Single-Dose Bioequivalence Study Comparing Two 2 mg Nicotine Lozenges

Smoking Cessation Clinical Trial

Official title:

A Single-Center, Single-Dose, Open-Label, Laboratory-Blind, Randomized, Two-Period Crossover Study to Determine the Bioequivalence of Two Nicotine Resinate Lozenge Formulations Containing Nicotine 2 mg in up to 42 Healthy Male and Female Smokers Under Fasting Conditions

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03432273
• Other study ID #: F-ZA113
• Status: Completed
• Phase: Phase 1
• Start date: February 19, 2018
• Est. completion date: March 27, 2018

Study information

• Verified date: August 2018
• Source: Fertin Pharma A/S
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to compare the pharmacokinetic (PK) profiles and assess bioequivalence between a new nicotine lozenge and a reference nicotine lozenge in healthy smokers.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: March 27, 2018
• Est. primary completion date: March 27, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Written consent given for participation in the study.

2. Healthy males and females, 18 to 55 years (inclusive) at screening.

3. Body Mass Index (BMI) between 18.5 and 30 kg/m2 (both inclusive).

4. Body mass not less than 50 kg.

5. Medical history, vital signs, physical examination, standard 12-lead electrocardiogram (ECG) and laboratory investigations must be clinically acceptable or within laboratory reference ranges for the relevant laboratory tests, unless the investigator considers the deviation to be irrelevant for the purpose of the study.

6. Females, if:

• Not of childbearing potential, e.g., has been surgically sterilized, undergone a hysterectomy, amenorrhea for = 12 months and considered post-menopausal, Note: in postmenopausal women, the value of the serum pregnancy test may be slightly increased. This test will be repeated to confirm the results. If there is no increase indicative of pregnancy, the female will be included in the study.

• Of childbearing potential, the following conditions are to be met:

Negative pregnancy test

If this test is positive, the subject will be excluded from the study. In the rare circumstance that a pregnancy is discovered after the subject received IMP, every attempt must be made to follow her to term.

Not lactating

Abstaining from sexual activity (if this is the usual lifestyle of the subject) or must agree to use an accepted method of contraception, and agree to continue with the same method throughout the study Examples of reliable methods of contraception include oral (documented that the dose has been stable for at least one month before the first intake of IMP), injectable or implantable contraceptives and non-hormonal intrauterine device.

In this study the concomitant use of hormonal contraceptives is allowed. Other methods, if considered by the investigator as reliable, will be accepted.

7. History of cigarette smoking of at least 10 cigarettes per day continuously for the past 3 months prior to screening and smokes first cigarette in more than 30 minutes after waking up in the morning.

8. No use of any tobacco or nicotine-containing products within 21 days of the first dose except cigarettes.

9. Have no interest in quitting smoking.

10. Have accepted to refrain from smoking for the duration of the study periods.

11. Exhaled CO concentration > 10 ppm at screening.

12. Successfully completed the dissolution training session prior to randomization.

13. Ability to communicate and comply with all study requirements including the study specific method of administration for the nicotine lozenges.

Exclusion Criteria:

1. Evidence of psychiatric disorder, antagonistic personality, poor motivation, emotional or intellectual problems likely to limit the validity of consent to participate in the study or limit the ability to comply with protocol requirements.

2. Any surgical or medical condition which may significantly alter the absorption, distribution, metabolism or excretion of any IMP substance.

3. Current alcohol use > 21 units of alcohol per week for males and > 14 units of alcohol per week for females or evidence of excessive alcohol use as indicated by an alcohol breathalyzer test result = 0.01%.

4. Regular exposure to substances of abuse (other than alcohol) within the past year.

5. Use of any medication, prescribed or over-the-counter or herbal remedies, within 2 weeks before the first administration of IMP except if this will not affect the outcome of the study in the opinion of the investigator.

In this study the concomitant use of hormonal contraceptives is allowed.

6. Expired CO levels greater than 10 ppm in the morning prior to dosing.

7. History of esophagitis, gastritis, peptic ulcer, gastro-esophageal reflux, gastrointestinal bleeding, rectal bleeding or other clinically significant gastrointestinal abnormalities within past 3 months.

8. History of cardiovascular disease such as uncontrolled hypertension, myocardial infarction, stroke or transient ischemic attack within the past 6 months prior to screening, congestive heart failure, angina pectoris, and arrhythmia.

9. Evidence of vasospastic disease (i.e., Buerger's disease) on medical history and physical examination.

10. Unable or unwilling to abstain from methylxanthines for 72 hours pre-dose.

11. Participation in another study with an experimental drug, where the last administration of the previous IMP was within 8 weeks (or within 5 elimination half-lives for chemical entities or 2 elimination half-lives for antibodies or insulin, whichever is the longer) before administration of IMP in this study, at the discretion of the investigator.

12. Treatment within the previous 3 months before the first administration of IMP with any drug with a well-defined potential for adversely affecting a major organ or system.

13. A major illness during the 3 months before commencement of the screening period.

14. History of hypersensitivity or allergy to the IMP or its excipients or any related medication.

15. History of bronchial asthma or any other bronchospastic disease.

16. History of convulsions.

17. History of porphyria.

18. Relevant history or laboratory or clinical findings indicative of acute or chronic disease, likely to influence study outcome.

19. Donation or loss of blood equal to or exceeding 500 mL during the 8 weeks before the first administration of IMP.

20. Diagnosis of hypotension made during the screening period.

21. Diagnosis of hypertension made during the screening period or current diagnosis of hypertension.

22. Resting pulse of > 100 beats per minute or < 40 beats per minute during the screening period, either supine or standing.

23. Positive testing for HIV, Hepatitis B and Hepatitis C.

24. Positive urine screen for drugs of abuse. In case of a positive result the urine screen for drugs of abuse may be repeated once at the discretion of the investigator.

25. Positive pregnancy test.

Related Conditions & MeSH terms

• Smoking Cessation

Intervention

Drug:
• Nicotine lozenge
Nicotine mint lozenge, 2 mg
• Nicotine lozenge
NiQuitin mint lozenge, 2 mg

Locations

Country	Name	City	State
South Africa	Bloemfontein Early Phase Clinical Unit, PAREXEL International (South Africa)	Bloemfontein

Sponsors (1)

Lead Sponsor	Collaborator
Fertin Pharma A/S

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cmax	Maximum observed plasma concentration (Cmax)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Primary	AUC0-t	Area under the plasma concentration versus time curve, from time zero to t, where t is the time of the last quantifiable concentration (AUC0-t)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Secondary	Tmax	Time to maximum observed plasma concentration (tmax)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Secondary	AUC0-inf	Area under the plasma concentration versus time curve, with extrapolation to infinity (AUC0-inf)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Secondary	?z	Terminal elimination rate constant (?z)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Secondary	t½.z	Apparent terminal elimination half-life (t½.z)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours
Secondary	kel	Apparent terminal elimination rate constant (kel)	Blood samples taken pre-dose and post-dose at 5, 10, 20, 30, 40, and 50 minutes, and 1, 1.25, 1.5, 2, 3, 6, 9, 12, 16 and 24 hours