Study of a Humanized Antibody Initiated 2 Months After an HLA Matched Allogenic Stem Cell Transplantation

NCT ID: NCT02921685

Last Updated: 2018-09-19

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-11-28
• Study Completion Date: 2020-04-28

Brief Summary

This study will determine the Maximal Tolerated Dose if any and the recommended dose for phase 2 of monalizumab, a monoclonal antibody directed against the CD94/NKG2A receptor, after allogenic stem cell transplantation. All patients will receive one single intravenous administration of one of the four doses of monalizumab.

Detailed Description

Allogeneic hematopoietic stem cell transplantation (Allo-HSCT) is a curative option for most of hematological malignancies, though the graft-versus-tumor (GVT) effect mediated by immune cells from the donor. However, the use of Allo-HSCT is limited by its toxicity, notably the graft-versus-host disease (GVHD) that is a major cause of non-relapse mortality (NRM). Conditioning regimens dramatically improved during the last fifteen years, with a decrease of both GVHD and NRM rates. Now, disease recurrence after Allo-HSCT is the first cause of treatment failure and remains a concern for approximately 30% of the patients.

Based on a safety immunologic platform (ATG based reduced toxicity conditioning regimens), it is needed to develop post Allo-HSCT strategies to decrease the incidence of relapse. In this context, the modulation of immune cell activity could play a role to prevent relapse. NK cells have a unique capacity to exert potent GVT effects without inducing GVHD. Moreover, NK cells recovery occurs early after Allo-HSCT and NK cells function are not severely impaired by the use of ciclosporin A, that is given for few months after Allo-HSCT as GVHD prophylaxis. Thus, NK cell modulation appears as a viable option for early immune intervention after Allo-HSCT.

Monalizumab (IPH2201), a monoclonal antibody has a non-depleting and purely blocking activity directed with high affinity and specificity against the CD94/NKG2A receptor expressed by subsets of NK cells, activated αβ CD8+ T cells, γδ-T cells and NK T cells. By suppressing the inhibitory signal transduced by NKG2A, IPH2201 enhances the anti-tumor functions, including cytolytic activity of these immune effector cells.The aim of the study is to determine the safety of IPH2201 after allogenic stem cell transplantation.

Conditions

Hematologic Malignancies

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Monalizumab

Monalizumab treatment will be initiated 75 to 100 days after hematopoietic stem cells transplantation. Patients will receive a single dose of monalizumab by intravenous route over 1 hour.

Group Type: EXPERIMENTAL

Monalizumab

Intervention Type: DRUG

Four dose levels will be tested.

Interventions

Monalizumab

Four dose levels will be tested.

Intervention Type: DRUG

Other Intervention Names

anti CD94/NKG2A; IPH2201

Eligibility Criteria

Inclusion Criteria

1. Patients presenting a hematological malignancy (acute myeloid leukemia, acute lymphoblastic leukemia, High risk R-IPSS myelodysplastic syndromes, multiple myeloma, chronic lymphoid leukemia, chronic myeloid leukemia, myeloproliferative neoplasm, Hodgkin lymphoma or Non-Hodgkin lymphoma) treated by allogeneic HSCT according to the following parameters :

• Donor : HLA matched related or unrelated (10/10) donor
• Graft : peripheral blood stem cells
• Conditioning : All types of conditioning reduced toxicity conditioning regimens ATG as in-vivo T-cell depletion
• GVHD prophylaxis by cyclosporine, still ongoing at full dose at the time of the inclusion

2. Patient being in one of the following post-graft situation at the time of inclusion:

• Acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL) patients: in morphological complete remission (CR) with less than 5% bone marrow blast count.
• High risk R-IPSS myelodysplastic syndromes patients: with at least marrow CR with less than 5% marrow blast count.
• Multiple myeloma patients: in at least very good partial response.
• Chronic Lymphoid Leukemia patients: in CR.
• Chronic Myeloid Leukemia patients: in hematological CR.
• Myeloproliferative neoplasm patients: no criteria for disease in acceleration phase.
• Hodgkin lymphoma or Non-Hodgkin lymphoma patients: in CR.

3. Age ≥ 18 and ≤ 70 years

4. ECOG = 0-1 or Karnofsky index ≥ 70%

5. Clinical laboratory values at screening

• Calculated creatinine clearance (according to MDRD) > 50 ml/min/1.73 m2
• Independence of red blood cell transfusion
• Platelet count > 75 x 109/l
• ANC > 1 x 109/l
• Bilirubin < 1.5 ULN
• ALT and AST < 3 ULN

6. Patients (male or female) who accept and are able to use contraceptive methods recognized as highly effective throughout the study and up to 5 months after the drug administration

7. Signed informed consent of the current clinical study, prior to any protocol-specific procedure

8. Patient affiliated to the national "Social Security" regimen or beneficiary of this regimen

1. Previous history of grade ≥ II acute GVHD (Glucksberg classification)

2. Current active disease or positive serology for HIV before grafting, and/or HCV with detectable viremia and/ or HBV with positive Hbs Antigen.

