- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00076388
Iressa Versus Docetaxel (Taxotere)
12. mai 2011 oppdatert av: AstraZeneca
A Randomized, Open-Label, Parallel Group, International, Multicenter, Phase III Study of Oral ZD1839 (IRESSA®) Versus Intravenous Docetaxel (TAXOTERE®) in Patients With Locally Advanced or Metastatic Recurrent Non-Small Cell Lung Cancer Who Have Previously Received Platinum-Based Chemotherapy
The purpose of this study is to compare the effects of ZD1839 or docetaxel in patients with advanced non-small cell lung cancer (NSCLC) that has recurred or progressed after receiving prior treatment with platinum-based chemotherapy.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering
1440
Fase
- Fase 3
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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Buenos Aires, Argentina
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Cordoba, Argentina
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El Palomar, Argentina
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Mar del Plata, Argentina
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Quilmes, Argentina
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Rosario, Argentina
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San Miguel de Tucuman, Argentina
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Santa Fe, Argentina
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Charleroi, Belgia
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Edegem, Belgia
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Genk, Belgia
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Godinne, Belgia
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Kortrijk, Belgia
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Leuven, Belgia
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Liège, Belgia
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Yvoir, Belgia
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RJ
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Rio de Janeiro, RJ, Brasil
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RS
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Porto Alegre, RS, Brasil
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SP
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Sao Paulo, SP, Brasil
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Alberta
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Edmonton, Alberta, Canada
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British Columbia
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Surrey, British Columbia, Canada
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New Brunswick
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Moncton, New Brunswick, Canada
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Nova Scotia
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Halifax, Nova Scotia, Canada
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Ontario
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Hamilton, Ontario, Canada
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London, Ontario, Canada
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Newmarket, Ontario, Canada
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St. Catherines, Ontario, Canada
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Sudbury, Ontario, Canada
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Toronto, Ontario, Canada
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York, Ontario, Canada
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Quebec
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Laval, Quebec, Canada
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Montreal, Quebec, Canada
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Ste-Foy, Quebec, Canada
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Aalborg, Danmark
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Arhus C, Danmark
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Glostrup, Danmark
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Herlev, Danmark
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København Ø, Danmark
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Vejle, Danmark
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Tallinn, Estland
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Tartu, Estland
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Manila, Filippinene
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Quezon City, Filippinene
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Alabama
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Birmingham, Alabama, Forente stater
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California
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Fountain Valley, California, Forente stater
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Los Angeles, California, Forente stater, 90048
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Santa Rosa, California, Forente stater
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Stockton, California, Forente stater, 95204
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Colorado
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Colorado Springs, Colorado, Forente stater
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Connecticut
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Norwich, Connecticut, Forente stater
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Delaware
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Newark, Delaware, Forente stater
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Florida
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Boca Raton, Florida, Forente stater
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Orlando, Florida, Forente stater, 32806
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Georgia
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Macon, Georgia, Forente stater
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Tucker, Georgia, Forente stater
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Illinois
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Skokie, Illinois, Forente stater, 60077
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Kentucky
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Knoxville, Kentucky, Forente stater
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Minnesota
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St. Louis Park, Minnesota, Forente stater
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New York
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Great Neck, New York, Forente stater, 11021
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Rochester, New York, Forente stater, 14621
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Syracuse, New York, Forente stater, 13210
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North Carolina
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Chapel Hill, North Carolina, Forente stater, 27599
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Charlotte, North Carolina, Forente stater
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Durham, North Carolina, Forente stater, 27710
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Ohio
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Cleveland, Ohio, Forente stater, 44195
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Oregon
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Portland, Oregon, Forente stater
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Pennsylvania
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Philadelphia, Pennsylvania, Forente stater
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Pittsburgh, Pennsylvania, Forente stater
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South Carolina
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Columbia, South Carolina, Forente stater
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Tennessee
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Nashville, Tennessee, Forente stater
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Texas
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Austin, Texas, Forente stater
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Dallas, Texas, Forente stater
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Houston, Texas, Forente stater, 77030-4009
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Tyler, Texas, Forente stater
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Utah
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Salt Lake City, Utah, Forente stater
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Virginia
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Fairfax, Virginia, Forente stater
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Washington
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Seattle, Washington, Forente stater
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Wisconsin
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Racine, Wisconsin, Forente stater
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Blois, Frankrike
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Boulogne Billancourt, Frankrike
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Caen Cedex, Frankrike
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Grenoble Cedex 09, Frankrike
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Le Mans, Frankrike
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Lille Cedex, Frankrike
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Nantes, Frankrike
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Niort, Frankrike
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Saint Herblain, Frankrike
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Vandoeuvre Les Nancy, Frankrike
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Vesoul Cedex, Frankrike
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Hong Kong, Hong Kong
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Jakarta, Indonesia
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Yogyakarta, Indonesia
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Napoli, Italia
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Roma, Italia
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Ancona
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La Torretta, Ancona, Italia
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BA
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Bari, BA, Italia
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BG
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Bergamo, BG, Italia
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BO
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Bologna, BO, Italia
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CN
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Cuneo, CN, Italia
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CT
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Catania, CT, Italia
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FO
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Forli', FO, Italia
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MI
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Melegnano, MI, Italia
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Rozzano, MI, Italia
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MO
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Modena, MO, Italia
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PR
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Parma, PR, Italia
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TO
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Torino, TO, Italia
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Beijing, Kina
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Guangzhou, Kina
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Shanghai, Kina
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Split, Kroatia
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Zagreb, Kroatia
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Riga, Latvia
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Kuala Lumpur, Malaysia
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Nilai, Malaysia
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Guadalajara, Mexico
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Monterrey, Mexico
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Morelia, Mexico
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Torreon, Mexico
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Singapore, Singapore
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Ljubliana, Slovenia
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Barcelona, Spania
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Gerona, Spania
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Madrid, Spania
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Málaga, Spania
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Sevilla, Spania
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Valencia, Spania
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Vitoria, Spania
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Zaragoza, Spania
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Alicante
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Elche, Alicante, Spania
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Bellinzona, Sveits
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St. Gallen, Sveits
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Zürich, Sveits
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Goteborg, Sverige
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Luleå, Sverige
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Skövde, Sverige
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Stockholm, Sverige
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Sundsvall, Sverige
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Umeå, Sverige
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Vasteras, Sverige
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Örebro, Sverige
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Östersund, Sverige
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Chiang Mai, Thailand
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Ankara, Tyrkia
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Istanbul, Tyrkia
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Izmir, Tyrkia
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Berlin, Tyskland
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Bonn, Tyskland
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Großhansdorf, Tyskland
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Köln, Tyskland
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Leverkusen, Tyskland
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Löwenstein, Tyskland
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Mannheim, Tyskland
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München, Tyskland
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Stuttgart, Tyskland
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Wiesbaden, Tyskland
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Baden-Württemberg
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Heidelberg, Baden-Württemberg, Tyskland
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Ulm, Baden-Württemberg, Tyskland
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Brandenburg
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Cottbus, Brandenburg, Tyskland
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Hessen
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Frankfurt, Hessen, Tyskland
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Nordrhein-Westfalen
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Düsseldorf, Nordrhein-Westfalen, Tyskland
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Rheinland-Pfalz
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Mainz, Rheinland-Pfalz, Tyskland
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Schleswig-Holstein
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Bad Segeberg, Schleswig-Holstein, Tyskland
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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
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Measurable (uni dimensional) disease by RECIST criteria in a lesion not previously irradiated or non measurable disease
- Locally advanced or metastatic NSCLC, not amenable to curative surgery or radiotherapy
- Advanced non-small cell lung cancer (NSCLC) that has recurred or progressed after receiving prior treatment with platinum-based chemotherapy
- WHO performance status (PS) 0-2
- Absolute Neutrophil Count (ANC) >1.5 x 109/liter (L) and platelets >100 x 109/L
- Life expectancy of at least 8 weeks
Exclusion Criteria:
- Prior ZD1839 therapy
- Prior docetaxel treatment for NSCLC
- Less than 14 days since completion of prior radiotherapy
- Less than 21 days since prior chemotherapy, immunotherapy or biological systemic anticancer therapy
- Evidence of clinically active Interstitial Lung Disease
- Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of basal cell carcinoma or cervical cancer in situ
- Newly diagnosed CNS metastases that have not yet been treated with surgery and/or radiation. Patients with previously diagnosed and treated CNS metastases or spinal cord compression may be considered if they have evidence of clinically SD (no steroid therapy or steroid dose being tapered) for at least 28 days
- Patients with pre existing peripheral neuropathy >= grade 2 (NCI CTC criteria)
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)
Hva måler studien?
Primære resultatmål
Resultatmål |
|---|
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To compare overall survival between ZD1839 and docetaxel
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Sekundære resultatmål
Resultatmål |
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To compare time to progression (TTP) between ZD1839 and docetaxel
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To compare progression-free rates at 4 months and 6 months between ZD1839 and docetaxel
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To compare the overall objective tumor response rate between ZD1839 and docetaxel
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To compare patient-reported functionality (PRF) and quality of life (QoL) between ZD1839 and docetaxel
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To compare safety and tolerability of ZD1839 and docetaxel
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studieleder: AstraZeneca Iressa Medical Science Director, MD, AstraZeneca
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.
Generelle publikasjoner
- Lombard A, Mistry H, Aarons L, Ogungbenro K. Dose individualisation in oncology using chemotherapy-induced neutropenia: Example of docetaxel in non-small cell lung cancer patients. Br J Clin Pharmacol. 2021 Apr;87(4):2053-2063. doi: 10.1111/bcp.14614. Epub 2020 Dec 19.
- Douillard JY, Shepherd FA, Hirsh V, Mok T, Socinski MA, Gervais R, Liao ML, Bischoff H, Reck M, Sellers MV, Watkins CL, Speake G, Armour AA, Kim ES. Molecular predictors of outcome with gefitinib and docetaxel in previously treated non-small-cell lung cancer: data from the randomized phase III INTEREST trial. J Clin Oncol. 2010 Feb 10;28(5):744-52. doi: 10.1200/JCO.2009.24.3030. Epub 2009 Dec 28.
- Kim ES, Hirsh V, Mok T, Socinski MA, Gervais R, Wu YL, Li LY, Watkins CL, Sellers MV, Lowe ES, Sun Y, Liao ML, Osterlind K, Reck M, Armour AA, Shepherd FA, Lippman SM, Douillard JY. Gefitinib versus docetaxel in previously treated non-small-cell lung cancer (INTEREST): a randomised phase III trial. Lancet. 2008 Nov 22;372(9652):1809-18. doi: 10.1016/S0140-6736(08)61758-4.
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. februar 2004
Primær fullføring (Faktiske)
1. mars 2007
Studiet fullført (Faktiske)
1. oktober 2007
Datoer for studieregistrering
Først innsendt
21. januar 2004
Først innsendt som oppfylte QC-kriteriene
22. januar 2004
Først lagt ut (Anslag)
23. januar 2004
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
13. mai 2011
Siste oppdatering sendt inn som oppfylte QC-kriteriene
12. mai 2011
Sist bekreftet
1. mai 2011
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Sykdommer i luftveiene
- Neoplasmer
- Lungesykdommer
- Neoplasmer etter nettsted
- Neoplasmer i luftveiene
- Thoracale neoplasmer
- Karsinom, bronkogent
- Bronkiale neoplasmer
- Lungeneoplasmer
- Karsinom, ikke-småcellet lunge
- Molekylære mekanismer for farmakologisk virkning
- Enzymhemmere
- Antineoplastiske midler
- Tubulin modulatorer
- Antimitotiske midler
- Mitosemodulatorer
- Proteinkinasehemmere
- Docetaxel
- Gefitinib
Andre studie-ID-numre
- D791GC00001
- EudraCT No: 2004-002943-28
- 1839IL/0721
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. .