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

Not Applicable
Recruiting
Conditions
Multiple Myeloma
Registration Number
NCT05945524
Lead Sponsor
University Hospital, Toulouse
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • With multiple myeloma
  • Who receive Teclistamab
  • Consent form signed
Exclusion Criteria
  • Patient under legal protection

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Response to teclistamab at 12 weeksat day 1 Cycle 4 (each cycle is 28 days)

response according to International Myeloma Working Group criteria

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (18)

CHU d'Amiens

🇫🇷

Amiens, France

CHU de Caen

🇫🇷

Caen, France

Polyclinique du Parc Drevon

🇫🇷

Dijon, France

CH Annecy Genevois

🇫🇷

Epagny Metz- Tessy, France

CHU de Lille

🇫🇷

Lille, France

Centre Léon Bérard

🇫🇷

Lyon, France

CHU de Montpellier

🇫🇷

Montpellier, France

Hôpital Saint-Louis

🇫🇷

Paris, France

Hôpital Saint-Antoine

🇫🇷

Paris, France

Hôpital Necker

🇫🇷

Paris, France

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CHU d'Amiens
🇫🇷Amiens, France
Lydia MONTES, MD
Contact
0222455482
montes.lydia@chu-amiens.fr

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