Safety and Efficacy Study of NTC-510 to Treat Pain Following Dental Surgery of Third Molars

This is a Phase 2a, randomized, double-blind, placebo-controlled, dose-ranging study to
evaluate the efficacy, concentration versus efficacy relationship, and safety of NTC-510 and
NTC-510A at doses of 2.0, 1.0, and 0.5 mg.

The study will consist of 4 phases: screening (within 28 days before check-in), check-in
(before surgery on Day 1), treatment (surgery, randomization, and treatment with study drug
on Day 1), and follow up (Days 6 to 8). During the screening phase, screening procedures
will be performed, subject eligibility will be determined, and written consent will be
obtained. Subjects will then undergo dental surgery to extract 1 or 2 third molars (with at
least 1 partial or complete bony mandibular extraction). The impaction score ([1] erupted in
tissue, [2] broken soft tissue, [3] partial bony impaction, and [4] full bony impaction)
will be collected for statistical adjustment should there be randomization imbalance. The
surgery will be conducted according to standard clinical unit procedures.

Inclusion Criteria:

- Subject is able to read, understand, and sign the approved informed consent form.

- Subject is an adult between 18 and 45 years of age, inclusive, who has been evaluated
and scheduled for an elective third molar surgical extraction (targeting 1 or 2 third
molars, at least 1 of which is mandibular and fully or partially impacted by bone).
Supernumerary or affected adjacent teeth may be removed at the surgeon's discretion.

- Subject has body mass index of 18.0 to 30.0 kg/m2, inclusive.

- Female subjects of childbearing potential must be using a medically acceptable form
of birth control for at least 1 month prior to screening (3 months on oral
contraceptives), e.g., oral or patch contraceptives, intrauterine device
(copper/hormonal), NuvaRing®, Depo-Provera®, or double-barrier method, and have a
negative pregnancy test prior to surgery. Female subjects of nonchildbearing
potential must be amenorrheic for at least 2 years or have had a hysterectomy and/or
bilateral oophorectomy.

- Subject must experience moderate to severe pain (i.e., rating of 2 or 3 on a 4-point
categorical PI scale [0 = none, 1 = mild, 2 = moderate, and 3 = severe] and a score
of ≥ 50 mm on a 100 mm VAS) within 5 hours after the dental extraction.

- Subject has been administered only 2% topical benzocaine, lidocaine with epinephrine,
and/or nitrous oxide as preoperative medication.

- Subject is determined by the investigator to be otherwise in good health and unlikely
to be at risk from participation in this study.

Exclusion Criteria:

- Female subject who is pregnant or lactating.

- Subject has a history of human immunodeficiency virus, hepatitis B, or hepatitis C
infection.

- Subject has participated in any clinical research study within the previous 8 weeks.

- Subject has a history of seizures and/or significant head trauma.

- Subject has an abnormal cardiac condition including any of the following:

- Medically significant disorders of cardiac rate and/or rhythm

- QTc interval > 450 msec (calculated using Fridericia's correction) or
uncorrected QT interval > 500 msec, PR interval > 240 msec or ≤ 110 msec,
evidence of second or third degree atrioventricular block, pathological Q-waves
(defined as Q-wave > 40 msec or depth > 0.5 mV), evidence of ventricular
pre-excitation, complete left bundle branch block, and/or resting heart rate
outside the range of 40 to 120 beats per minute

- Subject has evidence of clinically significant abnormal laboratory values including
the following:

- Impaired kidney function (i.e., serum creatinine ≥ 1.5 mg/dL)

- Impaired liver function (laboratory test values ≥ 3 times the upper limit of
normal [ULN] for aspartate aminotransferase or alanine aminotransferase, or
values > 2 times the ULN for alkaline phosphatase), or total bilirubin level >
1.5 times the ULN or, in the opinion of the investigator, liver function
impairment to the extent that the subject should not participate in this study

- Presence of Gilbert's Syndrome or any known hepatobiliary abnormalities

- Any other laboratory values judged as clinically significant by the investigator

- Subject has a history of chronic or sustained intake of opioid drugs in the preceding
12 months, or has taken any medication containing opioid compounds in the month
preceding entry to this trial.

- Subject has a history of alcohol or substance abuse or addiction within 2 years
before screening and/or routine consumption of 3 or more alcohol-containing beverages
per day. Subject has consumed alcohol within 3 days before administration of study
drug or cannot abstain for the duration of confinement to the clinical unit.

- Subject has a prior history of intolerance to opioid drugs, their excipients, or
related compounds.

- Subject has positive urine test for alcohol, cotinine, or drugs of abuse at screening
or check-in. If a subject is excluded for a positive drug screen due to prescribed
medication for pain from an infected molar, the subject may be rescreened after the
appropriate washout period.

- Subject has used any medication (with the exception of vitamins and contraceptives),
including over-the-counter medications, herbal and/or mineral supplements, dietary
supplements, or has ingested grapefruit-containing foods or beverages within 3 days
before administration of study drug, or cannot abstain for the duration of
confinement to the clinical unit.

- Subject has ingested caffeine-containing foods or beverages (e.g., coffee, tea,
chocolate, and colas) within 24 hours before administration of study drug or cannot
abstain for the duration of confinement to the clinical unit.

- Subject has smoked or used other nicotine products within 3 days before study drug
administration or cannot abstain for the duration of confinement to the clinical
unit.

- Subject has the presence of any conditions possibly affecting drug absorption (e.g.,
gastrectomy or malabsorption) or has taken oral medications that affect gastric acid
availability (including H2 antagonists, proton-pump inhibitors, and antacids) within
3 days before administration of study drug.

- Subject has any current dental or medical condition that could prevent safe
participation in this study.

- Subject has significant medical or psychiatric symptoms, cognitive impairment, or
other factors which, in the opinion of the investigator, would preclude compliance
with the protocol, adequate cooperation in the study, or obtaining informed consent.