Efficacy and Safety Study of Elagolix Versus Placebo or Leuprorelin Acetate in Endometriosis

Study Identifier
NBI-56418-0703
CT.gov Identifier
EudraCT Identifier
EUCTIS ID
Not available
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Study Complete

Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Endometriosis
  • Study Drug
  • Leuprorelin Acetate Depot
  • Elagolix
  • Placebo to Elagolix
  • Placebo to Leuprorelin Acetate
  • Phase
    Phase 2
    Sex
    Female
    Age
    18 - 45 Years

    Protocol Summary

    This study is designed to evaluate the safety and beneficial effects of elagolix (NBI-56418) compared to placebo and leuprorelin (an approved endometriosis therapy) over a three month period followed by an additional three months of treatment on elagolix.

    Study Locations

    No locations found.