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NCT04038359 · ClinicalTrials.gov registry record · Phase 2

A Phase 2 Study Comparing 2 Intermittent Dosing Schedules of Duvelisib in Participants With Indolent Non-Hodgkin Lymphoma

A Phase 2 study, sponsored by SecuraBio.

Completed
Registry status
Phase 2
Development phase
103
Enrollment target

NCT04038359: Completed Phase 2 study, sponsored by SecuraBio.

NCT04038359 is a Phase 2 study that has completed, run by SecuraBio. The registered enrollment target is 103 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04038359, a Phase 2 study, has completed, sponsored by SecuraBio.

COMPLETED
Registry status
Phase 2
Development phase
103 participants
Enrollment target

Study Summary

This study examined the effects of predefined 2-week duvelisib dose holidays on tumor responses and safety/tolerability.

Primary Outcome

ORR was defined as the percentage of participants achieving a complete response (CR) or partial response (PR) and assessed using the 2007 revised IWG criteria. The 2007 revised IWG criteria defined CR as the disappearance of all evidence of disease and PR as the regression of measurable disease and no new sites.

Interventions

  • DRUG Duvelisib

Trial Details

FieldValue
Enrollment Target 103 participants
Start Date 2019-09-24
Est. Completion 2023-07-24
Phase Phase 2
SecuraBio

15 total trials

What the finished NCT04038359 record still lists

NCT04038359 is an interventional study that assigns participants to a tested intervention. The registered 103 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% lower).

The record links to 0 conditions, and to 1 intervention - of which Duvelisib is the first listed.

NCT04038359 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04038359 about?

NCT04038359 is a clinical study titled "A Phase 2 Study Comparing 2 Intermittent Dosing Schedules of Duvelisib in Participants With Indolent Non-Hodgkin Lymphoma". This study examined the effects of predefined 2-week duvelisib dose holidays on tumor responses and safety/tolerability.

What is the current status of trial NCT04038359?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 103 participants. The study started on 2019-09-24. Estimated completion is 2023-07-24.

What interventions are being tested in trial NCT04038359?

The interventions under investigation include: Duvelisib (DRUG).

Who is sponsoring clinical trial NCT04038359?

This trial is sponsored by SecuraBio, which has 15 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04038359's enrollment target sits among peer trials

103 664th of 2000 higher than 1,333 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 NCT04038359, the US trial registry maintained by the National Library of Medicine. NCT04038359 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.