- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT06523556
Axatilimab s nebo bez azacitidinu k léčbě pacientů s pokročilou fází myeloproliferativních novotvarů, myeloproliferativními novotvary/myelodysplastickým syndromem překrývající se nebo vysoce rizikovou chronickou myelomonocytární leukémií
Studie fáze 1b/2 axatilimab (SNDX-6352) + azacitidin (AZA) v pokročilé fázi MPN, překrytí MPN/MDS nebo vysoce rizikové CMML
This phase Ib/II trial tests the best dose of axatilimab and effectiveness of axatilimab with or without azacitidine for the treatment of patients with advanced phase myeloproliferative neoplasms (MPN), myeloproliferative neoplasm/myelodysplastic syndrome (MPN/MDS) overlap or high risk chronic myelomonocytic leukemia (CMML). Axatilimab is an antibody that is cloned from a single white blood cell that is known to be able to recognize cancer cells and block a protein on the surface of the white blood cells that may be involved in cancer cell growth. By blocking the proteins, this may slow or halt the growth of the cancer. Azacitidine is in a class of medications called antimetabolites. It works by stopping or slowing the growth of cancer cells. Giving axatilimab with or without azacitidine may be safe and effective in treating patients with advanced phase MPN, MPN/MDS overlap or high risk CMML.
Přehled studie
Postavení
Podmínky
- Chronická myelomonocytární leukémie
- Refrakterní chronická myelomonocytární leukémie
- Myelodysplastický/myeloproliferativní novotvar
- Recidivující myelodysplastický/myeloproliferativní novotvar
- Atypická chronická myeloidní leukémie
- Recidivující myeloproliferativní novotvar
- Refrakterní myelodysplastický/myeloproliferativní novotvar
- Refrakterní myeloproliferativní novotvar
Detailní popis
PRIMARY OBJECTIVES:
I. To determine the recommended phase 2 dose (RP2D) of axatilimab in relapsed or refractory patients with advanced phase MPN, MPN/MDS overlap or high-risk CMML.
II. To evaluate the overall response rate of axatilimab + azacitidine (AZA) in newly diagnosed patients with advanced phase MPN, MPN/MDS overlap or high-risk CMML using Savona response criteria.
SECONDARY OBJECTIVES:
I. Determine the safety and tolerability of axatilimab + azacitidine combination therapy in those with newly diagnosed advanced phase MPN, MPN/MDS overlap or high-risk CMML.
II. Determine the quality of life in patients receiving axatilimab + AZA using a Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF).
III. Determine the effect of axatilimab + azacitidine on symptom relief which will be measured by transfusion burden (platelet and/or packed red blood cell), time in hospital, and immune related side effects specifically reactivation of tuberculosis (TB), infusion-related reactions, hepatotoxicity, pneumonia, pyrexia, sepsis, shortness of breath (SBO), hemoptysis, periorbital edema, fatigue, and pancreatitis.
EXPLORATORY OBJECTIVES:
I. To assess the pharmacokinetics of axatilimab in combination with AZA. II. To describe the prevalence and trajectories of patients' physical activity during treatment.
III. To perform detailed correlative studies related to genetic, biochemical, and immunologic changes that occur with axatilimab in combination with AZA.
OUTLINE: This is a phase I, dose-escalation study of axatilimab followed by a phase II study.
PHASE I: Patients receive axatilimab intravenously (IV) over 30 minutes on days 1 and 15 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At time of phase Ib completion, patients with clinical improvement may transition to phase II. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study.
PHASE II: Patients receive axatilimab IV over 30 minutes on days 1 and 15 and azacitidine IV over 10-40 minutes or subcutaneously (SC) on days 1-7 of each cycle. Cycles repeat every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients who achieve partial response (PR) or better may continue for up to 24 total cycles. Patients who achieve less than PR receive 2 additional cycles and, if PR or better is achieved, may complete up to 24 total cycles. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study.
After completion of study treatment, patients are followed up at 30 days and then every 6 months for up to 24 months after last dose of study medication.
