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NCT06251648 | NOT YET RECRUITING | Cancer


Acute Lymphoblastic Leukaemia Related to Lenalidomide (LenALL)
Sponsor:

University Hospital, Caen

Information provided by (Responsible Party):

Pierre-Marie MORICE, PharmD, PhD

Brief Summary:

Although lenalidomide (LEN) have proved effective in treating many cancers, few patients receiving LEN may experience rare but life-threatening adverse events such as Acute Lymphoblastic Leukaemia (ALL). Today, data about ALL are scarce. The objective was to investigate reports of ALL adverse events related to LEN in patients with cancer using the World Health Organization (WHO) pharmacovigilance database.

Condition or disease

Cancer

Intervention/treatment

Lenalidomide

Study Type : OBSERVATIONAL
Estimated Enrollment : 300 participants
Official Title : Acute Lymphoblastic Leukaemia Related to Lenalidomide in Patients With Cancer: an Observational and Retrospective Study Using the WHO's Pharmacovigilance Database
Actual Study Start Date : 2024-02-01
Estimated Primary Completion Date : 2024-02-15
Estimated Study Completion Date : 2024-03-31

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Case reported in the World Health Organization (WHO, also called VigiBase) at the time of the extraction
  • * Patients treated with at least LEN (L04AX04)
Exclusion Criteria
  • -Chronology not compatible between LEN and ALL

Acute Lymphoblastic Leukaemia Related to Lenalidomide (LenALL)

Location Details

NCT06251648


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Locations


Not yet recruiting

France,

chu's CAE N

Caen, France, 14033

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