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Phase I Study of HAL Formulations Applied to the Cervix in Healthy Volunteers

This study has been terminated.
Information provided by:
Photocure Identifier:
First received: July 3, 2007
Last updated: January 15, 2009
Last verified: January 2009
The purpose of the study is to determine the most effective formulation of HAL for release of hexaminolevulinate to the cervical epithelium at different doses.


Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: A Phase I Hexaminolevulinate (HAL) Dose-Finding Study Applying Different Formulations to the Cervix in Healthy Volunteers

Further study details as provided by Photocure:


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Healthy, pre-menopausal female volunteers

Exclusion Criteria:

  • Acute or chronic disease which could influence the study results
  Contacts and Locations
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Please refer to this study by its identifier: NCT00496171

Riks-Radium University Hospital
Oslo, Norway
Sponsors and Collaborators
Principal Investigator: Claes G Tropé, MD PhD Riks-Radium University Hospital
  More Information Identifier: NCT00496171     History of Changes
Other Study ID Numbers: PC CE102/07
Study First Received: July 3, 2007
Last Updated: January 15, 2009 processed this record on September 20, 2017