A Study of Subcutaneous Doses of HIP2B in Healthy Male Subjects

Primary Outcome:

To assess the tolerability and safety after subcutaneous single ascending doses of HIP2B in
healthy male subjects. Adverse events including local injection site reactions/pain will be
assessed during the study. Ongoing adverse events will be followed to resolution or for 30
days (whichever is sooner). Clinical laboratory evaluations including amylase and lipase
will be reviewed. Vital signs and ECGs will be used to evaluate subject safety.

Secondary Outcome:

To assess the pharmacokinetics (including Cmax, AUClast, AUC0-∞, tmax, t1/2, tlag) in
healthy male subjects after subcutaneous single ascending doses of HIP2B.

Inclusion Criteria:

- Subject is a healthy, male, between 19 and 45 years inclusive.

- Subject's body weight is between 50.0 and 100.0 kg inclusive and body mass index
(BMI) is between 18.0 and 31.6 kg/m2 inclusive.

- Subject is certified as healthy by a comprehensive clinical assessment (detailed
medical history and complete physical examination) by the study doctor.

- Subject has normal vital signs after 10 minutes resting in supine position:

- 95 mmHg ≤ systolic blood pressure ≤ 140 mmHg

- 45 mmHg ≤ diastolic blood pressure ≤ 90 mmHg

- 40 beats per minute ≤ heart rate ≤100 beats per minute

- Subject has a normal standard 12-lead ECG after 10 minutes resting in supine
position; 120 ms < PR < 220 ms, QRS < 120 ms, QTc ≤ 450 ms. Subject must be fasting.

- Laboratory parameters for the subject are within the normal range (or defined
screening threshold for the Investigative site), unless the Investigator considers an
abnormality to be not clinically significant for healthy subjects; however serum
creatinine, alkaline phosphatase, hepatic enzymes (AST/ ALT, amylase, lipase, and
fractional bilirubin (direct and indirect) should not exceed the upper laboratory
norm).

- Male subjects must continue to use their approved contraceptive method and to refrain
from donating semen for 30 days after participating in the study.

- The subject has given written informed consent prior to any study related procedures
being performed.

- The subject is not under any administrative or legal supervision.

Exclusion Criteria:

- The subject has any history or presence of clinically relevant cardiovascular,
pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurological,
osteo-muscular, articular, psychiatric, systemic, ocular, or infectious disease, or
signs of acute illness.

- The subject has frequent headaches and/or migraine, recurrent nausea and/or vomiting
(more than twice a month).

- The subject has significant blood loss or blood donation, within 56 days prior to IP
administration.

- The subject exhibits symptomatic hypotension, whatever the decrease in blood
pressure, or asymptomatic postural hypotension defined by a decrease in systolic
blood pressure ≥ 20 mmHg within 3 minutes when changing from the supine to the
standing position.

- The subject has the presence or history of drug hypersensitivity, or allergic disease
diagnosed and treated by a physician.

- The subject has a history or presence of drug or alcohol abuse (alcohol consumption >
2 drinks per day).

- The subject smokes more than 5 cigarettes or equivalent per day, unable to stop
smoking during the days the subject is confined or returning for study related
testing.

- Excessive consumption of beverages with xanthine bases (> 4 8 ounce glasses per day)
including energy drinks, weight loss drinks, protein mixes (i.e. for body building),
etc.

- Any medication, herbal supplement or other natural products (including St John's
Wort) within 14 days before the Day 1 visit or within 5 times the elimination
half-life or pharmacodynamic half-life of that drug, whichever is longest; any
vaccination within the last 28 days. This includes taking analgesics 2 days before
Day 1 visit which will interfere with pain assessment.

- Any subject who, in the judgment of the Investigator, is likely to be non-compliant
during the study, or unable to cooperate because of a language problem or poor mental
development.

- Any subject participating in another clinical trial of an investigational therapy
(including placebo) within 30 days of screening or 5 half-lives of the study
medication, whichever is longer.

- Any subject who cannot be contacted in case of emergency.

- Any subject who is the Investigator or any Sub-Investigator, Research Assistant,
Pharmacist, Study Coordinator, or other staff thereof, directly involved in the
conduct of the protocol.

- Any subject with a history or presence of any skin condition that would interfere
with injection site assessments (including tattoos) and no umbilical piercings.

- Positive results on urine drug screen (amphetamines/methamphetamines, barbiturates,
benzodiazepines, cannabinoids, cocaine, opiates).

- Positive urine ethanol test.

- Any subject with either amylase or lipase levels above the upper laboratory norm

- Any subject with previous history of pancreatitis or known gallbladder disease
(including gallstones and gallstone attacks; gallbladder removal will not exclude
subject from participating).

- Any subject with prior exposure to INGAP peptide