Open-Label Pharmacokinetic Study of Final Formulations of ATX-101

The objectives of this trial are to evaluate the safety and tolerability of ATX-101
injections and to characterize the pharmacokinetic profile of the two ATX-101 formulations
that are expected to be the final formulations. ATX-101 will be administered into the
submental fat as subcutaneous injections using the maximum proposed dosing regimen that is
intended for labeling.

Inclusion Criteria:

- Presence of sufficient submental fat into which 50 subcutaneous injections of ATX-101
spaced on a 1.0-cm grid can be safely administered based on the investigator's
judgment.

- Males or nonpregnant, nonlactating females who are aged 18 to 65 years, inclusive, on
the date of dosing with ATX-101. Females must have a negative serum human chorionic
gonadotropin (hCG) test result from a sample obtained during the screening period and
after admission to the research facility, but before the dose of study material.
Females of postmenopausal status must not have had menses for at least one year and
if younger than 55 years of age must have a serum FSH level ≥ 35 mIU/mL. Females of
childbearing potential must agree to practice adequate contraception, in the judgment
of the investigator, during the course of the trial.

- Serum hemoglobin test result of 11.0 g/dL or greater and negative hepatitis B,
hepatitis C, and HIV test result within 28 days before the dose of study material.

- Willing and able to comply with and understand the visit schedule and all of the
protocol-specified tests and procedures.

- Medically able to undergo the administration of study material as determined by
clinical and laboratory evaluations obtained within 28 days before dosing with study
material for which the investigator identifies no clinically significant abnormality.

- Signed informed consent obtained before any study-specific procedure is conducted.

Exclusion Criteria:

- History of any intervention to treat submental fat (e.g. liposuction, surgery, or
lipolytic agents).

- History of trauma associated with the chin or neck areas, which in the judgment of
the investigator may affect evaluation of safety of treatment.

- Loose skin in the neck or chin area for which reduction in submental fat may, in the
judgment of the investigator, result in a cosmetically unacceptable outcome.

- Prominent platysmal bands at rest that interfere with the evaluation of submental
fat.

- Evidence of any cause of enlargement in the submental area other than localized
subcutaneous fat.

- Body mass index (BMI) > 40.0 at the screening visit. Refer to Appendix B.

- Use of tobacco or nicotine-containing products within 3 months prior to dose.

- Any blood donation or significant blood loss within 56 days before the dose of study
material or plasma donation within 7 days before the dose of study material.

- A result on coagulation tests (PT, PTT) obtained within 28 days before the dose of
study material that indicates the presence of any clinically significant bleeding
disorder.

- Any medical condition that would interfere with the assessment of safety in this
trial or would compromise the ability of the subject to undergo study procedures or
to give informed consent.

- Treatment with fish oil, aspirin, or nonsteroidal anti-inflammatory agents (NSAIDS),
except acetaminophen, within 7 days before dosing, or any anticipated need for agents
with anticoagulative effects (e.g. warfarin, heparin) during the course of the trial.

- Treatment with oral anticoagulants (e.g. warfarin) within 30 days before dosing with
study material.

- Treatment with radio frequency, laser procedures, chemical peels, or dermal fillers
in the neck or chin area within 12 months before dosing with the study material, or
botulinum toxin injections in the neck or chin area within 6 months before dosing
with the study material.

- History of sensitivity to any components of the study material.

- History of drug or alcohol abuse, in the judgment of the investigator, within two
years before dosing with the study material.

- Presence of a positive urine drug or alcohol screening test result obtained from a
sample obtained during the screening period and/or after admission to the research
facility for the confinement period, but before dosing with the study material.

- Previous enrollment into a trial of ATX-101.

- Treatment with an investigational device or agent within 30 days before dosing.