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Spots Global Cancer Trial Database for Chemoprevention of Oral Premalignant Lesions

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Chemoprevention of Oral Premalignant Lesions

Official Title: Clinical Protocol For A Phase II Double-Blind, Placebo-Controlled, Randomized Study Of Celecoxib (Sc-58635) In Oral Premalignant Lesions, Investigator IND

Study ID: NCT00036283

Interventions

Celecoxib

Study Description

Brief Summary: Reduction in size and number of oral premalignant lesions

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Pfizer Investigational Site, Farmington, Connecticut, United States

Pfizer Investigational Site, Shreveport, Louisiana, United States

Pfizer Investigational Site, Ann Arbor, Michigan, United States

Pfizer Investigational Site, Minneapolis, Minnesota, United States

Pfizer Investigational Site, New York, New York, United States

Pfizer Investigational Site, Houston, Texas, United States

Pfizer Investigational Site, Seattle, Washington, United States

Contact Details

Name: Pfizer CT.gov Call Center

Affiliation: Pfizer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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