Single Dose Pharmacokinetics of Intranasal Fluticasone Delivered by a Fixed Combination With Azelastine (MP29 02) in Comparison to Two Different Fluticasone Nasal Sprays
Information source: MEDA Pharma GmbH & Co. KG
Information obtained from ClinicalTrials.gov on October 04, 2010
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Allergic Rhinitis
Intervention: Azelastine, Fluticasone (Drug); Fluticasone mono (Drug); Fluticasone (Drug)
Phase: Phase 1
Sponsored by: MEDA Pharma GmbH & Co. KG
Christine Kolb, Phone: +49 6172 888, Ext: 2511, Email: email@example.com
The primary objective is to assess the effect of azelastine hydrochloride (AZE) on the
relative bioavailability (AUC0-∞) of fluticasone propionate (FLU) when administered as fixed
AZE-FLU combination product (TEST) compared to a similar formulation without containing AZE
(i. e. FLU alone in the MP29-02 vehicle; REF).
The secondary objectives are to compare the relative bioavailability (AUC0-∞) of FLU when
administered either as fixed AZE-FLU combination product (TEST) or as marketed FLU product,
Fluticasone Propionate Nasal Spray, Roxane Laboratories (COMP); To compare the effects of
AZE on other pharmacokinetic parameters of FLU (AUC0 tlast, CL/f, Cmax, tmax, t½); To assess
Official title: Single Dose Pharmacokinetics of Intranasal Fluticasone Delivered by a Fixed Combination With Azelastine (MP29 02) in Comparison to Two Different Fluticasone Nasal Sprays Single-centre, Randomised, Open-label, Three-period, Six-sequence Cross-over Trial (William's Design)
Study design: Allocation: Randomized, Control: Active Control, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Effect of azelastine hydrochloride on the relative bioavailability of fluticasone
Effects of AZE on other pharmacokinetic parameters
This study will enrol healthy subjects. It is considered that study results are more
discriminative in healthy subjects than in rhinitis patients as there are no interferences
by varying rhinitis symptoms and respective differences in the status of the nasal mucosa
regarding the 3 study periods.
The time schedule for serum sampling (pre-dose and 8, 15, 30, 45 min, 1, 1¼, 1½, 2, 2½, 3,
4, 6, 8, 12, and 24 h p. a., time refer to the end of the second spray into the second
nostril of each administration) is derived from previous bioavailability studies assuming a
mean tmax of 1 h p. a. [P5] and a mean t1/2 of 3 h [L9]. Sampling times are expected to cover
an AUC0-tlast above 80% of the total AUC of fluticasone propionate (bioanalytical detection
method with a LLOQ of 0. 5 pg/mL).
Minimum age: 18 Years.
Maximum age: 45 Years.
1. Male or female healthy subjects of any Ethnic origin, age from 18 to 45 years.
2. Body mass index (BMI) from 18. 5 to 30. 0 kg/m2.
3. Use of adequate double contraception by female with childbearing potential (i. e.
women of child bearing potential using a highly effective method of birth control
defined as those which result in a low failure rate (i. e. <1% per year) when used
consistently and correctly such as implants, injectables, combined oral
contraceptives, hormonal IUDs) or surgically sterile (documented complete
hysterectomy or bi-tubal ligations; partial hysterectomy is not sufficient or
vasectomised partner). It must be ensured that the male partner uses a condom during
intercourse (if not surgically sterilized).
4. Use of adequate double contraception by male, who is a sexually active man and has
not been surgically sterilized, must consent that he uses a condom during intercourse
and ensures that his female partner practices adequate contraception (a highly
effective method of birth control defined as those which result in a low failure rate
(i. e. <1% per year) when used consistently and correctly such as implants,
injectables, combined oral contraceptives, hormonal IUDs) or surgically sterile
(documented complete hysterectomy or bi-tubal ligations; partial hysterectomy is not
5. Written informed consent.
6. Able to demonstrate correct nasal spray application technique at screening.
1. History of allergic reaction or sensitivity to fluticasone propionate, azelastine
hydrochloride or one of the excipients (e. g. benzalkoniumchloride, phenyl-ethyl
alcohol, microcrystalline cellulose).
