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ACTIVE NOT RECRUITING Phase 1

A Study Comparing Pre- and Post-Change Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma

NCT06425991 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the pharmacokinetics (processes by which drugs are absorbed, distributed in the body, and excreted) between teclistamab made from the current commercial manufacturing process (pre-change) and the new manufacturing process (post-change).

Interventions

  • DRUG Teclistamab

Study Locations (20)

Other

  • Flinders Medical Centre — Bedford Park
  • Box Hill Hospital — Box Hill
  • Royal Prince Alfred Hospital — Camperdown
  • Epworth Healthcare — Richmond
  • CHRU de Lille Hopital Claude Huriez — Lille
  • Hospices Civils de Lyon HCL — Lyon
  • CHU Nantes — Nantes
  • CHU de Bordeaux - Hospital Haut-Leveque — Pessac
  • Klinikum Chemnitz gGmbH — Chemnitz
  • Universitaetsklinikum Hamburg Eppendorf — Hamburg
  • Universitaetsklinikum Heidelberg — Heidelberg

Arizona

  • Banner MD Anderson Cancer Center — Gilbert

Colorado

  • Colorado Blood Cancer Institute — Denver

Florida

  • Cleveland Clinic Florida — Weston

Georgia

  • Augusta University- Georgia Cancer Center — Augusta

Indiana

  • St Francis Hospital & Health Centers Indiana Blood and Marrow Transplantation Franciscan Health — Indianapolis

Ohio

  • Cleveland Clinic — Cleveland

Texas

  • Baylor University Medical Center — Dallas

Trial Details

FieldValue
Enrollment Target 108 participants
Start Date 2024-06-07
Est. Completion 2027-03-03
Phase Phase 1

Sponsor

Janssen Research & Development

442 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06425991

The ClinicalTrials.gov registry entry for NCT06425991 describes a study currently listed as active not recruiting. It is categorized as Phase 1, 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 108 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 Relapsed or Refractory Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention — 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: NCT06425991 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, Arizona, Colorado. 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 NCT06425991 about?

NCT06425991 is a clinical study titled "A Study Comparing Pre- and Post-Change Teclistamab in Participants With Relapsed or Refractory Multiple Myeloma". The purpose of this study is to compare the pharmacokinetics (processes by which drugs are absorbed, distributed in the body, and excreted) between teclistamab made from the current commercial manufacturing process (pre-change) and the new manufacturing process (post-change).

What is the current status of trial NCT06425991?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 108 participants. The study started on 2024-06-07. Estimated completion is 2027-03-03.

What conditions does trial NCT06425991 study?

This clinical trial studies the following conditions: Relapsed or Refractory 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 NCT06425991?

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

Who is sponsoring clinical trial NCT06425991?

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 NCT06425991 being conducted?

This trial has 20 study locations across Arizona, Colorado, Florida, Georgia, Indiana. 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