🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Germany / NCT05748171
Recruiting Phase 2

A Study to Learn More About the Study Medicine Called Inotuzumab Ozogamicin (InO) in Children (1 to <18 Years) With First Relapse ALL

NCT05748171 · tracked via the Priya Life Science Germany tracker
Sponsor
Phase
Phase 2
Started
2023-05-17
Last updated
2026-09-24

Condition(s) studied

ACUTE LYMPHOBLASTIC LEUKEMIA

Investigational drug(s) / intervention(s)

Inotuzumab ozogamicin →ALLR3

Inotuzumab ozogamicin: Inotuzumab ozogamicin (BESPONSA™) is a CD22 targeted antibody drug conjugate (ADC) approved in several countries for the treatment of adults with relapsed or refractory B cell precursor acute lymphoblastic leukemia (ALL). The approved starting dose is 1.8mg/m2/cycle.

ALLR3: The ALLR3 chemotherapy regimen (vincristine, mitoxantrone, dexamethasone, and PEG-asparaginase \[or erwinia-asparaginase in the event of an allergic reaction to PEG-asparaginase\]) has been adopted by pediatric oncology groups as treatment for pediatric relapsed/refractory (R/R) acute lymphoblastic leukemia (ALL)

Study summary

This prospective, randomized, multicenter, open-label Phase 2 study is designed to evaluate the superiority of InO monotherapy vs ALLR3 after 1 cycle of induction treatment in paediatric participants (between 1 and \<18 years) with High Risk (HR) or very high risk (VHR) first bone marrow relapse CD22-positive BCP ALL, and to evaluate the safety and tolerability, PK and long-term efficacy. Treatment with study intervention will end after induction therapy; follow-up will continue for up to 5 years from randomization.

Eligibility

Sex
ALL
Min age
1 Year
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: 1. Male or female participants between 1 and \<18 years of age. 2. Morphologically confirmed diagnosis of first relapse HR or VHR BCP ALL; HR first relapse is defined as relapse occurring within 18 to 30 months of original diagnosis of ALL or within 6 months of completion of primary therapy, and lacking any identified very high-risk genetic abnormalities (Groeneveld-Krentz et al, 2019) (ie, KMT2A::AFF1 fusion \[t(4;11)(q21;q23)\], TCF3-HLF fusion \[t(17;19)(q22;p13)\], TCF3-PBX1 fusion \[t(1;19)(q23;p13.3)\], hypodiploidy \[\<40 chromosomes\] or masked low hypodiploidy (Molina et al, 2021), TP53 alteration). VHR first relapse is defined as relapse within 18 months of original diagnosis of ALL and/or with any of the following genetic abnormalities at original diagnosis or at relapse (Groeneveld-Krentz et al, 2019) (ie, KMT2A::AFF1 fusion \[t(4;11)(q21;q23)\], TCF3-HLF fusion \[t(17;19)(q22;p13)\], TCF3-PBX1 fusion \[t(1;19)(q23;p13.3)\], hypodiploidy \[\<40 chromosomes\] or masked low hypodiploidy (Molina et al, 2021), TP53 alteration). * CD22-positive ALL as defined by local institution; * Bone marrow involvement of ≥ 5% leukemic blasts (≥ M2 status). 3. Adequate serum chemistry parameters: * An eGFR in participants 1 to \<2 years of age, or eCrCl in those 2 to \<18 years of age, ≥30 mL/min using the recommended formula in Section 10.10.2. * AST and ALT ≤5 × institutional ULN at the time of randomization or pre-cytoreduction/general anesthesia; (Refer to Appendix 9 for France-specific requirement on the ALT/AST threshold); * Total bilirubin ≤1.5 × institutional ULN unless the participant has documented Gilbert's syndrome; 4. Prior history of thrombosis during corticosteroid use and/or asparaginase are eligible provided the patient receives anti-coagulant prophylaxis per institutional guidelines. 5. Cardiac shortening fraction ≥ 30% by echocardiogram or ejection fraction \>50% by MUGA. 6 Participants with combined bone marrow and testicular relapse are eligible assuming orchiectomy is performed prior to randomization or is planned at the end of induction therapy. 5.2. Exclusion Criteria 1. Any history of prior or ongoing hepatic SOS or prior liver failure \[defined as severe acute liver injury with encephalopathy and impaired synthetic function (INR of ≥1.5)\]. 2. Prior allo-HSCT or CAR T-cell therapy. 3. Isolated extramedullary leukemia. 4. Philadelphia-chromosome positive ALL, ie. BCR-ABL/t(9;22) present. 5. Prior therapy with a calicheamicin-conjugated antibody (eg, InO or gemtuzumab ozogamicin). 6. Participants with active, uncontrolled bacterial, fungal, or viral infection. 7. Hypersensitivity/allergy to both PEG-ASP and Erwinia-ASP

