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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT06465316 Not yet recruiting - Multiple Myeloma Clinical Trials

Testing Teclistamab (TECVAYLI) in Combination With Iberdomide for Hard-to-Treat Multiple Myeloma

Start date: August 16, 2024
Phase: Phase 1
Study type: Interventional

This phase Ib trial tests the safety, side effects, and best dose of iberdomide in combination with teclistamab in treating hard-to-treat multiple myeloma. Iberdomide is a medication that belongs to a group of drugs known as cereblon E3 ligase modulators. Iberdomide works by targeting and destroying proteins that help myeloma cancer cells to survive. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Immunotherapy with monoclonal antibodies, such as teclistamab, may help the body's immune system attack the cancer, and may interfere with the ability of cancer cells to grow and spread. Giving iberdomide in combination with teclistamab may be safe and tolerable in treating patients with multiple myeloma.

NCT ID: NCT06464991 Recruiting - Multiple Myeloma Clinical Trials

A Phase III Study of Eque-cel in Subjects With Len-refractory RRMM (FUMANBA-03)

FUMANBA-03
Start date: March 27, 2024
Phase: Phase 3
Study type: Interventional

This is a multicenter, randomized, controlled, open-label, phase III clinical study to evaluate the efficacy of Equecabtagene Autoleucel Injection versus standard therapy in subjects with lenalidomid-refractory RRMM who have received 1-2 lines of prior therapy.

NCT ID: NCT06463717 Recruiting - Multiple Myeloma Clinical Trials

Primary Multiple Myeloma Who Achieved MRD Negativity After Induction Therapy, ASCT or Not

Start date: December 1, 2023
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to compare the efficacy and safety of autologous hematopoietic stem-cell transplantation (ASCT) versus non ASCT regimens in primary multiple myeloma patients achieved MRD negativity after induction. The main question it aims to answer is: In primary multiple myeloma patients who achieved MRD negativity after induction, non ASCT regimens are not inferior to ASCT or not? Participants will receive ASCT or non ASCT regimen according to their own choice. Researchers will compare ASCT and non ASCT group see if any significant difference in efficacy and safety.

NCT ID: NCT06461988 Not yet recruiting - Multiple Myeloma Clinical Trials

Talquetamab & Lenalidomide as Post Stem Cell Transplant Maintenance in Multiple Myeloma

Start date: June 2024
Phase: Phase 2
Study type: Interventional

Multiple myeloma (MM) is a heterogenous plasma cell malignancy characterized by clonal proliferation of plasma cells and organ damage. Autologous transplantation with high dose chemotherapy is the standard of care in frontline treatment of eligible patients with MM.

NCT ID: NCT06457464 Not yet recruiting - Multiple Myeloma Clinical Trials

Clinical Outcomes and Prognostic Factors in Multiple Myeloma Patients

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

1. Description of the demographic, clinical, and laboratory characteristics of patients with MM admitted to the hematology unit of Assuit University Hospitals. 2. Determination of treatment outcomes and prognostic factors associated with survival rates.

NCT ID: NCT06435910 Recruiting - Clinical trials for Multiple Myeloma or Plasmacytoma

Engineered Dendritic Cell Vaccines for Multiple Myeloma

Start date: May 11, 2024
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the feasibility, safety, and efficacy of dendritic cell (DC) vaccines in the treatment of multiple myeloma (MM) or plasmacytoma based on immune-modified DC vaccines (DCvac). This approach is aimed to achieve prolonged maintenance of remission in multiple myeloma or plasmacytoma patients.

NCT ID: NCT06433947 Not yet recruiting - Clinical trials for Refractory Multiple Myeloma

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

Start date: June 2024
Phase: Phase 1
Study type: Interventional

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 refractory MM.

NCT ID: NCT06429150 Recruiting - Multiple Myeloma Clinical Trials

Frontline Combination CAR-T Cell Therapy for Multiple Myeloma or Plasmacytoma

Start date: May 11, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this clinical trial is to assess the feasibility, safety, and efficacy of CAR-T cell therapy targeting multiple cancer cell antigens in high-risk multiple myeloma or plasmacytoma as part of a frontline treatment regimen for patients. Another goal of the study is to learn more about the persistence and function of these CAR-T cells in the body.

NCT ID: NCT06425991 Recruiting - Clinical trials for Relapsed or Refractory Multiple Myeloma

A Study Comparing Pre- and Post-Change Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma

MajesTEC-10
Start date: June 7, 2024
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare the pharmacokinetics (processes by which drugs are absorbed, distributed in the body, and excreted) between teclistamab made from the current commercial manufacturing process (pre-change) and the new manufacturing process (post-change).

NCT ID: NCT06425276 Completed - Multiple Myeloma Clinical Trials

Evaluate Safety and Efficacy of High-dose Melphalan HCL for Injection in MM Patients With Auto-HSC Transplantation

Start date: July 24, 2020
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to learn if high-dose Melphalan HCl for Injection works to treat multiple myeloma. It will also learn about the safety of high dose Melphalan HCl for Injection. The main questions it aims to answer are: Does high-dose Melphalan HCl for Injection deplete bone marrow activity which results in a better outcome of patients'own stem cell (blood-forming cell) transplantation? What medical problems do participants have when taking high-dose Melphalan HCl for Injection? How fast is the high-dose Melphalan HCl for Injection cleared out from blood? Participants will: - Take high-dose Melphalan HCl for Injection for 2 days - Have stem cell transplantation one day after treatment - Stay in the hospital for at least 10days and visit the clinic once every week for the first month after transplantation and every month after for checkups and tests.