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Preliminary Evaluation of Safety and Efficacy by [14C] AC0010 Trail and Subsequent AC0010 Treatment

An Open-Label, Non-Randomized, Single-Center Study to Preliminary Evaluation of Safety and Efficacy of Patients Who Participant in [14C] AC0010 Trail and Subsequent Receiving AC0010 Treatment

The purpose of this study is to evaluate safety and efficacy of male Patients With Advanced NSCLC who participant in [14C] AC0010 ADME.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Detaljert beskrivelse

The purpose of this study is to evaluate safety and efficacy of male Patients With Advanced NSCLC who participant in [14C] AC0010 ADME (absorption, distribution, metabolism and excretion) trial and subsequent receiving AC0010 treatment.

Studietype

Intervensjonell

Registrering (Faktiske)

7

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Jiangsu
      • Nanjing, Jiangsu, Kina
        • Jiangsu Province Hospital

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

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

  • signed and dated informed consent
  • histologically or cytologically confirmed diagnosis of local advanced or recurrent NSCLC
  • failed to the treatment of EGFR-TKI and harbored T790M mutation
  • male, Age 18~ 65, have a body mass index (BMI)>19 kg/m2
  • Eastern Cooperative Oncology Group performance status(ECOG PS):0-1,Life expectancy of more than 3 months
  • main organs function is normal, laboratory values as listed below: blood test without blood transfusion within 14 days

    1. Haemoglobin >100 g/L
    2. Absolute neutrophil count ≥2.0x10^9/L or WBC ≥3.5 x10^9/L
    3. Platelet count ≥ 80x10^9/L
    4. Total bilirubin ≤1.5xULN
    5. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 2.5 times upper limit of normal (ULN)
    6. Serum creatinine ≤1.5xULN or creatinine clearance ratio ≥60 mL/ min
  • Any prior treatment (chemotherapy, radiotherapy or surgery) must be completed over 4 weeks(target therapy over 2 weeks) from the screening; Patients must have recovered from all toxicities related to prior anticancer therapies to grade ≤ 1 (CTCAE v 4.03)
  • International normalized ratio (INR) ≤ 1.5
  • Patients and their partners should be willing to use methods of contraception or total abstinence from start of dosing until 6 months after discontinuing of study treatment
  • Patients must withdraw from previous study of [14C] AC0010

Exclusion Criteria:

  • Prior treated with AC0010 or allergic to drug or its formulation ingredients
  • Patients receiving other anti-tumor therapy
  • Impairment of GI disease, renal disorders or liver disease that may significantly alter the absorption and metabolic of AC0010 (e.g., Unable to swallow, liver, kidney or gastrointestinal partial resection, chronic diarrhea and intestinal obstruction)
  • HCVAb positive, active hepatitis B (excluding HBV carriers), Hepatitis virus markers positive and receiving anti-virus drugs
  • Meningeal metastasis; brain metastasis with whole brain radiotherapy; prior received hormones or mannitol for the brain metastasis
  • Previous EGFR-TKI treatment related Interstitial lung disease history
  • Known human immunodeficiency virus infection (HIV), other acquired or congenital immunodeficiency disease, or a history of organ transplantation
  • Any severe and / or uncontrolled active infections
  • Patients receiving concomitant immunosuppressive agents or high-dose corticosteroids
  • Any severe and / or uncontrolled medical conditions
  • Patients being treated with drugs recognized as being inhibitors or inducers of the liver isoenzyme in the last 4 weeks prior to registration in the current study
  • Within 3 days prior to the treatment taking of dragon fruit, pomelo, grapefruit, orange, mango and other fruit may affect drug metabolizing enzymes or juice
  • Major surgery, incisional biopsy or traumatic injuries;
  • Within 4 weeks prior to the screening patients with bleeding ≥ grade 3, non-healing wound, sever ulcer or bone fracture
  • Patients received high dose irradiation treatment or other 14C-labeled drug within 1 year
  • Known a history of alcoholism or drug abuse
  • Investigator judgment that patient is unsuitable to participate in study

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
Eksperimentell: AC0010
each participant will be given AC0010 300mg bid
Oral dose of 300mg bid,the two doses are advised to be administered at an interval of 12 hours
Andre navn:
  • AC0010MA

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Objective Response Rate
Tidsramme: RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months
To assess the overall Objective Response Rate(ORR) of AC0010 in EGFR T790M mutation-positive patients with advanced NSCLC.
RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Progression Free Survival
Tidsramme: RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months
To assess the Progression Free Survival(PFS) of AC0010 in EGFR T790M mutation-positive patients with advanced NSCLC.
RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months
Disease control rate
Tidsramme: RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months
To assess the Disease control rate(DCR) of AC0010 in EGFR T790M mutation-positive patients with advanced NSCLC.
RECIST tumour assessments every 6 weeks from first dose until objective disease progression, up to approximately 11 months
Number of adverse events (AE) experienced by patients to assess safety
Tidsramme: From date of Signed informed consent forms until 30 days after disease progression, intolerable toxicity or withdrawal from study, approximately up to 18 months)
To assess the safety of AC0010 in EGFR T790M mutation-positive patients with advanced NSCLC.
From date of Signed informed consent forms until 30 days after disease progression, intolerable toxicity or withdrawal from study, approximately up to 18 months)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Lingxiang Liu, Doctor, The First Affiliated Hospital with Nanjing Medical University

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. november 2016

Primær fullføring (Faktiske)

1. juli 2018

Studiet fullført (Faktiske)

1. desember 2018

Datoer for studieregistrering

Først innsendt

19. desember 2016

Først innsendt som oppfylte QC-kriteriene

10. februar 2017

Først lagt ut (Faktiske)

15. februar 2017

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. februar 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

31. januar 2019

Sist bekreftet

1. januar 2019

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

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. .

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