RecruitingPhase 2NCT06489808

Linperlisib Combined With Immunochemotherapy in Relapsed/Refractory LBCL

An Open-label, Multicenter, Multi-cohort Clinical Study of Linperlisib Combined With Standard Immunochemotherapy in the Treatment of Relapsed/Refractory Large B-Cell Lymphoma Failing to First-line Therapy


Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Enrollment

89 participants

Start Date

May 28, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To evaluate the efficacy and safety of Linperlisib combined with standard immunochemotherapy in patients with R/R LBCL.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a drug called linperlisib (a PI3K inhibitor that blocks a growth pathway in cancer cells) in combination with immunotherapy and chemotherapy for people with large B-cell lymphoma that has returned or stopped responding to first-line treatment. **You may be eligible if...** - You have confirmed large B-cell lymphoma (a type of blood cancer) that has relapsed or stopped responding to first-line therapy - Your first-line treatment included anti-CD20 antibody (like rituximab) and anthracycline chemotherapy - You are otherwise eligible for further treatment **You may NOT be eligible if...** - You have already received more than one prior line of therapy for relapsed/refractory disease - You have received prior treatment that included this type of drug (PI3K inhibitor) - You have active infections or significant organ dysfunction - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGLinperlisib

Linperlisib RP2D D1-14

DRUGRituximab

rituximab 375 mg/m2 D0

DRUGGemcitabine

gemcitabine per regimen dosage

DRUGOxaliplatin

Oxaliplatin 130 mg/m2 D1

DRUGIfosfamide

Ifosfamide 5g/m2 D2

DRUGCarboplatin

Carboplatin AUC=5mg/mL · min (maximum absolute dose/cycle = 800 mg)

DRUGEtoposide

Etoposide 100mg/m2 D1-3

DRUGDexamethasone

Dexamethasone 40mg D1-4

DRUGCisplatin

Cisplatin 100mg/m2 D1, continuous intravenous infusion

DRUGAra-C

Ara-C 2g/m2 q12h D2

DRUGVinorelbine

Vinorelbine 20mg/m2 D1

DRUGMitoxantrone hydrochloride liposome

Mitoxantrone hydrochloride liposome 18mg/m2 D1


Locations(1)

Institute of Hematology & Blood Disease Hospital

Tianjin, Tianjin Municipality, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06489808


Related Trials