- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00907517
Study of SCH 900776 (MK-8776) With and Without Cytarabine in Participants With Acute Leukemias (P05247)
26. července 2018 aktualizováno: Merck Sharp & Dohme LLC
A Phase 1 Dose-Escalation Study of SCH 900776 in Combination With Cytarabine in Subjects With Acute Leukemias (Protocol No. P05247)
This study of SCH 900776 (MK-8776) will evaluate its safety and tolerability when given in combination with cytarabine to participants with acute leukemias.
Participants in the Dose-Escalation Part will be enrolled in cohorts that will receive sequentially higher doses of MK-8776 in combination with standard doses of cytarabine.
Only one combination treatment cycle of approximately 4 to 6 weeks is anticipated, but participants may receive additional cycles if clinically indicated after discussion between the Investigator and the Sponsor.
The recommended combination doses for a Phase 2 trial (RP2D) will be determined based on safety and biological activity.
Up to 10 to 15 additional participants will be studied at the combination RP2D.
Přehled studie
Postavení
Ukončeno
Podmínky
Intervence / Léčba
Typ studie
Intervenční
Zápis (Aktuální)
24
Fáze
- Fáze 1
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
18 let a starší (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Popis
Inclusion Criteria:
Must have a histologically or cytologically confirmed diagnosis of relapsed and/or refractory acute leukemia, including:
- acute myelogenous leukemia (AML), including AML arising from myelodysplasia (MDS) or myeloproliferative disorder (MPD);
- acute lymphocytic leukemia, including Philadelphia chromosome-positive (Ph+) ALL (Dose-Escalation Part only);
- chronic myelogenous leukemia (CML) in accelerated phase (AP) or blast crisis (BC) of either myeloid or lymphoid origin (Dose-Escalation Part only);
- treatment-related high-grade MDS (i.e. refractory anemia with excess blasts in transformation [RAEBT]);
- MPD in transformation [eg, CMMoL-T (5%-19% blasts)].
- Must have recurred or progressed following standard therapy or failed standard therapy, or have disease for which no standard therapy currently exists.
- Must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
- Females of childbearing potential must have a negative pregnancy test within 5 days prior to first dose of cytarabine.
- Females of childbearing potential and males whose sexual partner is of childbearing potential must agree to abstain from sexual intercourse or to use an acceptable method of contraception during the study and for 90 days following the last dose of study treatment.
- Must have adequate renal function as evidenced by a serum creatinine level <=1.5 x upper limit of normal (ULN) or a calculated creatinine clearance >=60 mL/min.
- Participants, except ones with known Gilbert's Syndrome, must have adequate hepatic function as evidenced by a serum bilirubin level <=1.5 mg/dL AND serum levels of aspartate and alanine aminotransferase (AST/ALT) <=5 x the ULN for the reference laboratory.
- Must have adequate cardiac function with a left ventricular ejection fraction (LVEF) of >=45% (echocardiogram or multiple-gated acquisition [MUGA] scan).
- Must be recovered from the effects of any prior surgery, radiotherapy, or systemic antineoplastic therapy.
- Participants who are refractory to or relapsed after prior allogeneic or autologous stem cell transplant are eligible.
Exclusion Criteria:
- Must not have known hypersensitivity to MK-8776 or cytarabine or to any of their excipients or have received therapy with another Checkpoint kinase 1 (CHK1) inhibitor.
- Must not have persistent, unresolved Common Terminology Criteria for Adverse Events version 3.0 (CTCAE v 3.0) ≥ Grade 2 drug-related toxicity (except alopecia, erectile impotence, hot flashes, decreased libido, hematologic toxicity) associated with previous treatment.
- Must not have known human immunodeficiency virus (HIV), hepatitis B or hepatitis C, or have a known history of liver cirrhosis or active alcohol abuse.
- Must not be New York Heart Association (NYHA) Class III (has marked limitation in activity due to symptoms, even during less than ordinary activity [e.g. walking short distances >20-100 m]; is comfortable only at rest) or Class IV (has severe limitations; experiences symptoms even while at rest; mostly bed bound).
- Must not have undergone major surgery within 3 weeks prior to first study drug administration after enrollment.
- Must not have known active central nervous system (CNS) or leptomeningeal leukemia.
- Must not have received radiation therapy within 2 weeks prior to first study treatment administration after enrollment or radiation therapy to >25% of bone marrow.
- Must not have received more than 4 prior induction regimens.
- Must not have a peripheral blast count ≥50,000/mm^3.
- Must not have active, uncontrolled graft versus host disease (GVHD) post-allogeneic stem cell transplant.
- Must not have had any of the following within 6 months prior to first study treatment administration after enrollment: myocardial infarction, severe/unstable angina pectoris, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, or seizure disorder.
- Must not have a known bleeding diathesis, e.g. hemophilia, or disseminated intravascular coagulation.
- Must not have an active, uncontrolled infection.
- Must not have a history of cytarabine-related neurotoxicity.
- Must not have a baseline corrected QT (QTc) interval >470 msec (i.e. CTCAE v 3.0 Grade ≥2).
- Must not currently be a smoker and/or must not be likely to smoke during the study.
- Females must not be breast-feeding, pregnant, or intend to become pregnant.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: MK-8776 10 mg/m^2 + Cytarabine 2 g/m^2
Participants received MK-8776 10 mg/m^2 intravenously (IV) on Days 2 and 3 and again on Days 11 and 12 PLUS cytarabine 2 g/m^2 IV via 72-hour continuous intravenous infusion (CIV) on Days 1 through 3 and repeated on Days 10 through 12 of a treatment cycle.
