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Clinical Trials in Germany / NCT05662904
Starting soon Phase 1

Genetic Ablation of CD33 in HSC to Broaden the Therapeutic Index of CD33-directed Immunotherapy in Patients with AML

NCT05662904 · tracked via the Priya Life Science Germany tracker
Phase
Phase 1
Started
2028-01
Last updated
2025-03-14

Condition(s) studied

Relapsed/Refractory Acute Myeloid Leukemia (AML)

Investigational drug(s) / intervention(s)

Donor-derived CD34+ HSC with CRISPR/Cas9-mediated CD33 deletionGemtuzumab Ozogamicin →

Donor-derived CD34+ HSC with CRISPR/Cas9-mediated CD33 deletion: CD33-deleted CD34+ hematopoietic stem cells derived from the initially matched family donor

Gemtuzumab Ozogamicin: Intrapatient intra-individual dose escalation Level 0: GO day 1 Level 1: GO day 1, day 4 Level 2: GO day 1, day 4, day 7 with repetition after 21 to 28 days up to 84 days.

Study summary

The study "GALAXY33" is an open-label, prospective, nonrandomized, one arm phase I clinical trial in which patients with relapsed AML after allogeneic hematopoietic stem cell transplantation will be transplanted with CD33-deleted CD34+ HSC derived from the initially matched family donor.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria: * confirmed AML according to the WHO classification * relapsed disease after allo-SCT from an HLA-identical family donor (≥ 2 months after allo-SCT at time of inclusion) * ≤ 29% of bone marrow blasts as detected by cytomorphology or immunohistochemistry * age ≥ 18 years * confirmed CD33 expression on leukemic blasts at current relapse (as detected by flow cytometry) * adequate organ function: * Renal function defined as: serum creatinine of ≤ 2x ULN or eGFR ≥ 30 mL/min/1.73 m2 * Liver function defined as: * ALT ≤ 3 times the ULN for the respective age * Bilirubin ≤ 2.0 mg/dl with the exception of patients with hyperbilirubinemia explained by Gilbert-Meulengracht syndrome (may be included if total bilirubin is ≤ 3.0 x ULN and direct bilirubin ≤ 1.5 x ULN) or extrahepatic disease (e.g. chronic hemolytic anemia) * Minimum level of pulmonary reserve defined as ≤ grade 1 dyspnea and pulse oxygenation \> 90% on room air * Hemodynamic stability and LVEF ≥ 40% as confirmed by echocardiogram * Absolute lymphocyte count (ALC) ≥ 100/mm3 Key Exclusion Criteria: * ECOG performance status \>2 * Confirmed CNS involvement * Acute or chronic Graft versus Host disease (GvHD) * Availability of other curative standard treatment options * Prior treatment with GO * Prior hepatic veno-occlusive disease (VOD) or sinusoidal obstruction syndrome (SOS) * Uncontrolled active hepatitis B or C * HIV-positivity * Uncontrolled bacterial, viral or fungal infection * Participation in another clinical trial at the time of screening * Organ dysfunction (liver, kidney, lung, heart) that is a contraindication for conditioning therapy * Severe concomitant disease (e.g. uncontrolled arterial hypertension, heart failure NYHA III-IV, uncontrolled diabetes mellitus, uncontrolled hyperlipidemia) * Unstable angina and/or myocardial infarction within 3 months prior to screening * Pregnant or nursing (lactating) women

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
University Hospital Dresden, Department of Medicine I Dresden Germany
University Hospital Heidelberg, Internal Medicine V Heidelberg Germany

More German Cancer Research Center trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05662904 on ClinicalTrials.gov ↗ ← All trials in Germany