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NCT03711578 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety Study of Tenalisib (RP6530), a Novel PI3K δ/γ Dual Inhibitor in Patients With Relapsed/Refractory Indolent Non-Hodgkin's Lymphoma (iNHL)

A Phase 2 study, sponsored by Rhizen Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT03711578: Completed Phase 2 study, sponsored by Rhizen Pharmaceuticals.

NCT03711578 is a Phase 2 study that has completed, run by Rhizen Pharmaceuticals. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03711578, a Phase 2 study, has completed, sponsored by Rhizen Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

To assess the anti-tumor activity and safety of Tenalisib in patients with relapsed/refractory indolent Non-Hodgkin's Lymphoma (iNHL),

Primary Outcome

ORR is defined as sum of CR and PR rates and will be assessed according to the Lugano Classification for initial evaluation, staging, and response assessment of Non-Hodgkin lymphoma. (Cheson-2014)

Interventions

  • DRUG Tenalisib,

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-11-25
Est. Completion 2020-10-16
Phase Phase 2
Rhizen Pharmaceuticals

7 total trials

What the finished NCT03711578 record still lists

NCT03711578 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

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

NCT03711578 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03711578 about?

NCT03711578 is a clinical study titled "Efficacy and Safety Study of Tenalisib (RP6530), a Novel PI3K δ/γ Dual Inhibitor in Patients With Relapsed/Refractory Indolent Non-Hodgkin's Lymphoma (iNHL)". To assess the anti-tumor activity and safety of Tenalisib in patients with relapsed/refractory indolent Non-Hodgkin's Lymphoma (iNHL),

What is the current status of trial NCT03711578?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2018-11-25. Estimated completion is 2020-10-16.

What interventions are being tested in trial NCT03711578?

The interventions under investigation include: Tenalisib, (DRUG).

Who is sponsoring clinical trial NCT03711578?

This trial is sponsored by Rhizen Pharmaceuticals, which has 7 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03711578's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 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 NCT03711578, the US trial registry maintained by the National Library of Medicine. NCT03711578 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.