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Terminated Phase 1 Interventional

Study to Assess Adverse Events and Change in Disease Activity of Intravenous (IV) Lemzoparlimab With or Without Oral/IV Dexamethasone and in Combination With Oral/IV/Subcutaneous Anti-Myeloma Regimens in Adult Participants With Multiple Myeloma

ClinicalTrials.gov ID: NCT04895410

Public ClinicalTrials.gov record NCT04895410. 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 May 14, 2026, 7:18 PM 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 1b, Dose Escalation and Expansion Study of Lemzoparlimab With or Without Dexamethasone and in Combination With Anti-Myeloma Regimens for the Treatment of Patients With Relapsed/Refractory Multiple Myeloma

Study identification

NCT ID
NCT04895410
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
8 participants

Conditions and interventions

Interventions

  • Carfilzomib Drug
  • Daratumumab Biological
  • Dexamethasone Drug
  • Lemzoparlimab Biological
  • Pomalidomide Drug

Drug · 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
Jan 16, 2022
Primary completion
Jun 23, 2022
Completion
Jun 23, 2022
Last update posted
Mar 5, 2023

2022

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Sylvester Comprehensive Cancer Center /ID# 228817 Miami Florida 33136-1002
Moffitt Cancer Center /ID# 229939 Tampa Florida 33612-9416
Norton Cancer Institute - St Matthews /ID# 229319 Louisville Kentucky 40207
Tulane Cancer Center Clinic /ID# 229832 New Orleans Louisiana 70112
University of Michigan Comprehensive Cancer Center Michigan Medicine /ID# 229309 Ann Arbor Michigan 48109
Henry Ford Health System /ID# 230341 Detroit Michigan 48202
Rutgers Cancer Institute of New Jersey /ID# 230174 New Brunswick New Jersey 08901
Columbia University Medical Center /ID# 229971 New York New York 10032-3729
Duke University Hospital /ID# 229564 Durham North Carolina 27710
Wake Forest Baptist Health /ID# 229996 Winston-Salem North Carolina 27157-0001
Perelman Center for Advanced Medicine - /ID# 228693 Philadelphia Pennsylvania 19104-5127
University of Virginia /ID# 229396 Charlottesville Virginia 22908

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04895410, 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 Mar 5, 2023 · Synced May 14, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04895410 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →