Study to Evaluate Pharmacokinetics Profile, Wearability, and Safety of 2 Progestin-Only Patches
NCT01623466 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 36
Last updated 2018-01-23
Summary
Pharmacokinetics, safety and wearability in two size patches of AG890 over eight weeks will be evaluated.
Conditions
- Healthy
Interventions
- DRUG
-
levonorgestrel
transdermal contraceptive delivery system
Sponsors & Collaborators
-
Agile Therapeutics
lead INDUSTRY
Principal Investigators
-
Elizabeth Garner, MD, PHD · Agile Therapeutics
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-07-31
- Primary Completion
- 2012-09-30
- Completion
- 2012-09-30
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