- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02171637
Dose Escalation Study of Oral Treatment With BIBW 2992 in Patients With Advanced Solid Tumors
20. juni 2014 oppdatert av: 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
Studieoversikt
Studietype
Intervensjonell
Registrering (Faktiske)
38
Fase
- Fase 1
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: BIBW 2992
|
escalating doses
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Maximum tolerated dose (MTD)
Tidsramme: 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
Tidsramme: up to 28 months
|
up to 28 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Area under the plasma concentration-time curve (AUC) for different time points
Tidsramme: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Predose plasma concentration (Cpre) for different time points
Tidsramme: Day 8 and 14
|
Day 8 and 14
|
|
Minimum measured plasma concentration (Cmin) for different time points
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Apparent clearance (CL/F) for different time points
Tidsramme: 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
Tidsramme: up to 384 hours after first drug administration
|
up to 384 hours after first drug administration
|
|
Accumulation ratio (RA)
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline and day 14
|
Baseline and day 14
|
|
Objective tumor responses
Tidsramme: 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
Tidsramme: up to 28 months
|
up to 28 months
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
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Hjelpsomme linker
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. november 2003
Primær fullføring (Faktiske)
1. februar 2006
Datoer for studieregistrering
Først innsendt
20. juni 2014
Først innsendt som oppfylte QC-kriteriene
20. juni 2014
Først lagt ut (Anslag)
24. juni 2014
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
24. juni 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. juni 2014
Sist bekreftet
1. juni 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 1200.1
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