3. Abnormal cardiac status with any of the following :

• Ejection fraction (measured by ultrasound or radionuclide imaging) < 50%
• Unstable angina
• Myocardial infarction within the last 6 months
• Presence or persistence of documented congestive heart failure (New York Heart Association functional classification III-IV)
• Arrhythmia requiring treatment and which is not stabilized by the treatment.
• QTc ≥ 450 ms (M) or 470 ms (F) (Bazett formula)

4. Previous other allogeneic hematopoietic transplantation or solid organ transplantation

5. Any other serious concurrent uncontrolled medical disorder within 4 weeks prior to IPH2201 administration

6. Use of systemic corticosteroids ongoing or within the last 1 week prior IPH2201 admin-istration

7. Use of any investigational agent within 3 months prior to first dosing (except procedure of conditioning regimen including registered drugs combinations, i.e. Busulfan and Fludarabine or Busulfan and Endoxan)

Exclusion Criteria

9. Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.

10. Pregnant or lactating women

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Innate Pharma

INDUSTRY

Sponsor Role: collaborator

Institut Paoli-Calmettes

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Didier BLAISE, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Institut Paoli-Calmettes

Locations

Institut Paoli Calmettes

Marseille, Bouches Du Rhônes, France

Site Status: RECRUITING

Countries

France

Central Contacts

Dominique GENRE, MD

Role: CONTACT

genred@ipc.unicancer.fr

33 4 91 22 37 78

Margot BERLINE, MSc, MBA

Role: CONTACT

boqueti@ipc.unicancer.fr

33 4 91 22 37 78

Facility Contacts

Dominique GENRE, MD

Role: primary

genred@ipc.unicancer.fr

33 4 91 22 37 78

Isabelle BOQUET, PhD

Role: backup

boqueti@ipc.unicancer.fr

33 4 91 22 37 78

References

Ruggeri L, Urbani E, Andre P, Mancusi A, Tosti A, Topini F, Blery M, Animobono L, Romagne F, Wagtmann N, Velardi A. Effects of anti-NKG2A antibody administration on leukemia and normal hematopoietic cells. Haematologica. 2016 May;101(5):626-33. doi: 10.3324/haematol.2015.135301. Epub 2015 Dec 31.

Reference Type: BACKGROUND

PMID: 26721894 (View on PubMed)

Godal R, Bachanova V, Gleason M, McCullar V, Yun GH, Cooley S, Verneris MR, McGlave PB, Miller JS. Natural killer cell killing of acute myelogenous leukemia and acute lymphoblastic leukemia blasts by killer cell immunoglobulin-like receptor-negative natural killer cells after NKG2A and LIR-1 blockade. Biol Blood Marrow Transplant. 2010 May;16(5):612-21. doi: 10.1016/j.bbmt.2010.01.019. Epub 2010 Feb 6.

Reference Type: BACKGROUND

PMID: 20139023 (View on PubMed)

Rathmann S, Glatzel S, Schonberg K, Uhrberg M, Follo M, Schulz-Huotari C, Kaymer M, Veelken H, Finke J, Fisch P. Expansion of NKG2A-LIR1- natural killer cells in HLA-matched, killer cell immunoglobulin-like receptors/HLA-ligand mismatched patients following hematopoietic cell transplantation. Biol Blood Marrow Transplant. 2010 Apr;16(4):469-81. doi: 10.1016/j.bbmt.2009.12.008. Epub 2010 Jan 4.

Reference Type: BACKGROUND

PMID: 20044012 (View on PubMed)

Pical-Izard C, Crocchiolo R, Granjeaud S, Kochbati E, Just-Landi S, Chabannon C, Frassati C, Picard C, Blaise D, Olive D, Fauriat C. Reconstitution of natural killer cells in HLA-matched HSCT after reduced-intensity conditioning: impact on clinical outcome. Biol Blood Marrow Transplant. 2015 Mar;21(3):429-39. doi: 10.1016/j.bbmt.2014.11.681. Epub 2015 Jan 9.

Reference Type: BACKGROUND

PMID: 25579888 (View on PubMed)

Related Links

http://www.institutpaolicalmettes.fr

Official web site of the sponsor

Other Identifiers

PIRAT-IPC 2015-018

Identifier Type: -

Identifier Source: org_study_id