Study of Glycopyrronium in Axillary Hyperhydrosis

This is a randomized, double-blind vehicle controlled study to assess the efficacy and safety
of glycopyrronium topical wipes compared to vehicle in subjects with axillary hyperhidrosis.

Safety will be assessed through lab tests, ECG, physical exams and vital signs.

Inclusion Criteria:

- Male or female ≥ 9 years of age.

- Primary, axillary hyperhidrosis of at least 6 months duration

- Hyperhidrosis Disease Severity Scale (HDSS) of 3 or 4 at Baseline

- Axillary Sweating Daily Diary (ASDD) ≥ 4 at Baseline

- Sweat production of at least 50 mg over 5 minutes in each axilla assessed
gravimetrically

Exclusion Criteria:

- Prior surgical procedure for hyperhidrosis.

- Prior axillary treatment with an anti-hyperhidrosis medical device (approved or
investigational).

- Prior treatment with botulinum toxin (e.g., Botox®) for axillary hyperhidrosis within
1 year of Baseline/Day 1.

- Previous active treatment in the Dermira DRM04-HH01 or DRM04-HH02 clinical trials.

- Axillary use of nonprescription antiperspirants within 1 week or prescription
antiperspirants within 2 weeks of Baseline.

- Subjects on new or regimens of psychotherapeutic medications that have changed within
2 months of baseline.

- Treatment with systemic anticholinergics within 4 weeks of the baseline visit unless
dosing has been stable for at least 4 months.

- Other treatment with glycopyrrolate within 4 weeks prior to Baseline.

- Secondary axillary hyperhidrosis or presence of a condition that may cause secondary
hyperhidrosis.

- History of Sjögren's syndrome or Sicca syndrome.

- History of glaucoma, inflammatory bowel disease, toxic megacolon, or febrile illness.

- Men with a history of urinary retention requiring catheterization due to prostatic
hypertrophy or severe obstructive symptoms of prostatic hypertrophy.

- History or presence of ventricular arrhythmias, atrial fibrillation, atrial flutter.

- Other systemic diseases or active uncontrolled infections, or any other condition
which, in the judgment of the Investigator, would put the subject at unacceptable risk
for participation in the study.