The duration of one treatment cycle was to be approximately 4 to 6 weeks (until hospital discharge).
|
IV infuze
Ostatní jména:
IV infusion
Ostatní jména:
|
|
Experimentální: MK-8776 20 mg/m^2 + Cytarabine 2 g/m^2
Participants received MK-8776 20 mg/m^2 IV on Days 2 and 3 and again on Days 11 and 12 PLUS cytarabine 2 g/m^2 IV via 72-hour CIV on Days 1 through 3 and repeated on Days 10 through 12 of a treatment cycle.
The duration of one treatment cycle was to be approximately 4 to 6 weeks (until hospital discharge).
|
IV infuze
Ostatní jména:
IV infusion
Ostatní jména:
|
|
Experimentální: MK-8776 40 mg/m^2 + Cytarabine 2 g/m^2
Participants received MK-8776 40 mg/m^2 IV on Days 2 and 3 and again on Days 11 and 12 PLUS cytarabine 2 g/m^2 IV via 72-hour CIV on Days 1 through 3 and repeated on Days 10 through 12 of a treatment cycle.
The duration of one treatment cycle was to be approximately 4 to 6 weeks (until hospital discharge).
|
IV infuze
Ostatní jména:
IV infusion
Ostatní jména:
|
|
Experimentální: MK-8776 56 mg/m^2 + Cytarabine 2 g/m^2
Participants received MK-8776 56 mg/m^2 IV on Days 2 and 3 and again on Days 11 and 12 PLUS cytarabine 2 g/m^2 IV via 72-hour CIV on Days 1 through 3 and repeated on Days 10 through 12 of a treatment cycle.
The duration of one treatment cycle was to be approximately 4 to 6 weeks (until hospital discharge).
|
IV infuze
Ostatní jména:
IV infusion
Ostatní jména:
|
|
Experimentální: MK-8776 140 mg + Cytarabine 2 g/m^2
Participants received MK-8776 140 mg flat dose IV on Days 2 and 3 and again on Days 11 and 12 PLUS cytarabine 2 g/m^2 IV via 72-hour CIV on Days 1 through 3 and repeated on Days 10 through 12 of a treatment cycle.
The duration of one treatment cycle was to be approximately 4 to 6 weeks (until hospital discharge).
|
IV infuze
Ostatní jména:
IV infusion
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Number of Participants Who Experienced a Dose-limiting Toxicity (DLT)
Časové okno: Throughout Cycle 1 (Up to 6 weeks)
|
Toxicity was assessed according to the Common Terminology Criteria for Adverse Events version 3.0 (CTCAE v 3.0).
DLTs in Cycle 1 consisted of any of the following: 1) Selected Grade 4 drug-related nonhematologic toxicities, 2) Selected Grade 3 drug-related nonhematologic toxicities that do not resolve to ≤ Grade 2 within 48 hours: Neurotoxicity of any duration, Nephrotoxicity of any duration, QT interval corrected by Fridericia (QTcF) prolongation of any duration, 3) Inability to administer Day 10 cytarabine therapy due to ongoing, uncontrolled serious or life-threatening toxicity.
The number of participants who experienced a DLT during Cycle 1 is summarized.
|
Throughout Cycle 1 (Up to 6 weeks)
|
|
Number of Participants Who Experienced an Adverse Event (AE)
Časové okno: Up to 45 days after last dose of study treatment (Up to 180 days)
|
An AE was defined as any untoward medical occurrence in a participant administered a study treatment and which does not necessarily have to have a causal relationship with this treatment.
An AE can be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a study treatment, whether or not considered related to this study treatment.
The number of participants who experienced an AE is summarized.
|
Up to 45 days after last dose of study treatment (Up to 180 days)
|
|
Number of Participants Who Discontinued Study Treatment Due to an AE
Časové okno: Up to 135 days
|
An AE was defined as any untoward medical occurrence in a participant administered a study treatment and which does not necessarily have to have a causal relationship with this treatment.
An AE can be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a study treatment, whether or not considered related to this study treatment.
The number of participants who discontinued study treatment due to an AE is summarized.
|
Up to 135 days
|
Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia (Aktuální)
29. července 2009
Primární dokončení (Aktuální)
13. června 2011
Dokončení studie (Aktuální)
13. června 2011
Termíny zápisu do studia
První předloženo
21. května 2009
První předloženo, které splnilo kritéria kontroly kvality
21. května 2009
První zveřejněno (Odhad)
22. května 2009
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
27. srpna 2018
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
26. července 2018
Naposledy ověřeno
1. července 2018
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Onemocnění imunitního systému
- Novotvary podle histologického typu
- Novotvary
- Lymfoproliferativní poruchy
- Lymfatická onemocnění
- Imunoproliferativní poruchy
- Nemoci kostní dřeně
- Hematologická onemocnění
- Myeloproliferativní poruchy
- Leukémie
- Leukémie, myeloidní
- Leukémie, myeloidní, akutní
- Lymfoblastická leukémie-lymfom prekurzorových buněk
- Leukémie, lymfoidní
- Leukémie, myeloidní, chronická, BCR-ABL pozitivní
- Leukémie, myeloidní, zrychlená fáze
- Fyziologické účinky léků
- Molekulární mechanismy farmakologického působení
- Antiinfekční látky
- Antivirová činidla
- Antimetabolity, Antineoplastika
- Antimetabolity
- Antineoplastická činidla
- Imunosupresivní látky
- Imunologické faktory
- Cytarabin
Další identifikační čísla studie
- P05247
- MK-8776-001 (Jiný identifikátor: Merck Protocol Number)
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Ano
Popis plánu IPD
https://www.merck.com/clinical-trials/pdf/ProcedureAccessClinicalTrialData.pdf
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 .