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NCT00680901CompletedPhase 3

LOGiC - Lapatinib Optimization Study in ErbB2 (HER2) Positive Gastric Cancer: A Phase III Global, Blinded Study Designed to Evaluate Clinical Endpoints and Safety of Chemotherapy Plus Lapatinib

A Phase III Study for ErbB2 Positive Advanced or Metastatic Gastric, Esophageal, or Gastroesophageal Junction Adenocarcinoma Treated With Capecitabine Plus Oxaliplatin With or Without Lapatinib

Source: ClinicalTrials.gov · Last updated 7 Aug 2025

Brief summary (registry, in English)

This was an international multi-center trial that enrolled patients with locally advanced, unresectable, or metastatic gastric, esophageal, or gastro-esophageal junction cancer whose tumors had amplification of the ErbB2 (HER2) gene. The trial investigated whether lapatinib, when added to the chemotherapy regimen, capecitabine plus oxaliplatin (CapeOx), extended the time to progression and overall survival. Tumor ErbB2 (HER2) status had to be known before trial entry. CapeOx was administered to all patients, and patients were randomly assigned to receive either lapatinib or placebo.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
545 (actual)
First submitted
15 May 2008
Start date
4 Jun 2008
Primary completion date
24 Sept 2012
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT00680901
EudraCT number
2007-005725-29

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 545
  • From 4 Jun 2008 to the primary completion date, 24 Sept 2012
  • 157 sites in 23 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent anti-cancer therapy (chemotherapy, radiation therapy other than for pain relief, immunotherapy, biologic therapy, hormonal therapy or surgery) while taking investigational treatment.
  • Prior palliative chemotherapy for the treatment of gastric cancer.
  • Prior treatment with oxaliplatin-based neoadjuvant or adjuvant chemotherapy completed \<12 months.

Other illness

  • Known history of active CNS disease.
  • Malabsorption syndrome or uncontrolled inflammatory gastrointestinal disease (such as Crohn's disease or ulcerative colitis).
  • Known history of uncontrolled or symptomatic angina, arrhythmias, or congestive heart failure.
  • Uncontrolled infection.
  • History of other malignancy. However, subjects who were disease-free for 5 years, or subjects with a history of a completely resected non-melanoma skin cancer or successfully treated in situ carcinoma, were eligible.

Other

  • Pregnant or lactating females at any time during the study.
  • Uncontrolled ascites.
  • Gastric carcinoid, epidermoid, sarcomas, or squamous cell carcinoma.

