD3 BsAb was classified with a score of 1. This is on account of only minimal clinical data present in regards to efficacy and safety."

Answered by AI

Are elderly patients excluded from this scientific experiment?

"This medical trial requires that participants are between the ages of 2 and 21."

Answered by AI

How many clinical facilities are actively participating in this trial?

"The trial is currently running at 13 different medical centres, including those in Boston, San Francisco and Pittsburgh. To minimize the amount of travel necessary to participate in this study, it's suggested that you choose a clinic located near your residence."

Answered by AI

Could you tell me the upper limit of participants that can join this medical experiment?

"36 willing and eligible patients are requested to participate in this study. Two of the approved sites for enrolling participants are Dana-Farber Cancer Institute (Boston, MA) and UCSF Benioff Children's Hospital (San Francisco, CA)."

Answered by AI
~1 spots leftby Apr 2025