- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02182141
An Dose Escalation Study of BIBF 1120 Administered in Patients With Relapsed or Refractory Multiple Myeloma
17. juli 2014 opdateret af: Boehringer Ingelheim
An Open Label Dose Escalation Study of BIBF 1120 Administered Orally for Four Weeks in Patients With Relapsed or Refractory Multiple Myeloma With Repeated Administration in Patients With Clinical Benefit
Maximum tolerated dose (MTD), safety, pharmacokinetics, efficacy of BIBF 1120, pharmacodynamics
Studieoversigt
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
17
Fase
- Fase 1
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Patients with confirmed diagnosis of multiple myeloma, who did not respond to or relapsed after either anthracyclines and pulsed glucocorticoids or high-dose therapy and who are currently not eligible for transplant modalities.
- Age 18 years or older
- Life expectancy of at least six months
- Patients have to give written informed consent (which must be consistent with ICH-GCP and local legislation)
- Eastern Cooperative Oncology Group (ECOG) performance score <2.
- Recovery from all therapy-related toxicities from previous chemo-, immuno- or radiotherapies.
Exclusion Criteria:
- History of relevant surgical procedures during the last four weeks prior to treatment with the trial drug, or active ulcers, fractures or injuries with incomplete healing
- Active infectious disease
- Uncontrolled, severe hypertension
- Gastrointestinal disorders anticipated to interfere with the resorption of the study drug
- Serious illness or concomitant non-oncological disease considered by the investigator to be incompatible with the protocol
- Absolute neutrophil count less than 1000 / mm³.
- Platelet count less than 30 000 / mm³
- Conjugated Bilirubin greater than 2 mg / dl (> 34 μmol/L, SI unit equivalent)
- Aspartate amino transferase (AST) and / or alanine amino transferase (ALT) greater than three times the upper limit of normal
- Endogenous creatinine clearance (ECC) <20 ml/min
- Women and men who are sexually active and unwilling to use a medically acceptable method of contraception
- Pregnancy or breastfeeding
- Treatment with other investigational drugs or participation in another clinical trial within the past four weeks before start of therapy or concomitantly with this trial (except for present trial drug)
- Patients unable to comply with the protocol
- Active alcohol or drug abuse
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: BIBF 1120
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Maximum tolerated dose (MTD)
Tidsramme: Up to 11 months
|
Up to 11 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Incidence and intensity of adverse events according to Common Toxicity Criteria (CTC) associated with increasing doses of BIBF 1120
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Change from baseline in laboratory parameters
Tidsramme: Baseline, up to 11 months
|
Baseline, up to 11 months
|
|
Objective tumor response in surrogate markers
Tidsramme: Baseline, up to 11 month
|
Baseline, up to 11 month
|
|
Concentration at 2h (C2,1)
Tidsramme: 2 hours after first administration
|
2 hours after first administration
|
|
Change from baseline in cellular protein tyrosine kinase inhibition
Tidsramme: Baseline, up to 11 months
|
Baseline, up to 11 months
|
|
Change from baseline in Eastern Cooperative Oncology Group (ECOG) performance score
Tidsramme: Baseline, up to 11 months
|
Baseline, up to 11 months
|
|
Change in vital signs
Tidsramme: up to 11 months
|
up to 11 months
|
|
Change from baseline in electrocardiogram (ECG)
Tidsramme: Baseline, up to 11 months
|
Baseline, up to 11 months
|
|
Predose concentration immediately before administration of the Nth dose over the dosing interval τ (Cpre,N)
Tidsramme: Up to day 28
|
Up to day 28
|
|
Area under the plasma concentration-time curve during the dosing interval τ (24 h) at steady state (AUCτ,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Plasma concentration at the time point immediately before dosing at steady state (Cpre,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Minimum plasma concentration during the dosing interval τ at steady state (Cmin,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Maximum plasma concentration during the dosing interval τ at steady state (Cmax,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Time to reach minimum plasma concentration during the dosing interval τ at steady state (tmin,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Time to reach maximum plasma concentration during the dosing interval τ at steady state (tmax,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Terminal half-life at steady state (t1/2,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Apparent plasma clearance at steady state (CL/F,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Mean residence time at steady state (MRTpo,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Apparent volume of distribution during the terminal phase at steady state (Vz/F,ss)
Tidsramme: Up to 11 months
|
Up to 11 months
|
|
Tumor response assessed according to the European Group for Blood and Marrow Transplantation (EBMT) criteria
Tidsramme: Up to 11 months
|
Up to 11 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Hjælpsomme links
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2003
Primær færdiggørelse (Faktiske)
1. marts 2005
Datoer for studieregistrering
Først indsendt
2. juli 2014
Først indsendt, der opfyldte QC-kriterier
7. juli 2014
Først opslået (Skøn)
8. juli 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
18. juli 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
17. juli 2014
Sidst verificeret
1. juli 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Karsygdomme
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- Myelomatose
- Neoplasmer, Plasmacelle
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Proteinkinasehæmmere
- Nintedanib
Andre undersøgelses-id-numre
- 1199.2
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .