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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.

Studieoversigt

Status

Afsluttet

Intervention / Behandling

Detaljeret 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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

7

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

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

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Han

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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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 navne:
  • AC0010MA

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

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

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. november 2016

Primær færdiggørelse (Faktiske)

1. juli 2018

Studieafslutning (Faktiske)

1. december 2018

Datoer for studieregistrering

Først indsendt

19. december 2016

Først indsendt, der opfyldte QC-kriterier

10. februar 2017

Først opslået (Faktiske)

15. februar 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

1. februar 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

31. januar 2019

Sidst verificeret

1. januar 2019

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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