Iberdomide Vs. Iberdomide Plus Isatuximab Maintenance Therapy Post ASCT in Newly Diagnosed Multiple Myeloma
- Conditions
- Multiple Myeloma
- Interventions
- Registration Number
- NCT06216158
- Lead Sponsor
- University of Heidelberg Medical Center
- Brief Summary
The goal of this clinical trial is to compare a maintenance therapy consisting of iberdomide and isatuximab with an iberdomide-only regimen. The trial is the subsequent maintenance therapy to GMMG-HD8/DSMM XIX trial for patients with newly-diagnosed multiple myeloma. The main question it aims to answer is:
• Will the addition of isatuximab lead to decreased amounts of measurable myeloma cells in the bone marrow after two years?
- Detailed Description
Prospective, multicentre, randomised, parallel group, open, phase III clinical trial for a maintenance therapy, for patients who underwent an induction therapy and autologous stem cell transplantation in the GMMG-HD8/DSMM XIX trial.
Investigational Medicinal Product: Iberdomid (oral), isatuximab (subcutaneous administration via a wearable injector system).
Randomisation will be performed centrally by GMMG/DSMM offices after verification of the eligibility of the patient. At the time of study inclusion, randomization will be performed into arm A (iberdomide) or arm B (iberdomide + isatuximab). Randomization will be stratified by centrally assessed MRD negativity status (yes vs. no vs. unknown); assessed by NGF from BMA; sensitivity of 10\^-5; independent of standard IMWG response) and number of HDM/ASCT (single vs. tandem).
Patients randomized in arm A will receive 39 cycles of the drug iberdomide, a Cereblon E3 Ubiquitin Ligase Modulating Drug (CELMoD®) that shares structural similarities to the immunomodulatory compounds (IMiDs) such as thalidomide and lenalidomide. Each cycle will last for 29 days. Patients in arm B will receive the same the 39 cycles of iberdomide plus monoclonal anti-CD38 antibody isatuximab subcutaneously. In both arms, patients will receive 20 mg dexamethasone in cycle 1, on the same days as the isatuximab administration in Arm B. End of study will be after 36 months of the maintenance therapy.
There is one primary objective:
- Demonstration of superiority of iberdomide plus isatuximab compared to iberdomide with respect to bone marrow minimal residual disease (MRD) negativity rates (sensitivity 2x10\^-6 via next-generation flow cytometry \[NGF\]) after two years of maintenance therapy.
There is one key secondary objective:
- PFS, defined as time from randomization to disease progression or death from any cause, whichever occurs first.
Further secondary objectives are:
* Rates of sustained MRD negativity (at sensitivity levels of 10-5 and 2x10\^-6 via NGF from BMA) after 1, 2 and 3 years of maintenance therapy.
* Conversion from MRD positive to negative (at sensitivity levels of 10\^-5 and 2x10\^-6 via NGF from BMA).
* Rates of best overall response to treatment (BOR).
* Rates of partial response (PR), very good partial response (VGPR), complete response (CR) and stringent complete response (sCR).
* Time-to-next-treatment (TTNT).
* PFS on subsequent line of therapy.
* Overall survival (OS).
* Improvement of IMWG response categories (PR, VGPR, CR, sCR).
* Proportions of patients in both treatment arms maintaining BOR and CR from baseline.
* Assessment of quality-of-life (QoL) via the EORTC-QLQC30, EORTC-QLQMY20, and EQ-5D-5L questionnaires.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 411
- Prior inclusion and treatment within the GMMG-HD8 / DSMM XIX trial
- Received at least one cycle high dose melphalan therapy (HDM) and autologous stem cell transplantation (ASCT)
- At least Partial Response (PR) according to IMWG criteria at inclusion in the trial
- Age of at least 18 years at trial inclusion
- WHO performance status of 0, 1, or 2
- Negative pregnancy test at inclusion (women of childbearing potential)
- For all men and women of childbearing potential: patients must be willing and capable to use adequate contraception during the complete therapy
- Ability of patient to understand character and individual consequences of the clinical trial
- Written informed consent (must be available before enrolment in the trial)
- Subjects with gastrointestinal disease that may significantly alter the absorption of iberdomide
- Patient has known hypersensitivity (or contraindication) to any of the components of study therapy that are not amenable to premedication with steroids or H1 blockers and that would prohibit further treatment with these agents (e.g. known intolerance or hypersensitivity to infused proteins products, sucrose, histidine, and polysorbate 80 as well as intolerance to arginine and Poloxamer 188)
- Patients with a history of serious allergic reaction to another immunomodulatory agent (thalidomide, lenalidomide, or pomalidomide)", as angioedema and severe dermatologic reactions, including Grade 4 rash and exfoliative or bullous rash
- Patients currently being treated with strong inhibitors or inducers of CYP3A4/5
- Systemic AL amyloidosis (except for localized AL amyloidosis limited to the skin or the bone marrow), plasma cell leukemia or polyneuropathy, organomegaly, endocrinopathy, monoclonal-protein and skin abnormalities or Waldenström macroglobulinemia.
