Study of Erenumab (AMG 334) in Women With Hot Flashes
Completed · Phase 1 · Has a placebo group
Conditions studied: Vasomotor Symptoms; Hot Flashes
In brief
The primary objective of this study was to evaluate the frequency of moderate to severe daily hot flashes 4 weeks after a single dose of erenumab (AMG 334) in women with hot flashes associated with menopause.
Key facts
- Study ID
- NCT01890109
- Run by
- Amgen
- People needed
- 103
- Starts
- 2013-05-13
- Expected to finish
- 2014-03-11
- Last updated by the study team
- 2019-01-14
Who can join
Age: 45 and older, up to 65. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- female subjects with hot flashes associated with menopause between 45 and 65 years of age, inclusive, with no history or evidence of clinically relevant medical disorders as determined by the investigator in consultation with the Amgen physician.
You may not qualify if…
- History or evidence of clinically significant disorder (including psychiatric), condition or disease that, in the opinion of the Investigator or Amgen physician would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.
Where it is running
- Research Site — San Diego, California, United States
- Research Site — Miami, Florida, United States
- Research Site — Winston-Salem, North Carolina, United States
- Eugene Andruczyk — Philadelphia, Pennsylvania, United States
- Research Site — Philadelphia, Pennsylvania, United States
- Research Site — Mt. Pleasant, South Carolina, United States
- Research Site — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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