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Trial Title: NDMM Patients Candidates for ASCT Comparing Extended VRD Plus vs. Isa-VRD vs. Isa-V-Iberdomide

NCT ID: NCT05558319

Condition: Newly Diagnosed Multiple Myeloma

Conditions: Official terms:
Multiple Myeloma
Dexamethasone
Lenalidomide
Bortezomib

Study type: Interventional

Study phase: Phase 3

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Bortezomib
Description: Bortezomib
Arm group label: Control arm (A)
Arm group label: EXPERIMENTAL ARM (B): Extended VRD and Early Rescue Intervention
Arm group label: EXPLORATORY ARM (C)

Intervention type: Drug
Intervention name: Isatuximab
Description: Isatuximab
Arm group label: Control arm (A)
Arm group label: EXPERIMENTAL ARM (B): Extended VRD and Early Rescue Intervention
Arm group label: EXPLORATORY ARM (C)

Intervention type: Drug
Intervention name: Iberdomide
Description: Iberdomide
Arm group label: EXPERIMENTAL ARM (B): Extended VRD and Early Rescue Intervention
Arm group label: EXPLORATORY ARM (C)

Intervention type: Drug
Intervention name: Lenalidomide
Description: Lenalidomide
Arm group label: Control arm (A)
Arm group label: EXPERIMENTAL ARM (B): Extended VRD and Early Rescue Intervention

Intervention type: Drug
Intervention name: Dexamethasone
Description: Dexamethasone
Arm group label: Control arm (A)
Arm group label: EXPERIMENTAL ARM (B): Extended VRD and Early Rescue Intervention
Arm group label: EXPLORATORY ARM (C)

Summary: This is a Phase III open-label, 3-arm, parallel, randomized, controlled trial. The allocation ratio 1:1:1 and outcome assessment are blind to group allocation. Patients will be randomized from 3 arms. Patients will receive VRD extended + ASCT plus ERI or Isatuximab-VRD + ASCT or Isatuximab-VID + ASCT.

