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Status:

TERMINATED

Study of LBH589 (Panobinostat) to Treat Malignant Brain Tumors

Lead Sponsor:

Neurological Surgery, P.C.

Conditions:

Recurrent Malignant Gliomas

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The drug LBH589 (panobinostat) is an experimental (investigational) drug that is being tested for recurrent (returning) malignant gliomas. An investigational drug is one that has not been approved by ...

Detailed Description

The prognosis for recurrent malignant gliomas remains dismal despite advances in neurological surgery, radiation oncology and chemotherapy. Median overall survival remains a mere 14.6 months and 2 yr ...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Recurrent malignant glioma with radiographic progression
  • No more than three prior therapies.
  • Male or female patients \>=18 years old
  • KPS \>=60.
  • Ability to provide written informed consent or consent obtained from responsible healthcare proxy.
  • Contrast-enhanced MRI within 2 weeks of enrollment.
  • Life expectancy \>= 8 weeks
  • Neutrophils \>1500/mm3
  • Platelets \> 100,000/mm3L
  • Hemoglobin \>=9 g/dL
  • AST/SGOT and ALT/SGPT \<= 2.5 x upper limit of normal (ULN) or \< 5.0 x ULN if the transaminase elevation is due to disease involvement
  • Serum bilirubin \<= 1.5 x ULN
  • Serum creatinine \<= 1.5 x ULN or 24-hour creatinine clearance \>= 50 ml/min
  • Total serum calcium or ionized calcium WNL
  • Serum potassium WNL
  • Serum sodium WNL
  • Serum albumin \>= LLN or 3g/dl
  • Elevated Alkaline Phosphatase due to bone metastasis can be enrolled
  • Baseline MUGA or ECHO must demonstrate LVEF \>= the LLN
  • TSH and free T4 WNL (patients may be on thyroid hormone replacement)
  • Women of childbearing potential (WOCBP) must have a negative serum pregnancy test within 7 days of the first administration of study treatment and must be willing to use two methods of contraception one of them being a barrier method during the study and for 3 months after last study drug administration.
  • No concurrent antitumor therapy.
  • No enzyme-inducing antiepileptic drugs.
  • No significant comorbidities
  • Patients must have recovered from toxic effects of prior therapy.
  • Exclusion criteria
  • Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer
  • Valproic acid for any medical condition during the study or within 5 days prior to first LBH589 treatment
  • Impaired cardiac function including:
  • Screening ECG with a QTc \> 450 msec
  • Congenital long QT syndrome
  • History of sustained ventricular tachycardia
  • History of ventricular fibrillation or torsades de pointes
  • Bradycardia \< 50 beats per minute. Patients with a pacemaker and heart rate \> = 50 beats per minute are eligible.
  • Myocardial infarction or unstable angina within 6 months
  • Congestive heart failure (NYHA class III or IV)
  • RBBB and LAH (bifascicular block)
  • Uncontrolled hypertension
  • Concomitant use of drugs with a risk of causing torsades de pointes Concomitant use of CYP3A4 inhibitors
  • Patients with unresolved diarrhea
  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter absorption of LBH589
  • Concurrent severe and/or uncontrolled medical conditions
  • Chemotherapy, any investigational drug or major surgery \< 4 weeks prior to starting study drug or have not recovered from side effects of such therapy.
  • Concomitant use of any anti-cancer therapy or radiation therapy.
  • Women who are pregnant or breast feeding or women of childbearing potential (WOCBP) not willing to use a double barrier method of contraception during the study and 3 months after the end of treatment. One of these methods of contraception must be a barrier method.
  • Male patients whose sexual partners are WOCBP not using a double method of contraception during the study and 3 months after the end of treatment. One of these methods must be a condom
  • History of another primary malignancy within 5 years other than curatively treated CIS of the cervix, or basal or squamous cell carcinoma of the skin
  • Known human immunodeficiency virus (HIV) or hepatitis C positivity
  • Significant history of non-compliance to medical regimens or inability to grant a reliable informed consent
  • More than three prior therapies
  • Hepatic or renal diseases or any diseases that will obscure toxicity or alter drug metabolism
  • Known active malignancies
  • Active infection requiring iv antibiotics
  • Systemic anticoagulants
  • Enzyme-inducing antiepileptic drugs

Exclusion

    Key Trial Info

    Start Date :

    November 1 2008

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    April 1 2009

    Estimated Enrollment :

    6 Patients enrolled

    Trial Details

    Trial ID

    NCT00848523

    Start Date

    November 1 2008

    End Date

    April 1 2009

    Last Update

    July 16 2010

    Active Locations (2)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (2 locations)

    1

    Long Island Brain Tumor Center at Neurological Surgery PC / Long Island Neuro-Oncology Associates

    Commack, New York, United States, 11725

    2

    Long Island Brain Tumor Center at Neurological Surgery PC / Long Island Neuro-Oncology Associates

    Great Neck, New York, United States, 11021