Multicenter Study to Investigate SER120 Nasal Spray Formulations in Patients With Nocturia - DB4

Completed · Phase 3 · Has a placebo group

Conditions studied: Nocturia

In brief

To investigate the efficacy and safety of SER120 nasal spray formulations in patients with nocturia

Key facts

Study ID

NCT01900704

Run by

Serenity Pharmaceuticals, Inc.

People needed

810

Starts

2013-08-01

Expected to finish

2015-04-01

Last updated by the study team

2020-11-09

Who can join

Age: 50 and older, up to 95. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female 50 years or older
• Nocturia of 6 or more months duration averaging greater than 2 nocturic episodes per night

You may not qualify if…

• CHF
• Diabetis Insipidus
• Renal insufficiency
• Hepatic insufficiency
• Incontinence
• Illnesses requiring systemic steroids
• Malignancy within the past 5 years
• Sleep apnea
• Nephrotic syndrome
• Unexplained pelvic mass
• Urinary bladder neurological dysfunction
• Urinary bladder surgery or radiotherapy
• Pregnant or breast feeding

Where it is running

• Stephen M. Auerbach, MD — Newport Beach, California, United States

Full record on ClinicalTrials.gov

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