CancerDrs Find care

Multiple Myeloma clinical trials in Utah

28 actively recruiting multiple myeloma trials at 9 sites across Utah.

Data from ClinicalTrials.gov · last refreshed

Phase 3 Recruiting Network

Lenalidomide, and Dexamethasone With or Without Daratumumab in Treating Patients With High-Risk Smoldering Myeloma

This phase III trial studies how well lenalidomide and dexamethasone works with or without daratumumab in treating patients with high-risk smoldering myeloma. Drugs used in chemotherapy, such as lenalidomide and dexamethasone, work in diff…

Sponsor: ECOG-ACRIN Cancer Research Group
NCT ID: NCT03937635
Sites in Utah:
  • American Fork Hospital / Huntsman Intermountain Cancer Center — American Fork, Utah
  • Sandra L Maxwell Cancer Center — Cedar City, Utah
  • Logan Regional Hospital — Logan, Utah
  • Intermountain Medical Center — Murray, Utah
  • McKay-Dee Hospital Center — Ogden, Utah
Phase 3 Recruiting Network

Testing the Use of Combination Therapy in Adult Patients With Newly Diagnosed Multiple Myeloma, the EQUATE Trial

This phase III trial compares the combination of four drugs (daratumumab, bortezomib, lenalidomide and dexamethasone) to the use of a three drug combination (daratumumab, lenalidomide and dexamethasone). Bortezomib may stop the growth of c…

Sponsor: ECOG-ACRIN Cancer Research Group
NCT ID: NCT04566328
Sites in Utah:
  • Huntsman Cancer Institute/University of Utah — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study of Teclistamab in Combination With Daratumumab and Lenalidomide (Tec-DR) and Talquetamab in Combination With Daratumumab and Lenalidomide (Tal-DR) in Participants With Newly Diagnosed Multiple Myeloma

The purpose of this study is to compare the efficacy of teclistamab in combination with daratumumab and lenalidomide (Tec-DR) and talquetamab in combination with daratumumab and lenalidomide (Tal-DR) versus daratumumab, lenalidomide, dexam…

Sponsor: Janssen Research & Development, LLC
NCT ID: NCT05552222
Sites in Utah:
  • Utah Cancer Specialists — Salt Lake City, Utah
  • Huntsman Cancer Institute — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study to Evaluate Mezigdomide, Bortezomib and Dexamethasone (MEZIVd) Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) in Participants With Relapsed or Refractory Multiple Myeloma (RRMM)

The purpose of this study is to compare the efficacy and safety of mezigdomide (CC-92480), bortezomib and dexamethasone (MeziVd) versus pomalidomide, bortezomib and dexamethasone (PVd) in participants with relapsed or refractory multiple m…

Sponsor: Celgene
NCT ID: NCT05519085
Sites in Utah:
  • Utah Cancer Specialists — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study Comparing Anitocabtagene Autoleucel to Standard of Care Therapy in Participants With Relapsed/ Refractory Multiple Myeloma

The goal of this study (iMMagine-3) is to compare the study drug, anitocabtagene autoleucel to standard of care therapy (SOCT) in participants with relapsed/refractory multiple myeloma who have received 1 to 3 prior lines of therapy, inclu…

Sponsor: Kite, A Gilead Company
NCT ID: NCT06413498
Sites in Utah:
  • Huntsman Cancer Institute, University of Utah — Salt Lake City, Utah
  • LDS Hospital — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study Comparing Talquetamab Plus Pomalidomide, Talquetamab Plus Teclistamab, and Elotuzumab, Pomalidomide, and Dexamethasone or Pomalidomide, Bortezomib, and Dexamethasone in Participants With Relapsed or Refractory Myeloma Who Have Received an Anti-CD38 Antibody and Lenalidomide

The purpose of this study is to compare the effectiveness of either talquetamab plus pomalidomide (Tal-P) or talquetamab plus teclistamab (Tal-Tec) with elotuzumab, pomalidomide, and dexamethasone (EPd) or pomalidomide, bortezomib, and dex…

Sponsor: Janssen Research & Development, LLC
NCT ID: NCT06208150
Sites in Utah:
  • Huntsman Cancer Institute — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study Comparing AZD0120, a Dual-targeted CAR-T Against B-cell Maturation Antigen (BCMA) and CD19, Versus Standard Regimens in Participants With Relapsed Refractory Multiple Myeloma (DURGA-4)

