A Study to Investigate the Absorption, Metabolism, Excretion, and Mass Balance of GC4419 in Healthy Adult Subjects

This is an open-label, single-dose, 1-period study.

On Day 1, a single 30 mg (~100 μCi) dose of [14C]GC4419 will be administered as an IV
infusion over 15 minutes. Blood, urine, and fecal samples will be collected to measure total
radioactivity (plasma, whole blood, urine, and fecal samples), for GC4419 and its metabolites
GC4520 and GC4570 concentrations (plasma, urine, and fecal samples), and for metabolic
profiling (plasma, urine, and fecal samples), as total amounts of radioactivity allow, for at
least 168 hours postdose (Day 8).

If discharge criteria are not met on Day 8, collection of blood will be collected
approximately every 72 hours, and urine and feces collection will continue in 24-hour
intervals thereafter (for determination of total radioactivity and metabolic profiling only)
until the discharge criteria are met or up to a maximum stay of 28 days (Day 29).

The clinic will attempt to contact all subjects (including subjects who terminate the study
early) using their standard procedures approximately 14 days after the last sample collection
to determine if any adverse event has occurred since the last sample collection.

Six (6), healthy, adult, non tobacco using, male subjects will be enrolled.

Inclusion Criteria:

1. Healthy, adult, male, 19-55 years of age, inclusive, at screening.

2. Continuous non-smoker who has not used nicotine containing products for at least 3
months prior to dosing and throughout the study.

3. Body mass index (BMI) ≥ 18.5 and ≤ 32.0 kg/m2 at screening.

4. No clinically significant medical history, physical examination, laboratory profiles,
vital signs or ECGs

5. A non-vasectomized subject must agree to use a condom with spermicide or abstain from
sexual intercourse during the study until 90 days beyond dosing.

6. Must agree not to donate sperm from dosing until 90 days after dosing.

7. Be willing and able to comply with the protocol.

Exclusion Criteria:

1. Subject is mentally or legally incapacitated

2. History or presence of clinically significant medical or psychiatric condition or
disease

3. History or presence of alcoholism or drug abuse within the past 2 years prior to
dosing.

4. History or presence of hypersensitivity or idiosyncratic reaction to the study drug or
related compounds.

5. Regularly has less than 1 bowel movement every 2 days.

6. Recent history (within 2 weeks of Day 1) of abnormal bowel habits

7. Positive results for human immunodeficiency virus (HIV), hepatitis B surface antigen
(HBsAg), or hepatitis C virus (HCV).

8. Blood pressure is less than 90/40 mmHg or greater than 140/90 mmHg

9. Heart rate is lower than 40 bpm or higher than 99 bpm

10. Unable to refrain from or anticipates the use of any drug, including prescription and
non prescription medications, herbal remedies, or vitamin supplements beginning 14
days prior to dosing and throughout the study.

11. Has been on a diet incompatible with the on study diet

12. Donation of blood or significant blood loss within 56 days prior to dosing.

13. Plasma donation within 7 days prior to dosing.

14. Has received radiolabeled substances or has been exposed to radiation sources over the
past 12 months or is likely to receive radiation exposure or radioisotopes within the
next 12 months such that participation in this study would increase their total
exposure beyond the recommended levels considered safe

15. Participation in another clinical study within 28 days prior to dosing.