Bone marrow sampling
OtherBone marrow sampling collected at 12 weeks after initiation treatment (day 1 cycle 4)
NCT Number: NCT05945524
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
CHU d'Amiens, Amiens, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Bone marrow sampling collected at 12 weeks after initiation treatment (day 1 cycle 4)
Time frame: at day 1 Cycle 4 (each cycle is 28 days)
response according to International Myeloma Working Group criteria
Contact information is provided by the study sponsor or research team.
University Hospital, Toulouse
Other
Acronym: ResisTec
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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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