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NCT06176729

Pola-R2 in Newly Diagnosed Non-fit Elderly DLBCL Patients

Recruiting now Phase 2 Last updated 20 December 2023
What this trial tests

Phase 2 trial testing Polatuzumab Vedotin, Rituximab, Lenalidomide in Diffuse Large B Cell Lymphoma in 30 participants. Currently enrolling.

Timeline
24 October 2023
Primary endpoint
24 October 2025
24 October 2027

Quick facts

Lead sponsorYan Zhang, MD
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date24 October 2023
Primary completion24 October 2025
Estimated completion24 October 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Yan Zhang, MD — full company profile →

Who can join

70 and older, any sex, with Diffuse Large B Cell Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a prospective, single-arm, phase II study, and the purpose of this study is to evaluate the efficacy and safety of Pola-R2 regimen in newly diagnosed elderly diffuse large B cell lymphoma classified into un-fit or frail group by comprehensive geriatric assessment(CGA).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Strategic Combinations of Antibody-Drug Conjugates from 2023 to 2025: From Dual Therapies to Innovative ADC-Based Regimens.
    Jang H, Chang JE. · · 2025 · PMID 41471096 · DOI 10.3390/pharmaceutics17121581
  2. Targeted Therapies and Immunotherapies for Diffuse Large B-Cell Lymphoma.
    Chaudhari J, Shah NN. · · 2025 · PMID 40805213 · DOI 10.3390/cancers17152517

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Other recruiting trials for Diffuse Large B Cell Lymphoma

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06176729.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing