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NCT04142619 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating Safety and Efficacy of UCART Targeting CS1 in Patients With Relapsed/Refractory Multiple Myeloma (MELANI-01)

A Phase 1 study, sponsored by Cellectis S.A..

Terminated
Registry status
Phase 1
Development phase
11
Enrollment target

NCT04142619 is a Phase 1 study that was terminated before completion, run by Cellectis S.A.. The registered enrollment target is 11 participants.

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The verdict

NCT04142619, a Phase 1 study, was terminated before completion, sponsored by Cellectis S.A..

TERMINATED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

This is a Phase I, FIH, open-label, dose escalation study evaluating Safety and Efficacy of UCART targeting CS1 in patients with Relapsed or Refractory Multiple Myeloma (MM). The purpose of this study is to evaluate the safety and clinical activity of UCARTCS1A and to determine the Maximum Tolerated Dose (MTD).

Interventions

  • BIOLOGICAL UCARTCS1A

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2019-11-21
Est. Completion 2023-06-18
Phase Phase 1

Sponsor

Cellectis S.A.

5 total trials

What the Registry Record Tells You About NCT04142619

The ClinicalTrials.gov registry entry for NCT04142619 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cellectis S.A., which has 5 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which UCARTCS1A is the first listed.

NCT04142619 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04142619 about?

NCT04142619 is a clinical study titled "Study Evaluating Safety and Efficacy of UCART Targeting CS1 in Patients With Relapsed/Refractory Multiple Myeloma (MELANI-01)". This is a Phase I, FIH, open-label, dose escalation study evaluating Safety and Efficacy of UCART targeting CS1 in patients with Relapsed or Refractory Multiple Myeloma (MM). The purpose of this study is to evaluate the safety and clinical activity of UCARTCS1A and to determine the Maximum Tolerated...

What is the current status of trial NCT04142619?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2019-11-21. Estimated completion is 2023-06-18.

What interventions are being tested in trial NCT04142619?

The interventions under investigation include: UCARTCS1A (BIOLOGICAL).

Who is sponsoring clinical trial NCT04142619?

This trial is sponsored by Cellectis S.A., which has 5 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.