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COMPLETED

A Study of Real-life Current Standards of Care in Patients With Relapsed and/or Refractory Multiple Myeloma Who Received at Least 3 Prior Lines of Therapy Including Proteasome Inhibitor (PI), Immunomodulatory Drug (IMID), and Cluster of Differentiation 38 (CD38) Monoclonal Antibody Treatment

NCT04035226 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to assess the safety and clinical response including overall response rate (ORR) of real-life standard-of-care (SOC) treatments under routine clinical practice, over a 24-month period, in patients with relapsed/refractory multiple myeloma (RRMM).

Conditions Studied

Interventions

  • OTHER No intervention

Study Locations (20)

Other

  • Grand Hopital de Charleroi, site Notre Dame — Charleroi
  • Universitair Ziekenhuis Antwerpen — Edegem
  • UZ Leuven — Leuven
  • Ucl de Mont-Godinne — Yvoir
  • Centre Hospitalier du Mans — Le Mans
  • Centre Hospitalier Régional Universitaire de Lille, Hôpital Claude Huriez — Lille
  • CHU de Montpellier Hopital Saint Eloi — Montpellier
  • C.H.U. Hotel Dieu - France — Nantes

California

  • Oncology Institute of Hope and Innovation — Glendale
  • Marin Cancer Center — Greenbrae

Missouri

  • Central Care Cancer Center — Bolivar
  • Washington University School Of Medicine — St Louis

New York

  • The Cancer Institute at St. Francis Hospital — East Hills
  • North Shore Hematology Oncology Associates, P.C. — East Setauket

Florida

  • Asclepes Research — Weeki Wachee

Illinois

  • Oncology Hematology Assoc of Central Illinois, P.C. d.b.a. Illinois CancerCare, P.C. — Peoria

Michigan

  • Providence Cancer Center — Southfield

Nevada

  • Optum Care — Las Vegas

Trial Details

FieldValue
Enrollment Target 254 participants
Start Date 2019-08-02
Est. Completion 2022-10-27

Sponsor

Janssen-Cilag

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04035226

The ClinicalTrials.gov registry entry for NCT04035226 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 254 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen-Cilag, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention — of which No intervention is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04035226 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, California, Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04035226 about?

NCT04035226 is a clinical study titled "A Study of Real-life Current Standards of Care in Patients With Relapsed and/or Refractory Multiple Myeloma Who Received at Least 3 Prior Lines of Therapy Including Proteasome Inhibitor (PI), Immunomodulatory Drug (IMID), and Cluster of Differentiation 38 (CD38) Monoclonal Antibody Treatment". The purpose of this study is to assess the safety and clinical response including overall response rate (ORR) of real-life standard-of-care (SOC) treatments under routine clinical practice, over a 24-month period, in patients with relapsed/refractory multiple myeloma (RRMM).

What is the current status of trial NCT04035226?

This trial is currently completed. The enrollment target is 254 participants. The study started on 2019-08-02. Estimated completion is 2022-10-27.

What conditions does trial NCT04035226 study?

This clinical trial studies the following conditions: Multiple Myeloma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04035226?

The interventions under investigation include: No intervention (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04035226?

This trial is sponsored by Janssen-Cilag, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04035226 being conducted?

This trial has 20 study locations across California, Florida, Illinois, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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