This is a randomised, multicentre, controlled, open-label, Phase III global study comparing the efficacy and safety of AZD0120 versus standard regimens (DKd \[daratumumab, carfilzomib, and dexamethasone\], DPd \[daratumumab, pomalidomide, …

Sponsor: AstraZeneca
NCT ID: NCT07391657
Sites in Utah:
  • Research Site — Salt Lake City, Utah
Phase 3 Recruiting Industry

A Study to Compare the Efficacy and Safety of BMS-986393 Versus Standard Regimens in Adult Participants With Relapsed or Refractory and Lenalidomide-exposed Multiple Myeloma (QUINTESSENTIAL-2)

The purpose of this study is to compare the efficacy and safety of arlo-cel (BMS-986393) versus standard regimens in adult participants with Relapsed or Refractory and Lenalidomide-exposed Multiple Myeloma.

Sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
NCT ID: NCT06615479
Sites in Utah:
  • Huntsman Cancer Institute — Salt Lake City, Utah
Phase 2 Recruiting Academic/Other

TAPUR: Testing the Use of Food and Drug Administration (FDA) Approved Drugs That Target a Specific Abnormality in a Tumor Gene in People With Advanced Stage Cancer

The purpose of the study is to learn from the real world practice of prescribing targeted therapies to patients with advanced cancer whose tumor harbors a genomic variant known to be a drug target or to predict sensitivity to a drug. NOTE:…

Sponsor: American Society of Clinical Oncology
NCT ID: NCT02693535
Sites in Utah:
  • Cedar City Hospital, SW Cancer Clinic, Sandra Maxwell Cancer Center — Cedar City, Utah
  • Intermountain Healthcare — Salt Lake City, Utah
  • Dixie Regional Medical Center-River Road Campus — St. George, Utah
Phase 2 Recruiting Industry

Study of Arlocabtagene Autoleucel (BMS-986393) a GPRC5D-directed CAR T Cell Therapy in Adult Participants With Relapsed or Refractory Multiple Myeloma

The purpose of this study is to evaluate the effectiveness and safety of Arlocabtagene Autoleucel (BMS-986393) in participants with relapsed or refractory multiple myeloma.

Sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
NCT ID: NCT06297226
Sites in Utah:
  • LDS Hospital — Salt Lake City, Utah
Phase 1, Phase 2 Recruiting Academic/Other

Testing the Combination of Two Approved Drugs and One Experimental Drug in Patients With Relapsed or Refractory Multiple Myeloma

This phase I/II trial tests the safety, side effects, best dose, and effectiveness of iberdomide in combination with belantamab mafodotin and dexamethasone in treating patients with multiple myeloma (MM) that has come back after a period o…

Sponsor: Alliance for Clinical Trials in Oncology
NCT ID: NCT06232044
Sites in Utah:
  • Huntsman Cancer Institute/University of Utah — Salt Lake City, Utah
Phase 1, Phase 2 Recruiting Industry

A Phase 1b/2 Study of Sonrotoclax (BGB-11417) as Monotherapy and in Various Combinations With Dexamethasone Plus Carfilzomib, Dexamethasone Plus Daratumumab, and Dexamethasone Plus Pomalidomide in Multiple Myeloma

The purpose of this study is to assess the safety, tolerability, and efficacy of sonrotoclax as monotherapy and in various combinations in patients with relapsed/refractory (R/R) multiple myeloma (MM) and chromosomal translocation t(11;14)…

Sponsor: BeOne Medicines
NCT ID: NCT04973605
Sites in Utah:
  • Huntsman Cancer Institute — Salt Lake City, Utah
Phase 2 Recruiting Academic/Other

Sequential Therapy in Multiple Myeloma Guided by MRD Assessments

This research study will determine the proportion of patients with lowest minimal residual disease (MRD) response obtainable after receiving 6 cycles of study treatment. Minimal residual disease is multiple myeloma cells below the level of…

Sponsor: University of Alabama at Birmingham
NCT ID: NCT05231629
Sites in Utah:
  • University of Utah — Salt Lake City, Utah
Phase 2 Recruiting Academic/Other

Impact of Budesonide on Incidence of ≥ Gr2 Diarrhea in Multiple Myeloma (MM) Patients Undergoing Autologous Stem Cell Transplant

A randomized placebo controlled, phase 2 study of budesonide in subjects with multiple myeloma undergoing autologous stem cell transplant (ACST). The study includes a run-in period with 20 patients.

