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BIBF 1120 and RAD001 in Solid Tumors - Phase I (BARIS)

19 maggio 2016 aggiornato da: Prof. Dr. Juergen Wolf, University of Cologne

BARIS - BIBF1120 and RAD001 in Solid Tumors. A Phase I Trial to Evaluate the Safety and Tolerability of Combined BIBF 1120 and RAD001 in Solid Tumors and to Determine the Maximum Tolerated Dose (MTD) of the Combination

BIBF1120 and RAD001 in solid tumors

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

A phase I trial to evaluate the safety and tolerability of combined BIBF 1120 and RAD001 in solid tumors and to determine the maximum tolerated dose (MTD) of the combination

Tipo di studio

Interventistico

Iscrizione (Effettivo)

18

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • NRW
      • Cologne, NRW, Germania, 50937
        • University Hospital of Cologne

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Histologically or cytologically proven solid tumor disease after failure of standard therapy regimen(s)
  2. Age > 18 years.
  3. ECOG performance status 0 to 1.
  4. Life expectancy of at least 12 weeks.
  5. Subjects with at least one measurable (CT or MRI) lesion.
  6. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements conducted within 7 days prior to screening:

    • Hemoglobin > 9.0 g/dl
    • Absolute neutrophil count (ANC) >1,500/mm3
    • Platelet count ³ 100,000/μl
    • Total bilirubin within normal limits
    • ALT and AST < 1.5 x upper limit of normal ( or < 2.5 x upper limit of normal in patients with liver involvement)
    • PT-INR/PTT < 1.5 x upper limit of normal [Patients who are being therapeutically anticoagulated with an agent such as coumadin or heparin will be allowed to participate provided that no prior evidence of underlying abnormality in these parameters exists.]
    • Serum creatinine < 1.5 x upper limit of normal or creatinine clearance (CrCl) ≥ 50 ml/min calculated by either Cockcroft-Gault or by 24 hours urine collection
  7. More than 14 days since previous chemotherapy, radiotherapy and surgery
  8. Negative urine or serum HCG in women of childbearing potential
  9. Signed and dated informed consent before the start of specific protocol procedures

Exclusion Criteria:

  1. Limited number of prior lines of treatment (including surgery and radiotherapy, if part of the standard therapy of the respective tumor entity)
  2. Prior treatment with BIBF 1120 or any other VEGFR inhibitor (bevacizumab is allowed)
  3. Prior treatment with RAD001 or any other mTOR inhibitor
  4. Known hypersensitivity to the trial drugs, to their excipients or to contrast media
  5. Chemo-, hormono-, radio-(except for brain and extremities) or immunotherapy or therapy with monoclonal antibodies or small tyrosine kinase inhibitors within the past 2 weeks prior to treatment with the trial drugs
  6. Persistence of clinically relevant therapy related toxicity from previous chemo and/or radiotherapy
  7. Active brain metastases (e.g. stable for <4 weeks, no adequate previous treatment with radiotherapy, symptomatic, requiring treatment with anticonvulsants; dexamethasone therapy will be allowed if administered as stable dose for at least one month before trial drug administration) or leptomeningeal metastases (documented by lumbar puncture)
  8. History of cardiac disease: congestive heart failure >NYHA class 2; active coronary artery disease (CAD), (MI more than 6 mo prior to study entry is allowed); cardiac arrhythmias requiring antiarrhythmic therapy (beta blockers or digoxin are permitted) or uncontrolled hypertension
  9. Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of BIBF1120 or RAD001 (e.g. ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection)
  10. History of HIV infection or previously seropositive for the virus
  11. History of Hepatitis B or/and C or previously seropositive for the Hepatitis B or/and C virus
  12. Radiographic evidence of cavitary or necrotic tumors
  13. Centrally located tumors with radiographic evidence (CT or MRI) of local invasion of major blood vessels
  14. Treatment with other investigational drugs or treatment in another clinical trial within the past 30 days before start of therapy or concomitantly with the trial
  15. Patients with seizure disorder requiring enzyme-inducing antiepileptics
  16. Therapeutic anticoagulation (except low-dose heparin and/or heparin flush as needed for maintenance of an indwelling intravenous devise) or antiplatelet therapy (except for low-dose therapy with acetylsalicylic acid ≤325mg per day)
  17. Major injuries within the past 10 days prior to start of study treatment with incomplete wound healing and/or planned surgery during the on-treatment study period
  18. Evidence or history of bleeding diasthesis or thrombosis, and known inherited predisposition to bleeding or thrombosis
  19. Proteinuria CTC AE grade 2 or greater
  20. Active serious infections
  21. Patients undergoing renal dialysis
  22. Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors [Ta, Tis & T1] or any cancer curatively treated > 3 years prior to study entry
  23. Serious illness or concomitant non-oncological disease such as neurologic, psychiatric, infectious disease or active ulcers (gastrointestinal tract, skin) or laboratory abnormality that may increase the risk associated with study participation or study drug administration and in the judgment of the investigator would make the patient inappropriate for entry into the study
  24. Patients who are sexually active and unwilling to use a medically acceptable method of contraception (e.g. such as implants, injectables, combined oral contraceptives, some intrauterine devices or vasectomized partner for participating females, condoms for participating males) during the trial and for at least three months after end of active therapy
  25. Pregnancy or breast feeding
  26. Psychological, familial, sociological or geographical factors potentially hampering compliance with the study protocol and follow-up schedule
  27. Active alcohol or drug abuse

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: BIBF 1120 + RAD001
Dose level 1: 1x 5mg Everolimus/d + 2x 150mg BIBF 1120/d. Dose level 2: 1x 5mg Everolimus/d + 2x 200mg BIBF 1120/d. Dose level 3: 1x 10mg Everolimus/d + 2x 200mg BIBF 1120/d
Altri nomi:
  • Everolimus, RAD001, Afinitor, BIBF 1120

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To determine the maximum tolerated dose (MTD) of RAD001 in combination with BIBF 1120 (150mg bid or 200mg bid) (endpoint: dose-limiting toxicities)
Lasso di tempo: Every visit
Documentation an estimation of adverse events
Every visit
To evaluate the tolerability of BIBF1120 and RAD001 in combination (endpoints: assessment of adverse events (AEs) according to CTC-AE V4.0)
Lasso di tempo: Every visit during the study
Documentation an estimation of adverse events
Every visit during the study

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To evaluate the clinical efficacy of the combination descriptively (endpoints: RR, progression free survival (PFS), overall survival (OS))
Lasso di tempo: Baseline and every six weeks during the study, after study every 6 months

CT will be done for evaluation of RR and PFS on day 57 and then every 6 weeks until progression.

For overall survival a telephone call every six months after study is continuation will be done

Baseline and every six weeks during the study, after study every 6 months
To analyze individual BIBF1120 pharmacokinetic (PK) parameters at steady-state (ss) of monotherapy and PK parameters of both BIBF1120 and RAD001 at ss of combination
Lasso di tempo: day 14, day 29
Blood collection for pharmacokinetic analysis
day 14, day 29
To assess changes in tumor vasculature a) early under BIBF1120 monotherapy, b) at ss of BIBF1120 monotherapy and c) at ss of combination therapy using dynamic contrast-enhanced MRI (DCE-MRI) (endpoints: IAUC, Ktrans, Kep, Ve)
Lasso di tempo: baseline, day 3, day 14, day 29
DCE MRI will be done
baseline, day 3, day 14, day 29
To correlate the clinical outcome with FGFR1-amplification status (endpoints: see above for clinical parameters)
Lasso di tempo: Screening
Documentation of histology
Screening

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Collaboratori

Investigatori

  • Investigatore principale: Juergen Wolf, Prof., University Hospital of Cologne

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 luglio 2012

Completamento primario (Effettivo)

1 ottobre 2014

Completamento dello studio (Effettivo)

1 maggio 2016

Date di iscrizione allo studio

Primo inviato

5 maggio 2011

Primo inviato che soddisfa i criteri di controllo qualità

5 maggio 2011

Primo Inserito (Stima)

6 maggio 2011

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

20 maggio 2016

Ultimo aggiornamento inviato che soddisfa i criteri QC

19 maggio 2016

Ultimo verificato

1 maggio 2016

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Tumori solidi

Prove cliniche su Everolimus + BIBF 1120

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