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NCT04790903 · ClinicalTrials.gov registry record · Phase 1

A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax in Combination With Polatuzumab Vedotin Plus Rituximab (R) and Cyclophosphamide, Doxorubicin, Prednisone (CHP) in Participants With Untreated BCL-2 Immunohistochemistry (IHC)-Positive Diffuse Large B-Cell Lymphoma (DLBCL)

A Phase 1 study, sponsored by Hoffmann-La Roche.

Terminated
Registry status
Phase 1
Development phase
50
Enrollment target

NCT04790903 is a Phase 1 study that was terminated before completion, run by Hoffmann-La Roche. The registered enrollment target is 50 participants.

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The verdict

NCT04790903, a Phase 1 study, was terminated before completion, sponsored by Hoffmann-La Roche.

TERMINATED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

This Phase Ib, open-label, multicenter study evaluates the safety, efficacy, and pharmacokinetics of venetoclax in combination with Pola + R-CHP in previously untreated participants with BCL-2 IHC-positive DLBCL. Approximately 50 participants will be enrolled in this study in five consecutive cohorts each consisting of approximately 10 participants.

Interventions

  • DRUG Venetoclax
  • DRUG Cyclophosphamide
  • DRUG Doxorubicin
  • DRUG Rituximab
  • DRUG Polatuzumab Vedotin

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2021-07-02
Est. Completion 2024-05-21
Phase Phase 1

Sponsor

Hoffmann-La Roche

909 total trials

What the Registry Record Tells You About NCT04790903

The ClinicalTrials.gov registry entry for NCT04790903 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 909 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Venetoclax is the first listed.

NCT04790903 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04790903 about?

NCT04790903 is a clinical study titled "A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax in Combination With Polatuzumab Vedotin Plus Rituximab (R) and Cyclophosphamide, Doxorubicin, Prednisone (CHP) in Participants With Untreated BCL-2 Immunohistochemistry (IHC)-Positive Diffuse Large B-Cell Lymphoma (DLBCL)". This Phase Ib, open-label, multicenter study evaluates the safety, efficacy, and pharmacokinetics of venetoclax in combination with Pola + R-CHP in previously untreated participants with BCL-2 IHC-positive DLBCL. Approximately 50 participants will be enrolled in this study in five consecutive cohort...

What is the current status of trial NCT04790903?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2021-07-02. Estimated completion is 2024-05-21.

What interventions are being tested in trial NCT04790903?

The interventions under investigation include: Venetoclax (DRUG), Cyclophosphamide (DRUG), Doxorubicin (DRUG), Rituximab (DRUG), Polatuzumab Vedotin (DRUG).

Who is sponsoring clinical trial NCT04790903?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

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.