Detailed description: Patients will receive induction treatment, which will consist: arm A (Isatuximab-VRD + ASCT) or arm B (VRD extended + ASCT plus ERI) or arm C (Isatuximab-VID + ASCT). After ASTC, patients will start consolidation which will be 2 cycles of similar treatment to induction. Continuous treatment will follow after consolidation and patients will receive: - arm A: Lenalidomide and monthly Isatuximab until progression, unacceptable toxicity, patient withdrawal, loss to follow up or death. During continuous treatment, dexamethasone 40 mg is used as a standardized premedication for Isatuximab. - arm B: after 6 cycles of induction VRD, ASCT and two consolidation VRDs, treatment continues with 10 additional cycles of VRD. During the extension cycles, VRD changes the bortezomib and dexamethasone regimen. In these10 cycles, both bortezomib and dexamethasone will be administered, at the same doses as the previous ones, but on a weekly schedule, on days 1, 8, 15 and 22 of each cycle. The lenalidomide regimen remains unchanged. - arm C: Iberdomide and monthly Isatuximab until progression, unacceptable toxicity, patient withdrawal, loss to follow up or death. During continuous treatment, dexamethasone 40 mg is used as a standardized premedication for Isatuximab. The primary objective is to compare the efficacy of extended VRD + ASCT plus ERI (Arm B) vs. Isatuximab-VRD + ASCT (Arm A) in terms of proportion of patients who are MRD-negative by next generation flow cytometry (NGF) after 18 cycles + ASCT. The primary endpoint, the MRD rate, takes as a reference the evaluation after the last extended VRD cycle, this is: 6 cycles for induction, 6 months for transplantation, 2 cycles for consolidation and 10 cycles until completing the 18 cycles of VRD, (in total about 24 months). For this reason,the primary endpoint in Arms A and C are established after a similar treatment time, which includes 4 cycles of induction, ASCT, 2 cycles of consolidation and 12 cycles of continuous treatment with Iberdomide plus Isatuximab (Dexamethasone to be determined).In patients of Arm B included in ERI, due to the great variability of the possible moments of incorporation in this therapeutic program, only rules are established for the moment and the realization or not of the transplant. The evaluation of the results will be carried out separately in the patients included, butalso in conjunction with the rest of the patients in Arm B to know the effect of the global strategy. After the evaluation of the primary endpoint, continuous/maintenance treatment continues in Arms A, B and C, including patients in ARM B assigned to the ERI program. Obtaining conventional CR in either arm will require a BM analysis for MRD. In the case of stable response or improvement without RC, MRD controls have been pre-established. Due to the lack of data on tolerance and adherence to long-term treatment with Isatuximab and Iberdomide, changes in the therapeutic programs, for this reason, a complete revision of the therapeutic program has been predetermined at the moment in which the last patient included in the clinical trial reaches 36 months of treatment. At this point, taking into account the updated knowledge about continuous or maintenance treatments, the strategies for a second clinical trial or an extension of this clinical trial will be defined.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Patient is, in the investigator's opinion, willing and able to comply with the protocol requirements. 2. Patient must be able to understand the study procedures. 3. Patient has given voluntary written informed consent before performance of any studyrelated procedure non part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to their future medical care. 4. Newly diagnosed multiple myeloma patient who requires start active treatment according to the 2014 IMWG criteria, namely clonal bone marrow plasma cells ≥10% or biopsy-proven bony or extramedullary plasmacytoma and any one or more of the following myeloma defining events: evidence of end organ damage that can be attributed to the underlying plasma cell proliferative disorder, specifically: Hypercalcaemia, Anaemia, Renal Insufficiency, or Bone lesions (one or more osteolytic lesions on skeletal radiography, CT, or PET-CT), and any one or more of the following biomarkers: clonal BMPC% ≥60%, i/u free light ratio ≥100 or > 1 focal lesions on MRI or PET/CT) [Lancet Oncol. 2014;15(12): e538-e548]. 5. Patient must have a measurable secretory disease defined as either serum monoclonal protein of ≥ 0,5 g/dl or urine monoclonal (light chain) protein ≥ 200 mg/24 h. For patients whose disease is only measurable by serum FLC, the involved FLC should be ≥ 10mg/dL (100 mg/L), with an abnormal serum FLC ratio. 6. Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2. 7. Patient must be ≤ 65 years of age. 8. Patient must have adequate organ function, defined as follows: - Absolute neutrophil count (ANC) ≥1.0 X 109/L without G-CSF use in the prior 7 days - Hemoglobin ≥8.0 g/dL (prior red blood cell (RBC) transfusion or recombinant human erythropoietin use is permitted) - Platelets ≥ 75 x 109/L in participants in whom <50% of bone marrow nucleated cells are plasma cells and ≥ 50×109/L in participants in whom ≥50% of bone marrow nucleated cells are plasma cells (without transfusion support or thrombopoietin receptor agonist within 7 days before the laboratory test). - Calcium Corrected serum calcium ≤13.5 mg/dL (≤3.4 mmol/L); or free ionized calcium ≤6.5 mg/dL (≤1.6 mmol/L). - Total bilirubin ≤2 X ULN - ALT ≤2.5 X ULN - AST ≤2.5 X ULN - Renal: eGFRa: ≥40 mL/min/ 1.73 m2 - Cardiac: LVEF (echo) ≥ 50% 9. Female patient: contraceptive use should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. A female patient is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies: - Is not a woman of childbearing potential (WOCBP), i.e., fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilization methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy OR - Is a WOCBP and - She understands the potential teratogenic risk to the unborn child - She understands the need for effective contraception as stated in the protocol, without interruption, 28 days before starting study treatment, throughout the entire duration of study treatment, during dose interruptions and for at least 28 days after the last dose of study treatment. - She understands and agrees to inform the Investigator if a change or stop of method of contraception is needed. - She must be capable of complying with effective contraceptive measures. - She is informed and understands the potential consequences of pregnancy and the need to notify her study doctor immediately if there is a risk of pregnancy. - She understands the need to commence study treatment as soon as it is dispensed following a negative pregnancy test. - She understands and accepts the need to undergo pregnancy testing based on the frequency outlined in this plan and in the Informed Consent. - She acknowledges she understands the hazards iberdomide or lenalidomide can cause to an unborn fetus and the necessary precautions associated with the use of study drugs. The Investigator must ensure that a WOCBP: i) Complies with the conditions of the pregnancy prevention plan, including confirmation that she has an adequate level of understanding. ii) Acknowledges the aforementioned requirements. A WOCBP must have a negative highly sensitive serum pregnancy test (as required by local regulations) within 72 hours before the first dose of study drug. Nonchildbearing potential is defined as follows (by other than medical reasons): - Has not achieved menarche at some point. - Has undergone a hysterectomy or bilateral oophorectomy. - Has been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (ie, has had menses at any time in the preceding 24 consecutive months). 