- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01210911
Metformin Combined With Chemotherapy for Pancreatic Cancer (GEM)
A Phase II, Randomized, Placebo Controlled Study to Evaluate the Efficacy of the Combination of Gemcitabine, Erlotinib and Metformin in Patients With Locally Advanced and Metastatic Pancreatic Cancer
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
In this phase II randomized, placebo controlled study, patients with locally advanced or metastatic pancreatic cancer will be randomized to treatment with gemcitabine, erlotinib and metformin, or gemcitabine, erlotinib and placebo.
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without treatment. Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food. Metformin/ placebo will be administered at a dose of 500 mg twice daily. If well tolerated the dose will be increased to 1000 mg twice daily in the second week.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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-
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Amsterdam, Olanda, 1105AZ
- Academic Medical Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Signed informed content obtained prior to treatment
- Cytological or histological confirmed carcinoma of the pancreas
- Metastatic cancer
- Measurable lesion according to RECIST criteria
- ECOG/ WHO performance 0-2
- Age > 18 years
- Adequate renal function (creatinine < 150 µmol/L and/ or a creatinine clearance > 60 ml/ L)
- Adequate liver function (bilirubin < 1.5 times upper limit of normal, ALAT or ASAT < 5.0 times upper limit of normal in case of liver metastases and < 2.5 the upper limit of normal in absence of liver metastases).
- Adequate bone marrow function (WBC > 3.0 x 10 9/L, platelets > 100 x 10 9/L)
- Mentally, physically, and geographically able to undergo treatment and follow up
Exclusion Criteria:
- Clinical or radiological evidence of CNS metastases
- Pregnancy (positive serum pregnancy test) and lactation
- Serious concomitant systemic disorder that would compromise the safety of the patient, at the discretion of the investigator
Patients who have any severe and/or uncontrolled medical conditions:
- unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction ≤ 6 months prior to randomization, serious uncontrolled cardiac arrhythmia
- uncontrolled diabetes as defined by fasting serum glucose >2X ULN.
- active or uncontrolled severe infection.
- cirrhosis, chronic active hepatitis or chronic persistent hepatitis
- severely impaired lung function
- Previous treatment with erlotinib
- Previous treatment with gemcitabine for metastatic disease
- Previous treatment with gemcitabine combined with radiotherapy for locally advanced pancreatic cancer within 6 months prior to study entry
- Patients with a known hypersensitivity to metformin
- Use of metformin in the previous 6 months
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Gemcitabine, erlotinib and metformin
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine.
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food.
Metformin will be administered at a dose of 500 mg twice daily.
If well tolerated the dose will be increased to 1000 mg twice daily in the second week.
|
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine
Altri nomi:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
Altri nomi:
Metformin will be administered at a dose of 500 mg twice daily for the first week.
If tolerated well, the dose will be increased up to 1000 mg twice daily in the second week.
Altri nomi:
|
|
Comparatore placebo: Gemcitabine, erlotinib and placebo
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine.
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food.
PLacebo will be administered at a dose of 500 mg twice daily.
If well tolerated the dose will be increased to 1000 mg twice daily in the second week.
|
Gemcitabine at a dose of 1000 mg/m2 (iv, 30 minutes) will be given weekly, for 3 weeks, followed by one week without gemcitabine
Altri nomi:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
Altri nomi:
Placebo will be administered at a dose of 500 mg twice daily for the first week.
If tolerated well, the dose will be increased up to 1000 mg twice daily in the second week.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Survival after 6 months
Lasso di tempo: 6 months after completion of the study
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6 months after completion of the study
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Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Progression free survival
Lasso di tempo: 6 months after the completion of the study
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6 months after the completion of the study
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Objective response rate
Lasso di tempo: expected treatment duration 2- 6 months
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expected treatment duration 2- 6 months
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toxicity profile
Lasso di tempo: during study and 4 weeks after stop study medication
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during study and 4 weeks after stop study medication
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Hanneke Wilmink, MD, PhD, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie dell'apparato digerente
- Neoplasie
- Neoplasie per sede
- Malattie del sistema endocrino
- Neoplasie dell'apparato digerente
- Neoplasie delle ghiandole endocrine
- Malattie pancreatiche
- Neoplasie pancreatiche
- Agenti ipoglicemizzanti
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Agenti antinfettivi
- Agenti antivirali
- Inibitori enzimatici
- Antimetaboliti, Antineoplastici
- Antimetaboliti
- Agenti antineoplastici
- Agenti immunosoppressivi
- Fattori immunologici
- Inibitori della chinasi proteica
- Gemcitabina
- Erlotinib cloridrato
- Metformina
Altri numeri di identificazione dello studio
- AMCmedonc10/003
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .