- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT02115386
Trial to Evaluate the Improvement of Chronic Low-grade AEs in Patients With Ph+ CML With Optimal Response to Imatinib When Switched to Nilotinib (MACS1532)
Open-label Multicenter Trial to Evaluate the Improvement of Chronic Low-grade Adverse Events Experienced by Patients With Ph+ Chronic Myelogenous Leukemia in Chronic Phase (CML-CP) With Optimal Response to Imatinib When Switched From Imatinib to Nilotinib Treatment
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Faza 3
Kontakty i lokalizacje
Lokalizacje studiów
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Moscow, Federacja Rosyjska, 125167
- Novartis Investigative Site
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion criteria:
Male or female patients ≥ 18 years of age 2. ECOG ≤ 2 3. Diagnosis of CML-CP < 15% blasts in peripheral blood and bone marrow
- < 30% blasts plus promyelocytes in peripheral blood and bone marrow
- < 20% basophiles in the peripheral blood
- ≥ 100 x 109 /L platelets
- No evidence of extramedullary leukemic involvement, with the exception of hepatosplenomegaly. 4. Minimal treatment duration before inclusion is 6 months. 5. Optimal response to imatinib at the time of inclusion according to LeukemiaNet 2009 criteria defined as:
- Patients treated with imatinib for ≥6 and <12 months must be in MCR Patients treated with imatinib for ≥12 and <18 months must be in CCR
- Patients treated with imatinib for ≥18 months must be in MMR (MMR response defined either as 3 log reduction of bcr-abl/abl ratio or as 0,1% by IS). 6. Initial treatment with 400mg imatinib with current treatment with imatinib 400 or 300 mg QD 7. Imatinib dose interruptions are allowed prior to inclusion but should not exceed 28 consecutive days 8. Persistent Grade 1- 2 non-hematological adverse events for at least 2 months despite best supportive care. Toxicity was to be evaluated by treating physician using CTCAE criteria. 9. In case of several types of non-hematological AEs no one can exceed grade 2 and at least one should last at least 2 months. 10. Adequate end organ function defined by:
- Total bilirubin < 1.5 x ULN
- AST and ALT < 2.5 x ULN
- Creatinine < 1.5 x ULN
- Serum amylase and lipase ≤ 1.5x ULN
- Alkaline phosphatase ≤ 2.5 x ULN unless considered tumor related 11. Serum potassium, magnesium, phosphorus and calcium values within normal range or corrected to within normal limits with supplements prior to first dose of study medication. 12. Patients must have an imatinib washout period of at least 3 days and not to exceed 7 days prior to the first dose of nilotinib. 13. Ability to provide written informed consent prior to any study related screening procedures being done
Exclusion criteria:
- Patients who have experienced any Grade 3 or higher non-hematologic toxicity 30 days prior to screening
- Loss of response (hematologic, cytogenetic, molecular) any time prior to inclusion
- Prior accelerated phase or blast phase CML
- Previously documented T315I mutation
- Chromosomal abnormalities (trisomy 8) and/or clonal evolution other than Ph+.
- Previous treatment with imatinib >400 mg any time prior to inclusion.
- Previous treatment with any other tyrosine kinase inhibitors except for only imatinib
Impaired cardiac function including any of the following:
- LVEF < 45% as determined by echocardiogram reading or MUGA
- Complete left bundle branch block
- Long QT syndrome or a known family history of long QT syndrome
- History or presence of clinically significant ventricular or atrial tachyarrhythmias
- Clinically significant resting bradycardia (< 50 beats per minute)
- QTcF > 450 msec on baseline ECG. If QTcF > 450 and electrolytes are not within normal ranges, electrolytes were to be corrected and then the patient re-screened for QTcF
- Myocardial infarction within 1 year of starting study drug
Other clinically significant heart disease (e.g., unstable angina, congestive heart failure, or uncontrolled hypertension) 9. Patients receiving therapy with inhibitors of CYP3A4 or medications that prolong the QT interval and cannot be either discontinued or switched to a different medication prior to starting study drug. 10. Treatment with strong CYP3A4 inducers (e.g. phenytoin, carbamazepine, rifampin, rifabutin, rifapentin, phenobarbital, St. John's Wort), that cannot be discontinued or switched to a different medication prior to starting study drug. 11. Impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug. 12. History of acute pancreatitis within 1 year of study entry. 13. Known cytopathologically confirmed CNS infiltration (in absence of suspicion of CNS involvement, lumbar puncture not required). 14. Any other malignancy that is clinically significant or requires active intervention.
15. Severe or uncontrolled medical conditions (i.e., uncontrolled diabetes, active or uncontrolled infection). 16. Acute or chronic liver or severe renal disease considered unrelated to cancer.
17. History of significant congenital or acquired bleeding disorder unrelated to cancer.
18. Previous radiotherapy to ≥ 25% of the bone marrow. 19. Major surgery within 4 weeks prior to Day 1 of study or patients who have not recovered from prior surgery. 20. Treatment with other investigational agents within 30 days of Day 1. 21. History of non-compliance to medical regimens or inability to grant consent 22. Women who are pregnant, breast feeding, or of childbearing potential without a negative urinary test at baseline
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Nilotinib
Dosage was 300 mg BID daily taken orally without food.
