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NCT01742793 · ClinicalTrials.gov registry record · Phase 1

An Open Label, International, Multi-centre, Phase I/IIa Study of Lenalidomide (Revlimid) and Romidepsin (Istodax) for Relapsed /Refractory Hodgkin Lymphoma, Mature T-cell Lymphoma and Multiple Myeloma. (RId Study)

A Phase 1 study, sponsored by Yale University.

Terminated
Registry status
Phase 1
Development phase
12
Enrollment target

NCT01742793: Clinical Trial Phase 1 study, sponsored by Yale University.

NCT01742793 is a Phase 1 study that was terminated before completion, run by Yale University. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01742793, a Phase 1 study, was terminated before completion, sponsored by Yale University.

TERMINATED
Registry status
Phase 1
Development phase
12 participants
Enrollment target

Study Summary

The study hypothesis is that lenalidomide and romidepsin (and dexamethasone for patients with myeloma) will have an acceptable toxicity profile and that in combination will have sufficient activity in the target population (including those previously refractory to HDACi monotherapy) to warrant further investigation.

Primary Outcome

Overall response rate is a combination of partial response and complete response according to specific response criteria that will be used throughout the study.

Interventions

  • DRUG lenalidomide (Revlimid) and romidepsin (Istodax)

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2012-10
Est. Completion 2016-08
Phase Phase 1
Yale University

1,492 total trials

Why NCT01742793 stopped before completion

NCT01742793 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 1 intervention - of which lenalidomide (Revlimid) and romidepsin (Istodax) is the first listed.

NCT01742793 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01742793 about?

NCT01742793 is a clinical study titled "An Open Label, International, Multi-centre, Phase I/IIa Study of Lenalidomide (Revlimid) and Romidepsin (Istodax) for Relapsed /Refractory Hodgkin Lymphoma, Mature T-cell Lymphoma and Multiple Myeloma. (RId Study)". The study hypothesis is that lenalidomide and romidepsin (and dexamethasone for patients with myeloma) will have an acceptable toxicity profile and that in combination will have sufficient activity in the target population (including those previously refractory to HDACi monotherapy) to warrant furth...

What is the current status of trial NCT01742793?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2012-10. Estimated completion is 2016-08.

What interventions are being tested in trial NCT01742793?

The interventions under investigation include: lenalidomide (Revlimid) and romidepsin (Istodax) (DRUG).

Who is sponsoring clinical trial NCT01742793?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01742793's enrollment target sits among peer trials

12 1852nd of 2000 higher than 90 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT01742793, the US trial registry maintained by the National Library of Medicine. NCT01742793 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.