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- Klinische proef NCT02171637
Dose Escalation Study of Oral Treatment With BIBW 2992 in Patients With Advanced Solid Tumors
20 juni 2014 bijgewerkt door: Boehringer Ingelheim
A Phase I Open Label Dose Escalation Study of Once-daily Oral Treatment With BIBW 2992 for 14 Days in Patients With Advanced Solid Tumors
Evaluation of maximum Tolerated Dose (MTD), safety, pharmacokinetics, efficacy of BIBW 2992, pharmacodynamic modulation of biomarkers, correlation of Epidermal Growth Factor Receptor (EGFR) and Human EGF-like Receptor number 2 (HER2) immunohistochemical status with objective tumour responses
Studie Overzicht
Studietype
Ingrijpend
Inschrijving (Werkelijk)
38
Fase
- Fase 1
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Male or female patients with confirmed diagnosis of advanced, non resectable and / or metastatic solid tumors, of types historically known to express EGFR and/or HER2, who have failed conventional treatment, or for whom no therapy of proven efficacy exists, or who are not amenable to established forms of treatment
- Age 18 years or older
- Life expectancy of at least three (3) months
- Written informed consent given that is consistent with International Conference on Harmonization - Good Clinical Practice (ICH-GCP) guidelines
- Eastern Cooperative Oncology Group (ECOG) performance score 0, 1, or 2
- Patients must have resolution of prior chemo-, hormone, immuno-, or radiotherapy-related toxicities to CTC Grade < 1
- Patients have to be recovered from previous surgery
- Paraffin-embedded tumor material must be accessible for analysis of EGFR and HER2-status.
- The additional 12 patients that were to be recruited at the MTD also had to fulfill the following criterion: Measurable tumor deposits (RECIST: Response Evaluation Criteria in Solid Tumors) by one or more techniques (X-ray, CT, MRI)
Exclusion Criteria:
- Active infectious disease
- Gastrointestinal disorders that might interfere with the absorption of the study drug or chronic diarrhea
- Serious illness or concomitant non-oncological disease considered by the investigator to be incompatible with the protocol
- Brain metastases requiring therapy as based on clinical symptoms
- Impaired cardiac left ventricular function with resting ejection fraction CTC Grade ≥ 1
- Absolute neutrophil count (ANC) less than 1500 / mm3
- Platelet count less than 100 000 / mm3
- Bilirubin greater than 1.5 mg / dl (> 26 μmol / L, SI unit equivalent)
- Aspartate amino transferase (AST) and / or alanine amino transferase (ALT) greater than three times the upper limit of normal (if related to liver metastases greater than five times the upper limit of normal)
- Serum creatinine greater than 1.5 mg / dl (> 132 μmol / L, SI (Systeme International) unit equivalent)
- Women and men who are sexually active and unwilling to use a medically acceptable method of contraception
- Pregnancy or breast-feeding
- Treatment with other investigational drugs; chemotherapy, immunotherapy, radiotherapy or hormone therapy (excluding LHRH agonists, other hormones taken for breast cancer, or bisphosphonates) or participation in another clinical study within the past four weeks before start of therapy or concomitantly with this study
- Patients unable to comply with the protocol
- Active alcohol or drug abuse
RETREATMENT CRITERIA
The patient may be eligible for re-treatment after the previous course finished. The patient will not be eligible if the following criteria are met.
- Patients with clinical signs of disease progression or if an X-ray, CT or MRI was done and the test showed progressive disease
- Cardiac left ventricular function CTC Grade ≥ 2 at any time during the previous course
- Patients fulfilling any of the Exclusion Criteria as mentioned under exclusion criteria on Day 29 of the previous course
- Patients not recovered from any dose-limiting toxicity (DLT) 14 days after the last administration of BIBW 2992 in the previous course. Recovery is defined as a return to baseline level or CTC Grade 1, whichever is higher
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: BIBW 2992
|
escalating doses
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Maximum tolerated dose (MTD)
Tijdsspanne: up to 28 months
|
up to 28 months
|
|
Incidence and intensity of Adverse Events (AE) according to Common Terminology Criteria for Adverse Events (CTCAE) associated with increasing doses of BIBW 2992
Tijdsspanne: up to 28 months
|
up to 28 months
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Area under the plasma concentration-time curve (AUC) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Predose plasma concentration (Cpre) for different time points
Tijdsspanne: Day 8 and 14
|
Day 8 and 14
|
|
Minimum measured plasma concentration (Cmin) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Maximum measured plasma concentration (Cmax) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Time from dosing to the minimum plasma concentration (tmin) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Time from dosing to the maximum plasma concentration (tmax) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Terminal half-life (t1/2) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Mean residence time after oral administration (MRTpo) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Apparent clearance (CL/F) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Apparent volume of distribution during the terminal phase (Vz/F) for different time points
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Accumulation ratio (RA)
Tijdsspanne: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Modulation of biomarker (EGFR, p-EGFR, p-MAPK (mitogen-activated protein kinase), p-Akt, Ki-67, p-27KIP1) in skin biopsies prior to administration of BIBW 2992 and at the end of the first treatment period
Tijdsspanne: Baseline and day 14
|
Baseline and day 14
|
|
Modulation of biomarker (EGFR, p-EGFR, HER2, p-MAPK, p-Akt, Ki-67, p-27KIP1) in tumor biopsies prior to administration of BIBW 2992 and at the end of the first treatment period in 6 or more patients treated at the MTD
Tijdsspanne: Baseline and day 14
|
Baseline and day 14
|
|
Objective tumor responses
Tijdsspanne: every 8 weeks up to 28 months
|
every 8 weeks up to 28 months
|
|
Correlation of EGFR, HER2, estrogen receptor and progesterone receptor immunohistochemical status as based on tumor biopsies or excisions obtained prior to this trial with objective tumor responses
Tijdsspanne: up to 28 months
|
up to 28 months
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Nuttige links
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 november 2003
Primaire voltooiing (Werkelijk)
1 februari 2006
Studieregistratiedata
Eerst ingediend
20 juni 2014
Eerst ingediend dat voldeed aan de QC-criteria
20 juni 2014
Eerst geplaatst (Schatting)
24 juni 2014
Updates van studierecords
Laatste update geplaatst (Schatting)
24 juni 2014
Laatste update ingediend die voldeed aan QC-criteria
20 juni 2014
Laatst geverifieerd
1 juni 2014
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 1200.1
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