Who the study is looking for

  • Histologically confirmed gastric adenocarcinoma or adenocarcinoma of the esophagus or gastro-esophageal junction.
  • Gastric cancer that is unresectable due to locally advanced (defined as stage IV: T4N1-3 or TanyN3), metastatic, or locally recurrent disease; Esophageal cancer that is unresectable due to locally advanced (T3N1 or T4Nany), metastatic or locally recurrent disease.
  • Measurable or non-measurable, but radiologically evaluable disease, according to RECIST.
  • HER2 amplification by FISH assessed by the local or designated central laboratory; Subjects with unknown HER2 status were not eligible.
  • Adequate organ function, as defined in the study protocol, assessed within 14 days prior randomization.
  • Cardiac ejection fraction within institutional range of normal as measured by echocardiogram (ECHO).
  • Prior/Concurrent Therapy:
    • At least 3 weeks following major surgery, such as gastrectomy, and were recovered from any related toxicity More than 5 years since prior chemotherapy for malignancy other than GC. At least 4 weeks since prior radiotherapy
    • More than 5 years since prior biologic or hormonal therapy or immunotherapy for malignancy other than gastric carcinoma.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (157)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
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Buenos AiresArgentinaUnknown status
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CipollettiArgentinaUnknown status
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Ciudad Aut6noma de Buenos AiresArgentinaUnknown status
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La RiojaArgentinaUnknown status
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NeuquénArgentinaUnknown status
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QuilmesArgentinaUnknown status
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RosarioArgentinaUnknown status
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San Miguel de TucumánArgentinaUnknown status
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Santa FeArgentinaUnknown status
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BarretosBrazilUnknown status
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Belo HorizonteBrazilUnknown status
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FlorianópolisBrazilUnknown status
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JaúBrazilUnknown status
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Porto AlegreBrazilUnknown status
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Rio de JaneiroBrazilUnknown status
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Santo AndréBrazilUnknown status
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São PauloBrazilUnknown status
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EdmontonCanadaUnknown status
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LondonCanadaUnknown status
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MontrealCanadaUnknown status
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Saint JohnCanadaUnknown status
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TorontoCanadaUnknown status
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VancouverCanadaUnknown status
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SantiagoChileUnknown status
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TemucoChileUnknown status
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Viña del MarChileUnknown status
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BeijingChinaUnknown status
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ChangchunChinaUnknown status
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ChengduChinaUnknown status
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FuzhouChinaUnknown status
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GuangzhouChinaUnknown status
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HangzhouChinaUnknown status
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HarbinChinaUnknown status
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HefeiChinaUnknown status
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NanjingChinaUnknown status
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QingdaoChinaUnknown status
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ShanghaiChinaUnknown status
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TianjinChinaUnknown status
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TallinnEstoniaUnknown status
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TartuEstoniaUnknown status
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PokfulamHong Kong SAR ChinaUnknown status
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TuenmenHong Kong SAR ChinaUnknown status
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GyőrHungaryUnknown status
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KaposvárHungaryUnknown status
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KecskemétHungaryUnknown status
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MiskolcHungaryUnknown status
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PécsHungaryUnknown status
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SzegedHungaryUnknown status
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SzolnokHungaryUnknown status
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BeershebaIsraelUnknown status
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HaifaIsraelUnknown status
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JerusalemIsraelUnknown status
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Petah TikvaIsraelUnknown status
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Ramat GanIsraelUnknown status
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RehovotIsraelUnknown status
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Tel AvivIsraelUnknown status
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ZrifinIsraelUnknown status
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CoimbatoreIndiaUnknown status
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KochiIndiaUnknown status
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KolkataIndiaUnknown status
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NagpurIndiaUnknown status
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New DelhiIndiaUnknown status
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ParelIndiaUnknown status
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PuneIndiaUnknown status
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TrivandrumIndiaUnknown status
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BariItalyUnknown status
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BergamoItalyUnknown status
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CesenaItalyUnknown status
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FlorenceItalyUnknown status
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GenoaItalyUnknown status
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L’AquilaItalyUnknown status
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Meldola (FC)ItalyUnknown status
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ModenaItalyUnknown status
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ParmaItalyUnknown status
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PesasroItalyUnknown status
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PiacenzaItalyUnknown status
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Province of MacerataItalyUnknown status
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RiminiItalyUnknown status
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Rionero in Vulture (PZ)ItalyUnknown status
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RomeItalyUnknown status
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Treviglio (BG)ItalyUnknown status
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UdineItalyUnknown status
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BusanSouth KoreaUnknown status
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DaeguSouth KoreaUnknown status
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HwasunSouth KoreaUnknown status
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Seodaemun-gu, SeoulSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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SuwonSouth KoreaUnknown status
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Suwon, Kyonggi-doSouth KoreaUnknown status
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Acapulco de JuárezMexicoUnknown status
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Mexico CityMexicoUnknown status
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Oaxaca CityMexicoUnknown status
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AmsterdamNetherlandsUnknown status
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LeeuwardenNetherlandsUnknown status
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NijmegenNetherlandsUnknown status
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CallaoPeruUnknown status
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LimaPeruUnknown status
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GdanskPolandUnknown status
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KrakowPolandUnknown status
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OlsztynPolandUnknown status
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PłockPolandUnknown status
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PoznanPolandUnknown status
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RybnikPolandUnknown status
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SłupskPolandUnknown status
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SzczecinPolandUnknown status
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TorunPolandUnknown status
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WarsawPolandUnknown status
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San JuanPuerto RicoUnknown status
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ChelyabinskRussiaUnknown status
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KirovRussiaUnknown status
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KurskRussiaUnknown status
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MoscowRussiaUnknown status
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OmskRussiaUnknown status
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RyazanRussiaUnknown status
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Saint PetersburgRussiaUnknown status
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SaratovRussiaUnknown status
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SochiRussiaUnknown status
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StavropolRussiaUnknown status
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UfaRussiaUnknown status
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BangkokThailandUnknown status
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Hatyai, SongkhlaThailandUnknown status
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TainanTaiwanUnknown status
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TaipeiTaiwanUnknown status
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Taoyuan CountyTaiwanUnknown status
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CherkasyUkraineUnknown status
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ChernivtsiUkraineUnknown status
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DniproUkraineUnknown status
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DnipropetrovskUkraineUnknown status
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DonetskUkraineUnknown status
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Ivano-FrankivskUkraineUnknown status
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KharkivUkraineUnknown status
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Kryvyi RihUkraineUnknown status
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KyivUkraineUnknown status
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LutskUkraineUnknown status
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LvivUkraineUnknown status
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OdesaUkraineUnknown status
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PlyutyUkraineUnknown status
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SimferopilUkraineUnknown status
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SimferopolUkraineUnknown status
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SumyUkraineUnknown status
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TernopilUkraineUnknown status
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UzhhorodUkraineUnknown status
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VinnitsiaUkraineUnknown status
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ZaporizhzhyaUkraineUnknown status
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AlhambraUnited StatesUnknown status
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FullertonUnited StatesUnknown status
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HendersonUnited StatesUnknown status
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La VerneUnited StatesUnknown status
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NorthridgeUnited StatesUnknown status
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OxnardUnited StatesUnknown status
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Redondo BeachUnited StatesUnknown status
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Santa MariaUnited StatesUnknown status
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Santa MonicaUnited StatesUnknown status
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Terre HauteUnited StatesUnknown status
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AnkaraTurkey (Türkiye)Unknown status
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GaziantepTurkey (Türkiye)Unknown status
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TrabzonTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.