Atlas Trials

Comparing Bioavailability When Preservative-free Makena® (Hydroxyprogesterone Caproate Injection, 250 mg/mL) is Administered as an Intramuscular Manual Injection or as a Subcutaneous Injection Using an Auto-injector in Healthy Post-menopausal Women

Clinical trial NCT02940522 · COMPLETED

Trial details

NCT number
NCT02940522
Sponsor
AMAG Pharmaceuticals, Inc.
Status
COMPLETED
Phase
Phase 1
Study type
INTERVENTIONAL
Comparing Bioavailability When Makena® is Administered in Healthy Post-menopausal Women
Start date
2016-09-01
Primary completion
2016-12-01
Enrollment
122

View on ClinicalTrials.gov

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