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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03502876
Other study ID # RESISTANCE A L'IBRUTINIB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 2, 2017
Est. completion date December 31, 2019

Study information

Verified date May 2020
Source French Innovative Leukemia Organisation
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Assessment of the mutational profile of the residual clone and the distribution of lymphocyte subpopulations at 3 years of treatment with ibrutinib

This project has an epidemiological part: to establish the percentage of patients, in a real-life situation, still undergoing treatment 3 years after its initiation, as well as a biological part: to determine the evolution of the clone and the prevalence of BTK mutations and PLCg2 in the absence of clinical or biological criteria for scalability.


Description:

Observationnal and biological study


Recruitment information / eligibility

Status Completed
Enrollment 198
Est. completion date December 31, 2019
Est. primary completion date December 31, 2018
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients included in the ATU (epidemiology)

- under treatment at 3 years of ibrutinib

- more than 18 years old

Exclusion Criteria:

- no ibrutinib treatment

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France FILO French Innovative Leukemia Organization Tours
France Project manager Tours

Sponsors (1)

Lead Sponsor Collaborator
French Innovative Leukemia Organisation

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ibrutinib resistance In the long term, this study will help to draft new recommendations from FILO-LLC concerning the detection of resistance and the management of patients. under treatment at 3 years of ibrutinib
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