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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

Toestand

Voltooid

Conditie

Interventie / Behandeling

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.

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

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