A Study Comparing JNJ-68284528, a CAR-T Therapy Directed Against B-cell Maturation Antigen (BCMA), Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) or Daratumumab, Pomalidomide and Dexamethasone (DPd) in Participants With Relapsed and Lenalidomide-Refractory Multiple Myeloma

Running, not enrolling · Phase 3

Conditions studied: Multiple Myeloma

In brief

The purpose of this study is to compare the efficacy of ciltacabtagene autoleucel (cilta-cel) with standard therapy, either Pomalidomide, Bortezomib and Dexamethasone (PVd) or Daratumumab, Pomalidomide and Dexamethasone (DPd).

Key facts

Study ID

NCT04181827

Run by

Janssen Research & Development, LLC

People needed

419

Starts

2020-06-12

Expected to finish

2027-03-31

Last updated by the study team

2026-07-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Measurable disease at screening as defined by any of the following: (a) Serum monoclonal paraprotein (M-protein) level greater than or equal to (>=) 0.5 gram per deciliter (g/dL) or urine M-protein level >=200 milligram (mg)/24 hours; or (b) Light chain multiple myeloma without measurable M-protein in the serum or the urine: Serum free light chain >=10 mg/dL and abnormal serum free light chain ratio
• Have received 1 to 3 prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory drug (IMiD)
• Have documented evidence of PD by International Myeloma Working Group (IMWG) criteria based on investigator's determination on or within 6 months of their last regimen
• Be refractory to lenalidomide per IMWG consensus guidelines (failure to achieve minimal response or progression on or within 60 days of completing lenalidomide therapy). Progression on or within 60 days of the last dose of lenalidomide given as maintenance will meet this criterion. For participants with more than 1 prior line of therapy, there is no requirement to be lenalidomide refractory to the most recent line of prior therapy. However, participants must be refractory to lenalidomide in at least one prior line
• Have clinical laboratory values meeting the following criteria during the Screening Phase (re testing is allowed but the below criteria must be met in the latest test prior to randomization):
• Hemoglobin >=8 gram per deciliter (g/dL) (without prior RBC transfusion within 7 days before the laboratory test; recombinant human erythropoietin use is permitted);
• Absolute neutrophil count (ANC) >=1 * 10\^9 per liter (L) (without recombinant human granulocyte colony-stimulating factor [G-CSF] within 7 days and without pegylated G-CSF within 14 days of the laboratory test);
• Platelet count >=75 * 10\^9/L (without prior platelet transfusion within 7 days before the laboratory test) in participants in whom less than (<) 50 percent (%) of bone marrow nucleated cells are plasma cells; platelet count >=50 * 10\^9/L (without prior platelet transfusion within 7 days before the laboratory test) in participants in whom >=50% of bone marrow nucleated cells are plasma cells;
• Lymphocyte count >=0.3 * 10\^9/L;
• Aspartate aminotransferase (AST) less than or equal to (<=)3 * upper limit of normal (ULN);
• Alanine aminotransferase (ALT) <=3 * ULN;
• Total bilirubin <=2.0 * ULN; except in participants with congenital bilirubinemia, such as Gilbert syndrome (in which case direct bilirubin <=1.5 * ULN is required);
• Estimated glomerular filtration rate >=40 milliliter per minute (mL/min) per 1.73 meter square (m\^2) (to be calculated using the Modification of Diet in Renal Disease [MDRD] formula)

You may not qualify if…

• Prior treatment with chimeric antigen receptor T-cell (CAR-T) therapy directed at any target
• Any previous therapy that is targeted to B-cell maturation antigen (BCMA)
• Ongoing toxicity from previous anticancer therapy that has not resolved to baseline levels or to Grade 1 or less; except for alopecia
• Participants with Grade 1 peripheral neuropathy with pain or Grade 2 or higher peripheral neuropathy will not be permitted to receive pomalidomide, bortezomib, and dexamethasone (PVd) as standard therapy or bridging therapy; however, participants may receive daratumumab, pomalidomide, and dexamethasone (DPd) as standard therapy or bridging therapy
• Received a cumulative dose of corticosteroids equivalent to >=70 mg of prednisone within the 7 days prior to randomization
• Monoclonal antibody treatment within 21 days
• Cytotoxic therapy within 14 days
• Proteasome inhibitor therapy within 14 days
• Immunomodulatory drug (IMiD) therapy within 7 days

Where it is running

• Mayo Clinic Cancer Center-Scottsdale — Phoenix, Arizona, United States
• Stanford University Medical Center — Stanford, California, United States
• Colorado Blood Cancer Institute — Denver, Colorado, United States
• Yale New Haven Hospital — New Haven, Connecticut, United States
• University Of Miami Leonard M Mille School Of Medicine SCCC — Miami, Florida, United States
• University of Iowa Hospitals and Clinics — Iowa City, Iowa, United States
• University of Kansas — Westwood, Kansas, United States
• University Of Maryland Medical Center — Baltimore, Maryland, United States
• Mayo Clinic - Rochester — Rochester, Minnesota, United States
• Washington University School Of Medicine — St Louis, Missouri, United States
• Hackensack University Medical Center — Hackensack, New Jersey, United States
• Memorial Sloan-Kettering Cancer Center — New York, New York, United States
• University of Rochester Medical Center — Rochester, New York, United States
• Duke University Medical Center — Durham, North Carolina, United States
• The Ohio State University — Columbus, Ohio, United States
• Huntsman Cancer Institute — Salt Lake City, Utah, United States
• Wisconsin Institutes for Medical Research — Madison, Wisconsin, United States
• Medical College Of Wisconsin — Milwaukee, Wisconsin, United States
• Royal Adelaide Hospital — Adelaide, Australia
• Royal Prince Alfred Hospital — Camperdown, Australia
• Royal Brisbane and Womens Hospital — Herston, Australia
• Peter MacCallum Cancer Centre — Melbourne, Australia
• Alfred Health — Melbourne, Australia
• Fiona Stanley Hospital — Murdoch, Australia
• University of Alabama at Birmingham — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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