Clinical Trials Logo

Lymphoma clinical trials

View clinical trials related to Lymphoma.

Filter by:

NCT ID: NCT06436677 Recruiting - Clinical trials for Cutaneous T Cell Lymphoma

A Study of Molecular Subtyping-based Therapeutic Strategies for Cutaneous T-cell Lymphoma

AMITY
Start date: May 9, 2024
Phase:
Study type: Observational [Patient Registry]

Cutaneous T-cell lymphoma (CTCL) is a group of diseases resulting from clonal hyperplasia of memory T cells in the skin. The increasing incidence and high treatment costs have posed significant challenges to public health and the economy. Current treatment guidelines only provide partial control, leading to varying remission times and recurrence rates. This study aims to use molecular subtyping and immunohistochemistry to guide treatment selection for CTCL patients, aiming to prolong clinical benefit, improve treatment safety, and reduce economic burden.

NCT ID: NCT06433362 Recruiting - Clinical trials for Peripheral T Cell Lymphoma

CMOEP in the Treatment of Untreated Peripheral T-cell Lymphoma

Start date: June 1, 2024
Phase: Phase 2
Study type: Interventional

This is a prospective, single arm, multicenter study to evaluate the safety and efficacy of CMOEP in patients with untreated peripheral T-cell lymphoma.

NCT ID: NCT06422247 Recruiting - Clinical trials for Peripheral T-cell Lymphoma

Observational Study in Japanese Patients With Peripheral T-Cell Lymphoma Who Received Second-Line Therapy

Start date: June 14, 2024
Phase:
Study type: Observational

The purpose of this study is to describe the therapeutic practices and the prognosis of patients with relapsed or refractory peripheral T-cell lymphoma in Japan

NCT ID: NCT06421948 Recruiting - Clinical trials for Peripheral T-cell Lymphoma

Linperlisib Combined With Chidamide in Patients With PTCL

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

The goal of this clinical trial is to determine the maximum tolerated dose (MTD) of PI3Kδ inhibitor linperlisib when combined with fixed dose of HDAC inhibitor chidamide in participants with peripheral T-cell lymphoma (PTCL), and to compare the combination of linperlisib and chidamide to standard CHOP (cyclophosphamide, doxorubicin/epirubicin, vincristine, and prednisone) regimen chemotherapy in the frontline treatment of PTCL to see which therapy is better.

NCT ID: NCT06421805 Recruiting - Lymphoma Clinical Trials

Establishing Prospective Mediastinal Tumor Database of PUMCH

MTDPUMCH
Start date: January 1, 2012
Phase:
Study type: Observational [Patient Registry]

This study aims to prospectively document the population characteristics, imaging findings, pathological features, prognostic factors, etc., of patients with mediastinal tumors. Clinical information will be structured and processed, and it is recommended to establish a mediastinal tumors database at Peking Union Medical College Hospital. The goal is to provide support for the quality of diagnosis and treatment, clinical protocols, and medical decision-making related to mediastinal tumors.

NCT ID: NCT06415708 Recruiting - B Cell Lymphoma Clinical Trials

Obinutuzumab Combined With Bendamustine in the Treatment of Mature B-cell Lymphoma

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

This is a prospective, single-center, single-arm clinical study to evaluate the efficacy and safety of maintenance therapy with obinutuzumab for 2 years in patients ≥ 18 years of age with newly diagnosed mature B-cell lymphoma (including follicular lymphoma[FL], marginal zone cell lymphoma[MZL] , waldenström macroglobulinemia[WM], hairy-cell leukemia variant[HCL-v]) who achieved ≥ PR after 6 cycles of obinutuzumab in combination with bendamustine.

NCT ID: NCT06406556 Recruiting - Clinical trials for Extranodal NK/T-cell Lymphoma

Safety & Efficacy of Peg-ASP-based CCRT in Early Stage ENKTL

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

The purpose of this multi-center, single arm, phase Ⅱ clinical trail is to evaluate the efficacy and toxicity of concurrent chemoradiotherapy by using single-drug pegaspargase for patients with ENKTL in stage IE to IIE.

NCT ID: NCT06395870 Recruiting - Clinical trials for B-Cell Non-Hodgkin Lymphoma-Refractory

Targeting CD19/CD20 Dual-targeted Cell in Patients With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

Start date: May 9, 2024
Phase: Phase 1
Study type: Interventional

A phase I, open-label clinical study to evaluate the safety, tolerability, and efficacy of LUCAR-G39D, a dual-targeted cell preparation targeting CD19/CD20, in patients with relapsed/refractory B-cell non-Hodgkin lymphoma.

NCT ID: NCT06393738 Recruiting - Clinical trials for Relapsed/Refractory (R/R) Mature B Cell Non Hodgkin Lymphoma (NHL)

A Study of ARV-393 in Relapsed/Refractory Non-Hodgkin Lymphoma.

Start date: April 30, 2024
Phase: Phase 1
Study type: Interventional

This clinical trial is studying the safety and potential anti-tumor activity of an investigational drug called ARV-393 in patients diagnosed with advanced Relapsed/Refractory non-Hodgkin's lymphoma to determine if ARV-393 may be a possible treatment option. ARV-393 is thought to work by breaking down a protein present in many types of non-Hodgkins lymphomas, which may prevent, slow or stop tumor growth. This is the first time ARV-393 will be used by people. The investigational drug will be given as an oral tablet.

NCT ID: NCT06393361 Recruiting - Clinical trials for PD-1 Inhibitor Failed Patients With Classical Hodgkin Lymphoma

Chidamide+Decitabine Plus Anti-PD-1 Antibody in PD-1 Inhibitor Failed Patients With Classical Hodgkin Lymphoma.

Start date: June 1, 2024
Phase: Phase 2
Study type: Interventional

The issue of therapy after PD-1 inhibitor failure is unresolved in classic Hodgkin lymphoma. Preliminary clinical observations have shown that patients might benefit from Chidamide+Decitabine plus anti-PD-1 antibody. This open-label, randomized, phase 2 study aims to evaluate the efficacy of Chidamide+Decitabine plus anti-PD-1 and the standard of care, which includes anti-PD-1 antibody, in patients with classical Hodgkin lymphoma who have experienced failure with PD-1 inhibitor. The primary objective of the study is to evaluate the 12-month progression-free survival rates.