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supplied in 150 mg capsules to be taken orally
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Number of Participants With Improvement of Grades of Persistent Non-hematological Adverse Event (AE) for Grade 1 and 2 at 6 Months
Ramy czasowe: at 6 month after switching from imatinib to nilotinib
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Improvement was defined as decreasing of grade of non-hematological toxicity from 2 to <2 or from 1 to <1.
In case of multiple low-grade non-hematological toxicities improvement was defined as an improvement of at least one non-hematological AE and no worsening of any other persistent non-hematological AEs.
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at 6 month after switching from imatinib to nilotinib
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Number of Participants With Improvement of Grades of Persistent Non-hematological Adverse Event (AE) for Grade 1 and 2 at 3 Months
Ramy czasowe: at 3 month after switching from imatinib to nilotinib
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Improvement was defined as decreasing of grade of non-hematological toxicity from 2 to <2 or from 1 to <1.
In case of multiple low-grade non-hematological toxicities improvement was defined as an improvement of at least one non-hematological AE and no worsening of any other persistent non-hematological AEs.
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at 3 month after switching from imatinib to nilotinib
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Number of Participants With Complete Cytogenetic Response (CCyR)
Ramy czasowe: at months 6,12 and 24 after switching from imatinib to nilotinib
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Cytogenetic response will be assessed as the percentage of Ph+ metaphases in the bone marrow and is defined as the following: Complete (CCyR) - 0% Ph+ metaphases.
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at months 6,12 and 24 after switching from imatinib to nilotinib
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Number of Participants With a Major Molecular Response
Ramy czasowe: Months 1, 3, 6, early termination
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MMR was defined as a ≥ 3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤ 0.1 % BCR-ABL/ABL % by international scale as measured by RQ-PCR, confirmed by duplicate analysis of the same sample.
Molecular response was described for all time points except screening where response was estimated.
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Months 1, 3, 6, early termination
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Time to and Duration of CCyR and MMR After Switch From Imatinib to Nilotinib at 24 Months
Ramy czasowe: at 24 Months
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to evaluate time to achievement and duration of CCyR and MMR after switching from imatinib to nilotinib
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at 24 Months
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Time to First Improvement of Persistant Chronic Low-grade Non-hematologic AEs at 24 Months After Switch From Imatinib to Nilotinib
Ramy czasowe: first improvement of AEs after switch to 24 Months
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Evaluate time to first improvement of low-grade non-hematologic adverse events, experienced by patients treated with imatinib and persistent despite of best supportive measures after switching to nilotinib therapy.
Optimal improvement is defined as AE grade decreasing to 0.
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first improvement of AEs after switch to 24 Months
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Lisiting by Participant of EORTC-QLQ-C30 for Quality of Life
Ramy czasowe: Screening, months 1, 3, 6, after switch to nilotinib
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EORTC-QLQ-C30 was administered to evaluate quality of life changes after switching to nilotinib.
Scores ranged from 1 (very poor) to 6 (excellent)
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Screening, months 1, 3, 6, after switch to nilotinib
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Współpracownicy i badacze
Sponsor
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- CAMN107ARU02
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Novartis is committed to sharing access to patient-level data and supporting clinical documents from eligible studies with qualified external researchers. Requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to protect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Philadelphia Positive (Ph+) Chronic Myeloid Leukemia
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Novartis PharmaceuticalsZakończonyPhiladelphia Positive (Ph+) przewlekła białaczka szpikowaStany Zjednoczone, Francja, Republika Korei, Tajlandia, Włochy, Holandia, Indyk, Węgry, Federacja Rosyjska, Hiszpania, Zjednoczone Królestwo, Japonia, Malezja
Badania kliniczne na Nilotinib
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Rina PlattnerNational Cancer Institute (NCI); NovartisRekrutacyjnyCzerniak przerzutowy | Mutacja genu BRAFStany Zjednoczone
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University Hospital, BordeauxZakończonyBiałaczka, szpikowa, przewlekła, BCR-ABL dodatniaFrancja
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European LeukemiaNetLudwig-Maximilians - University of Munich; Heidelberg UniversityAktywny, nie rekrutującyPrzewlekła białaczka szpikowaNiemcy, Holandia
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Novartis PharmaceuticalsNie dostępnyPrzewlekła białaczka szpikowa (CML)
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Georgetown UniversityNational Institutes of Health (NIH)ZakończonyDemencja z ciałami Lewy'egoStany Zjednoczone
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Massachusetts General HospitalZakończony
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Andrew J. Wagner, MD, PhDMassachusetts General Hospital; Novartis; Brigham and Women's HospitalZakończonyGuz olbrzymiokomórkowy pochewki ścięgna | Barwione kosmkowo-guzkowe zapalenie błony maziowej | Guz olbrzymiokomórkowy typu rozlanegoStany Zjednoczone
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Assiut UniversityJeszcze nie rekrutacjaPrzewlekła białaczka szpikowa
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Georgetown UniversityZakończonyChoroba Parkinsona | Choroba Parkinsona Z DemencjąStany Zjednoczone
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Novartis PharmaceuticalsZakończony