- Previous systemic anti-myeloma treatment other than administered within the GMMG-HD8 / DSMM XIX trial (including up to two cycles cycle high dose melphalan therapy (HDM) and autologous stem cell transplantation (ASCT). Local, consolidative radiotherapy for myeloma disease is permitted unless performed in case of progressive disease according to IMWG criteria
- Severe cardiac dysfunction (NYHA classification III-IV)
- Significant hepatic dysfunction (ASAT and/or ALAT ≥ 3 times normal level and/or serum bilirubin ≥ 1.5 times normal level if not due to hereditary abnormalities as Gilbert's disease), unless related to MM or HDM/ASCT.
- Patients with active or uncontrolled hepatitis B or C or detectable liver disease due to hepatitis B or C. In case of history of hepatitis B or C, it must be clarified whether it has been overcome and negative circulating HBV-DNA or HCV-RNA must be provided. Positive hepatitis B status may only be acceptable in absence of circulating HBV-DNA or signs of chronic or acute infection and if an adequate prophylaxis is being implemented during the course of the study. Prophylaxis for patients with history of hepatitis B or C should be set on a patient individual basis.
- HIV positivity
- Patients with active, uncontrolled infections
- Patients with severe renal insufficiency (Creatinine Clearance < 30ml/min) or requiring hemodialysis
- Patients with peripheral neuropathy or neuropathic pain, grade 2 or higher (as defined by the NCI Common Terminology Criteria for Adverse Events (NCI CTCAE, version 5.0)
- Patients with a history of any active malignancy during the past 5 years with the exception of following malignancies after curative therapy: basal cell carcinoma of the skin, squamous cell skin carcinoma, stage 0 cervical carcinoma or any in situ malignancy. A history of an early stage malignancy during the past 5 years may be acceptable, however, in this case the GMMG study office has to be consulted prior to study inclusion
- Patients with acute diffuse infiltrative pulmonary and/or pericardial disease
- Autoimmune haemolytic anaemia with positive indirect Coombs test or immune thrombocytopenia
- Platelet count < 75 x 109/l
- Haemoglobin ≤ 8.0 g/dl, unless related to MM
- Absolute neutrophil count (ANC) < 1.0 x 109/l (the use of colony stimulating factors within 14 days before the test is not allowed)
- Corrected serum calcium > 14 mg/dl (> 3.5 mmol/l)
- Unable or unwilling to undergo thromboprophylaxis
- Pregnancy and lactation
- Participant has any concurrent severe and/or uncontrolled medical condition or psychiatric disease that is likely to interfere with study procedures or results, or that in the opinion of the investigator would constitute a hazard for participating in this study or that confounds the ability to interpret data from the study
- Subjects, who are committed to an institution by virtue of an order issued either by the judicial or the administrative authorities
- Participation in other interventional clinical trials. This does not include long-term follow-up periods without active drug treatment of previous studies during the last 6 months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Arm A: Iberdomide Iberdomide 36 months of oral iberdomide administration; In cycle 1, dexamethasone is added as pre-medication Arm B: Iberdomide plus isatuximab Iberdomide 36 months of oral iberdomide plus subcutaneous isatuximab administration; In cycle 1, dexamethasone is added as pre-medication Arm B: Iberdomide plus isatuximab Dexamethasone 36 months of oral iberdomide plus subcutaneous isatuximab administration; In cycle 1, dexamethasone is added as pre-medication Arm B: Iberdomide plus isatuximab Isatuximab 36 months of oral iberdomide plus subcutaneous isatuximab administration; In cycle 1, dexamethasone is added as pre-medication Arm A: Iberdomide Dexamethasone 36 months of oral iberdomide administration; In cycle 1, dexamethasone is added as pre-medication
- Primary Outcome Measures
Name Time Method Demonstration of superiority of iberdomide plus isatuximab compared to iberdomide with respect to bone marrow minimal residual disease (MRD). 24 months after start of maintenance therapy The primary objective of this trial is to compare the two-year MRD negativity rate (sensitivity 2x10\^-6 via next-generation flow cytometry \[NGF\]; from bone marrow aspirate) when treated with iberdomide plus isatuximab, with the MRD negativity after treatment with iberdomide only.
- Secondary Outcome Measures
Name Time Method Progression-free survival (PFS) from date of randomization. From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months PFS, defined as time from randomization to disease progression or death from any cause, whichever occurs first.
