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RECRUITING Phase 3

A Study Comparing Talquetamab Plus Pomalidomide, Talquetamab Plus Teclistamab, and Elotuzumab, Pomalidomide, and Dexamethasone or Pomalidomide, Bortezomib, and Dexamethasone in Participants With Relapsed or Refractory Myeloma Who Have Received an Anti-CD38 Antibody and Lenalidomide

NCT06208150 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the effectiveness of either talquetamab plus pomalidomide (Tal-P) or talquetamab plus teclistamab (Tal-Tec) with elotuzumab, pomalidomide, and dexamethasone (EPd) or pomalidomide, bortezomib, and dexamethasone (PVd).

Conditions Studied

Interventions

  • DRUG Teclistamab
  • DRUG Dexamethasone
  • DRUG Pomalidomide
  • DRUG Talquetamab
  • DRUG Elotuzumab

Study Locations (20)

Maryland

  • Luminis Health Center for Cancer and Blood Disorders — Annapolis
  • University of Maryland School of Medicine — Baltimore
  • The Sidney Kimmel Comprehensive Cancer Center at John Hopkins — Baltimore

Michigan

  • University of Michigan — Ann Arbor
  • Henry Ford Cancer Institute — Detroit
  • Henry Ford Health Providence Southfield Hospital — Southfield

California

  • UCSF Fresno — Clovis
  • UCLA — Santa Monica

Florida

  • Memorial Healthcare System — Hollywood
  • Moffitt Cancer Center — Tampa

Georgia

  • Winship Cancer Institute Emory University — Atlanta
  • City of Hope Cancer Center — Newnan

Connecticut

  • Yale University School Of Medicine — New Haven

Delaware

  • Medical Oncology Hematology Consultants, PA — Newark

Idaho

  • Kootenai Health — Coeur d'Alene

Trial Details

FieldValue
Enrollment Target 795 participants
Start Date 2024-01-22
Est. Completion 2028-03-31
Phase Phase 3

Sponsor

Janssen Research & Development

442 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06208150

The ClinicalTrials.gov registry entry for NCT06208150 describes a study currently listed as recruiting. It is categorized as Phase 3, 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 795 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen Research & Development, which has 442 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 5 interventions — of which Teclistamab 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: NCT06208150 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Maryland, Michigan, California. 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 NCT06208150 about?

NCT06208150 is a clinical study titled "A Study Comparing Talquetamab Plus Pomalidomide, Talquetamab Plus Teclistamab, and Elotuzumab, Pomalidomide, and Dexamethasone or Pomalidomide, Bortezomib, and Dexamethasone in Participants With Relapsed or Refractory Myeloma Who Have Received an Anti-CD38 Antibody and Lenalidomide". The purpose of this study is to compare the effectiveness of either talquetamab plus pomalidomide (Tal-P) or talquetamab plus teclistamab (Tal-Tec) with elotuzumab, pomalidomide, and dexamethasone (EPd) or pomalidomide, bortezomib, and dexamethasone (PVd).

What is the current status of trial NCT06208150?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 795 participants. The study started on 2024-01-22. Estimated completion is 2028-03-31.

What conditions does trial NCT06208150 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 NCT06208150?

The interventions under investigation include: Teclistamab (DRUG), Dexamethasone (DRUG), Pomalidomide (DRUG), Talquetamab (DRUG), Elotuzumab (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06208150?

This trial is sponsored by Janssen Research & Development, which has 442 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06208150 being conducted?

This trial has 20 study locations across California, Connecticut, Delaware, Florida, Georgia. 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