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NCT Number: NCT05945524

Analysis of the Resistance and Sensitivity Mechanisms to Teclistamab by Focusing on Single Immune Cell Examination

The aim of this study is to discover the immune and oncogenomic features that distinguish patients who respond to teclistamab from patients who are primarily resistant. Moreover, phenotypic and genotypic characteristics that occur with secondary resistance to teclistamab will be analyzed.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU d'Amiens, Amiens, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • With multiple myeloma
  • Who receive Teclistamab
  • Consent form signed

Exclusion criteria

  • Patient under legal protection

Treatment and study plan

Bone marrow sampling

Other

Bone marrow sampling collected at 12 weeks after initiation treatment (day 1 cycle 4)

Primary outcomes

  1. Response to teclistamab at 12 weeks

    Time frame: at day 1 Cycle 4 (each cycle is 28 days)

    response according to International Myeloma Working Group criteria

Study contacts

Contact information is provided by the study sponsor or research team.

Hervé AVET LOISEAU, MD, PhD

CONTACT

[email protected]

+33 531 156 142 ext. 33

Sponsors and collaborators

Lead sponsor

University Hospital, Toulouse

Other

Registry information

Acronym: ResisTec

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jul 14, 2023
Registry last updated
Apr 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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