A Pilot Study of EM-1421 for the Treatment of Cervical Intraepithelial Neoplasia
Completed · Phase 1/Phase 2
Conditions studied: Cervical Intraepithelial Neoplasia
In brief
The primary objective of this study is to determine pilot safety and efficacy data for a topical formulation of EM-1421 applied to the cervix of patients with CIN 1, 2, or 3.
Key facts
- Study ID
- NCT00154089
- Run by
- Erimos Pharmaceuticals
- People needed
- 8
- Starts
- 2004-11-01
- Expected to finish
- 2006-12-01
- Last updated by the study team
- 2016-02-23
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age or older
- Negative pregnancy test
- Biopsy confirmed CIN 1, 2, or 3
You may not qualify if…
- Pregnancy or breast feeding
Where it is running
- University of Maryland, Dept. of Family Medicine — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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