Working… Menu
Trial record 13 of 25 for:    "Acute Lymphocytic Leukemia" | "inotuzumab ozogamicin"

Study of Inotuzumab Ozogamicin Combined to Chemotherapy in Older Patients With Philadelphia Chromosome-negative CD22+ B-cell Precursor ALL (EWALL-INO)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03249870
Recruitment Status : Recruiting
First Posted : August 15, 2017
Last Update Posted : April 5, 2018
Information provided by (Responsible Party):
Patrice Chevallier, Nantes University Hospital

Brief Summary:
The aim of the present EWALL-INO study is to confirm very promising results obtained with a combination of INO and mild chemotherapy in older de novo CD22+ B-ALL patients. For that purpose, safety and efficacy of a weekly INO administration combined to mild-intensity chemotherapy will be evaluated in a cohort of patients aged more than 55 years with newly diagnosed previously untreated Ph-negative (CD22+) BCP-ALL. Conversely to the MDACC miniHCVD-INO study and in order to lower the overall toxicity of the combination, INO will be given as part of the remission induction treatment phase during the first 2 treatment cycles only, in combination with corticosteroid, vincristine, cyclophosphamide and intrathecal prophylaxis only; then, all responding patients will received standard INO-free chemotherapy as consolidation and maintenance.

Condition or disease Intervention/treatment Phase
Acute Lymphoblastic Leukemia (ALL) - Philadelphia Chromosome (Ph)-Negative CD22+ B-cell Precursor (BCP) Drug: Inotuzumab ozogamicin (INO) Phase 2

Detailed Description:

INO schedule of administration will be as described in the refractory/relapsed INO-VATE study for the first cycle, with sequential day 1/8/15 doses of 0.8, 0.5 and 0.5 mg/m2, respectively. Reduced dose of INO will be used for the second and last cycle (0.5 mg/m2 on day 1/8). This was retained in order:

  1. to minimize potential toxicities, including liver disorders and prolonged thrombocytopenia; and
  2. to allow delivery of subsequent chemotherapy consolidations cycles.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 130 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2 Study of Inotuzumab Ozogamicin (INO) Combined to Chemotherapy in Older Patients With Philadelphia Chromosome-negative CD22+ B-cell Precursor Acute Lymphoblastic Leukemia
Actual Study Start Date : December 28, 2017
Estimated Primary Completion Date : October 2021
Estimated Study Completion Date : October 2021

Arm Intervention/treatment
Experimental: Inotuzumab ozogamicin (INO) Drug: Inotuzumab ozogamicin (INO)

INO schedule of administration is as follows:

  • First induction course: 0.8 mg/m² on day 1, 0.5 mg/m² on day 8, and 0.5 mg/m² on day 15
  • Second induction course: 0.5 mg/m² on day 1, and 0.5 mg/m² on day 8

Primary Outcome Measures :
  1. Assessment of overall survival (OS) [ Time Frame: one year ]
    The primary objective of the trial is to assess overall survival (OS) observed at 1 year after administration of INO and chemotherapy in older Ph-negative BCP-ALL patients.

Secondary Outcome Measures :
  1. Assessment of adverse events (AEs) [ Time Frame: 3 months ]
    Type, duration and frequency of AEs up to 3 months of induction course 1 or 2

  2. Rate of complete remission (CR / CRp) [ Time Frame: 35 days ]
    CR/CRp response rate after INO-based induction course 1 and 2

  3. Assessment of Minimal residual disease (MRD) [ Time Frame: 35 days ]
    Flow cytometry and Ig-TCR MRD levels, after INO-based induction course 1 and 2 and impact on outcomes

  4. Rate of early death [ Time Frame: 100 days ]
    Early death (ED) rate at 30, 60 and 100 day from treatment initiation

  5. Composite measure for Duration of response (DOR), Disease-free survival (DFS) and cumulative incidence of relapse (CIR) [ Time Frame: one year ]
    Duration of response (DOR), Disease-free survival (DFS) and cumulative incidence of relapse (CIR)

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   55 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patients aged more than 55 years old,
  • With confirmed diagnosis of BCP-ALL according to World Health Organisation (WHO) criteria expressing the CD22 antigen by flow cytometry (20% or more positive blast cells),
  • Without central nervous system (CNS) involvement,
  • Without BCR-ABL fusion by standard cytogenetics, Fluorescence In Situ Hybridization (FISH) analysis and/or RT-PCR,
  • Previously untreated,
  • Eligible to intensive chemotherapy, due to general health status,
  • ECOG performance status ≤ 2,
  • Patients must have the following laboratory values unless considered due to leukemia: AST and ALT ≤ 2.5 x upper the limit of normal (ULN); estimated GFR ≥ 50 mL/min using the MDRD equation; total and direct serum bilirubin ≤ 1.5 x ULN; electrolyte panel within normal ranges for the institution unless attributed to the underlying disease.
  • Written informed consent obtained prior to any screening procedures.
  • Eligible for National Health Insurance in France.