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 2
- Fáze 1
Kontakty a umístění
Studijní kontakt
- Jméno: The Ohio State University Comprehensive Cancer Center
- Telefonní číslo: 800-293-5066
- E-mail: OSUCCCClinicaltrials@osumc.edu
Studijní místa
-
-
Ohio
-
Columbus, Ohio, Spojené státy, 43210
- Nábor
- Ohio State University Comprehensive Cancer Center
-
Kontakt:
- Uma M. Borate
- Telefonní číslo: 614-293-3316
- E-mail: Uma.Borate@osumc.edu
-
Vrchní vyšetřovatel:
- Uma M. Borate
-
-
Oregon
-
Portland, Oregon, Spojené státy, 97239
- Nábor
- Oregon Health & Science University
-
Kontakt:
- Knight Cancer Institute Clinical Trials
- Telefonní číslo: 503-494-1080
- E-mail: trials@ohsu.edu
-
Kontakt:
- Ted Braun, MD, PhD
- Telefonní číslo: 503-494-1080
- E-mail: braunt@ohsu.edu
-
Vrchní vyšetřovatel:
- Ted Braun, MD, PhD
-
-
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
-
Signed informed consent must be obtained prior to participation in the study
-
Age ≥ 18 years at the date of signing the informed consent form (ICF)
-
Morphologically confirmed diagnosis of the following based on 2016 World Health Organization (WHO) classification (Arber et al 2016): Phase 1b, patients with relapsed or refractory of any of the following; phase 2, patients with newly diagnosed of any of the following:
- Chronic myelomonocytic leukemia (CMML), classified as intermediate-2, OR high-risk per the CMML Specific Prognostic Scoring System (CPSS) Molecular Model
- Atypical chronic myelocytic leukemia (aCML)
- MDS/MPN unclassified (MDS/MPN-U)
- Myeloproliferative neoplasm accelerated phase (MPN-AP)
- MPN-AP requires a previous diagnosis of polycythemia vera (PV), essential thrombocythemia (ET), or primary myelofibrosis (PMF) with intermediate-2 or high risk disease according to International Prostate Symptom Score (IPSS) as well as progression on or failure to respond to at least one line of therapy.
- Myelodysplastic syndrome/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T) or MDS/MPN with SF3B1 mutation and thrombocytosis (MDS/MPN-SF3B1-T).
- Not suitable for immediate myeloablative/intensive chemotherapy based on investigator assessment of age, comorbidities, local guidelines, institutional practice (any or all of these)
-
PHASE Ib (RELAPSE [R]/ REFRACTORY [R]): Relapse/refractory patients who have received at least two cycles of disease directed therapy (prior therapies can include hypomethylating agents [HMAs], HMA combination therapies, and other disease directed therapies)
-
PHASE II (NEWLY DIAGNOSED PHASE): Newly diagnosed patients without prior treatment, including intensive induction chemotherapy. However, previous treatment with hydroxyurea, ruxolitinib, and/or up to 2 cycles of HMAs (decitabine, azacitidine, oral decitabine [INQOVI]) is permitted
-
Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2
-
Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 × upper limit of normal (ULN)
-
Total bilirubin ≤ 1.5 × ULN (except in the setting of isolated Gilbert syndrome)
-
Estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73m^2 (estimation based on Modification of Diet in Renal Disease [MDRD] formula, by local laboratory)
-
Patient is able to communicate with the investigator and has the ability to comply with the requirements of the study procedures
-
Women of childbearing potential and men, if not surgically sterilized, should use adequate contraception from 14 days prior to study entry and until 90 days after the last follow-up visit. Adequate contraception is defined as using hormonal contraceptives or an intrauterine device combined with at least 1 of the following forms of contraception: a diaphragm or cervical cap, or a condom
Exclusion Criteria:
-
Diagnosis of acute myeloid leukemia (AML) including acute promyelocytic leukemia and extra-medullary AML based on WHO 2016 classification (Arber et al 2016)
-
Patients who are candidates for myeloablative or intensive chemotherapy treatment or who do not provide consent for this treatment
-
History of organ transplant or allogenic hematopoietic stem cell transplant
-
Participants with prior malignancy, except:
- Participants with history of adequately treated malignancy for which no anticancer systemic therapy (namely chemotherapy, radiotherapy or surgery) is ongoing or required during the course of the study.
