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ACTIVE NOT RECRUITING Phase 3

An Open-Label Study Comparing Glofitamab and Polatuzumab Vedotin + Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone Versus Pola-R-CHP in Previously Untreated Patients With Large B-Cell Lymphoma

NCT06047080 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the efficacy and safety of glofitamab in combination with polatuzumab vedotin plus rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) vs Pola-R-CHP in participants with previously untreated CD20-positive large B-cell lymphoma (LBCL).

Conditions Studied

Interventions

  • DRUG Cyclophosphamide
  • DRUG Glofitamab
  • DRUG Doxorubicin
  • DRUG Rituximab
  • DRUG Polatuzumab vedotin

Study Locations (20)

California

  • Kaiser Permanente - Anaheim (E. La Palma) — Anaheim
  • University of California, San Francisco-Fresno — Clovis
  • City of Hope National Medical Center — Duarte
  • City of Hope - Lennar Foundation Cancer Center — Irvine
  • Valkyrie Clinical Trials — Los Angeles
  • UCLA Jonsson Comprehensive Cancer Center — Los Angeles
  • Kaiser Permanente - Roseville — Roseville
  • Kaiser Permanente - Santa Clara — Santa Clara
  • Stanford Univ School of Med — Stanford
  • Kaiser Permanente Medical Ctr — Vallejo

Colorado

  • University of Colorado Cancer Center — Aurora
  • Rocky Mountain Cancer Center - Denver — Littleton

Florida

  • Miami Cancer Institute of Baptist Health, Inc. — Miami
  • Memorial Cancer Institute at Memorial West — Pembroke Pines

Illinois

  • Robert H. Lurie Comprehensive Cancer Center of Northwestern University — Chicago
  • Illinois Cancer Care — Peoria

Alaska

  • Alaska Oncology & Hematology, LLC — Anchorage

Connecticut

  • Yale University School Of Medicine — New Haven

District of Columbia

  • Medstar Franklin Square Medical Center — Washington D.C.

Hawaii

  • Hawaii Cancer Care — Honolulu

Trial Details

FieldValue
Enrollment Target 1,130 participants
Start Date 2023-09-18
Est. Completion 2030-10-30
Phase Phase 3

Sponsor

Hoffmann-La Roche

758 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06047080

The ClinicalTrials.gov registry entry for NCT06047080 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hoffmann-La Roche, which has 758 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Large B-Cell Lymphoma appearing as the primary indexed condition, and to 5 interventions — of which Cyclophosphamide is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06047080 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Colorado, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06047080 about?

NCT06047080 is a clinical study titled "An Open-Label Study Comparing Glofitamab and Polatuzumab Vedotin + Rituximab, Cyclophosphamide, Doxorubicin, and Prednisone Versus Pola-R-CHP in Previously Untreated Patients With Large B-Cell Lymphoma". The purpose of this study is to compare the efficacy and safety of glofitamab in combination with polatuzumab vedotin plus rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) vs Pola-R-CHP in participants with previously untreated CD20-positive large B-cell lymphoma (LBCL).

What is the current status of trial NCT06047080?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 1,130 participants. The study started on 2023-09-18. Estimated completion is 2030-10-30.

What conditions does trial NCT06047080 study?

This clinical trial studies the following conditions: Large B-Cell Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06047080?

The interventions under investigation include: Cyclophosphamide (DRUG), Glofitamab (DRUG), Doxorubicin (DRUG), Rituximab (DRUG), Polatuzumab vedotin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06047080?

This trial is sponsored by Hoffmann-La Roche, which has 758 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06047080 being conducted?

This trial has 20 study locations across Alaska, California, Colorado, Connecticut, District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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