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En randomisert fase 3-studie av pemetrexed og cisplatin versus gemcitabin og cisplatin hos pasienter med lokalt avansert eller metastatisk ikke-småcellet lungekreft

10. september 2019 oppdatert av: Eli Lilly and Company

En randomisert fase 3-studie av ALIMTA og cisplatin versus GEMZAR og cisplatin hos pasienter med lokalt avansert eller metastatisk ikke-småcellet lungekreft

Denne studien er en randomisert fase 3-studie som sammenligner pemetrexed og cisplatin kombinasjon med gemcitabin og cisplatin for behandling av ikke-småcellet lungekreft (NCSLC). Gemcitabin pluss cisplatin er for tiden standardbehandlingen for NSCLC. Det antas at pemetrexed pluss cisplatin kan være like effektive og kan ha færre bivirkninger enn standardbehandlingen.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

1713

Fase

  • Fase 3

Kontakter og plasseringer

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

Studiesteder

      • Bahia Blanca, Argentina
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      • Buenos Aires, Argentina
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      • Bedford Park, Australia
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      • Camperdown, Australia
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      • Chermisdie, Australia
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      • Fitzroy, Australia
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      • Hornsby, Australia
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      • Nedlands, Australia
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      • South Brisbane, Australia
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      • St Leonards, Australia
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      • Leuven, Belgia
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      • Liege, Belgia
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      • Florianopolis, Brasil
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      • Porto Alegre, Brasil
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      • Rio De Janeiro, Brasil
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      • Salvador, Brasil
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      • Sao Paulo, Brasil
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    • British Columbia
      • North Vancouver, British Columbia, Canada
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    • Ontario
      • Brampton, Ontario, Canada
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      • Toronto, Ontario, Canada
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    • Quebec
      • Sainte-Foy, Quebec, Canada
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      • Herlev, Danmark
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      • Odense, Danmark
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      • Helsinki, Finland
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      • Tampere, Finland
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    • California
      • Sacramento, California, Forente stater
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      • Torrance, California, Forente stater
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    • Florida
      • Jacksonville, Florida, Forente stater
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    • Georgia
      • Macon, Georgia, Forente stater
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    • Kansas
      • Wichita, Kansas, Forente stater
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    • Kentucky
      • Lexington, Kentucky, Forente stater
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    • Maine
      • Scarborough, Maine, Forente stater
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    • Minnesota
      • Duluth, Minnesota, Forente stater
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    • Missouri
      • Saint Louis, Missouri, Forente stater
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    • Montana
      • Billings, Montana, Forente stater
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    • New Jersey
      • Hackensack, New Jersey, Forente stater
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    • North Carolina
      • Hickory, North Carolina, Forente stater
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    • Oregon
      • Portland, Oregon, Forente stater
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    • South Carolina
      • Columbia, South Carolina, Forente stater
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    • Tennessee
      • Nashville, Tennessee, Forente stater
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    • Texas
      • Arlington, Texas, Forente stater
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    • Virginia
      • Richmond, Virginia, Forente stater
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
    • Washington
      • Seattle, Washington, Forente stater
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Bordeaux, Frankrike
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      • Grenoble, Frankrike
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      • Marseille, Frankrike
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      • Montpellier, Frankrike
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      • Paris, Frankrike
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      • Saint Herblain, Frankrike
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      • Strasbourg, Frankrike
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      • Vandoeuvre-les-Nancy, Frankrike
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      • Athens, Hellas
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      • Heraklion, Hellas
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      • Patras, Hellas
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      • Bangalore, India
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      • Cochin, India
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      • Hyderabad, India
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      • Mumbai, India
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      • New Dehli, India
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      • Pune, India
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      • Kfar Saba, Israel
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      • Tel-Aviv, Israel
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      • Tel-Hashomer, Israel
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      • Ancona, Italia
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      • Bergamo, Italia
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      • Bologna, Italia
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      • Forli, Italia
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      • Genova, Italia
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      • Livorno, Italia
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      • Modena, Italia
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      • Orbassano, Italia
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      • Roma, Italia
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      • Taormina, Italia
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      • Goyang-Si, Korea, Republikken
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      • Seoul, Korea, Republikken
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      • Ciudad Obregon, Mexico
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      • Guadalajara, Mexico
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      • Leon, Mexico
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      • Mexicali, Mexico
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      • Mexico City, Mexico
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      • Alkmaar, Nederland
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      • Amstelveen, Nederland
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      • Amsterdam, Nederland
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      • Arnhem, Nederland
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      • Den Bosch, Nederland
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      • Eindhoven, Nederland
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      • Harderwijk, Nederland
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      • Heerlen, Nederland
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      • Krakow, Polen
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      • Lodz, Polen
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      • Szczecin-Zdunowo, Polen
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      • Warszawa, Polen
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Coimbra, Portugal
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Lisboa, Portugal
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Porto, Portugal
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Santa Maria Da Feira, Portugal
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • San Juan, Puerto Rico
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Alicante, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Badalona, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Barcelona, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Madrid, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Pamplona, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Sabadell, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Santander, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Zaragoza, Spania
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Aberdeen, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Bangor, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Chelmsford, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Fulham, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Plymouth, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Sutton, Storbritannia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Goteborg, Sverige
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Lund, Sverige
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Stockholm, Sverige
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Niao Sung Hsiang, Taiwan
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Taichung, Taiwan
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Taipei, Taiwan
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Tao-Yuan, Taiwan
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Ankara, Tyrkia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Antalya, Tyrkia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Istanbul, Tyrkia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Izmir, Tyrkia
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Mannheim, Tyskland
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Budapest, Ungarn
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Deszk, Ungarn
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Pecs, Ungarn
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Graz, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Grimmenstein, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Innsbruck, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Leoben, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Linz, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • St. Poelten, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Vienna, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician
      • Wels, Østerrike
        • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician

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 og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inklusjonskriterier:

  • Diagnostisering av NSCLC stadium IIIB som ikke mottar kurativ behandling eller stadium IV.
  • Ingen tidligere kjemoterapi for lungekreft.
  • Pasienter må ha minst én endimensjonalt målbar lesjon.
  • Tidligere strålebehandling til mindre enn 25 % av benmargen, hele bekkenet ikke tillatt. Stråling skal være gjennomført minst 4 uker før studieopptak.

Ekskluderingskriterier:

  • Behandling med et hvilket som helst medikament innen de siste 30 dagene som ikke har fått myndighetsgodkjenning.
  • Alvorlig hjertetilstand.
  • Alvorlig medisinsk lidelse i tillegg til NSCLC som ville gjøre det vanskelig for pasienten å fullføre studien.
  • Manglende evne eller vilje til å ta tilskudd av folsyre eller vitamin B12.
  • Tilstedeværelse av væskeretensjon som ikke kan kontrolleres av drenering.

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: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: B
75 mg/m2, IV, q 21 dager x 6 sykluser
1250 mg/m2, IV, dag 1 og 8 kv 21 dager x 6 sykluser
Andre navn:
  • Gemzar
  • LY188011
Eksperimentell: EN
500 mg/m2, IV q 21 dager x 6 sykluser
Andre navn:
  • Alimta
  • LY231514
75 mg/m2, IV, q 21 dager x 6 sykluser

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Total overlevelse
Tidsramme: baseline til dato for død uansett årsak
baseline til dato for død uansett årsak

Sekundære resultatmål

Resultatmål
Tidsramme
Varighet av svar
Tidsramme: tidspunkt for respons på progressiv sykdom
tidspunkt for respons på progressiv sykdom
Tid for progressiv sykdom
Tidsramme: baseline til målt progressiv sykdom
baseline til målt progressiv sykdom
Progresjonsfri overlevelse
Tidsramme: baseline til målt progressiv sykdom
baseline til målt progressiv sykdom
Tid til behandlingssvikt
Tidsramme: grunnlinje til å avslutte behandlingen
grunnlinje til å avslutte behandlingen

Samarbeidspartnere og etterforskere

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

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

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. juli 2004

Primær fullføring (Faktiske)

1. januar 2007

Studiet fullført (Faktiske)

1. mars 2008

Datoer for studieregistrering

Først innsendt

12. juli 2004

Først innsendt som oppfylte QC-kriteriene

15. juli 2004

Først lagt ut (Anslag)

16. juli 2004

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

12. september 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. september 2019

Sist bekreftet

1. september 2019

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Anonymiserte individuelle pasientnivådata vil bli gitt i et sikkert tilgangsmiljø ved godkjenning av et forskningsforslag og en signert datadelingsavtale.

IPD-delingstidsramme

Data er tilgjengelig 6 måneder etter den primære publisering og godkjenning av indikasjonen studert i USA og EU, avhengig av hva som er senere. Data vil være tilgjengelig på ubestemt tid for forespørsel.

Tilgangskriterier for IPD-deling

Et forskningsforslag må godkjennes av et uavhengig granskningspanel og forskere må signere en datadelingsavtale.

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • SEVJE
  • CSR

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. .

Abonnere