About Research
Study #51923
Are You a Good Fit?
Men & Women
Between the ages of 22 and 65 years.
Smoker of at least 10 cigarettes per day for at least 12 months prior to screening.
BMI (Body Mass Index) between 18 and 40 kg/m2.
Must not use THC or illicit drugs.
- Receive up to $6,050 for your participation in this study
What are the Time Requirements?
Group 1
Visit DatesHow Much: $6,050
Group 2
Visit DatesHow Much: $6,050
Group 3
Visit DatesHow Much: $6,050
Group 4
Visit DatesHow Much: $6,050
BMI Calculator
All study dates are tentative and subject to change.
o Female subjects who are heterosexually active and of childbearing potential (e.g., neither surgically sterile at least 6 months prior to first check-in nor postmenopausal with amenorrhea for at least 12 months prior to first check-in with follicle-stimulating hormone [FSH] levels consistent with postmenopausal status) must have been using one of the following forms of contraception for the time indicated and agree to continue using it through completion of the study:
hormonal (e.g., oral, vaginal ring, transdermal patch, implant, injection) consistently for at least 3 months prior to first check-in, when used in combination with male condoms with spermicide (use of NuvaRing® is at the
Principal Investigator’s discretion).
double barrier (e.g., condom with spermicide or diaphragm with spermicide) consistently for at least 2 weeks prior to first check-in
intrauterine device or system (utilize Principal Investigator discretion regarding use of hormonal or nonhormonal devices) for at least 3 months prior to first check-in.
exclusive partner who is clinically sterile (i.e., documented infertility or surgical sterilization; see below for additional information on sterility) or has been vasectomized for at least 6 months (inclusive) prior to first
check-in.
• Note: Sexual abstinence, defined as refraining from intercourse, is allowed when this is in line with the preferred and usual lifestyle of the subject. Female subjects of childbearing potential who are not currently
engaging in heterosexual intercourse must agree to use one of the above methods of birth control through completion of study, if:
o they have heterosexual intercourse during the study.
• Female subjects who are of nonchildbearing potential must have undergone one of the following sterilization procedures at least 6 months prior to first check-in:
o Hysteroscopic sterilization (including Essure® or similar nonsurgical
sterilization procedures)
o Bilateral tubal ligation or bilateral salpingectomy.
o Hysterectomy
o Bilateral Oophorectomy
• Or be postmenopausal with amenorrhea for at least 12 months prior to first check-in:
o and have FSH levels consistent with postmenopausal status.
If you have previously submitted an application, call 417-831-2048 to enroll. Or click on the button below to submit your application now.