A Safety and Efficacy Study of Dexmedetomidine in Patients Requiring Sedation During Monitored Anesthesia Care (MAC)

Monitored anesthesia care (MAC) is a specific anesthesia service that involves an
anesthesiologist administering sedatives and analgesics to a patient while monitoring
his/her vital signs. MAC is often used to supplement local and regional anesthesia for
non-intubated patients undergoing non-invasive procedures and minor surgery. The goal of MAC
is to relieve anxiety by inducing a minimally depressed level of consciousness while the
patient is able to continuously and independently maintain a patent airway and to respond
appropriately to verbal commands.

Respiratory depression is the major concern with most of the medications (midazolam,
fentanyl, propofol) currently used for MAC. There is clearly an unmet need for a sedative
agent that can safely be used during MAC in both healthy and high risk populations with
limited adverse side effects. A medication that can attenuate anxiety and the stress
response associated with surgery and procedures without causing respiratory depression is
highly desirable. A medication that reduces the total amount of opioids administered during
a procedure could substantially reduce complications. Such a medication could be used either
alone or in combination with other agents, thereby reducing the dose and side effects of the
other agents.

Dexmedetomidine (DEX) has sympatholytic, sedative, analgesic, and anxiolytic effects that
attenuate the catecholamine response to perioperative stress. DEX has not been associated
with respiratory depression when used alone, despite sometimes deep levels of sedation.

An estimated 325 patients (260 DEX, 65 PBO) requiring MAC sedation for an elective
surgery/procedure will be randomized at approximately 25 investigative sites.

Inclusion Criteria:

- Adult (≥18 years of age)

- American Society of Anesthesiologists (ASA) Physical Status I, II, III, or IV.

- If female, subject is non-lactating and is either:

1. Not of childbearing potential, defined as post-menopausal for at least 1 year or
surgically sterile due to bilateral tubal ligation, bilateral oophorectomy or
hysterectomy.

2. Of childbearing potential but is not pregnant at time of baseline and is
practicing one of the following methods of birth control: oral or parenteral
contraceptives, double-barrier method, vasectomized partner, or abstinence from
sexual intercourse.

- Subject requires monitored anesthesia care (MAC) in an operating room (OR) or
procedure room with an anesthesiologist in attendance.

- Subject requires one of the following types of elective surgeries/procedures expected
to take longer than 30 minutes:

- Orthopedic

- Ophthalmic

- Plastic

- Vascular stents

- Breast biopsies

- AV fistulas

- Excision of lesion.

- Subject requires local anesthetic block.

- Subject (or subject's legally authorized representative) has voluntarily signed and
dated the informed consent document approved by the Institutional Review Board.

Exclusion Criteria:

- Subject has received general anesthesia within 7 days prior to study entry, has
received any experimental drug within 30 days prior to study drug administration, or
has been previously enrolled in this study.

- Subject requires endotracheal intubation or laryngeal mask airway (LMA)

- Subject has central nervous system (CNS) disease with an anticipated potential for
increased intracranial pressure, an uncontrolled seizure disorder, and/or known
psychiatric illness that could confound a normal response to sedative treatment.

- Subject requires epidural or spinal anesthesia.

- Subject has received treatment with an alpha-2 agonist or antagonist within 14 days
of the scheduled surgery/procedure.

- Subject for whom opiates, benzodiazepines, dexmedetomidine, or other alpha-2 agonists
are contraindicated.

- Subject has received an intravenous (IV) opioid within one hour, or a by mouth
(PO)/intramuscular (IM) opioid within 4 hours, of the start of study drug
administration.

- Subject has acute unstable angina, acute myocardial infarction documented by
laboratory findings in the past 6 weeks, heart rate <50 bpm, systolic blood pressure
(SBP) <90 mmHg, or third-degree heart block unless patient has a pacemaker.

- Subject has known elevated serum glutamic pyruvic transaminase (SGPT/Alanine
aminotransferase [ALT]) and/or serum glutamic oxaloacetic transaminase
(SGOT/aspartate Aminotransferase [AST]) values of ≥2 times the upper limit of normal
within the 2 months prior to screening, and/or a history of liver failure.

- Subject has any other condition or factor which, in the Investigator's opinion, might
increase the risk to the subject.