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Study of Lenvatinib in Combination With Everolimus in Participants With Unresectable Advanced or Metastatic Renal Cell Carcinoma (RCC)

7 marzo 2019 aggiornato da: 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.

Panoramica dello studio

Stato

Completato

Tipo di studio

Interventistico

Iscrizione (Effettivo)

7

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Chiba, Giappone
        • Eisai Trial Site #1
      • Tokyo, Giappone
        • Eisai Trial Site #2
      • Tokyo, Giappone
        • Eisai Trial Site #1

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

20 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Voluntary agreement to provide written informed consent of this study.
  2. Willing and able to comply with all aspects of the protocol after being fully informed of the content.
  3. Males or females aged greater than or equal to 20 years at the time of informed consent.
  4. Histological or cytological confirmation of RCC.
  5. Participants must have confirmed diagnosis of unresectable advanced and/or metastatic RCC.
  6. Disease progression following vascular endothelial growth factor (VEGF) targeted therapy.
  7. Eastern Cooperative Oncology Group Performance Status (ECOG-PS) of 0 to 1.
  8. Adequately controlled blood pressure with or without the use of antihypertensive agents.
  9. Participants with adequate function of major organs.
  10. Adequate blood coagulation function, defined as international normalized ratio (INR) less than or equal to 1.5.
  11. Survival expectation of 3 months or longer after study enrollment.
  12. Participants with adequate washout period from the end of prior treatment to the start of study drug administration.
  13. 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.
  14. Male participants and their female partners must meet the criteria above.

Exclusion Criteria:

  1. 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.
  2. Prior exposure to lenvatinib.
  3. Participants who have not recovered from toxicities to less than or equal to Grade 1 as a result of prior anticancer therapy, except alopecia.
  4. Major surgery within 3 weeks prior to the first dose of lenvatinib.
  5. Participants with a urine protein greater than or equal to 1 gram per 24 hours (g/24 hours).
  6. Uncontrollable diabetes as defined by fasting glucose greater than 1.5* upper limit of normal (ULN).
  7. Fasting total cholesterol greater than 7.75 millimole per liter (mmol/L) (greater than 300 milligram per decilitre [mg/dL]).
  8. Fasting triglycerides greater than 2.5 * ULN.
  9. Any condition that might affect the absorption of lenvatinib and/or everolimus.
  10. Significant cardiovascular impairment.
  11. Bleeding or thrombotic disorders or use of anticoagulants requiring therapeutic INR monitoring.
  12. Active hemoptysis.
  13. Active infections that require systemic treatment.
  14. Human immunodeficiency virus (HIV) positive.
  15. Hepatitis B virus (HBV).
  16. A history of interstitial pneumonia with clinical manifestation or as confirmed by means of diagnostic imaging.
  17. 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.
  18. 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).
  19. 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.
  20. Females who are pregnant or breastfeeding (not eligible even she discontinues breastfeeding).
  21. Any medical or other condition which, in the opinion of the investigator, would preclude participation in a clinical trial.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Lenvatinib plus Everolimus
Altri nomi:
  • Lenvatinib più Everolimus per via orale una volta al giorno

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants Who Experienced Any Dose Limiting Toxicity (DLT)
Lasso di tempo: From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
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).
From first dose of study drug up to Cycle 1 Day 28 (Cycle length=28 days)
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Lasso di tempo: Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)
Baseline up to 30 days after the last dose of study drug (up to approximately 21.5 months)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Cmax: Maximum Observed Plasma Concentration for Levatinib and Everolimus
Lasso di tempo: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Css,Max: Maximum Observed Plasma Concentration at Steady State for Levatinib and Everolimus
Lasso di tempo: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Levatinib and Everolimus
Lasso di tempo: Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Tss,Max: Time to Reach the Maximum Plasma Concentration (Cmax) at Steady State for Levatinib and Everolimus
Lasso di tempo: Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
AUC 0-t: Area Under the Concentration-time Curve From Zero (Pre-dose) to Time of Last Quantifiable Concentration for Levatinib and Everolimus
Lasso di tempo: Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Cycle 1 Day 1 and Cycle 1 Day 15 predose and at 1, 2, 4 ,8, and 24 hours postdose (Cycle length=28 days)
Number of Participants With Best Overall Response (BOR)
Lasso di tempo: 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)
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
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)
Objective Response Rate (ORR)
Lasso di tempo: 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)
ORR was defined as the percentage of participants who achieved BOR of CR or PR. ORR was assessed using RECIST 1.1.
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)
Disease Control Rate (DCR)
Lasso di tempo: 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)
DCR was defined as the percentage of participants who achieved BOR of CR, PR, or SD. DCR was assessed based on RECIST 1.1.
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)
Number of Participants With the Minimum Percent Change From Baseline in the Sum of Diameters of Target Lesions
Lasso di tempo: Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)
Baseline up to first tumor assessment at which diameter of target lesions were available (up to approximately 23 months)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 luglio 2015

Completamento primario (Effettivo)

29 maggio 2017

Completamento dello studio (Effettivo)

29 maggio 2017

Date di iscrizione allo studio

Primo inviato

22 maggio 2015

Primo inviato che soddisfa i criteri di controllo qualità

22 maggio 2015

Primo Inserito (Stima)

27 maggio 2015

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

19 marzo 2019

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 marzo 2019

Ultimo verificato

1 settembre 2018

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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