Study identifier: NCT07061145 Synced from ClinicalTrials.gov · August 05, 2026
● Study status: Recruiting

A Potential Relationship Between Treatment With Tyrosine Kinase Inhibitors and Erectile Dysfunction in Male Patients With Chronic Myeloid Leukemia

Condition: Chronic Myelocytic Leukemia · Erectile Dysfunctions · CVD - Cardiovascular Disease  ·  Sponsor: Azienda USL Reggio Emilia - IRCCS

PhaseN/A
Planned participants350
Who can joinMale, 18 Years to 75 Years
Healthy volunteersNo

About this study

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by the presence of the Philadelphia chromosome, resulting in the constitutive activation of the BCR-ABL1 tyrosine kinase. The advent of tyrosine kinase inhibitors (TKIs) has revolutionized the management of CML, trasforming it from a fatal disease to a chronic condition with excellent long-term outcomes for the majority of patients. The introduction of tyrosine kinase inhibitor (TKI) based treatment for CML has revolutionized the management of this previously fatal disease, achieving sustained disease-control in more than 90% of patients. However, as patients with CML are often required to undergo lifelong TKI therapy to maintain disease control, concerns regarding the long-term safety and tolerability of these agents have emerged. The efficacy of second and third-generation TKIs exceeds the efficacy of imatinib, owing to their potent impact on wild-type BCR-ABL1 and various BCR-ABL1 mutants, along with additional drug targets. Furthermore, TKIs exhibit activity on non-kinase targets (es. oxidoreductase NQO2 for nilotinib and imatinib). The prolonged treatment duration and expanded TKIs repertoire have led the emergence of various unexpected non-hematologic adverse events (AE), notably vascular adverse events (VAEs). Recent evidence indicates a relatively high incidence of severe arterial changes in TKI-treated patients, with VAEs frequency correlating with TKI dosage and treatment duration. How…

This description comes directly from the study's public registry record.

Talk to the study team

Isabella Capodanno, MD  ·  0522295511  ·  isabella.capodanno@ausl.re.it

Maria Pina Faruolo  ·  0522295511  ·  mariapina.faruolo@ausl.re.it

Always discuss trial participation with your own doctor first.

Locations (1)

Azienda USL IRCCS di Reggio EmiliaReggio Emilia, RE, ItalyRecruiting

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