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NCT04762160 · ClinicalTrials.gov registry record · Phase 2

SYMPHONY-2, A Trial to Examine Combination of Tazemetostat With Rituximab in Subjects With Relapsed/Refractory Follicular Lymphoma

A Phase 2 study, sponsored by Epizyme.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT04762160: Clinical Trial Phase 2 study, sponsored by Epizyme.

NCT04762160 is a Phase 2 study that was terminated before completion, run by Epizyme. The registered enrollment target is 5 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04762160, a Phase 2 study, was terminated before completion, sponsored by Epizyme.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

This study evaluates the safety and efficacy of combining the EZH2 inhibitor tazemetostat with rituximab in R/R FL subjects previously treated with at least 2 standard prior systemic treatment regimens where at least 1 anti-CD20-based regimen was used.

Primary Outcome

ORR was defined as the percentage of participants with WT EZH2 status who achieved a complete response (CR) or partial response (PR) according to the 2014 Lugano Classification as assessed by investigator and blinded independent review committee (IRC). CR = complete metabolic response per positron emission tomography-computed tomography (PET-CT) based response or complete radiologic response per CT-based response. PR = partial metabolic response per PET-CT-based response or partial remission per

Interventions

  • DRUG Tazemetostat
  • COMBINATION_PRODUCT Rituximab

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2020-12-15
Est. Completion 2022-03-22
Phase Phase 2
Epizyme

16 total trials

Why NCT04762160 stopped before completion

NCT04762160 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Tazemetostat is the first listed.

NCT04762160 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04762160 about?

NCT04762160 is a clinical study titled "SYMPHONY-2, A Trial to Examine Combination of Tazemetostat With Rituximab in Subjects With Relapsed/Refractory Follicular Lymphoma". This study evaluates the safety and efficacy of combining the EZH2 inhibitor tazemetostat with rituximab in R/R FL subjects previously treated with at least 2 standard prior systemic treatment regimens where at least 1 anti-CD20-based regimen was used.

What is the current status of trial NCT04762160?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2020-12-15. Estimated completion is 2022-03-22.

What interventions are being tested in trial NCT04762160?

The interventions under investigation include: Tazemetostat (DRUG), Rituximab (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT04762160?

This trial is sponsored by Epizyme, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04762160's enrollment target sits among peer trials

5 2000th of 2000 the lowest 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 NCT04762160, the US trial registry maintained by the National Library of Medicine. NCT04762160 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.