- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT02454478
Study of Lenvatinib in Combination With Everolimus in Participants With Unresectable Advanced or Metastatic Renal Cell Carcinoma (RCC)
7. března 2019 aktualizováno: Eisai Co., Ltd.
Phase 1 Study of Lenvatinib in Combination With Everolimus in Subjects With Unresectable Advanced or Metastatic RCC
Phase 1 study to investigate the tolerability and safety of lenvatinib in combination with Everolimus in participants with unresectable advanced or metastatic RCC.
Přehled studie
Postavení
Dokončeno
Podmínky
Intervence / Léčba
Typ studie
Intervenční
Zápis (Aktuální)
7
Fáze
- Fáze 1
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní místa
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-
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Chiba, Japonsko
- Eisai Trial Site #1
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Tokyo, Japonsko
- Eisai Trial Site #2
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Tokyo, Japonsko
- Eisai Trial Site #1
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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
20 let a starší (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Popis
Inclusion Criteria:
- Voluntary agreement to provide written informed consent of this study.
- Willing and able to comply with all aspects of the protocol after being fully informed of the content.
- Males or females aged greater than or equal to 20 years at the time of informed consent.
- Histological or cytological confirmation of RCC.
- Participants must have confirmed diagnosis of unresectable advanced and/or metastatic RCC.
- Disease progression following vascular endothelial growth factor (VEGF) targeted therapy.
- Eastern Cooperative Oncology Group Performance Status (ECOG-PS) of 0 to 1.
- Adequately controlled blood pressure with or without the use of antihypertensive agents.
- Participants with adequate function of major organs.
- Adequate blood coagulation function, defined as international normalized ratio (INR) less than or equal to 1.5.
- Survival expectation of 3 months or longer after study enrollment.
- Participants with adequate washout period from the end of prior treatment to the start of study drug administration.
- Females of childbearing potential must not have had unprotected sexual intercourse within 28 days before participant registration and must agree to use a highly effective method of contraception throughout the entire study period and for 30 days after final administration of investigational drug. If currently abstinent, the participant must agree to use a double-barrier method as described above if she becomes sexually active during this study period or for 30 days after investigational drug discontinuation. Females who are using hormonal contraceptives must have been on a stable dose of the same hormonal contraceptive product for at least 4 weeks before administration and must continue to use the same contraceptive during this study and for 30 days after investigational drug discontinuation.
- Male participants and their female partners must meet the criteria above.
Exclusion Criteria:
- Participants with central nervous system (CNS) metastases are not eligible, unless they have completed local therapy and have discontinued the use of corticosteroids for this indication for at least 4 weeks before starting treatment in this study. Any signs (example, radiologic) or symptoms of brain metastases must be stable for at least 4 weeks before starting study treatment.
- Prior exposure to lenvatinib.
- Participants who have not recovered from toxicities to less than or equal to Grade 1 as a result of prior anticancer therapy, except alopecia.
- Major surgery within 3 weeks prior to the first dose of lenvatinib.
- Participants with a urine protein greater than or equal to 1 gram per 24 hours (g/24 hours).
- Uncontrollable diabetes as defined by fasting glucose greater than 1.5* upper limit of normal (ULN).
- Fasting total cholesterol greater than 7.75 millimole per liter (mmol/L) (greater than 300 milligram per decilitre [mg/dL]).
- Fasting triglycerides greater than 2.5 * ULN.
- Any condition that might affect the absorption of lenvatinib and/or everolimus.
- Significant cardiovascular impairment.
- Bleeding or thrombotic disorders or use of anticoagulants requiring therapeutic INR monitoring.
- Active hemoptysis.
- Active infections that require systemic treatment.
- Human immunodeficiency virus (HIV) positive.
- Hepatitis B virus (HBV).
- A history of interstitial pneumonia with clinical manifestation or as confirmed by means of diagnostic imaging.
- Medical need for the continued use of potent or moderate inhibitors of cytochrome P450 3A (CYP3A) or P-gp, or potent or moderate inducer of CYP3A.
- Known intolerance to lenvatinib (or any of the excipients) or known hypersensitivity to everolimus (or any of the excipients) or rapmycins (sirolimus, temsirolimus and so on).
- Alcohol or drug dependency or abuse, inability to comply with every aspects of the study protocol, or any physical or mental conditions that in the opinion of the investigators would preclude the participant's participation in the study.
- Females who are pregnant or breastfeeding (not eligible even she discontinues breastfeeding).
- Any medical or other condition which, in the opinion of the investigator, would preclude participation in a clinical trial.
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: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
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Experimentální: Lenvatinib plus Everolimus
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Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Number of Participants Who Experienced Any Dose Limiting Toxicity (DLT)
Časové okno: From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
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DLT was defined as toxicity related to the combination therapy and was graded according to Common Terminology Criteria for Adverse Events version 4.03 (CTCAE v4.03).
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From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
|
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Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Časové okno: Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)
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Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Cmax: Maximum Observed Plasma Concentration for Levatinib and Everolimus
Časové okno: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Css,Max: Maximum Observed Plasma Concentration at Steady State for Levatinib and Everolimus
Časové okno: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Levatinib and Everolimus
Časové okno: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Tss,Max: Time to Reach the Maximum Plasma Concentration (Cmax) at Steady State for Levatinib and Everolimus
Časové okno: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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AUC 0-t: Area Under the Concentration-time Curve From Zero (Pre-dose) to Time of Last Quantifiable Concentration for Levatinib and Everolimus
Časové okno: Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
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Number of Participants With Best Overall Response (BOR)
Časové okno: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
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BOR included complete response (CR), partial response (PR), stable disease (SD), and PD (progressive disease).
BOR was assessed using Response Evaluation Criteria in Solid Tumor (RECIST) 1.1
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From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
|
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Objective Response Rate (ORR)
Časové okno: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
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ORR was defined as the percentage of participants who achieved BOR of CR or PR.
ORR was assessed using RECIST 1.1.
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From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
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Disease Control Rate (DCR)
Časové okno: From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
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DCR was defined as the percentage of participants who achieved BOR of CR, PR, or SD.
DCR was assessed based on RECIST 1.1.
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From first dose of study drug until PD, development of unacceptable toxicity, participant requests to discontinue, withdrawal of consent or study termination (up to approximately 23 months)
|
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Number of Participants With the Minimum Percent Change From Baseline in the Sum of Diameters of Target Lesions
Časové okno: Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)
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Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)
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Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
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)
1. července 2015
Primární dokončení (Aktuální)
29. května 2017
Dokončení studie (Aktuální)
29. května 2017
Termíny zápisu do studia
První předloženo
22. května 2015
První předloženo, které splnilo kritéria kontroly kvality
22. května 2015
První zveřejněno (Odhad)
27. května 2015
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
19. března 2019
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
7. března 2019
Naposledy ověřeno
1. září 2018
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Novotvary podle histologického typu
- Novotvary
- Urologické novotvary
- Urogenitální novotvary
- Novotvary podle místa
- Onemocnění ledvin
- Urologická onemocnění
- Adenokarcinom
- Novotvary, žlázové a epiteliální
- Novotvary ledvin
- Karcinom, renální buňka
- Karcinom
- Fyziologické účinky léků
- Molekulární mechanismy farmakologického působení
- Inhibitory enzymů
- Antineoplastická činidla
- Imunosupresivní látky
- Imunologické faktory
- Inhibitory proteinkinázy
- Everolimus
- Lenvatinib
Další identifikační čísla studie
- E7080-J081-112
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 .