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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT05545202 Not yet recruiting - Multiple Myeloma Clinical Trials

A Randomized, Comparative, Double-blind Trial of Pentaisomaltose and Dimethyl Sulphoxide for Cryoprotection of Hematopoietic Stem Cells in Subjects With Multiple Myeloma or Malignant Lymphoma With a Need for Autologous Transplantation

Start date: April 30, 2024
Phase: Phase 4
Study type: Interventional

A randomized, comparative, double-blind trial of pentaisomaltose and dimethyl sulphoxide for cryoprotection of hematopoietic stem cells in subjects with multiple myeloma or malignant lymphoma with a need for autologous transplantation

NCT ID: NCT05530096 Not yet recruiting - Multiple Myeloma Clinical Trials

Telo Genomics Technology to Detect & Profile Multiple Myeloma MRD

TELO - DMRD
Start date: January 2023
Phase:
Study type: Observational [Patient Registry]

The purpose : Detect and profile Multiple myeloma Measurable Residual Disease(MRD) prognostics for monitoring post-transplant Multiple Myeloma (MM) Patients receiving maintenance therapy.

NCT ID: NCT05498545 Not yet recruiting - Clinical trials for Relapsed/Refractory Multiple Myeloma

Universal BCMA-targeted LUCAR-B68 Cells in Patients With Relapsed/Refractory Multiple Myeloma

Start date: September 2022
Phase: Phase 1
Study type: Interventional

A Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of Universal BCMA-targeted LUCAR-B68 Cells Product in Patients With Relapsed/Refractory Multiple Myeloma

NCT ID: NCT05495620 Not yet recruiting - Clinical trials for Multiple Myeloma in Relapse

Long-term KRd in Relapsed and/or Refractory Multiple Myeloma

Start date: August 1, 2022
Phase:
Study type: Observational

Research question: Is KRd therapy effective and safe in the real-world Asian patients? Primay objective: To evaluate the effectiveness of KRd in RRMM patients Secondary objectives: To evaluate the effectiveness of investigational treatment strategy by - PFS difference according to the high-risk disease subgroups and previous treatment - OS - Overall response rate and clinical benefit rate - Duration of response To evaluate the safety and tolerability of KRd in RRMM patients

NCT ID: NCT05439538 Not yet recruiting - Clinical trials for Multiple Myeloma(MM)

Serum NGAL IN Patients With Multiple Myeloma

Start date: October 1, 2022
Phase:
Study type: Observational

The aim of this study was to evaluate SERUM neutrophil gelatinase-associated lipocalin, emerging indicator of tubular damage and examine their relationship with established measures of renal function (serum creatinine, and estimated glomerular filtration rate, eGFR) among MM patients with and without renal impairment (RI), and at various stages of MM progression.

NCT ID: NCT05429515 Not yet recruiting - Multiple Myeloma Clinical Trials

Effect of HFR-SUPRA in the Treatment of Multiple Myeloma-related Acute Kidney Injury

Start date: July 1, 2022
Phase: Phase 4
Study type: Interventional

In patients with multiple myeloma-related acute kidney injury, compare the renal outcome of chemotherapy combined with HFR-SUPRA to chemotherapy combined with hemodialysis.

NCT ID: NCT05353907 Not yet recruiting - Myeloma Clinical Trials

Dual-Energy Computed Tomography for Improving Imaging Assessment of Multiple Myeloma

DECIMA
Start date: June 2022
Phase:
Study type: Observational

Up to 30% of patients with newly diagnosed/suspected myeloma cannot undergo or do not tolerate whole body MRI (WB-MRI). A number of factors may be contributory. First, WB-MRI protocols can take in excess of 1 hour. Patients must remain still within a narrow bore scanner with multiple MRI coils that can be claustrophobic. Second, there is significant acoustic noise that can be heard despite the use of ear protection. Third, 80% of patients will experience bone pain or fracture at some point during their illness, affecting their comfort within the scanner. Fourth, patients also have higher anxiety. One review reported up to 30% of patients experienced considerable apprehension and up to 10% severe psychological distress when undergoing MRI. Finally, myeloma is predominantly an illness of the elderly and co-morbid conditions decrease patients' ability to tolerate a long scan. When WB-MRI cannot be performed, NICE recommend whole-body computed tomography (WB-CT), which the investigators know offers decreased diagnostic performance in terms of marrow assessment and focal lesion detection. The investigators believe that using a novel CT technique - dual-energy CT (DECT) - may offer better diagnostic performance over standard WB-CT in myeloma patients. What the investigators seek to do in this study is to evaluate the sensitivity and specificity of DECT in a cohort of untreated patients; and compare the performance of DECT to simulated standard CT (data simulated from the DECT) and also to WB-MRI (reference standard alongside bone marrow biopsy results. The investigators will assess both subjective visual analysis of DECT images as well as CT quantitative values for the bone marrow. Secondary objectives include assessment of patient experience across both imaging tests and assessment of intra & inter observer variability in subjective visual analysis

NCT ID: NCT05331313 Not yet recruiting - Multiple Myeloma Clinical Trials

The Aim is to Identify Recurrent Genomic Mutations and/or Predisposing Polymorphisms in Patients With Sporadic Cases of Multiple Myeloma

MMSPORADGEN
Start date: December 1, 2022
Phase:
Study type: Observational

There is a growing body of data suggesting that the the risk of developing multiple myeloma, or myelomagenesis, is associated with genetic alterations occurring in the tumor cells. A limited number of candidate genes and polymorphisms have been reported in patients with this disease. In this study the investigators will compare the genetic information obtained on purified abnormal plasmocytes obtained from patients with multiple myeloma with available public databases in an effort to identify and if possible validate the role of certain mutations and/or polymorphisms in myelomagenesis. Plasmocytes will be obtained by immunomagnetic enrichment using CD138+ beads.

NCT ID: NCT05325801 Not yet recruiting - Multiple Myeloma Clinical Trials

A Study of CAR-T Cells Targeting Both BCMA and GPRC5D in Treatment of Relapsed or Refractory Multiple Myeloma

Start date: April 2022
Phase: Phase 1
Study type: Interventional

An Open-Label, Dose Finding Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of BMCA and GPRC5D dual target CAR-T cells therapy in Patients with relapsed or refractory multiple myeloma

NCT ID: NCT05308875 Not yet recruiting - Multiple Myeloma Clinical Trials

Efficacy and Safety Evaluation of PD1-BCMA-CART

Start date: March 1, 2024
Phase: N/A
Study type: Interventional

This trial aims to evaluate the safety and efficacy of PD1-BCMA-CART in treating patients with relapsed or refractory multiple myeloma.