Study of Levotofisopam 50 mg Three Times a Day (TID) Administered for 7 Days on Hyperuricemia and Gout

The primary objectives of this study are (1) to evaluate the safety and tolerability of
levotofisopam in patients with hyperuricemia and gout, and (2) to evaluate the effect of
treatment with levotofisopam on serum urate levels in these patients.

Inclusion Criteria:

- Provide voluntary, signed informed consent.

- Male or postmenopausal or surgically sterile females, 18 to 65 years of age,
inclusive. Female participants must have been amenorrheic for a minimum of 12 months
and must have a negative pregnancy test result within 3 days before administration of
levotofisopam. Surgically sterile females are defined as those who have had a
hysterectomy, bilateral ovariectomy, or bilateral tubal ligation. Male subjects must
agree to practice a medically acceptable form of contraception for the duration of
the study and for 30 days after receiving the last dose of levotofisopam.

- Physician diagnosis of gout with at least one gout flare in the last 6 months, at
least one chronically swollen joint due to gout, or presence of a tophus.

- Serum urate level ≥ 8.0 mg/dL and ≤ 12.0 mg/dL after having stopped all
urate-lowering therapy for at least 10 days. Serum urate level must also be > 7.7
mg/dL and ≤ 12.0 mg/dL on Day -3 and on Day -2.

- Willing and able to discontinue urate-lowering therapy starting at the screening
visit (14-21 days before receiving study drug) through to the follow-up visit (up to
10 days after discharge from the study unit), for a total time off urate-lowering
therapy of up to approximately 5 weeks.

- In the opinion of the investigator, able to participate in all scheduled evaluations,
likely to complete all required tests, and likely to be compliant.

- Medications permitted for the treatment of non-excluded medical conditions (other
than gout) must be at stable doses for at least 14 days prior to baseline.

- Permitted concurrent general medical conditions must be stable and well controlled.

- Written and oral fluency in the English language.

Exclusion Criteria:

- Previous treatment with racemic tofisopam (RS-tofisopam), levotofisopam
(S-tofisopam), or dextofisopam (R-tofisopam).

- Known or suspected hypersensitivity to any benzodiazepine.

- History of two or more clinically significant drug allergies.

- Clinically significant infection within 30 days prior to screening or between screen
and admission.

- History or presence of clinically significant medical disease that might compromise
the study or be detrimental to the patient, such as hepatitis (patient excluded if
hepatitis A was present within 2 years before screening or if there is any history of
hepatitis B or C), human immunodeficiency virus (HIV) infection, uncontrolled
diabetes mellitus, cirrhosis, active biliary disease (bile ducts or gallbladder), or
moderate or severe chronic kidney disease (estimated glomerular filtration rate < 60
mL/min/1.73 m2).

- Presence of a gout flare during screening or the procedure window.

- History or presence of nephrolithiasis.

- History or presence of malignancy other than localized basal cell cancer, squamous
cell skin cancer, or cancer in situ that has been resected within 5 years.

- Clinically significant head trauma with loss of consciousness within 10 years prior
to screen.

- Myocardial infarction, congestive heart failure, or known coronary artery disease
within 5 years prior to screen.

- Any history of cerebrovascular accident.

- History of seizure disorder other than a single childhood febrile seizure.

- Alcohol or psychoactive substance abuse or dependence, as defined by DSM-IV, within 1
year prior to screen, or alcohol use exceeding 21 units per week (on average) in the
3 months preceding screen.

- Used any tobacco- or nicotine-containing product more days than not within 30 days
prior to screening or between screen and admission.

- Regular consumption (e.g., more days than not) of excessive quantities of
caffeine-containing beverages (e.g., more than eight cups of coffee or equivalent per
day) within 30 days prior to screening or between screen and admission.

- History of suicide attempt, any suicidal behavior within 6 months prior to screening
or between screen and baseline, or, in the opinion of the investigator, clinically
significant risk of suicide or violent behavior.

- History or presence of a clinically significant psychiatric disorder or symptom
(e.g., delusions, hallucinations) that is likely to compromise the study (e.g.,
confound study results) or be detrimental to the patient.

- History of difficulty donating blood, or history or presence of clinically
significant bleeding or hemorrhagic tendencies.

- Donation of blood or plasma within 90 days prior to screening or between screening
and admission.

- Uncontrolled hypertension (systolic blood pressure > 160 mmHg and/or diastolic > 95
mmHg) or heart rate either < 50 BPM or > 100 BPM at any evaluation prior to the first
dose of test drug.

- Pregnancy, lactation, a positive pregnancy test result during the screening or
admission evaluation.

- A clinically significant abnormality on the screening physical examination, 12-lead
electrocardiogram (ECG), or laboratory evaluations.

- A corrected QT (QTcF) value > 450 msec (males) or > 470 msec (females) at screening,
admission (Day -3), or baseline (Day -1).

- Aspartate aminotransferase or alanine aminotransferase levels > 2 times upper limit
of normal (ULN), alkaline phosphatase > 1.5 times ULN, creatinine outside the limits
of normal, triglycerides > 500 mg/dL, or thyroid-stimulating hormone (TSH) levels
greater than 6.0 µIU/L at screening, admission (Day -3), or Day -2.

- A finding of opiates, amphetamines, cocaine, cannabis, or phencyclidine on the urine
drug screen (UDS). Any other positive UDS result must be discussed by the
investigator and medical monitor prior to potentially allowing participation of the
subject in the study.

- A positive HIV, hepatitis B, or hepatitis C test.

- Inability to take or tolerate colchicine for gout flare prophylaxis (0.6 mg QD or
BID).

- Required use of any of the following from the screening visit through the follow-up
visit: aspirin or other nonsteroidal antiinflammatory drugs (other than paracetamol,
as noted below), diuretics, medications with known urate-lowering effects (including,
but not limited to, fenofibrate, losartan, or vitamin C > 500 mg/day), or
urate-lowering therapy other than levotofisopam.

- Dietary requirements inconsistent with the study unit's standardized diet.

- Body mass index ≥ 35.

- Use of any investigational treatment within 30 days prior to screening or between
screen and admission.

- Use of any psychopharmacologic drug or substance within 7 days of screening or
between screen and admission.

- Use of potent CYP3A4 inhibitors or potent CYP3A4 inducers within 7 days prior to
screening or between screen and admission.

- An estimated 24-hour uric acid excretion > 1,000 mg/day.