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NCT06594939 · ClinicalTrials.gov registry record · Phase 2

Mosunetuzumab and Polatuzumab Vedotin With Split-Dose CHP Chemotherapy for Elderly Patients With Diffuse Large B-Cell Lymphoma

A Phase 2 study, sponsored by Medical College of Wisconsin.

Not yet
Registry status
Phase 2
Development phase
31
Enrollment target

NCT06594939: Clinical Trial Phase 2 study, sponsored by Medical College of Wisconsin.

NCT06594939 is a Phase 2 study that has not yet begun recruiting, run by Medical College of Wisconsin. The registered enrollment target is 31 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06594939, a Phase 2 study, has not yet begun recruiting, sponsored by Medical College of Wisconsin.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
31 participants
Enrollment target

Study Summary

This single-arm, interventional phase 2 study is designed to evaluate whether the inclusion of mosunetuzumab subcutaneous and polatuzumab vedotin (Mosun-Pola) to a split-dose CHP chemotherapy backbone will improve outcomes for elderly patients with a new diagnosis of diffuse large B-cell lymphoma.

Primary Outcome

This is defined as the number of subjects achieving a complete response at the end of treatment using the Lugano criteria.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Mosunetuzumab
  • DRUG Doxorubicin
  • DRUG Prednisone
  • DRUG Polatuzumab Vedotin

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2026-06
Est. Completion 2029-12
Phase Phase 2
Medical College of Wisconsin

447 total trials

What is known before NCT06594939 opens enrollment

NCT06594939 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

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

NCT06594939 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06594939 about?

NCT06594939 is a clinical study titled "Mosunetuzumab and Polatuzumab Vedotin With Split-Dose CHP Chemotherapy for Elderly Patients With Diffuse Large B-Cell Lymphoma". This single-arm, interventional phase 2 study is designed to evaluate whether the inclusion of mosunetuzumab subcutaneous and polatuzumab vedotin (Mosun-Pola) to a split-dose CHP chemotherapy backbone will improve outcomes for elderly patients with a new diagnosis of diffuse large B-cell lymphoma.

What is the current status of trial NCT06594939?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2026-06. Estimated completion is 2029-12.

What interventions are being tested in trial NCT06594939?

The interventions under investigation include: Cyclophosphamide (DRUG), Mosunetuzumab (DRUG), Doxorubicin (DRUG), Prednisone (DRUG), Polatuzumab Vedotin (DRUG).

Who is sponsoring clinical trial NCT06594939?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06594939's enrollment target sits among peer trials

31 1578th of 2000 higher than 419 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06594939, the US trial registry maintained by the National Library of Medicine. NCT06594939 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.