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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01428310
Other study ID # RCP-006
Secondary ID
Status Completed
Phase Phase 1
First received September 1, 2011
Last updated October 29, 2015
Start date September 2011
Est. completion date December 2011

Study information

Verified date October 2015
Source Rock Creek Pharmaceuticals, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study will consist of 2 phases. Phase 1 will be a one day crossover study to see the effects of study product on a smoker's desire to smoke, measured by changes in scores on questionnaires given over time. Phase 2 will be a two-week extension, in which subjects will self-administer the study product and visit the study site for assessment of desire to smoke and collection of samples for the evaluation of smoking-related biomarkers.


Recruitment information / eligibility

Status Completed
Enrollment 109
Est. completion date December 2011
Est. primary completion date October 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 23 Years to 72 Years
Eligibility Inclusion Criteria:

- healthy adult smokers

- using at least 1 pack of cigarettes per day, for at least 5 years

Exclusion Criteria:

- allergy to study product components

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Anatabloc(TM)
one dissolvable bit, one time, after a period of abstinence from smoking
CigRx(R)
one dissolvable bit, one time, after a period of abstinence from smoking

Locations

Country Name City State
United States Comfort Inn Martinsburg West Virginia

Sponsors (1)

Lead Sponsor Collaborator
Rock Creek Pharmaceuticals, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary effect on subject's craving to smoke craving is assessed by changes in questionnaire answers over time 5 hours No
Secondary adverse events related to study product collection of information on adverse events related to study product 5 hours No
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