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Evaluation of efficacy, safety and tolerability of Targretin capsules in patients with advanced or metastatic non-small cell lung cancer - Article


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Ethosuximide Capsules

Zarontin



Clinical Trial: Evaluation of efficacy, safety and tolerability of Targretin capsules in patients with advanced or metastatic non-small cell lung cancer

This study is no longer recruiting patients.

Sponsored by: Ligand Pharmaceuticals
Information provided by: Ligand Pharmaceuticals

Purpose

Ligand Pharmaceuticals Inc. is studying the use of Targretin capsules (bexarotene) in combination with standard chemotherapy for the treatment of metastatic non-small cell lung cancer in patients who have not yet received chemotherapy for their lung cancer.

Condition Treatment or Intervention Phase
Non-small cell lung cancer
 Drug: bexarotene
Phase III

MedlinePlus related topics:  Lung Cancer

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Randomized Phase III Trial Comparing Targretin Capsules/Cisplatin/Vinorelbine Versus Cisplatin/Vinorelbine in Chemotherapy-Naive Patients with Advanced or Metastatic Non-Small Cell Lung Cancer

Further Study Details: 

Expected Total Enrollment:  600

Ligand Pharmaceuticals Inc. is studying the use of Targretin capsules (bexarotene) in combination with Cisplatin and Vinorelbine for the treatment of metastatic non-small cell lung cancer in patients who have not yet received chemotherapy for their lung cancer. In these studies, every patient receives a platinum-containing chemotherapy every four weeks for at least four chemotherapy cycles (approximately four months). Half of the patients are randomly assigned to receive Targretin capsules once daily in addition to the chemotherapy. The other half is randomized to receive a standard platinum-containing chemotherapy without Targretin capsules.

Eligibility

Genders Eligible for Study:  Both

Criteria

Patients must have:

Patients must be able to complete at least four cycles of combination chemotherapy (i.e., approximately four months)

Patients must not have had:


Location Information


Alabama
      Brookwood Medical Center, Birmingham,  Alabama,  35209,  United States

Arizona
      Southern Arizona VA Healthcare System, Tucson,  Arizona,  85723,  United States

California
      Arroyo Research Inc., Pasadena,  California,  91105,  United States

      Desert Hematology-Oncology Medical Group, Inc., Rancho Mirage,  California,  92270,  United States

Florida
      New Hope Cancer Center, Hudson,  Florida,  34667,  United States

      University of Florida, Gainsville,  Florida,  32610,  United States

      Bay Area Cancer Consultants, Palm Harbor,  Florida,  34684,  United States

      Veterans Affairs Medical Center, Miami,  Florida,  33125,  United States

Illinois
      Northwest Medical Specialists, Arlington Heights,  Illinois,  60004,  United States

Louisiana
      Jayne Gurtler, M.D., APMC, Metairie,  Louisiana,  70006,  United States

      Louisiana State University Health Science Center, New Orleans,  Louisiana,  70112,  United States

Michigan
      St. Joseph Mercy Oakland Hospital, Pontiac,  Michigan,  48341,  United States

Missouri
      Capitol Comprehensive Cancer Care Clinic, Jefferson City,  Missouri,  65109,  United States

New York
      SUNY Downstate Medical Center, Brooklyn,  New York,  11203,  United States

      VA Western New York Health Care System, Buffalo,  New York,  14215,  United States

Ohio
      Hematology-Oncology Associates, Toledo,  Ohio,  43623,  United States

Oklahoma
      Tariq Mahmood, Midwest City,  Oklahoma,  73110,  United States

Tennessee
      University Oncology & Hematology Associates, Chattanooga,  Tennessee,  37404,  United States

Wisconsin
      Marshfield Medical Research Foundation, Marshfield,  Wisconsin,  54449,  United States

      Medical Associates Health Centers, Menomonee Falls,  Wisconsin,  53051,  United States

Australia, Australian Capital Territory
      Canberra Hospital, Garran,  Australian Capital Territory,  2605,  Australia

Australia, New South Wales
      Port Macquarie Base Hospital, Port Macquarie,  New South Wales,  2444,  Australia

      Southern Medical Daycare Centre, Wollongong,  New South Wales,  2500,  Australia

Australia, South Australia
      Burnside War Memorial Hospital, Toorak Gardens,  South Australia,  5065,  Australia

      Queen Elizabeth Hospital, Woodville,  South Australia,  5011,  Australia

Australia, Tasmania
      Royal Hobart Hospital, Hobart,  Tasmania,  7001,  Australia

Australia, Victoria
      Box Hill Hospital, Box Hill,  Victoria,  3128,  Australia

      Border Medical Oncology, Wodonga,  Victoria,  3690,  Australia

Canada, Alberta
      Tom Baker Cancer Centre, Calgary,  Alberta,  T2N 4N2,  Canada

Canada, Manitoba
      Cancer Care Manitoba, Winnepeg,  Manitoba,  R3E 0V9,  Canada

Canada, Nova Scotia
      QEII Health Sciences Center, Halifax,  Nova Scotia,  B3H 1V7,  Canada

Canada, Ontario
      Ottawa Regional Cancer Centre, Ottawa,  Ontario,  K1H 1C4,  Canada

Czech Republic
      Nemocnice odd. Onkologie, Ceske Budejovice,  370 87,  Czech Republic

      Pneumologicka klinika 1. LF UK, Praha-6-Veleslavin,  CZ-160 00,  Czech Republic

      Klinika pneumologie a hrudni chirurgie 3.LF, Praha-8,  CZ-180 00,  Czech Republic

France, Cedex
      Centre Hospitalier Francois Maillot, Briey,  Cedex,  54150,  France

      Centre Hospitalier General de Belfort, Belfort,  Cedex,  90016,  France

      Centre Hospitalier Intercommunal de la Haute-Saone, Vesoul,  Cedex,  70014,  France

      Institut Jean Godinot, Reims,  Cedex,  51100,  France

Greece
      University Hospital of Patras, Rio,  26500,  Greece

      7th Pneumonology Clinic, Sotiria Hospital for Diseases of the Chest, Athens,  11527,  Greece

      6th Pneumonology Department, Sotiria Hospital for Diseases of the Chest, Athens,  11527,  Greece

Greece, Alexandroupolis
      University Hospital of Alexandroupolis, Dragana,  Alexandroupolis,  68100,  Greece

Greece, Crete
      University General Hospital of Heraklion, Heraklion,  Crete,  Greece

Greece, Thessaloniki
      1st Pulmonary Clinic of G. Papanikolaou Hospital, Exochi,  Thessaloniki,  57010,  Greece

      2nd Pulmonary Clinic of G. Papanikolaou Hospital, Exochi,  Thessaloniki,  57010,  Greece

Hungary
      Fovarosi Onkormanyzat Uzsoki utcai, Korhaza, Budapest,  1145,  Hungary

      Koranyi National Institute for Pulmonology, Budapest,  1529,  Hungary

      Csongrad Megyei Onkormanyzat Mellkasi, Deszk,  6772,  Hungary

      Semmelweis University Department of Pulmonology, Budapest,  1125,  Hungary

Israel
      Barzilai Medical Centre, Ashkelon,  78308,  Israel

      Kaplan Medical Center, Rehovot,  76100,  Israel

      Assaf Harofeh Medical Center, Zerifin,  70300,  Israel

      Meir Hospital, Kfar Sava,  44281,  Israel

      Hadassah Medical Center, Jerusalem,  19200,  Israel

      Sheba Medical Center, Tel Hashomer,  52620,  Israel

      Tel-Aviv Sovrasky Medical Center, Tel Aviv,  64239,  Israel

Poland
      Akademii Medycznej w Gdansku, Gdansk,  80-216,  Poland

      Centrum Onkologii Instytut im. M. Sklodowskiej-Curie, Krakow,  31-115,  Poland

      Wielkopolskie Centrum Chorob Pluc I Gruzlicy, Poznan,  66-569,  Poland

      Instytut Gruzlicy i Chorob Pluc, Warsaw,  01-138,  Poland

      Regionalne Centrum Onkologii, Bialystok,  15-027,  Poland

Russian Federation
      Research Institute of Oncology n.a. Hertzen, Moscow,  12584,  Russian Federation

      City Oncology Clinical Center, Moscow,  107005,  Russian Federation

      Central Clinical Hospital n.a. Semashko, Moscow,  129128,  Russian Federation

      Russian Oncology Research Center n.a. Blokhin, Moscow,  115478,  Russian Federation

      City Oncology Hospital #62, Moscow,  143423,  Russian Federation

      City Oncology Center, St Petersburg,  197022,  Russian Federation

      Research Institute of Oncology n.a. Petrov, St Petersburg,  197758,  Russian Federation

      St. Petersburg Pavlov State Medical University, St Petersburg,  197089,  Russian Federation

      Arkhangelsk Regional Oncology Center, Arkhangelsk,  163045,  Russian Federation

United Kingdom, Aberdeen
      Aberdeen Royal Infirmary, Foresterhill,  Aberdeen,  AB25 2ZN,  United Kingdom

United Kingdom, England
      Chelsea & Westminster Hospital, London,  England,  SW10 9NH,  United Kingdom

      Bristol Hematology and Oncology Centre, Bristol,  England,  BS2 8ED,  United Kingdom

      Guys & St. Thomas' Cancer Centre, London,  England,  SE1 9RT,  United Kingdom

      Leicester Royal Infirmary, Leicester,  England,  LE1 5WW,  United Kingdom

United Kingdom, Scotland
      University of Edinburgh, Edinburgh,  Scotland,  EH4 2XU,  United Kingdom

Study chairs or principal investigators

Mack Mabry, M.D.,  Study Director,  Ligand Pharmaceuticals   

More Information

http://www.Ligand.com

Study ID Numbers:  L1069-49
Record last reviewed:  September 2004
Last Updated:  October 13, 2004
Record first received:  December 31, 2002
ClinicalTrials.gov Identifier:  NCT00050973
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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November 18, 2008



Page Updated: June 1, 2005
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