Exclusion Criteria:

  • Concurrent therapy with any other investigational agent or cytotoxic drug,
  • Prior documented chronic liver disease,
  • Active Hepatitis B Virus (HBV) or Hepatitis C Virus (HCV) or positive HIV serology,
  • Female patients who are pregnant or breast feeding or patients of childbearing potential not willing to use a double barrier method of contraception during the study and for 3 months following the last dose of maintenance.
  • Male patients whose sexual partner(s) are women of childbearing potential who are not willing to use a double barrier method of contraception, one of which includes a condom, during the study and for 3 months following the last dose of maintenance.
  • Any of concurrent severe and/or uncontrolled medical condition, which could compromise participation in the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03249870

Layout table for location contacts
Contact: Assitan KONE +33 1 39 23 97 75
Contact: Laure MORISSET +33 1 39 23 97 85

Layout table for location information
CH Amiens sud Recruiting
Amiens, France
Contact: Grusson         
CHU Angers Recruiting
Angers, France
Contact: Hunault         
CHU Besançon Recruiting
Besançon, France
Contact: Berceanu         
Hopital Avicenne Recruiting
Bobigny, France
Contact: Braun         
Hopital Duchenne Recruiting
Boulogne-sur-Mer, France
Contact: Choufi         
CHU Caen Recruiting
Caen, France
Contact: Chantepie         
CH metropole Savois_ chambery Recruiting
Chambéry, France
Contact: Sutton         
HIA Percy Recruiting
Clamart, France
Contact: Konopacki         
CHU Clermond Ferrand Recruiting
Clermont-Ferrand, France
Contact: Cacheux         
Hopital Mondor Recruiting
Créteil, France
Contact: Maury         
Hopital Dijon Recruiting
Dijon, France
Contact: Caillot         
CHU Grenoble Recruiting
Grenoble, France
Contact: Thiebaut         
CH Versailles Recruiting
Le Chesnay, France
Contact: Rousselot         
CHU Limoges Recruiting
Limoges, France
Contact: Turlure         
Centre Leon Berard Recruiting
Lyon, France
Contact: Gilis         
IPC Recruiting
Marseille, France
Contact: Vey         
CH Meaux Recruiting
Meaux, France
Contact: Frayfer         
CH Montpellier Recruiting
Montpellier, France
Contact: Hicheri         
CHU Nantes Recruiting
Nantes, France
Contact: Chevallier         
Centre Lacassagne Recruiting
Nice, France
Contact: Gastaud         
CHU Nice Recruiting
Nice, France
Contact: Cluzeau         
CHR Orléans Recruiting
Orléans, France
Contact: Alexis         
Hopital Necker Recruiting
Paris, France
Contact: Marcais         
Hopital St Antoine Recruiting
Paris, France
Contact: Isnard         
Hopital St Louis Recruiting
Paris, France
Contact: Dombret         
CHU Haut Leveque Recruiting
Pessac, France
Contact: Leguay         
CH Lyon Sud Recruiting
Pierre-Bénite, France
Contact: Thomas         
CH Reims Recruiting
Reims, France
Contact: Himberlin         
CH Roubaix Recruiting
Roubaix, France
Contact: Plantier         
Centre H Becquerel Rouen Recruiting
Rouen, France
Contact: Lepretre         
Institut de cancerologie Recruiting
Saint-Priest-en-Jarez, France
Contact: Tavernier         
CHU Strasbourg Recruiting
Strasbourg, France
Contact: Bilger         
IUCT Oncopole Recruiting
Toulouse, France
Contact: Huguet         
CH Valenciennes Recruiting
Valenciennes, France
Contact: Fernandes         
CHRU Nancy Recruiting
Vandœuvre-lès-Nancy, France
Contact: Roth Guepin         
Sponsors and Collaborators
Versailles Hospital
Layout table for investigator information
Principal Investigator: Patrice CHEVALLIER, MD Nantes University Hospital

Layout table for additonal information
Responsible Party: Patrice Chevallier, MD, PhD, Nantes University Hospital Identifier: NCT03249870     History of Changes
Other Study ID Numbers: P16/11- EWALL INO
2016-004942-27 ( EudraCT Number )
First Posted: August 15, 2017    Key Record Dates
Last Update Posted: April 5, 2018
Last Verified: April 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Inotuzumab Ozogamicin
Leukemia, Lymphoid
Philadelphia Chromosome
Neoplasms by Histologic Type
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Translocation, Genetic
Chromosome Aberrations
Pathologic Processes
Antineoplastic Agents