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)
engraftement of gene edited CD34+HSC — on day 28 successful engraftement of gene edited CD34+HSC in the bone marrow
dose-limiting toxicity — until EOS (day 90) dose-limiting toxicity (DLT) of Gemtuzumab-Ozogamicin
toxicities according to the Common Terminology Criteria for Adverse Events (CTCAE v5.0) — until EOS (day 90) frequency and grade of AEs with gene-edited HSC transplantation
Trial sites (2)
Facility
City
Region
Status
University Hospital Dresden, Department of Medicine I
Dresden
Germany
University Hospital Heidelberg, Internal Medicine V
Heidelberg
Germany
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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.
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