- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05776979
Post-Transplant Maintenance Therapy With Isatuximab Plus Lenalidomide for High-Risk Multiple Myeloma Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objectives:
Primary Objectives
1. Compare progression-free survival at 3 years with historical control rate of 50%.
Primary endpoint
1. Progression-free survival at 3 years, measured from the date of transplant to the date of progression or death.
Secondary objectives:
- Assess minimal residual disease (MRD) rate at 12 months after starting Isatuximab maintenance therapy
- Assess overall best response rate (defined as the occurrence of VGPR or better and CR/sCR) before the 4th Isatuximab cycle, and at 12, 24, and 36 months after starting maintenance therapy
- Assess MRD rate before 4th Isatuximab cycle and at 24 months after starting maintenance therapy
- Assess duration of response (DOR)
- Assess overall survival (OS)
- Assess safety
Study Type
Enrollment (Estimated)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: Muzzaffar Qazilbash, MD
- Phone Number: (713) 745-3458
- Email: mqazilba@mdanderson.org
Study Locations
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Texas
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Houston, Texas, United States, 77030
- Recruiting
- M D Anderson Cancer Center
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Principal Investigator:
- Muzaffar Qazilbash, MD
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Contact:
- Muzaffar Qazilbash, MD
- Phone Number: 713-745-3458
- Email: mqazilba@mdanderson.org
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Adult patients 18 to 70 years old, with newly diagnosed symptomatic (according to the revised 2014 IMWG criteria as summarized in Appendix A) myeloma. Patients must have measurable disease at diagnosis defined by any of the following:
- Serum M-protein ≥1 g/dL (for IgA ≥0.5 g/dL) or urine M-protein ≥200 mg/24 hours
- For oligosecretory myeloma, involved serum free light chain (FLC) level ≥10 mg/dL, provided serum FLC ratio is abnormal
- For non-secretory myeloma, > 1 focal lesions measurable by imaging
Subjects must have high-risk myeloma defined as followed:
- R-ISS stage II or III patients (Appendix B)
- ISS stage III (Appendix B)
- ≥ 3 copies +1q21 in patients with ISS Stage II/III or R-ISS Stage II/III
- Presence of del(17p) cytogenetic abnormality regardless of ISS/R-ISS Stage
- Presence of at least 2 high-risk genetic abnormalities [del(17p), t(4;14), t(14;16), t(14;20), +1q21] regardless of ISS/R-ISS stage
- English and non-English speaking patients are eligible.
- Karnofsky performance score of at least 70% and/or ECOG PS ≤2
Underwent ASCT using a conditioning regimen consisting of Busulfan and Melphalan with adequate cell count recovery after transplant without the need for growth factor support or transfusions within 7 days from the lab test
- Absolute neutrophil count (ANC) ≥1000 /µL
- Hemoglobin ≥8 g/dL
- Platelet count ≥50,000 /µL
- Patients must have achieved partial response (PR) or better prior to starting maintenance therapy.
Adequate major organ system function as demonstrated by:
- Serum creatinine clearance equal or more than 30 ml/min (calculated with Cockcroft- Gault formula).
- Total bilirubin equal or less than 2.0 mg/dL (equal or less than 3.0 mg/dL for patients with Gilbert's disease).
- ALT or AST equal or less than 3 times the upper normal for adults.
- Patient or patient's legal representative, parent(s) or guardian should provide written Internal Review Board (IRB)-approved informed consent.
- Female patients included must not be pregnant or lactating. Females of childbearing potential must have (before starting treatment) a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10-14 days prior to and again within 24 hours prior to starting Isatuximab and with each cycle of study treatment. Females of childbearing potential must refrain from becoming pregnant and commit to either apply highly effective method of birth control (two reliable methods of birth control) or continue abstinence from heterosexual intercourse during study period and for at least 5 months after last dose of Isatuximab. Patients who receive Lenalidomide should continue to follow REVLIMID REMSTM requirements.
- Men of reproductive potential must agree to follow accepted birth control methods and refrain from sperm donation for the duration of the study and for at least 5 months after last dose of Isatuximab. Patients who receive Lenalidomide should continue to follow REVLIMID REMSTM requirements.
Exclusion Criteria
- Progression of myeloma, as defined by the IMWG criteria (Appendix C), prior to initiation of maintenance therapy
- Patients receiving any other investigational agents within 14 days or 5 half-lives of the investigational drug prior to initiation of study intervention. Exceptions can be granted after discussing with PI.
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to any of the study drugs. Hypersensitivity or history of intolerance to steroids, mannitol, pregelatinized starch, sodium stearyl fumarate, histidine (as base and hydrochloride salt), arginine hydrochloride, poloxamer 188, sucrose or any of the other components of study intervention that are not amenable to premedication with steroids and H2 blockers or would prohibit further treatment with these agents.
- Known hypersensitivity or desquamating rash to either thalidomide or lenalidomide.
- Participants must not have an active infection requiring treatment.
- Participants must not have an uncontrolled intercurrent illness including, but not limited to, an uncontrolled hypertension (systolic >170, diastolic >100 despite antihypertensive therapy), symptomatic congestive heart failure (Class III or IV as defined by the New York Heart Association (NYHA) functional classification system), acute coronary syndrome, liver cirrhosis, and/or cognitive impairments/psychiatric illness/social situations that would limit compliance with study requirements. PI is the final arbiter of this criterion.
- Major surgery within 4 weeks before initiating study treatment.
- HIV-positive patients and/or active hepatitis A, B or C infections.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: isatuximab plus lenalidomide after an autologous stem cell transplantation (ASCT)
Both isatuximab and lenalidomide are FDA approved and commercially available for the treatment of relapsed or refractory MM (MM that has come back or stopped responding to treatment).
Participants will begin taking the study drugs about 60-180 days after your ASCT.
Participants may receive the study drugs for about 3 years.
After that, participants will have follow-up visits 1 time a year for the 3 years after your last dose of study drugs
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Given by vein over about 75 minutes
Other Names:
Given by PO
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5
Time Frame: through study completion; an average of 1 year.
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through study completion; an average of 1 year.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Muzzaffar Qazilbash, MD, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Immune System Diseases
- Neoplasms by Histologic Type
- Neoplasms
- Lymphoproliferative Disorders
- Immunoproliferative Disorders
- Hematologic Diseases
- Hemorrhagic Disorders
- Hemostatic Disorders
- Paraproteinemias
- Blood Protein Disorders
- Multiple Myeloma
- Neoplasms, Plasma Cell
- Physiological Effects of Drugs
- Antineoplastic Agents
- Immunologic Factors
- Angiogenesis Inhibitors
- Angiogenesis Modulating Agents
- Growth Substances
- Growth Inhibitors
- Lenalidomide
Other Study ID Numbers
- 2022-0028
- NCI-2023-02219 (Other Identifier: NCI-CTRP Clinical Trials Registry)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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