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Trial · NCT06176729

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

NCT06176729, Phase 2, Recruiting, Yan Zhang, MD

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Pola-R2 in Newly Diagnosed Non-fit Elderly DLBCL Patients. Trials, record NCT06176729. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06176729

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Pola-R2 in Newly Diagnosed Non-fit Elderly DLBCL Patients
NCT number
NCT06176729
Status
Recruiting
Phases
Phase 2
Enrollment
30 participants, estimated
Lead sponsor
Yan Zhang, MD
Conditions
Diffuse Large B Cell Lymphoma
Interventions
Polatuzumab Vedotin, Rituximab, Lenalidomide
First posted
2023-12-20
Last updated
2023-12-20

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primarycomplete remission rateevaluated every 3 months,up to 24 monthsproportion of patients achieving complete remission
Secondaryoverall remission rateevaluated every 3 months,up to 24 monthsproportion of patients achieving at least partial remission
Secondary2 year progression-free survival rate2 years after last patient includedtime from treatment to the time of disease progression or death of any reason
Secondary2 year overall survival rate2 years after last patient includedtime from treatment to the time of death of any reason
Secondaryany adverse event occurred during this study2 years after last patient includedsafety

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06176729

GET https://conductscience.org/api/trials/v1/NCT06176729/registered