- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02536586
A Study of LY3023414 in Japanese Participants With Advanced Cancer
20. juli 2018 oppdatert av: Eli Lilly and Company
A Phase 1 Study of LY3023414 in Japanese Patients With Advanced Malignancies
The main purpose of this study is to evaluate the tolerability of an investigational drug known as LY3023414 in Japanese participants with advanced cancer or cancer that has spread to another part(s) of the body.
The study will also explore the safety of the drug.
It will measure how much of the drug gets into the blood steam and how long the body takes to get rid of it.
It will investigate anti-cancer activity.
Studieoversikt
Studietype
Intervensjonell
Registrering (Faktiske)
12
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Chiba, Japan, 277 8577
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician.
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Tokyo, Japan, 104-0045,
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri, 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician.
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
20 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria
- Have histological or cytological evidence of a diagnosis of solid tumor that is advanced and/or metastatic and must be, in the judgment of the investigator, an appropriate candidate for experimental therapy after available standard therapies have failed or for whom standard therapy would not be appropriate.
- Have the presence of measurable or non-measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
- Have adequate organ and coagulation function.
- Have discontinued all previous cancer therapies, and any agents that have not received regulatory approval for any indication, for at least 21 days or 5 half-lives prior to study treatment, whichever is shorter, and recovered from the acute effects of therapy. Participants must have discontinued mitomycin-C or nitrosourea therapy for at least 42 days.
- Are able to swallow capsules.
- Males must agree to use medically approved barrier contraceptive precautions during the study and for 3 months following the last dose of study drug.
- Females with childbearing potential: Must agree to use medically approved contraceptive precautions during the study and for 3 months following the last dose of study drug, must have had a negative serum or urine pregnancy test ≤7 days before the first dose of study drug.
- A breastfeeding woman must not be breastfeeding. If a female who stops breastfeeding enters the study, breastfeeding must cease from the day of the first study drug administration until at least 3 months after the last administration.
Exclusion Criteria
- Have serious pre-existing medical conditions.
- Have symptomatic central nervous system malignancy or metastasis.
- Have known acute or chronic leukemia or current hematologic malignancies that, in the judgment of the investigator and sponsor, may affect the interpretation of results.
- Have a known active fungal, bacterial, and/or known viral infection.
- Intolerance to any previous treatment with any phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) inhibitor. Treatment with any PI3K/AKT/mTOR inhibitor must have discontinued for at least 21 days or 5 half-lives prior to first study drug administration, whichever is shorter, and participants must have recovered from the acute effects of therapy.
- Have a second primary malignancy that, in the judgment of the investigator, and sponsor may affect the interpretation of results.
- Participants with active alcohol abuse, as determined by the investigator.
- Have a history of heart failure according to New York Heart Association Class ≥3.
- Have corrected QT (QTc) interval of >470 milliseconds (msec) on screening electrocardiogram (ECG).
- Have insulin-dependent diabetes mellitus or a history of gestational diabetes mellitus.
- Have any evidence of clinically active interstitial lung disease (ILD).
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: LY3023414
LY3023414 administered orally, twice daily in 21-day cycles.
Treatment will continue until disease progression, development of unacceptable toxicity, or other discontinuation criteria are met.
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LY3023414 administered orally.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
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Number of Participants with LY3023414 Dose-Limiting Toxicities (DLT)
Tidsramme: Cycle 1 (21 days)
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Cycle 1 (21 days)
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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Pharmacokinetics (PK): Area Under the Plasma Concentration-Time Curve (AUC) of LY3023414
Tidsramme: Predose Cycle 1 through predose Cycle 3. (Cycle = 21 days.)
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Predose Cycle 1 through predose Cycle 3. (Cycle = 21 days.)
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Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3023414
Tidsramme: Predose Cycle 1 through predose Cycle 3. (Cycle = 21 days.)
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Predose Cycle 1 through predose Cycle 3. (Cycle = 21 days.)
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Proportion of Participants With Best Overall Response (OR) of Partial Response (PR) or Complete Response (CR) (Overall Response Rate [ORR])
Tidsramme: Baseline through study completion (estimated as up to five months)
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Baseline through study completion (estimated as up to five months)
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. september 2015
Primær fullføring (Faktiske)
9. februar 2017
Studiet fullført (Faktiske)
9. februar 2017
Datoer for studieregistrering
Først innsendt
28. august 2015
Først innsendt som oppfylte QC-kriteriene
28. august 2015
Først lagt ut (Anslag)
1. september 2015
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
24. juli 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. juli 2018
Sist bekreftet
1. juli 2018
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- 15838
- I6A-JE-CBBH (Annen identifikator: Eli Lilly and Company)
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .