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Retrospective Observational Research Study to Describe the Real World Use of Bosutinib in a Single Centre in Scotland
Retrospective Observational Research Study to Describe the Real World Use of Bosutinib in a Single Centre in Scotland

NCT05363488

CompletedN/A

Sponsor: Pfizer

Conditions: Myeloid Leukemia

Interventions: Bosutinib

Countries: United Kingdom

This study will describe the efficacy and safety of bosutinib in patients with chronic myeloid leukaemia (CML) used in a real world clinical practice setting.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

* Patients with a diagnosis of Ph+ CML aged ≥18 years at bosutinib initiation.
* Patients prescribed bosutinib (irrespective of the phase of their disease) EITHER in normal clinical practice since it received marketing authorisation (27 March 2013) by the EMA OR via the compassionate use programme prior to marketing authorization.
* Where required, evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study.

Exclusion Criteria:

* Patients prescribed bosutinib as part of an interventional clinical trial programme.
* Patients initiated on bosutinib less than 3 months prior to data collection taking place.
* Patients prescribed bosutinib as exclusively post-allograft therapy.
Locations (1)
  • Glasgow, United Kingdom