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NCT04594798 · ClinicalTrials.gov registry record · Phase 2

A Study of Polatuzumab Vedotin, Rituximab and Dose Attenuated CHP in Older Patients With DLBCL

A Phase 2 study of Lymphoma, B-Cell and DLBCL, sponsored by University of Rochester.

Active
Registry status
Phase 2
Development phase
39
Enrollment target
1
Study location

NCT04594798 is a Phase 2 study of Lymphoma, B-Cell and DLBCL that is active but no longer recruiting, run by University of Rochester. The registered enrollment target is 39 participants, below the 200-participant average among 31 other Lymphoma, B-Cell trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04594798, a Phase 2 study of Lymphoma, B-Cell and DLBCL, is active but no longer recruiting, sponsored by University of Rochester.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
39 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to test the effectiveness and safety of polatuzumab vedotin in combination with R-miniCHP in patients 75 years and older with DLBCL.

Conditions Studied

Interventions

  • DRUG Cyclophosphamide
  • DRUG Doxorubicin
  • DRUG Rituximab
  • DRUG Prednisone
  • DRUG Polatuzumab vedotin

Study Locations (1)

New York

  • University of Rochester - Rochester

Trial Details

FieldValue
Enrollment Target 39 participants
Start Date 2021-09-20
Est. Completion 2026-07-31
Phase Phase 2

Sponsor

University of Rochester

636 total trials

What the Registry Record Tells You About NCT04594798

The ClinicalTrials.gov registry entry for NCT04594798 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 39 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 200-participant average among 31 other Lymphoma, B-Cell trials with a reported enrollment target (80% lower). The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Lymphoma, B-Cell appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT04594798 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT04594798 about?

NCT04594798 is a clinical study titled "A Study of Polatuzumab Vedotin, Rituximab and Dose Attenuated CHP in Older Patients With DLBCL". The purpose of this study is to test the effectiveness and safety of polatuzumab vedotin in combination with R-miniCHP in patients 75 years and older with DLBCL.

What is the current status of trial NCT04594798?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 39 participants. The study started on 2021-09-20. Estimated completion is 2026-07-31.

What conditions does trial NCT04594798 study?

This clinical trial studies the following conditions: Lymphoma, B-Cell, DLBCL.

What interventions are being tested in trial NCT04594798?

The interventions under investigation include: Cyclophosphamide (DRUG), Doxorubicin (DRUG), Rituximab (DRUG), Prednisone (DRUG), Polatuzumab vedotin (DRUG).

Who is sponsoring clinical trial NCT04594798?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04594798 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.