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

19 de mayo de 2016 actualizado por: 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

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

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 de estudio

Intervencionista

Inscripción (Actual)

18

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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
Otros nombres:
  • Everolimus, RAD001, Afinitor, BIBF 1120

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
To determine the maximum tolerated dose (MTD) of RAD001 in combination with BIBF 1120 (150mg bid or 200mg bid) (endpoint: dose-limiting toxicities)
Periodo de tiempo: 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)
Periodo de tiempo: Every visit during the study
Documentation an estimation of adverse events
Every visit during the study

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
To evaluate the clinical efficacy of the combination descriptively (endpoints: RR, progression free survival (PFS), overall survival (OS))
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: Screening
Documentation of histology
Screening

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Investigador principal: Juergen Wolf, Prof., University Hospital of Cologne

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de julio de 2012

Finalización primaria (Actual)

1 de octubre de 2014

Finalización del estudio (Actual)

1 de mayo de 2016

Fechas de registro del estudio

Enviado por primera vez

5 de mayo de 2011

Primero enviado que cumplió con los criterios de control de calidad

5 de mayo de 2011

Publicado por primera vez (Estimar)

6 de mayo de 2011

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

20 de mayo de 2016

Última actualización enviada que cumplió con los criterios de control de calidad

19 de mayo de 2016

Última verificación

1 de mayo de 2016

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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