Glivec® (Imatinib Mesylate, STI571) in Monotherapy Versus Glivec®-Interferon Alpha in the Treatment of Chronic-Phase Chronic Myeloid Leukaemia
Launched by PETHEMA FOUNDATION · Oct 20, 2006
Trial Information
Current as of June 03, 2025
Completed
Keywords
ClinConnect Summary
Open, prospective, multicentre, phase IV, comparative and randomised study
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients with newly-diagnosed chronic-phase Ph-positive chronic myeloid leukaemia (maximum 3 months as of the diagnosis of the disease, with the date of the cytogenetic study regarded as such).
- • 2. Age between 18 and 72 years (both included).
- • 3. Performance status \< 2 on the ECOG scale (see Annex 3).
- • 4. Secure written or oral informed consent in the presence of a witness and consent for biological samples (annexes 5 and 6).
- Exclusion Criteria:
- • 1. Criteria of acceleration or blastic crisis (see Annex 7).
- • 2. When there is a compatible family donor in patients aged under 40 years or a non-relative donor in patients aged under 30 years (in whom allogenic transplant is still regarded as first-line treatment), the possibility of performing an allogenic transplant as first therapeutic option should be considered. In any case, as this aspect is still a matter of debate, it is left up to each group to take the relevant decision depending on the institution's policy.
- • 3. Administration of other treatments before inclusion in the protocol (a maximum of 3 months of monotherapy with hydroxyurea is permitted).
- • 4. Altered hepatic or renal function (SGOT, SGPT, total bilirubin and creatinine \> 1.5 times the upper limit of normality).
- • 5. Uncontrolled diseases, such as thyroidal dysfunction, diabetes mellitus, angina pectoralis, serious heart failure (functional class III/IV of the New York Heart Association classification), neuropsychiatric infection or disease (see annex 15).
- • 6. Positive serology for HIV.
- • 7. Record of cancer in the last 5 years (barring basal cell skin carcinoma and cervical carcinoma in situ).
- • 8. Pregnancy or breastfeeding
About Pethema Foundation
Pethema Foundation is a prominent clinical trial sponsor dedicated to advancing research in hematology and oncology. Focused on improving patient outcomes, the foundation collaborates with leading medical institutions and researchers to design and implement innovative clinical studies. By fostering partnerships and leveraging cutting-edge methodologies, Pethema Foundation aims to accelerate the development of novel therapeutic approaches and enhance the understanding of blood-related diseases. Their commitment to scientific excellence and patient-centered research positions them as a vital contributor to the field of medical science.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Valencia, , Spain
Madrid, , Spain
Barcelona, , Spain
Valencia, , Spain
Madrid, , Spain
Valencia, , Spain
Valencia, , Spain
Palma De Mallorca, , Spain
Salamanca, , Spain
Pamplona, Navarra, Spain
Lleida, , Spain
Sevilla, , Spain
Barcelona, , Spain
Jerez De La Frontera, , Spain
Murcia, , Spain
Palma De Mallorca, Mallorca, Spain
Barcelona, , Spain
Santander, , Spain
Tortosa, Tarragona, Spain
Barcelona, , Spain
Córdoba, , Spain
La Coruña, , Spain
Málaga, , Spain
Málaga, , Spain
Madrid, , Spain
Oviedo, Asturias, Spain
Tenerife, Islas Canarias, Spain
Madrid, , Spain
Oviedo, , Spain
Mataró, Barcelona, Spain
Sabadell, Barcelona, Spain
Terrassa, Barcelona, Spain
Alcorcón, Madrid, Spain
Pamplona, Navarra, Spain
Avila, , Spain
Barcelona, , Spain
Barcelona, , Spain
Cáceres, , Spain
Granada, , Spain
Huelva, , Spain
Jaen, , Spain
Madrid, , Spain
Madrid, , Spain
Madrid, , Spain
Madrid, , Spain
O'barco De Valdeorras, , Spain
Palencia, , Spain
Segovia, , Spain
Tarragona, , Spain
Vigo, , Spain
Vigo, , Spain
Zamora, , Spain
Patients applied
Trial Officials
Cervantes Francisco, Dr
Study Chair
Hospital Clinic of Barcelona
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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