2. Any evidence of clinically relevant acute or chronic cardiovascular, pulmonary,
hepatic, renal, gastrointestinal, haematological, endocrine, metabolic, mental,
neurological, or other disease at screening.
3. Positive ß-HCG pregnancy test, or established pregnancy, breast-feeding or planned
pregnancy during the study.
Lack of suitability for the study:
4. History of haemophilia or coagulation disease.
5. Significant history of orthostatic hypotension, fainting or blackouts.
6. Existence of any surgical or medical condition, which might significantly alter the
absorption, distribution, metabolism, or excretion of study drug.
7. Chronic or clinically relevant acute infections (e. g. of the respiratory tract
including sinusitis and rhinitis), acute rhinorrhoea or febrile disease the week
8. Clinical chemical, haematological or any other laboratory parameters clinically
relevant outside the reference range (e. g. elevated liver enzymes, renal laboratory
parameters, and coagulation abnormalities such as abnormalities of platelet count,
prothrombin time, or activated partial thromboplastin time).
9. Positive results in HIV, HCV and HBsAg tests.
10. ECG abnormalities of clinical relevance, in particular abnormal prolongations of
QT/QTc- or PQ-interval (i. e. QTc according to Fridericia ≥ 450 ms, PQ ≥ 220 ms).
11. Resting heart rate in the awake subject below 45 BPM or above 90 BPM, systolic blood
pressure below 100 mmHg or above 145 mmHg, diastolic blood pressure above 95 mmHg.
12. Regular therapy with corticosteroids (e. g. fluticasone propionate) or antihistamines
(e. g. azelastine hydrochloride).
13. Any concurrent medication or any medication within 2 weeks preceding the start of the
study (single intake/use of drugs may be accepted, if judged by the investigator to
have no clinical relevance and no influence on study outcome).
14. Exposure to any cytochrome P450 3A4 inhibiting or inducing drug (e. g. ritonavir,
ketoconazole, itraconazole, erythromycin, rifampicin, St. John's wort (Hypericum
perforatum) etc.) diets (charcoal grilled meat, brussels sprouts, broccoli) or
beverages (e. g. grapefruit juice) within 14 days prior to study enrolment, or
anticipated consumption of such products during that period or at any time throughout
15. History of any nasal surgery or known clinically relevant abnormalities, such as
rhinitis medicamentosa, polyposis, septum deviation with clinical symptoms, or nasal
16. Known perennial airway allergies or vasomotor rhinitis. Known seasonal airway
allergies which are clinically relevant acute within the last six weeks prior to the
start of the study or might become acute during the study period.
17. History of malignancy within the past five years.
18. Blood donation within the last 2 months prior to the start of the study.
19. Present or history of drug or alcohol abuse within the last three years. Regular
daily consumption of more than half a litre of usual beer or 0. 25 L of wine per day
or the equivalent quantity of approximately 30 g of alcohol in another form.
20. Current smoker or smoking during the last year.
21. Exposure to an investigational medicinal product within the last 3 months.
22. Subject reports a regular xanthine consumption of > 5 cups of coffee or black tea per
day (or equivalent xanthine consumption of ≥ 500 mg xanthine per day using other
23. Subject is vegetarian or reports other strict dietary habits which would preclude the
subject's acceptance of standardized meals.
24. Lack of ability or willingness to give informed consent.
25. Lack of willingness to have personal study related data collected, archived or
transmitted according to protocol.
26. Lack of willingness or inability to co-operate adequately.
27. Anticipated non-availability for study visits/procedures.
28. Vulnerable subjects (such as persons kept in detention).
Locations and Contacts
Christine Kolb, Phone: +49 6172 888, Ext: 2511, Email: firstname.lastname@example.org
ClinPharmCologne, Cologne, NRW 51063, Germany; Recruiting
Hartmut Dietrich, MD, Phone: +49 221 6472, Ext: 324, Email: email@example.com
Angela Kentrat, MD, Phone: +49 221 6472, Ext: 671, Email: firstname.lastname@example.org
Hartmut Dietrich, MD, Principal Investigator
Starting date: August 2010
Last updated: September 2, 2010