CI

At a glance

ClinicalIndex Comparison Record
Phase 2Not Yet Recruiting· 50 target
Drug / intervention
SR-GDPdrug
Likely dose
SR-GDP 40mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06062641
NCT06062641Phase 2Not Yet Recruiting

Selinexor Combined With R-GDP Regimen for TP53-altered Relapsed/Refractory Diffuse Large B-cell Lymphoma: a Single Arm, Single Center, Phase II Study

Ruijin Hospital·interventional·Posted Oct 2, 2023·Updated Nov 7, 2023

In Brief

A Phase 2 clinical trial evaluating SR-GDP for Relapsed or Refractory B-cell Lymphoma. Not yet recruiting, targeting 50 participants across 1 site.

Detailed Summary

To evaluate the efficacy and safety of selinexor combined with R-GDP regimen in the treatment of patients with TP53-altered relapsed or refractory B-cell lymphoma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2Not Yet Recruiting
2024202520262027
First PostedOct 2, 2023
Enrollment StartOct 30, 2023
Primary CompletionApr 30, 2024
Study CompletionSep 30, 2027
TodayJul 1, 2026
Enrollment to primary: 6 monthsPosted 2.7 years ago

Interventions

SR-GDPdrug

Selinexor 40mg/d,po d1,8,15; rituximab 375mg/m2, iv d1; gemcitabine 1g/m2, iv d1,8; cisplatin 25mg/m2, iv d1-3; dexamethasone 40mg,po/iv d1-4 (If patient\>70y, the dosage should be changed to 20mg). Each cycle lasts for 21 days, with a maximum of 6 cycles of combination therapy. For patients who achieved PR or better response at the end of combination therapy, they will start receiving single-agent selinexor 40mg treatment (qw) in cycles of 28 days until disease progression (PD) or unacceptable toxicity occurs.