Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT02926222 : Regorafenib in Relapsed Glioblastoma
PhasePhase 2
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

- Male or female ? 18 years of age

- Histologically confirmed de novo glioblastoma multiforme (grade IV)

- First recurrence after adjuvant treatment (surgery followed by radiotherapy and
temozolomide chemotherapy with or without bevacizumab) in patients who have not
received further therapeutic interventions

- For patients not undergoing a second surgery at the time of relapse, recurrent
disease must include at least one bi?dimensionally measurable contrast?enhancing
lesion with clearly defined margins by MRI scan, with minimal diameters of 10 mm,
visible on 2 or more axial slices 5 mm apart, based on an MRI scan done within 2
weeks prior to randomization

- Documented progression of disease as defined by RANO criteria at least 12 weeks after
completion of radiotherapy, unless the recurrence is outside the radiation field or
has been histologically documented

- Have adequate bone marrow function, liver function, and renal function, as measured
by the following laboratory assessments conducted within 7 days prior to the
initiation of study treatment:

- Hemoglobin >9.0 g/dl

- Absolute neutrophil count (ANC) >1500/mm3 without transfusions or granulocyte
colony stimulating factor and other hematopoietic growth factors

- Platelet count ?100,000/?l

- White blood cell count (WBC) >3.0 x 109/L

- Total bilirubin <1.5 times the upper limit of normal

- ALT and AST <3 x upper limit of normal (<5 x upper limit of normal for patients
with liver involvement of their cancer and/or have bone metastasis)

- Serum creatinine <1.5 x upper limit of normal

- Alkaline phosphatase <2.5 x ULN (<5 x upper limit of normal for patients with
liver involvement of their cancer and/or have bone metastasis)

- 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 per medical history)

- Lipase ? 1.5 x the ULN

- Glomerular filtration rate ? 30 mL/min/1.73 m2 according to the Modified Diet in
Renal Disease abbreviated formula

- Analyses of MGMT methylation status on tumoral tissue at first surgery (at own
institution)

- Understand, be willing to give consent, and sign the written informed consent form
(ICF) prior to undergoing any study-specific procedure

- If female and of childbearing potential, have a negative result on a pregnancy test
performed a maximum of 7 days before initiation of study treatment

- If female and of childbearing potential, or if male, agree to use adequate
contraception (eg, intrauterine device, oral contraceptive, or double-barrier method)
based on the judgment of the investigator or a designated associate from the date on
which the ICF is signed until 8 weeks after the last dose of study drug

- World Health Organization (WHO) Performance status ? 1 (or Karnofsky performance
status (KPS) ?70)) within 14 days prior to the initiation of study treatment

- Stable or decreasing dosage of steroids for 7 days prior to the baseline MRI scan.

- Patients may have undergone surgery for the recurrence; the histological report must
document a glioblastoma recurrence. If operated:

- at least 28 days and maximum 42 days interval from the surgery is required prior
to administration of study drugs and patients should have fully recovered

- Exclusion Criteria:

- Are taking strong cytochrome P (CYP) CYP3A4 inhibitors (eg, clarithromycin,
indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, posaconazole,
ritonavir, saquinavir, telithromycin, voriconazole) or strong CYP3A4 inducers (eg,
carbamazepine, phenobarbital, phenytoin, rifampin, St. John's Wort)

- Radiotherapy within 12 weeks prior to the diagnosis of progression, if the lesion is
in the radiation field,

- Have had systemic anticancer therapy including cytotoxic therapy, signal transduction
inhibitors, immunotherapy, and/or hormonal therapy within 4 weeks prior to initiation
of study treatment

- Positioning of carmustin wafers during first or second surgery

- Other active or inactive malignancy (except for carcinoma in situ of the cervix, of
the prostate or basal cell carcinoma). Malignancy will be considered inactive if
patients are in complete remission for at least 3 years prior to study entry

- Have had prior treatment with regorafenib or any other VEGFR-targeting kinase
inhibitor

- Have had a major surgical procedure, open biopsy, or significant traumatic injury
within 28 days prior to initiation of study treatment

- Are pregnant

- Are breastfeeding

- Are unable to swallow oral tablets (crushing of study treatment tablets is not
allowed)

- Have congestive heart failure classified as New York Heart Association Class 2 or
higher

- Have had unstable angina (angina symptoms at rest) or new-onset angina ? 3 months
prior to screening.

- Have had a myocardial infarction < 6 months prior to initiation of study treatment

- Have cardiac arrhythmias requiring anti-arrhythmic therapy, with the exception of
beta blockers or digoxin

- Have uncontrolled hypertension (systolic blood pressure [SBP] > 140 mmHg or diastolic
blood pressure [DBP] > 90 mmHg) despite optimal medical management

- Have had arterial thrombotic or embolic events such as cerebrovascular accident
(including transient ischemic attacks), or pulmonary embolism within 6 months prior
to the initiation of study treatment

- Have an ongoing infection with severity of Grade 2 or above (NCI-CTCAE v 4.0)

- Have a known history of human immunodeficiency virus infection

- Have either active or chronic hepatitis B or C requiring treatment with antiviral
therapy

- Have a history of organ allograft

- Have evidence or history of any bleeding diathesis (including mild hemophilia),
irrespective of severity

- Have had a hemorrhage or a bleeding event ? Grade 3 (NCI-CTCAE v 4.0) within 4 weeks
prior to the initiation of study treatment

- Have a non-healing wound, ulcer, or bone fracture

- Have renal failure requiring hemodialysis or peritoneal dialysis

- Have dehydration ? Grade 1 (NCI-CTCAE v 4.0)

- Have interstitial lung disease with ongoing signs and symptoms at the time informed
consent is obtained

- Have persistent proteinuria > 3.5 g/24 hours measured by urine protein creatinine
ratio from a random urine sample (Grade 3, NCI-CTCAE v 4.0)

- Have any other serious or unstable illness, or medical, psychological, or social
condition, that could jeopardize the safety of the subject and/or his/her compliance
with study procedures, or may interfere with the subject's participation in the study
or evaluation of the study results

- Have a known hypersensitivity to any of the study drugs, study drug classes, or
excipients in the formulation of the study drugs

- Have any malabsorption condition

- Recurrent disease located outside of the brain
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT02926222      |      Link to official Clinicaltrials.gov listing
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