10. Male patient: contraceptive use should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. Male patient is eligible to participate if he agrees to the following from the time of first dose of study until 6 months after the last dose of iberdomide or lenalidomide to allow for clearance of any altered sperm: - Understand the potential teratogenic risk if engaged in sexual activity with a pregnant female or a WOCBP. - Understand the need for the use of a condom even if he has had a vasectomy, if engaged in sexual activity with a pregnant female or a FCBP - Understand the potential teratogenic risk, so the subject should not donate semen or sperm.. Understand that the effects on fertility are currently unknown, therefore all family planning options and/or alternatives should be thoroughly discussed with the study doctor prior to receiving iberdomide. 11. All prior treatment-related toxicities (defined by National Cancer Institute- Common Toxicity Criteria for Adverse Events (NCI-CTCAE), version 5.0 must be ≤ Grade 1 at the time of enrolment except for alopecia. Exclusion Criteria: 1. Patient has a diagnosis of primary amyloidosis, monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), plasma cell leukemia or active POEMS syndrome at the time of screening. 2. Patient has had clinical evidence of central nervous system (CNS) or pulmonary leukostasis, disseminated intravascular coagulation, or CNS multiple myeloma. 3. Prior history of malignancies, other than multiple myeloma (except for basal or squamous cell carcinoma of the skin, carcinoma in situ of the cervix or the breast), unless the patient has been free of the disease for ≥ 5 years. 4. Any serious medical condition that places the subject at an unacceptable risk if he or she participates in this study; subjects with conditions requiring chronic steroid or immunosuppressive treatment, such as rheumatoid arthritis, multiple sclerosis and/or lupus, that likely need additional steroid or immunosuppressive treatments in addition to the study treatment. 5. Pregnant or breastfeeding females. 6. Men and women of reproductive potential who are not using effective contraceptive methods (double barrier method, intrauterine device, oral contraception). 7. Patient is simultaneously enrolled in other interventional clinical trial. 8. Patient has used an investigational drug within 28 days or five half-lives, whichever is longer, preceding the first dose of study drug. 9. Patient must not have received prior radiotherapy (except localized palliative radiotherapy for pain, palliation or fracture) within 2 weeks of start of study therapy. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis. 10. Major surgery (except kyphoplasty) ≤ 4 weeks prior to initiating protocol therapy. 11. Patient has peripheral neuropathy or neuropathic pain grade 1 with pain or ≥2, as defined by the National Cancer Institute Terminology Criteria for Adverse Events (NCI CTCAE) Version 5.0. 12. Patient evidence of cardiovascular risk including any of the following: - Myocardial infarction within 6 months before randomization, or an unstable or uncontrolled disease/condition related to or affecting cardiac function (eg, unstable angina, congestive heart failure, New York Heart Association Class III-IV). - Uncontrolled cardiac arrhythmia. - Screening 12-lead ECG showing a baseline interval QTcF> 470 msec (exception: subjects with pacemaker). - Patients with uncontrolled hypertension. 13. Patients who have current unstable liver or biliary disease defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice, or cirrhosis. Note: Stable chronic liver disease (including Gilbert's syndrome or asymptomatic gallstones) or hepatobiliary involvement of malignancy is acceptable if otherwise meets entry criteria. 14. Presence of active renal condition (infection, requirement for dialysis or any other condition that could affect patient's safety). Participants with isolated proteinuria resulting from MM are eligible, provided they fulfil inclusion criteria. 15. Evidence of active mucosal or internal bleeding. 16. Any serious medical condition or psychiatric illness that would interfere in understanding of the informed consent form. 17. Uncontrolled endocrine diseases (i.e. diabetes mellitus, hypothyroidism or hyperthyroidism) (i.e. requiring relevant changes in medication within the last month, or hospital admission within the last 3 months). 18. Patient with acute diffuse infiltrative pulmonary disease and/or pericardial disease. 19. Patient with severe chronic obstructive pulmonary disease (COPD) or asthma with forced expiratory volume in the first minute (FEV1) less than 50%. 20. History of interstitial lung disease or ongoing interstitial lung disease. 21. Subject has gastrointestinal disease that may significantly alter the absorption of iberdomide and/or other oral study treatment. 22. Patient has an active infection requiring systemic antibiotic, antiviral, or antifungal treatment at the time of starting treatment. 23. Patient has known HIV infection. 24. Patient has positive hepatitis B surface antigen (HBsAg), or hepatitis B core antibody (HBcAb) at screening or within 3 months prior to first dose of study treatment. 25. Patient has positive hepatitis C antibody test result or positive hepatitis C RNA test result at screening or within 3 months prior to first dose of study treatment. Note: Participants with positive Hepatitis C antibody due to prior resolved disease can be enrolled, only if a confirmatory negative Hepatitis C RNA test is obtained. Note: Hepatitis RNA testing is optional and participants with negative Hepatitis C antibody test are not required. 26. Patient require concurrent administration of a strong inhibitor or inducer of cytochrome P450 (CYP3A4/5) (including within 14 days of initiating study treatment). 27. Patient has a known immediate or delayed hypersensitivity reaction or idiosyncratic reactions to iberdomide or drugs chemically related to iberdomide. 28. Patient has a known immediate or delayed hypersensitivity reaction or idiosyncratic reactions to isatuximab or drugs chemically related to isatuximab, hypersensitivity reactions, or idiosyncratic reactions to other molecular antibodies. 29. Patient has a known immediate or delayed hypersensitivity reaction or idiosyncratic reactions to lenalidomide or dexamethasone or drugs chemically related to lenalidomide or dexamethasone.

Gender: All

Minimum age: 18 Years

Maximum age: 65 Years

Healthy volunteers: No

Locations:

Facility:
Name: Hospital Principe de Asturias

Address:
City: Alcalá de Henares
Country: Spain

Contact:
Last name: Julio García Suárez
Email: jgsuarez@salud.madrid.org

Investigator:
Last name: Julio García Suárez, Dr
Email: Principal Investigator

Facility:
Name: Hospital Universitario Quirón Salud Madrid

Address:
City: Pozuelo De Alarcón
Zip: 28223
Country: Spain

Contact:
Last name: Carmen Martínez Chamorro
Email: carmenmartinezchamorro@quironsalud.es ; carmenmartinezchanomorro@hotmail.com

Investigator:
Last name: Carmen Martínez Chamorro
Email: Principal Investigator

Facility:
Name: Clinica Universidad Navarra (CUN)

Address:
City: Pamplona
Zip: 31008
Country: Spain

Contact:
Last name: Jesus San Miguel Izquierdo
Email: sanmiguel@unav.es

Investigator:
Last name: Jesus San Miguel Izquierdo
Email: Principal Investigator

Facility:
Name: Hospital General Universitario de Albacete

Address:
City: Albacete
Country: Spain

Contact:
Last name: Irene Gómez Catalán
Email: irenevonu12@gmail.com

Investigator:
Last name: Irene Gómez Catalán
Email: Principal Investigator

Facility:
Name: Hospital Germans Trias i Pujol (ICO BADALONA)

Address:
City: Badalona
Country: Spain

Contact:
Last name: Albert Oriol Rocafiguera
Email: aoriol@iconcologia.net

Investigator:
Last name: Albert Oriol Rocafiguera
Email: Principal Investigator

Facility:
Name: Hospital Clinic i Provincial de Barcelona

Address:
City: Barcelona
Country: Spain

Contact:
Last name: Laura Rosiñol, Dr

Phone: 93 2275400
Email: LROSINOL@clinic.cat

Investigator:
Last name: Laura Rosiñol
Email: Principal Investigator

Facility:
Name: Hospital de la Santa Creu i Sant Pau

Address:
City: Barcelona
Country: Spain

Contact:
Last name: Miguel Granell Gorrochategui, Dr

Phone: 93 5565647
Email: MGranell@santpau.cat

Investigator:
Last name: Miguel Granell Gorrochategui
Email: Principal Investigator

Facility:
Name: Hospital Universitari Vall d´Hebron

Address:
City: Barcelona
Country: Spain

Contact:
Last name: Mercedes Gironella Mesa, Dr

Phone: 93 2746100
Email: mgironel@gmail.com; mgironel@vhebron.net

Investigator:
Last name: Mercedes Gironella Mesa
Email: Principal Investigator

Facility:
Name: ICO L´Hospitalet

Address:
City: Barcelona
Country: Spain

Contact:
Last name: Anna Sureda Balari, Dr

Phone: 93 2607750
Email: asureda@iconcologia.net

Investigator:
Last name: Anna Sureda Balari
Email: Principal Investigator

Facility:
Name: Hospital Universitario de Cruces

Address:
City: Bilbao
Country: Spain

Contact:
Last name: Elena Amutio Díez, Dr

Phone: 946 006320
Email: mariaelena.amutiodiez@osakidetza.net

Investigator:
Last name: Elena Amutio Díez
Email: Principal Investigator

Facility:
Name: Hospital Universitario de Burgos

Address:
City: Burgos
Zip: 09006
Country: Spain

Contact:
Last name: Francisco Javier Díaz Gálvez
Email: fcdiaz@saludcastillayleon.es