Sponsor: University of Utah
NCT ID: NCT05405387
Sites in Utah:
  • Huntsman Cancer Institute at the University of Utah — Salt Lake City, Utah
Phase 2 Recruiting Academic/Other

Use of Isatuximab, Dexamethasone and Lenalidomide in a Go-Slow Fashion for Ultra-Frail Patients With Multiple Myeloma

Historically, the frailest patients with multiple myeloma are under-represented in clinical trials, and have very high rates of treatment discontinuation, and early treatment mortality. The investigators hypothesize that a go-slow gentle a…

Sponsor: University of Utah
NCT ID: NCT06517017
Sites in Utah:
  • Huntsman Cancer Institute at the University of Utah — Salt Lake City, Utah
Phase 1 Recruiting Industry

A Study to Learn About the Effects of Cemsidomide in Combination With Elranatamab in Relapsed/Refractory Multiple Myeloma Subjects

The main purpose of the study is to understand the safety and tolerability of cemsidomide when given along with elranatamab in subjects with relapsed or refractory multiple myeloma. The first part of the study will evaluate different dose …

Sponsor: C4 Therapeutics, Inc.
NCT ID: NCT07280013
Sites in Utah:
  • Huntsman Cancer Institute, University of Utah — Salt Lake City, Utah
Phase 1 Recruiting Industry

CRISPR-Edited Allogeneic Anti-BCMA CAR-T Cell Therapy in Patients With Relapsed/Refractory Multiple Myeloma

This is a Phase 1 study to evaluate the safety of CB-011 (the study treatment), an allogeneic chimeric antigen receptor (CAR-T) cell therapy that targets the B cell maturation antigen (BCMA), to determine the best dose of CB-011, and to as…

Sponsor: Caribou Biosciences, Inc.
NCT ID: NCT05722418
Sites in Utah:
  • Huntsman Cancer Institute, University of Utah — Salt Lake City, Utah
Phase 1 Recruiting Industry

Study to Assess Safety and Tolerability of OPN-6602 in Subjects With Relapsed and/or Refractory Multiple Myeloma

Phase 1b, open-label study evaluating the safety, tolerability, pharmacokinetics, preliminary antitumor activity, and pharmacodynamics of OPN-6602 monotherapy and in combination with dexamethasone in subjects with relapsed and/or refractor…

Sponsor: Opna Bio LLC
NCT ID: NCT06433947
Sites in Utah:
  • Huntsman Cancer Center Institute University of Utah — Salt Lake City, Utah
Phase 1 Recruiting Industry

Study of Oral Administration of LP-118 in Patients With Relapsed or Refractory CLL, SLL, MDS, MDS/MPN, AML, CMML-2, MPN-BP, ALL, MF, NHL, RT, MM or T-PLL.

This is a Phase 1, multi-center, open-label study with a dose-escalation phase (Phase 1a) and a cohort expansion phase (Phase 1b), to evaluate the safety, tolerability, and PK profile of LP-118 under a once daily oral dosing schedule in up…

Sponsor: Newave Pharmaceutical Inc
NCT ID: NCT04771572
Sites in Utah:
  • University of Utah — Salt Lake City, Utah
Recruiting NIH

Collection of Tissue Samples for Cancer Research

Background: -Patients who are being evaluated and/or treated at the NIH Clinical Center and adult patients at participating sites will be entered onto this tissue procurement protocol for collection of tissue specimens. Objectives: * To ob…

Sponsor: National Cancer Institute (NCI)
NCT ID: NCT00900198
Sites in Utah:
  • University of Utah — Salt Lake City, Utah
Recruiting Academic/Other

Screening for AL Amyloidosis in Smoldering Multiple Myeloma

In this multicenter study, we will recruit 400 patients 40 years of age or older at 15 centers with a diagnosis of smoldering multiple myeloma (SMM), a group of patients for whom standard of care is observation not treatment. The main goal…

Sponsor: Tufts Medical Center
NCT ID: NCT06365060
Sites in Utah:
  • University of Utah, Huntsman Cancer Hospital — Salt Lake City, Utah

Showing 25 of 28 trials with sites in Utah. See all multiple myeloma trials →

Medical disclaimer: This page aggregates public ClinicalTrials.gov data. It is not medical advice. Always confirm eligibility and enrollment details with the trial site or your oncologist.

Source: ClinicalTrials.gov API v2 · Last checked: 2026-04-20