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Completed Phase 2 Interventional Results available

Efficacy and Safety Study of bb2121 in Subjects With Relapsed and Refractory Multiple Myeloma

ClinicalTrials.gov ID: NCT03361748

Public ClinicalTrials.gov record NCT03361748. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 1:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter Study to Determine the Efficacy and Safety of bb2121 in Subjects With Relapsed and Refractory Multiple Myeloma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open label, single-arm, multicenter, Phase 2 study to evaluate the efficacy and safety of bb2121 in subjects with relapsed and refractory multiple myeloma. A leukapheresis procedure will be performed to manufacture bb2121 chimeric antigen receptor (CAR) modified T cells. Prior to bb2121 infusion subjects will receive lymphodepleting therapy with fludarabine and cyclophosphamide.

Study identification

NCT ID
NCT03361748
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
149 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 12, 2017
Primary completion
Dec 19, 2023
Completion
Dec 19, 2023
Last update posted
May 22, 2025

2017 – 2023

United States locations

U.S. sites
18
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Local Institution - 108 San Francisco California 94143
University of California - San Francisco San Francisco California 94143
Emory University Atlanta Georgia 30322
Local Institution - 103 Atlanta Georgia 30322
Local Institution - 107 Boston Massachusetts 02114
Dana Farber Cancer Institute Boston Massachusetts 02115
Massachusetts General Hospital Boston Massachusetts 02214
Local Institution - 106 Boston Massachusetts 02215
Local Institution - 105 Rochester Minnesota 55905
Mayo Clinic Rochester Minnesota 55905
Hackensack University Medical Center Hackensack New Jersey 07601
Local Institution - 102 Hackensack New Jersey 07601
Local Institution - 109 New York New York 10029
Mt. Sinai Medical Center New York New York 10029
Local Institution - 101 Nashville Tennessee 37203
Sarah Cannon Research Institute Nashville Tennessee 37203
Local Institution - 104 Dallas Texas 75390
University of Texas Southwestern Medical Center Dallas Texas 75390

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03361748, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 22, 2025 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03361748 live on ClinicalTrials.gov.

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