Investigator:
Last name: Francisco Javier Díaz Gálvez
Email: Principal Investigator

Facility:
Name: Complejo Hospitalario de Cáceres

Address:
City: Cáceres
Country: Spain

Contact:
Last name: Ignacio Casas Avilés, Dr

Phone: 927 256200
Email: ignacio.casas@salud-juntaex.es

Investigator:
Last name: Ignacio Casas Avilés
Email: Principal Investigator

Facility:
Name: Hospital Universitario de Cabueñes

Address:
City: Gijón
Country: Spain

Contact:
Last name: María Esther González García

Phone: + 34 985 18 50 00
Email: esthergongar@yahoo.es

Investigator:
Last name: María Esther González García
Email: Principal Investigator

Facility:
Name: Hospital Universitari Dr. Josep Trueta (ICO Girona)

Address:
City: Girona
Country: Spain

Contact:
Last name: Yolanda González Montes, Dr

Phone: 972 225833
Email: ygonzalez@iconcologia.net

Investigator:
Last name: Yolanda González Montes
Email: Principal Investigator

Facility:
Name: Hospital Universitario Virgen de las Nieves

Address:
City: Granada
Country: Spain

Contact:
Last name: María Esther Clavero Sánchez
Email: eclaverosa@hotmail.com

Investigator:
Last name: María Esther Clavero Sánchez
Email: Principal Investigator

Facility:
Name: Hospital Universitario de Guadalajara

Address:
City: Guadalajara
Country: Spain

Contact:
Last name: Dunia de Miguel Llorente
Email: duniamll@hotmail.com

Investigator:
Last name: Dunia de Miguel Llorente
Email: Principal Investigator

Facility:
Name: H.Universitario de Jerez de la Frontera

Address:
City: Jerez De La Frontera
Country: Spain

Contact:
Last name: Sebastián Garzón López, Dr
Email: sebastianf.garzon.sspa@juntadeandalucia.es

Investigator:
Last name: Sebastian Garzón López
Email: Principal Investigator

Facility:
Name: Hospital Universitario de Canarias

Address:
City: La Laguna
Country: Spain

Contact:
Last name: Sunil Lakhwani
Email: mthernan@ull.es/mailto:sunillakhwani@hotmail.com

Investigator:
Last name: Sunil Lakhwani
Email: Principal Investigator

Investigator:
Last name: Miguel Teodoro Hernández
Email: Principal Investigator

Facility:
Name: Complejo Asistencial Universitario de León

Address:
City: León
Country: Spain

Contact:
Last name: Fernando Escalante Barrigón, Dr

Phone: 987 237400
Email: fescalanteb@yahoo.es

Investigator:
Last name: Fernando Escalante Barrigón
Email: Principal Investigator

Facility:
Name: Hospital Arnau de Vilanova (Lleida)

Address:
City: Lleida
Country: Spain

Contact:
Last name: Antoni Garcia Guiñon
Email: agarciag.lleida.ics@gencat.cat

Investigator:
Last name: Antoni Garcia Guiñon
Email: Principal Investigator

Facility:
Name: Hospital San Pedro

Address:
City: Logroño
Country: Spain

Contact:
Last name: María José Nájera Irazu, Dr

Phone: 941 298000
Email: mjnajera@riojasalud.es

Investigator:
Last name: María José Nájera Irazu
Email: Principal Investigator

Facility:
Name: Complejo Hospitalario Lucus Augusti

Address:
City: Lugo
Country: Spain

Contact:
Last name: Esperanza Lavilla Rubia, Dr

Phone: 982 296000
Email: Esperanza.Lavilla.Rubira@sergas.es

Investigator:
Last name: Esperanza Lavilla Rubia
Email: Principal Investigator

Facility:
Name: Fundación Jiménez Díaz-Ute