Trial Locations
- Locations (53)
Helios Klinikum Bad Saarow
🇩🇪Bad Saarow, Germany
Vivantes Klinikum Neukölln, Klinik für Hämatologie und Onkologie
🇩🇪Berlin, Germany
Helios Klinikum Berlin-Buch
🇩🇪Berlin, Germany
Vivantes Klinikum Spandau
🇩🇪Berlin, Germany
Evangelisches Klinikum Bethel
🇩🇪Bielefeld, Germany
Johanniter Krankenhaus
🇩🇪Bonn, Germany
Universitätsklinikum Bonn
🇩🇪Bonn, Germany
Klinikum Chemnitz
🇩🇪Chemnitz, Germany
Carl-Thiem-Klinikum Cottbus gGmbH, 2. Medizinische Klinik
🇩🇪Cottbus, Germany
Charité, III. Medizinische Abteilung
🇩🇪Berlin, Germany
Malteser Krankenhaus
🇩🇪Flensburg, Germany
Onkologische Schwerpunktpraxis
🇩🇪Heidelberg, Germany
Gemeinschaftsklinikum Mittelrhein Koblenz
🇩🇪Koblenz, Germany
Rotkreuzklinikum
🇩🇪München, Germany
Robert-Bosch-Krankenhaus
🇩🇪Stuttgart, Germany
Uniklinik RWTH Aachen, Klinik für Hämatologie, Onkologie, Hämostaseologie und Stammzelltransplantation
🇩🇪Aachen, Germany
Klinikum Darmstadt GmbH, Medizinische Klinik V
🇩🇪Darmstadt, Germany
St. Johannes Hospital Dortmund
🇩🇪Dortmund, Germany
Universitätsklinikum Carl Gustav Carus Dresden
🇩🇪Dresden, Germany
Universitätsklinikum Düsseldorf
🇩🇪Düsseldorf, Germany
Marien Hospital Düsseldorf GmbH, Klinik für Onkologie, Hämatalogie und Palliativmedizin
🇩🇪Düsseldorf, Germany
KEM I Evang. Kliniken Essen-Mitte gGmbH, Evangelisches Krankenhaus Essen-Werden gGmbH, Klinik für Hämatologie, Onkologie und Stammzelltransplantation
🇩🇪Essen, Germany
Centrum für Hämatologie und Onkologie Bethanien
🇩🇪Frankfurt am Main, Germany
Universitätsmedizin Greifswald
🇩🇪Greifswald, Germany
Katholisches Krankenhaus Hagen
🇩🇪Hagen, Germany
Universitätsmedizin Halle
🇩🇪Halle, Germany
Universitätsklinikum Hamburg-Eppendorf, Zentrum für Onkologie
🇩🇪Hamburg, Germany
Onkologische Schwerpunktpraxis Heidelberg
🇩🇪Heidelberg, Germany
Universitätsklinikum Heidelberg, Medizinische Klinik V
🇩🇪Heidelberg, Germany
SLK Kliniken Heilbronn, Medizinische Klinik III
🇩🇪Heilbronn, Germany
Universitätsklinikum des Saarlandes, Klinik für Innere Medizin 1
🇩🇪Homburg, Germany
Philipps-Universität Marburg Hämatologie/Onkologie
🇩🇪Marburg, Germany
Klinikum Hochsauerland
🇩🇪Meschede, Germany
Kliniken Ostalb
🇩🇪Mutlangen, Germany
Klinikum der Friedrich-Schiller-Universität Jena, Klinik für Innere Medizin II, Abteilung Hämatologie und internistische Onkologie
🇩🇪Jena, Germany
Westpfalz-Klinikum
🇩🇪Kaiserslautern, Germany
Klinikverbund Allgäu, Klinikum Kempten, Hämatologie / Onkologie
🇩🇪Kempten, Germany
Oncocare, Gemeinschaftspraxis für Hämatologie und Onkologie
🇩🇪Lebach, Germany
Klinikum der Stadt Ludwigshafen
🇩🇪Ludwigshafen, Germany
Universitätsklinikum Schleswig-Holstein
🇩🇪Lübeck, Germany
Universitätsklinikum Magdeburg
🇩🇪Magdeburg, Germany
Universitätsklinikum Mannheim, III. Medizinische Klinik
🇩🇪Mannheim, Germany
Kliniken Maria Hilf
🇩🇪Mönchengladbach, Germany
Klinikum rechts der Isar der TU München
🇩🇪München, Germany
Klinikum Oldenburg
🇩🇪Oldenburg, Germany
Krankenhaus Barmherzige Brüder Regensburg, Klinik für Onkologie und Hämatologie
🇩🇪Regensburg, Germany
Universitätsklinikum Regensburg
🇩🇪Regensburg, Germany
Onkologische Schwerpunktpraxis Speyer
🇩🇪Speyer, Germany
Klinikum der Landeshauptstadt Stuttgart - Katharinenhospital
🇩🇪Stuttgart, Germany
Universitätsklinikum Tübingen
🇩🇪Tübingen, Germany
Schwarzwald Baar Klinikum
🇩🇪Villingen-Schwenningen, Germany
University of Würzburg, Med. Klinik und Poliklinik II
🇩🇪Würzburg, Germany
Brüderkrankenhaus St. Josef
🇩🇪Paderborn, Germany