TAU-2014-1: Mibefradil and Hypofractionated Re-Irradiation Therapy in Recurrent GBM

Glioblastoma Multiforme (GBM) Clinical Trial

Official title:

TAU-2014-1: Phase I Trial of Mibefradil Dihydrochloride With Hypofractionated Re-Irradiation Therapy in Treating Patients With Recurrent Glioblastoma Multiforme (GBM)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02202993
• Other study ID #: 1406014067
• Status: Completed
• Phase: Phase 1
• Start date: August 2014
• Est. completion date: September 29, 2017

Study information

• Verified date: April 2019
• Source: Cavion, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a dose-escalation study that will assess the safety and determine the maximum tolerated dose (MTD) of mibefradil dihydrochloride, a partially selective T-type calcium channel blocker, combined with hypofractionated radiation therapy (RT) in subjects with recurrent glioblastoma multiforme (GBM).

Description:

Patients will receive mibefradil dihydrochloride, which will be dose escalated from 150mg/day until the maximum tolerated dose (MTD) is determined, or until a dose of 350 mg/day is reached using a standard 3 + 3 design. Mibefradil dihydrochloride will be dosed orally in 4 divided doses per day for 17 consecutive days to the MTD. The MTD will be determined according to dose-limiting toxicities (DLTs) graded using the Common Terminology Criteria for Adverse Events version 4.0. Radiation therapy (RT) consists of 5 fractions of 600 centigray (cGy) each, delivered over 2 consecutive weeks for a total dose of 3,000 cGy, using stereotactic, intensity-modulated radiation therapy (IMRT).

The primary endpoint of the study is to determine the MTD of mibefradil dihydrochloride when given with concurrent hypofractionated RT. Secondary and tertiary endpoints include evaluating the efficacy of mibefradil dihydrochloride and RT in terms of progression-free survival (PFS) and overall survival (OS), and to perform translational research on resected tumor tissue.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: September 29, 2017
• Est. primary completion date: September 29, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Sign written informed consent.

• Histologically proven glioblastoma multiforme (GBM) that is progressive or recurrent following standard radiation therapy (RT) and temozolomide (i.e., at least "biopsy-proven" recurrent disease). Previous salvage therapies after first recurrence are permitted.

• Measurable contrast-enhancing progressive or recurrent GBM (single or multiple lesions) by MRI imaging with an interval of greater than or equal to 6 months between recurrence and completion of prior radiotherapy.

• Patients who have not passed an interval of at least 6 months may still be eligible if they meet the following criteria: convincing histologic evidence of disease recurrence which is not thought to predominantly represent radionecrosis, standard focal external beam radiation therapy (EBRT) treatment with acceptable doses to tumor and normal tissue which suggest re-irradiation is feasible.

• Prior history of standard dose focal RT to 60 Gy in 30 fractions or 59.4 Gy in 1.8 Gy fractions, or equivalent or lower doses. Patients who have received prior treatment with non-standard RT dose and fractionation schemes are still eligible, provided they have only received a single course of RT. However, subjects treated with interstitial brachytherapy or single-fraction stereotactic radiosurgery are not eligible for this trial.

• Karnofsky performance status =60%

• Clinical laboratory:

• absolute neutrophil count >1,500/microliter (mcL)

• platelets >100,000/mcL

• hemoglobin > 9 g/ dL serum bilirubin < 1.5 times the upper limit of normal (ULN); unless due to Gilbert's syndrome (in which <2 times ULN acceptable)

• serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) < 2.5 times ULN

• serum Creatinine < 1.5 times ULN

• Women of childbearing potential and men must agree to use adequate contraception.

• Women of childbearing potential must have a negative pregnancy test prior to treatment.

• Recovered to Common Toxicity Criteria for Adverse Effects (CTCAE) grade = 2 from prior therapy toxicities

• 30 days since previous treatment of brain tumor with any other agents.

• Stable or decreasing corticosteroid regimen (no increase for 7 days) prior to the start of treatment.

• >18 years of age

Exclusion Criteria:

• Concurrent malignancy except curatively treated non-melanoma skin cancer or carcinoma in situ of the cervix, breast, or bladder. Subjects with prior malignancies must be disease-free for = five years.

• Biopsy-confirmed exclusive radionecrosis after initial GBM therapy.

• Receipt of other investigational agents or anti-cancer agents within 30 days

• Serious concurrent infection or medical illness, which would jeopardize the ability of the subject to receive treatment safely.

• Systolic blood pressure <100 mm Hg, diastolic <60 mm Hg.

• Requirement for calcium channel blocker for blood pressure control that cannot be switched to an antihypertensive with an alternative mechanism of action. Permitted anti-hypertensive medications include: chlorothiazide, hydrochlorothiazide, atenolol, nadolol, enalapril, lisinopril, eprosartan, and irbesartan.

• Known, active hepatitis.

• corrected QT (QTc) interval = 450 milliseconds (mSec) for males or =470 mSec for females. PR interval > 250 mSec for males and females

• High-grade (second degree or above) atria-ventricular (AV) block or persistent sinus bradycardia of less than 50 beats per minute (BPM).

• Known HIV-positivity

• Pregnant and/or lactating women

• Anti-arrhythmia medication other than beta-blockers or digoxin.

• Treatment with concurrent enzyme-inducing anti-epileptic drugs (EIAEDs).

• Treatment with unfractionated heparin. Patients taking an anticoagulant must use warfarin or a low molecular weight heparin.

• Treatment with specified drugs that are substrates of cytochrome 3A4 (CYP3A4), cytochrome 2D6 (CYP2D6), cytochrome 1A2 (CYP1A2)

Related Conditions & MeSH terms

• Glioblastoma
• Glioblastoma Multiforme (GBM)

Intervention

Drug:
• Mibefradil with Radiation
Patients will receive mibefradil dihydrochloride, which will be dose escalated from 150mg/day until the maximum tolerated dose (MTD) is determined, or until a dose of 350 mg/day is reached using a standard 3 + 3 design. Mibefradil dihydrochloride will be dosed orally in 4 divided doses per day for 17 consecutive days to the MTD. This will be given concurrently with hypofractionated radiation therapy.

Locations

Country	Name	City	State
United States	Yale University	New Haven	Connecticut

Sponsors (2)

Lead Sponsor	Collaborator
Cavion, Inc.	Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Intra-tumoral concentration of mibefradil dihydrochloride		27 months
Other	Western blot characterization of resected tumor tissue following 5 days of mibefradil dihydrochloride		27 months
Primary	Dose limiting toxicities		Monitored continuously, 27 months
Primary	Maximum tolerated dose		Monitored continuously, 27 months
Secondary	Adverse events		27 months
Secondary	Mibefradil dihydrochloride steady state plasma concentrations		27 months
Secondary	Progression-free survival of treated patients		27 months
Secondary	Overall survival of treated patients		27 months