Safety Study of Mibefradil When Given Four Times a Day in Healthy Volunteers

This study will establish the safety, detailed pharmacokinetics, and, possibly, maximum
tolerated dose (MTD) of ascending doses of mibefradil administered four times a day (QID) in
healthy volunteers. The knowledge gained will then guide the details of a study of Interlaced
Therapy™ in patients with recurrent High Grade Glioma (HGG). Non-clinical studies are
currently on-going in the efficacy of Interlaced Therapy™ in ovarian cancer, pancreatic
cancer, and intracranial malignancy.

Inclusion Criteria:

1. Normal healthy volunteers aged 19 to 55 years, male or female, and willing and able to
sign informed consent;

2. Females must have a negative pregnancy test at screening and be practicing a suitable
method of birth control so that, in the opinion of the Investigator, they will not
become pregnant during the course of the study, or females can be postmenopausal (no
menstrual period for one year) or surgically sterilized. Females must either be
sexually inactive (abstinent) for 14 days prior to Screening and remain so through 30
days following the final dosing of the study drug or have been using one of the
following acceptable methods of birth control for the times specified:

- Barrier method (condom or diaphragm) with spermicidal for at least 14 days prior
to Screening through Day -1 through 30 days following the final dosing of the
study drug;

- Surgical sterilization (vasectomy) of partner at least 6 months prior to Day -1;
or

- Females of non-childbearing potential have undergone one of the following
sterilization procedures at least 6 months prior to Day -1: bilateral tubal
ligation, hysterectomy, hysterectomy with unilateral or bilateral oophorectomy,
or bilateral oophorectomy.

3. Male subjects must continue to use their approved contraceptive method for 60 days
after participating in the study.

4. Has a body mass index (BMI) between 18.0 and 32.0 kg/m², inclusive; and

5. Have no acute illnesses or chronic health issues that require medication.

Exclusion Criteria:

1. History of investigational drug use within 30 days of this study;

2. Subject has a clinically significant disorder that, in the opinion of the
Investigator, could result in the subject's inability to understand and comply with
the requirements of the study;

3. History of hypertension, treated or untreated, or screening BP >140 mm Hg systolic or
>90 mm Hg diastolic;

4. Currently or within the last 14 days taking any medications (prescription,
nonprescription, or herbal or Chinese remedies) including oral contraceptives and
hormone replacement therapy;

5. Subject has a history of impaired hepatic function that, in the Investigator's
opinion, contraindicates participation in this study; or the subject has any other
abnormal laboratory value of clinical significance for this study in the Investigators
opinion;

6. Current smoker (more than 10 cigarettes/day) for 6 months;

7. Subject has a creatinine clearance (CLcr) of less than 70 mL/min as calculated by the

Cockroft-Gault equation:

CLcr = ((140 - age) x body mass x [0.85 if female]) / (72 x creatinine)

where age is given in years, body mass is given in kg, and creatinine is given in
mg/dL;

8. Subject has a history, signs, or symptoms of ischemic cardiac, cerebrovascular, or
peripheral vascular syndromes or other significant underlying cardiovascular disease
that are clinically significant in the Investigator's opinion. This includes any known
cardiac rhythm disorder or ECG abnormality;

9. Subject, in the Investigator's opinion, is likely to have unrecognized cardiovascular
disease, based on history or the presence of risk factors;

10. Subject is currently taking or had taken in the previous 14 days, herbal preparations
containing St. John's Wort (Hypericum perforatum);

11. Subject has a history of allergic reactions to calcium channel antagonists;

12. Females who are pregnant, actively trying to become pregnant, or lactating. Females
must be practicing a suitable method of birth control (adequate barrier method of
birth control; abstinence) so that, in the opinion of the Investigator, they will not
become pregnant during the course of the study, or females can be postmenopausal (no
menstrual period for one year) or surgically sterilized;

13. Subject had a recent history (in the past 3 months) suggestive of evidence of alcohol
or drug abuse or dependence, or has any unaccounted-for drug or alcohol in the
original drug screen (tested positive);

14. Allergy to latex or rubber;

15. Hemoglobin under laboratory lower limit of normal; or

16. Significant blood loss of 500 mL or greater or blood donation within 56 days prior to
Day 1. Subjects cannot donate plasma within 5 days prior to Day 1.