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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT06099912 Not yet recruiting - Multiple Myeloma Clinical Trials

Dynamic Frailty Assessment for Guiding the Treatment in Older Adults With Newly Diagnosed Multiple Myeloma

DFA
Start date: July 1, 2024
Phase:
Study type: Observational

Investigators designed the single-center, prospective real-world based clinical study with the aim of applying the standardized geriatric assessment system IMWG-FS internationally for dynamic frailty assessment of elderly newly diagnosed multiple myeloma(NDMM), guiding therapeutic decision based on their fit/frail status (fit → intensive; frail → mild), to observe their treatment tolerance, treatment related adverse events(TRAE), treatment discontinued(TD), and survival(progression survivaland overall survival).

NCT ID: NCT06095752 Recruiting - Multiple Myeloma Clinical Trials

Multiple Myeloma Prognostic Indices

Start date: November 1, 2023
Phase:
Study type: Observational

The aim of this study was to evaluate the impact of albumin / fibrinogen ratio, blood viscosity and RDW on the prognosis of a newly diagnosed MM patients

NCT ID: NCT06087653 Recruiting - Multiple Myeloma Clinical Trials

Safety, Efficacy, and Pharmacokinetics of Continuous Subcutaneous Lenalidomide in Multiple Myeloma (MM)

Start date: October 2, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Primary Objective • Assess the safety and tolerability of low-dose lenalidomide administered by continuous subcutaneous (SC) infusion (STAR-LLD) in combination with dexamethasone and a proteasome inhibitor (PI). Secondary Objectives - To assess the immunologic activity of natural killer (NK) cells and T cells for innate and humoral immunity. - To establish the pharmacokinetic (PK) profile of STAR-LLD at a defined infusion rate targeting steady-state blood concentrations. - To determine pharmacodynamic (PD) changes with STAR-LLD in a panel of biomarkers associated with clinical response to lenalidomide. - Evaluate changes in efficacy indicators including objective response rate (ORR), progression-free survival (PFS), and duration of response (DOR). Exploratory Objective - To assess the impact of STAR-LLD on patient reported symptoms and outcomes. Primary Endpoints - The grade, frequency, and relationship of treatment-emergent adverse events (TEAEs) including adverse events of special interest (AESIs): (gastrointestinal [GI] toxicity, fatigue, hematologic toxicity, rash (non-infusion site). - The observation of dose-limiting toxicities (DLTs) of STAR-LLD during Cycle 1. Secondary Endpoints - Immune profiles, functional assays for NK cell activation and antigen specific T-cell activity. - Blood concentrations of lenalidomide at on Day 1 and at steady state. - Changes in biomarkers during treatment. - Rate of complete response, very good partial response (VGPR), partial response (PR), stable disease (SD), and progressive disease. - Determination of ORR, PFS, and DOR

NCT ID: NCT06084962 Recruiting - Clinical trials for Relapse/Refractory Multiple Myeloma

A Study of DeepTag-GPRC5D Targeted CAR-T Cells Therapy for Refractory/Relapsed Multiple Myeloma

Start date: October 20, 2023
Phase: Phase 1
Study type: Interventional

Clinical Trial for the safety and efficacy of DeepTag-GPRC5D targeted CAR-T cells therapy for refractory/relapsed multiple myeloma

NCT ID: NCT06083207 Not yet recruiting - Multiple Myeloma Clinical Trials

A Study of IBI3003 in Subjects With Relapsed or Refractory Multiple Myeloma

Start date: February 1, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

This is a phase 1/2 multicenter, open-label, first-in-human study of IBI3003. It includes a phase 1 dose escalation and expansion section to identify maximum tolerated dose(MTD)/recommended Phase 2 Dose(RP2D) of IBI3003, plans to enroll 23~116 subjects, and a phase 2 stage to explore efficacy, safety and tolerability of IBI3003 at RP2D in multiple myeloma.

NCT ID: NCT06082596 Completed - Clinical trials for Relapsed or Refractory Multiple Myeloma

Study of BEBT-908 in Subjects With Advanced Hematological Tumors

Start date: March 2, 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study was to evaluate the safety and tolerance of BEBT-908 for injection in the treatment of recurrent refractory malignant lymphoma, multiple myeloma and chronic lymphoblastic leukemia, and to obtain the pharmacokinetic data and preliminary efficacy of BEBT-908 for injection, and to explore the relationship between the safety and efficacy of BEBT-908 for injection and related biomarkers.

NCT ID: NCT06073353 Recruiting - Multiple Myeloma Clinical Trials

Psychosocial Mobile Application (THRIVE-M) for Patients With Multiple Myeloma

THRIVE-M
Start date: December 1, 2023
Phase: N/A
Study type: Interventional

This clinical trial aims to evaluate whether a psychosocial mobile application (THRIVE-M), is efficacious for improving quality of life, psychological distress, and fatigue in patients living with multiple myeloma compared to usual care.

NCT ID: NCT06068400 Recruiting - Clinical trials for Multiple Myeloma in Relapse

Clinical Study to Evaluate the Safety and Efficacy of CAR-T in the Treatment of Multiple Myeloma

Start date: September 13, 2023
Phase: N/A
Study type: Interventional

This is a single arm, single center clinical study evaluating the safety and efficacy of CAR-T treatment for multiple myeloma.

NCT ID: NCT06066359 Recruiting - Myeloma Clinical Trials

Phase I/II Trial of Cord Blood-Derived NK Cells Genetically Engineered With NY-ESO-1 TCR/IL-15 Cell Receptor for Relapsed/Refractory Multiple Myeloma

Start date: November 30, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

To find the recommended dose of NY-ESO-1 TCR/IL-15 NK cells that can be given to patients with relapsed or refractory MM. To learn if the dose of NY-ESO-1 TCR/IL-15 NK cells found in Part A can help to control the disease.

NCT ID: NCT06066346 Recruiting - Multiple Myeloma Clinical Trials

A Study of Talquetamab for People With Multiple Myeloma Who Have Received BCMA CAR T-Cell Therapy

Start date: September 27, 2023
Phase: Phase 2
Study type: Interventional

The researchers are doing this study to find out whether talquetamab is an effective treatment after BCMA CAR Tcell therapy for people with relapsed or refractory multiple myeloma. All participants in this study will have already received the BCMA CAR T-cell therapy ide-cel for their disease.