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NCT03915184 · ClinicalTrials.gov registry record · Phase 1

Clinical Trial to Evaluate Zevor-cel (CT053) in Patients With Relapsed and/or Refractory Multiple Myeloma (LUMMICAR STUDY 2)

A Phase 1 study of Multiple Myeloma, sponsored by CARsgen Therapeutics Co..

Active
Registry status
Phase 1
Development phase
105
Enrollment target
13
Study locations

NCT03915184 is a Phase 1 study of Multiple Myeloma that is active but no longer recruiting, run by CARsgen Therapeutics Co.. The registered enrollment target is 105 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (81% lower). The trial reports 13 study locations across 11 states.

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The verdict

NCT03915184, a Phase 1 study of Multiple Myeloma, is active but no longer recruiting, sponsored by CARsgen Therapeutics Co..

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
105 participants
Enrollment target
13
Study locations

Study Summary

A phase 1b/2, open label, multi-center, Clinical Study of Chimeric Antigen Receptor T Cells targeting BCMA in patients with relapsed and or refractory multiple myeloma.

Conditions Studied

Interventions

  • BIOLOGICAL zevor-cel

Study Locations (13)

Texas

  • UT Southwestern Medical Center - Dallas
  • MD Anderson - Houston
  • Methodist Hosptial - Houston

Arizona

  • Mayo Clinic Hospital - Phoenix

California

  • UCSF - San Francisco

Colorado

  • Colorado Blood Cancer Institute - Denver

Florida

  • Moffitt Cancer Center - Tampa

Massachusetts

  • Dana Farber Cancer Center - Boston

Minnesota

  • Mayo - Rochester

Tennessee

  • TriStar CMC - Nashville

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2019-09-25
Est. Completion 2034-12-31
Phase Phase 1

Sponsor

CARsgen Therapeutics Co.

2 total trials

What the Registry Record Tells You About NCT03915184

The ClinicalTrials.gov registry entry for NCT03915184 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (81% lower). The listed sponsor is CARsgen Therapeutics Co., which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention - of which zevor-cel is the first listed.

NCT03915184 reports 13 study locations spanning 11 distinct geographic areas - top geographies include Texas, Arizona, California.

Frequently Asked Questions

What is clinical trial NCT03915184 about?

NCT03915184 is a clinical study titled "Clinical Trial to Evaluate Zevor-cel (CT053) in Patients With Relapsed and/or Refractory Multiple Myeloma (LUMMICAR STUDY 2)". A phase 1b/2, open label, multi-center, Clinical Study of Chimeric Antigen Receptor T Cells targeting BCMA in patients with relapsed and or refractory multiple myeloma.

What is the current status of trial NCT03915184?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 105 participants. The study started on 2019-09-25. Estimated completion is 2034-12-31.

What conditions does trial NCT03915184 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT03915184?

The interventions under investigation include: zevor-cel (BIOLOGICAL).

Who is sponsoring clinical trial NCT03915184?

This trial is sponsored by CARsgen Therapeutics Co., which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03915184 being conducted?

This trial has 13 study locations across Arizona, California, Colorado, Florida, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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