- Participants who are receiving adjuvant therapy such as hormone therapy are eligible. However, participants who developed therapy related neoplasms are not eligible
-
Previous known allergy/sensitivity to components of axatilimab
-
History of acute or chronic pancreatitis
-
History of myositis
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Crossover Assignment
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: Phase I (Axatilimab)
Patients receive axatilimab IV over 30 minutes on days 1 and 15 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. At time of phase Ib completion, patients with clinical improvement may transition to phase II. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study. |
Undergo blood sample collection
Ostatní jména:
Given IV
Ostatní jména:
Undergo bone marrow biopsy and aspiration |
|
Experimentální: Phase II (Axatilimab and azacitidine)
Patients receive axatilimab IV over 30 minutes on days 1 and 15 and azacitidine IV over 10-40 minutes or SC on days 1-7 of each cycle. Cycles repeat every 28 days for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients who achieve PR or better may continue for up to 24 total cycles. Patients who achieve less than PR receive 2 additional cycles and, if PR or better is achieved, may complete up to 24 total cycles. Patients undergo bone marrow biopsy and aspiration and blood sample collection throughout the study. |
Undergo blood sample collection
Ostatní jména:
Given IV or SC
Ostatní jména:
Ancillary study Given IV
Ostatní jména:
Undergo bone marrow biopsy and aspiration |
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of dose limiting toxicities
Časové okno: Up to 42 days after the first dose of study medication
|
Includes hematologic and non-hematologic toxicities |
Up to 42 days after the first dose of study medication
|
|
Overall response rate
Časové okno: Up to 5 years
|
The number of participants whose best response (according to the 2006 International Working Group response criteria) over the efficacy analysis period is a complete response or partial response will be tallied to estimate the overall response rate and provide a 95% exact confidence interval, according to the Clopper-Pearson method. |
Up to 5 years
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Incidence of adverse events
Časové okno: Up to 30 days after end of treatment
|
Adverse events will be tabulated by toxicity grade and relationship with study medication and assessed by Common Terminology Criteria for Adverse Events version 5.0. |
Up to 30 days after end of treatment
|
|
Quality of life measured by Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF)
Časové okno: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine (AZA) and will be determined using a Modified Myeloproliferative Neoplasm Symptom Assessment Form (MPNSAF) score. The MPNSAF score has a range from 0 to 100 with 100 representing the highest level of symptom severity. Descriptive statistics, means and standard deviations or medians and ranges will be applied to summarize the MPNSAF score. |
Up to 5 years
|
|
Number of platelet transfusions
Časové okno: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
|
Number of packed red blood cell transfusions
Časové okno: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
|
Time in hospital
Časové okno: Up to 5 years
|
Will be assessed in patients receiving axatilimab + azacitidine and will be determined by descriptive statistics. |
Up to 5 years
|
Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: Uma M Borate, MD, Ohio State University Comprehensive Cancer Center
Publikace a užitečné odkazy
Užitečné odkazy
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Patologické procesy
- Novotvary
- Chronické onemocnění
- Atributy nemoci
- Novotvary podle histologického typu
- Hematologická onemocnění
- Leukémie, myeloidní
- Nemoci kostní dřeně
- Leukémie
- Patologické stavy, příznaky a symptomy
- Hemická a lymfatická onemocnění
- Leukémie, myelomonocytární, chronická
- Myeloproliferativní poruchy
- Myelodysplastická-myeloproliferativní onemocnění
- Leukémie, myeloidní, chronická, atypická, BCR-ABL negativní
- Organické chemikálie
- Heterocyklické sloučeniny, 1 kruh
- Heterocyklické sloučeniny
- Vyšetřovací techniky
- Klinické laboratorní techniky
- Diagnostické techniky a postupy
- Diagnóza
- Chirurgické postupy, operativní
- Cytologické techniky
- Nukleové kyseliny, nukleotidy a nukleosidy
- Cytodiagnosis
- Cytidin
- Pyrimidinové nukleosidy
- Pyrimidiny
- Diagnostické techniky, chirurgické
- Aza sloučeniny
- Nukleosidy
- Ribonukleosidy
- Azacitidin
- Biopsie
- Manipulace se vzorkem
- axatilimab
Další identifikační čísla studie
- OSU-23442
- NCI-2024-05515 (Identifikátor registru: CTRP (Clinical Trial Reporting Program))
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .