Multiple Myeloma Clinical Trials in Hackensack, New Jersey
8 studies are recruiting for multiple myeloma in Hackensack, New Jersey right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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A Study to Determine the Recommended Dose and Schedule, and Evaluate the Safety and Preliminary Efficacy of Mezigdomide in Combination With Elranatamab in Participants With Relapsed and/or Refractory Multiple Myeloma
The purpose of this study is to evaluate the preliminary safety and determine the RP2D of mezigdomide in combination with elranatamab in participants with relapsed and refractory multiple myeloma (RRMM).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hackensack University Medical Center, Hackensack, New Jersey
- Locations
- 22 in total
- Run by
- Celgene
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A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel
The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- Hackensack University Medical Center, Hackensack, New Jersey
- Locations
- 50 in total
- Run by
- Janssen Research & Development, LLC
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A Study of an MMSET Inhibitor in Patients With Relapsed and Refractory Multiple Myeloma
A Phase I study to evaluate the safety of a novel, orally available, selective, and potent small molecule inhibitor of the histone lysine methyl transferase MMSET (also known as NSD2/WHSC1) to prevent the dimethylation of H3K36 in adult patients with relapsed or refractory multiple myeloma (RRMM).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hackensack University Medical Center, Hackensack, New Jersey
- Locations
- 26 in total
- Run by
- K36 Therapeutics, Inc.
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A Study to Evaluate the Safety, Effectiveness and Tolerable Dose of Arlocabtagene Autoleucel (BMS-986393) in Novel Combinations in Participants With Relapsed and/or Refractory Multiple Myeloma
The purpose of this study is to establish a safe and tolerable dose of arlocabtagene autoleucel (BMS-986393) in combinations with alnuctamab, mezigdomide, iberdomide, and elranatamab in participants with relapsed and/or refractory multiple myeloma (RRMM).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- John Theurer Cancer Center at Hackensack University Medical Center, Hackensack, New Jersey
- Locations
- 19 in total
- Run by
- Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
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Selinexor and Backbone Treatments of Multiple Myeloma Patients
This study will independently assess the efficacy and safety of 11 combination therapies in 12 arms, in dose-escalation/-evaluation and expansion phases, for the treatment of patients with relapsed/refractory multiple myeloma (RRMM) and newly diagnosed multiple myeloma (NDMM). The combinations to b…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hackensack University Medical Center - John Theurer Cancer Center, Hackensack, New Jersey
- Locations
- 25 in total
- Run by
- Karyopharm Therapeutics Inc
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A Study of Belantamab Mafodotin Administered in Combination With Lenalidomide and Dexamethasone (BRd) Versus Daratumumab, Lenalidomide, and Dexamethasone (DRd) in Participants With Newly Diagnosed Multiple Myeloma (NDMM) Who Are Ineligible for Autologous Stem Cell Transplantation (TI-NDMM)
The purpose of this Phase 3 study is to evaluate if BRd prolongs progression free survival (PFS) and/or improves minimal residual disease (MRD) negative status compared with DRd in participants with TI-NDMM.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- GSK Investigational Site, Hackensack, New Jersey
- Locations
- 181 in total
- Run by
- GlaxoSmithKline
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Carfilzomib Based Chemotherapy Mobilization for Autologous Stem Cell Transplants in Multiple Myeloma
This phase I study utilizes a 3+3 design with escalating cohorts of Carfilzomib at 20mg/m2, 27mg/m2, 36mg/m2, 45mg/m2, 56mg/m2, and 70mg/m2 to be administered concomitantly with Cyclophosphamide 2 gm/m2, Dexamethasone and Granulocyte colony-stimulating factor (G-CSF)
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Hackensack Meridian Health - John Theurer Cancer Center, Hackensack, New Jersey
- Run by
- Hackensack Meridian Health
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A Study to Evaluate Safety, Drug Levels and Effectiveness of CC-92480 (BMS-986348) in Combination With Other Treatments in Participants With Relapsed or Refractory Multiple Myeloma
The purpose of this study is to assess the safety, tolerability and preliminary effectiveness of CC-92480 (BMS-986348) in novel therapeutic combinations for the treatment of Relapsed or Refractory Multiple Myeloma (RRMM).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- John Theurer Cancer Center at Hackensack UMC, Hackensack, New Jersey
- Locations
- 17 in total
- Run by
- Bristol-Myers Squibb
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
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