Effects of AFQ056 & Nicotine in Reducing Cigarette Smoking

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Smoking Abstinence

See also
Status	Clinical Trial	Phase
Completed	`NCT05385055` - Reduction of Exposure, Inflammation, and Oxidative Stress Following at Least 2 Years of Switching to THS Use Compared to Cigarette Smoking
Completed	`NCT01210586` - Tobacco Cessation in Postmenopausal Women	N/A
Enrolling by invitation	`NCT05382221` - Breathe 2 Project 3: Comprehensive Chronic Care	N/A
Recruiting	`NCT03556774` - Boosting Chinese Healthcare Service Providers' Utilization of Smoking Cessation Interventions by 'WeChat WeQuit' Program	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT05385055 - Reduction of Exposure, Inflammation, and Oxidative Stress Following at Least 2 Years of Switching to THS Use Compared to Cigarette Smoking

Completed

NCT01210586 - Tobacco Cessation in Postmenopausal Women

N/A

Enrolling by invitation

NCT05382221 - Breathe 2 Project 3: Comprehensive Chronic Care

N/A

Recruiting

NCT03556774 - Boosting Chinese Healthcare Service Providers' Utilization of Smoking Cessation Interventions by 'WeChat WeQuit' Program

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00414752
Study type	Interventional
Source	Novartis
Contact
Status	Completed
Phase	Phase 1
Start date	September 2006

Effects of AFQ056 and Nicotine in Reducing Cigarette Smoking

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms