CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 51 enrolled
Drug / intervention
Gemtuzumab Ozogamicindrug
Likely dose
Gemtuzumab Ozogamicin 3 mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03727750
NCT03727750Phase 4Completed

A SINGLE ARM, OPEN-LABEL, PHASE 4 STUDY EVALUATING QT INTERVAL, PHARMACOKINETICS, AND SAFETY OF GEMTUZUMAB OZOGAMICIN (MYLOTARG (TRADEMARKER)) AS A SINGLE-AGENT REGIMEN IN PATIENTS WITH RELAPSED OR REFRACTORY CD33-POSITIVE ACUTE MYELOID LEUKEMIA

Pfizer·interventional·Posted Nov 1, 2018·Updated Mar 25, 2022

In Brief

A Phase 4 clinical trial evaluating Gemtuzumab Ozogamicin for ECG and 2 related conditions. Completed, enrolled 51 participants across 24 sites in 6 countries.

Detailed Summary

This is a single-arm, open-label, Phase 4 study evaluating the effect of GO on the QTc, pharmacokinetics, safety, and immunogenicity of GO as a single-agent monotherapy in adult and pediatric patients with relapsed or refractory CD33-positive AML.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Hungary, Poland, Spain, United Kingdom, United States
Collaborators--

Timeline

Phase 4CompletedFinished
20192020202120222023202420252026
First PostedNov 1, 2018
Enrollment StartJul 3, 2019
Primary CompletionApr 27, 2021
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 7.7 years ago

Interventions

Gemtuzumab Ozogamicindrug

Three doses of GO 3 mg/m2 (up to one vial) as a 2 hour intravenous infusion on Cycle 1 Days 1, 4, and 7. A second cycle of GO 3mg/m² (up to one vial) on Cycle 2 Days 1, 4, and 7 will be allowed at the investigator's discretion for patients who meet the criteria