Primary outcome measure(s)

Trial sites (65)

FacilityCityRegionStatus
St. Anna Kinderspital Vienna Austria Recruiting
Cliniques universitaires Saint-Luc Brussels Bruxelles-capitale, Région de Recruiting
UZ Gent Ghent Oost-vlaanderen Recruiting
UZ Leuven Leuven Vlaams-brabant Recruiting
Detska nemocnice FN Brno Brno Brno-město Recruiting
Fakultni Nemocnice Motol a Homolka Prague Czechia Recruiting
Rigshospitalet Copenhagen Capital Region Recruiting
Helsinki university hospital Helsinki Finland Recruiting
Centre Hospitalier Universitaire de Nice - Hôpital l'Archet Nice Alpes-maritimes Recruiting
CHU Strasbourg-Hautepierre, Service d'hematologie oncologie pediatrique, pediatrie 3 Strasbourg Alsace Recruiting
Bordeaux University Hospital - Pellegrin Bordeaux Aquitaine Recruiting
CHU de Toulouse - Hôpital des Enfants - Hemato-Immuno-Oncologie Toulouse Haute-garonne Recruiting
Centre Hospitalier Régional Universitaire de Nancy - Hôpitaux de Brabois Vandœuvre-lès-Nancy Meurthe-et-moselle Recruiting
Hôpital Jeanne de Flandre - CHRU Lille NORD Recruiting
Assistance Publique - Hopitaux de Paris (AP-HP) - Hopital Robert Debre - Centre Hospitalo Universita Paris Paris Recruiting
Institut d'Hématologie et d'Oncologie Pédiatrique Lyon France Recruiting
CHU de Nantes - Hôpital Mère - Enfants Nantes France Recruiting
Hôpital Armand Trousseau Paris France Recruiting
CHRU De Rennes - Hôpital Sud Rennes France Recruiting
Universitaetsklinikum Freiburg Freiburg im Breisgau Baden-Wurttemberg Recruiting
Universitaetsklinikum Ulm Ulm Baden-Wurttemberg Recruiting
Universitaetsklinikum Wuerzburg Würzburg Bavaria Recruiting
Universitätsklinikum Frankfurt Goethe-Universität Frankfurt am Main Hesse Recruiting
Medizinische Hochschule Hannover Hanover Lower Saxony Recruiting
Universitaetsklinikum Essen Essen North Rhine-Westphalia Recruiting
Universitätsklinikum Münster - Albert Schweitzer Campus Münster North Rhine-Westphalia Recruiting
Universitaetsklinikum Schleswig-Holstein Campus Kiel Kiel Schleswig-Holstein Recruiting
Charité Campus Virchow-Klinikum Berlin Germany Recruiting
Universitaetsklinikum Duesseldorf Düsseldorf Germany Recruiting
Universitätsklinikum Gießen Giessen Germany Recruiting
Universitaetsklinikum Hamburg-Eppendorf Hamburg Germany Recruiting
Medizinische Hochschule Hannover Hanover Germany Recruiting
Universitätsklinikum Jena Jena Germany Recruiting
Schneider Children's Medical Center Petah Tikva Central District Recruiting
The Edmond and Lily Safra Children's Hospital; The Chaim Sheba Medical Center Ramat Gan Central District Recruiting
Rambam Health Care Campus Haifa Northern District Recruiting
Tel-Aviv Sourasky Medical Center Dana-Dwek Children's Hospital Tel Aviv TELL ABĪB Recruiting
Azienda Ospedaliera di Rilievo Nazional Santobono Pausilipon Naples Campania Recruiting
IRCCS Istituto Giannina Gaslini Genoa Liguria Recruiting
Fondazione IRCCS San Gerardo dei Tintori Monza Lombardy Recruiting

+ 25 more sites — see the full list on the official registry below.

More Pfizer trials in Germany

Other trials for the same condition

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 NCT05748171 on ClinicalTrials.gov ↗ ← All trials in Germany