- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
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.
Studietype
Registrering (Faktiske)
Fase
- Fase 2
Kontakter og plasseringer
Studiesteder
-
-
-
Amsterdam, Nederland, 1105AZ
- Academic Medical Center
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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
Andre navn:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
Andre navn:
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.
Andre navn:
|
|
Placebo komparator: 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
Andre navn:
Erlotinib will be administered at a daily dose of 100 mg at least one hour before or 2 hours after the ingestion of food
Andre navn:
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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Survival after 6 months
Tidsramme: 6 months after completion of the study
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6 months after completion of the study
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Progression free survival
Tidsramme: 6 months after the completion of the study
|
6 months after the completion of the study
|
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Objective response rate
Tidsramme: expected treatment duration 2- 6 months
|
expected treatment duration 2- 6 months
|
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toxicity profile
Tidsramme: 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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Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: Hanneke Wilmink, MD, PhD, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i fordøyelsessystemet
- Neoplasmer
- Neoplasmer etter nettsted
- Sykdommer i det endokrine systemet
- Neoplasmer i fordøyelsessystemet
- Neoplasmer i endokrine kjertel
- Pankreassykdommer
- Neoplasmer i bukspyttkjertelen
- Hypoglykemiske midler
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Anti-infeksjonsmidler
- Antivirale midler
- Enzymhemmere
- Antimetabolitter, antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Proteinkinasehemmere
- Gemcitabin
- Erlotinib hydroklorid
- Metformin
Andre studie-ID-numre
- AMCmedonc10/003
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