Sensitivity of Pharmacokinetics to Differences in Aerodynamic Particle Size Distribution
| Status: | Completed |
|---|---|
| Conditions: | Asthma |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 18 - 50 |
| Updated: | 12/30/2018 |
| Start Date: | November 2016 |
| End Date: | January 20, 2018 |
Evaluation of the Sensitivity of Pharmacokinetics to Differences in the Aerodynamic Particle Size Distribution of Three Different Formulations of Fluticasone Propionate Dry Powder Inhalers
When a drug company first develops a drug, the company has to show the Food and Drug
Administration (FDA) that the drug is safe and effective. If FDA concludes that the drug is
safe and effective, FDA approves the drug. The company can then sell the drug, which the
company does using "trade name." Only the drug company that developed the "trade name" drug
is allowed to sell it. However, other drug companies can create their own version of the
"trade name" drug, which usually happens after the patents for the "trade name" product run
out. These drugs, often called "generic drugs," potentially will be less expensive for the
patient. In order to sell generic drugs, drug companies must show that their generic version
is the same as the "trade name" drug in a number of ways. For example, they generally have to
show that their product is intended to be used to treat the same diseases or conditions, that
it has the same label, and that the product has the same active ingredient as the "trade
name" drug. The generic company also has to show that generic product is "bioequivalent" to
the trade name drug, meaning that the generic product gets to the part of the body where the
drug works at the same rate that the trade name drug does. How to show how much drug gets to
the part of the body where it works, and how fast, depends on the type of product the drug
is. The primary aim of this research study is to aid the FDA in finding methods to ensure
that the versions of generic drugs that are inhaled (for example, drugs used to treat asthma)
are bioequivalent to the trade name drug. As a part of the research study, pharmacokinetic
(PK) studies (studies measuring drug levels in the blood over time after inhalation) will be
done using three different versions of fluticasone propionate (FP, a drug routinely used in
asthmatic patients) administered using a dry powder inhaler (DPI, an inhalation device that
delivers the drug as a dry powder). The results from this study will help FDA ensure that
generic products are the same as the trade name drugs.
Administration (FDA) that the drug is safe and effective. If FDA concludes that the drug is
safe and effective, FDA approves the drug. The company can then sell the drug, which the
company does using "trade name." Only the drug company that developed the "trade name" drug
is allowed to sell it. However, other drug companies can create their own version of the
"trade name" drug, which usually happens after the patents for the "trade name" product run
out. These drugs, often called "generic drugs," potentially will be less expensive for the
patient. In order to sell generic drugs, drug companies must show that their generic version
is the same as the "trade name" drug in a number of ways. For example, they generally have to
show that their product is intended to be used to treat the same diseases or conditions, that
it has the same label, and that the product has the same active ingredient as the "trade
name" drug. The generic company also has to show that generic product is "bioequivalent" to
the trade name drug, meaning that the generic product gets to the part of the body where the
drug works at the same rate that the trade name drug does. How to show how much drug gets to
the part of the body where it works, and how fast, depends on the type of product the drug
is. The primary aim of this research study is to aid the FDA in finding methods to ensure
that the versions of generic drugs that are inhaled (for example, drugs used to treat asthma)
are bioequivalent to the trade name drug. As a part of the research study, pharmacokinetic
(PK) studies (studies measuring drug levels in the blood over time after inhalation) will be
done using three different versions of fluticasone propionate (FP, a drug routinely used in
asthmatic patients) administered using a dry powder inhaler (DPI, an inhalation device that
delivers the drug as a dry powder). The results from this study will help FDA ensure that
generic products are the same as the trade name drugs.
Formulation Development
The aim of the pharmaceutical development was to manufacture three Dry powder Inhalation
(DPI) formulations containing Fluticasone Propionate in an Plastiape Monodose DPI device,
which provide distinct in vitro deposition patterns on a Next Generation Impactor. NGI is a
high performance cascade impactor used to characterize aerosol particles by particle size. It
is desirable to develop three formulations with the same emitted dose (ED), impactor size
mass (ISM) but different mass median aerodynamic diameter (MMAD). Meeting these design
criteria for the formulations would help to see if pharmacokinetic parameters are sensitive
to regional differences in drug deposition whilst having the dose deposited in the lung from
different formulations being the same.The three formulation developed are labeled Fluticasone
Propionate Drug formulation 1 through 3.
Study Procedures and scheduling
The study is comprised of 5 visits in total - a screening visit and 4 treatment visits. At
least 5 days should lapse between the treatment visits.
Screening Visit During the screening visit, the inclusion and exclusion criteria will be
reviewed to ensure the volunteer is appropriate for the study. The informed consent will be
reviewed with the volunteer by a member of the study team and the volunteer will be
encouraged to ask questions to ensure the volunteer has a good understanding of the study. If
the volunteer is eligible and agrees to participate, the volunteer will be asked to sign the
informed consent form prior to any study specific procedures including randomization. After
the volunteer signs the informed consent, the volunteer will be interviewed and demographic
data, medical history and concomitant medications will be collected and recorded. A physical
examination will be performed after the vital sign measurements are obtained. A pregnancy
test for female volunteers will be obtained. Spirometry testing and inhalation training will
be performed by a qualified study clinician/investigator to ensure the suitability of
volunteers. Laboratory tests including a Complete Blood Count (CBC), urinalysis and metabolic
panel will be collected via venipuncture and processed in the lab. Screening tests will be
performed within 14 days of treatment visit 1 and no later than 2 days before treatment visit
1. All screening results will be evaluated by the study clinician/investigator against the
inclusion/exclusion criteria to confirm the eligibility of the volunteers.
Inhalation training: Inhalation training will be performed by a qualified study clinician at
the screening visit and at each study visit. The training will be accomplished by
instructions and subsequent inhalation via training devices containing empty capsules. The
instructions on how to use the device correctly are similar to the Foradil Aerolizer DPI
product information label. (http://www.rxlist.com/foradil-drug/medication-guide.htm )
Treatment Visits 1, 2, 3 and 4 Eligible volunteers will be asked to return for treatment
visit 1. A minimum period of 5 days should lapse between the subsequent treatment visits.
Each treatment visit is scheduled for 28 hours over two days. The study will be conducted at
the University of Florida (UF) CRC (Clinical Research Center). It is an outpatient study and
the volunteer will be asked to come back the following day for the 24 hour blood sample. The
volunteer will be asked to stay in an outpatient room during the treatment visit. The same
activities are carried out at the other treatment visits.
At each treatment visit, eligibility criteria will be reviewed and confirmed to ensure
volunteer is appropriate for study. Changes in medical history including concomitant
medications will be documented. Vital signs will be obtained. Inhalation training will be
provided to the volunteers as mentioned in the section above. An IV catheter will be inserted
in a vein located in the forearm region of the volunteer. The IV catheter is used to avoid
multiple pricks while collecting blood samples. The IV catheter is not used for the
administration of the drug. The volunteer inhales 5 times from a given inhaler during each
treatment visit. Each inhaler will be used only once and by only one volunteer to ensure the
volunteer's safety from infectious agents. The schedule below summarizes the procedures
performed at the screening visit and a single treatment visit.
Blood sample collection Blood samples will be drawn by inserting an indwelling catheter into
the volunteer's median cubital vein in the forearm region. Blood samples will be taken 15
minutes prior to the dosing of the product (pre-dose sample) and 5, 10, 15, 20, 30, 45, 60
minutes, 1.5, 2, 3, 4, 6, 8, 10, 12, 14 and 24 hours post dosing. At each time point 9ml of
blood sample will be collected of which the first 1ml will be discarded and the remaining 8
ml will be stored in a vacutainer tube for plasma preparation and storage.
The aim of the pharmaceutical development was to manufacture three Dry powder Inhalation
(DPI) formulations containing Fluticasone Propionate in an Plastiape Monodose DPI device,
which provide distinct in vitro deposition patterns on a Next Generation Impactor. NGI is a
high performance cascade impactor used to characterize aerosol particles by particle size. It
is desirable to develop three formulations with the same emitted dose (ED), impactor size
mass (ISM) but different mass median aerodynamic diameter (MMAD). Meeting these design
criteria for the formulations would help to see if pharmacokinetic parameters are sensitive
to regional differences in drug deposition whilst having the dose deposited in the lung from
different formulations being the same.The three formulation developed are labeled Fluticasone
Propionate Drug formulation 1 through 3.
Study Procedures and scheduling
The study is comprised of 5 visits in total - a screening visit and 4 treatment visits. At
least 5 days should lapse between the treatment visits.
Screening Visit During the screening visit, the inclusion and exclusion criteria will be
reviewed to ensure the volunteer is appropriate for the study. The informed consent will be
reviewed with the volunteer by a member of the study team and the volunteer will be
encouraged to ask questions to ensure the volunteer has a good understanding of the study. If
the volunteer is eligible and agrees to participate, the volunteer will be asked to sign the
informed consent form prior to any study specific procedures including randomization. After
the volunteer signs the informed consent, the volunteer will be interviewed and demographic
data, medical history and concomitant medications will be collected and recorded. A physical
examination will be performed after the vital sign measurements are obtained. A pregnancy
test for female volunteers will be obtained. Spirometry testing and inhalation training will
be performed by a qualified study clinician/investigator to ensure the suitability of
volunteers. Laboratory tests including a Complete Blood Count (CBC), urinalysis and metabolic
panel will be collected via venipuncture and processed in the lab. Screening tests will be
performed within 14 days of treatment visit 1 and no later than 2 days before treatment visit
1. All screening results will be evaluated by the study clinician/investigator against the
inclusion/exclusion criteria to confirm the eligibility of the volunteers.
Inhalation training: Inhalation training will be performed by a qualified study clinician at
the screening visit and at each study visit. The training will be accomplished by
instructions and subsequent inhalation via training devices containing empty capsules. The
instructions on how to use the device correctly are similar to the Foradil Aerolizer DPI
product information label. (http://www.rxlist.com/foradil-drug/medication-guide.htm )
Treatment Visits 1, 2, 3 and 4 Eligible volunteers will be asked to return for treatment
visit 1. A minimum period of 5 days should lapse between the subsequent treatment visits.
Each treatment visit is scheduled for 28 hours over two days. The study will be conducted at
the University of Florida (UF) CRC (Clinical Research Center). It is an outpatient study and
the volunteer will be asked to come back the following day for the 24 hour blood sample. The
volunteer will be asked to stay in an outpatient room during the treatment visit. The same
activities are carried out at the other treatment visits.
At each treatment visit, eligibility criteria will be reviewed and confirmed to ensure
volunteer is appropriate for study. Changes in medical history including concomitant
medications will be documented. Vital signs will be obtained. Inhalation training will be
provided to the volunteers as mentioned in the section above. An IV catheter will be inserted
in a vein located in the forearm region of the volunteer. The IV catheter is used to avoid
multiple pricks while collecting blood samples. The IV catheter is not used for the
administration of the drug. The volunteer inhales 5 times from a given inhaler during each
treatment visit. Each inhaler will be used only once and by only one volunteer to ensure the
volunteer's safety from infectious agents. The schedule below summarizes the procedures
performed at the screening visit and a single treatment visit.
Blood sample collection Blood samples will be drawn by inserting an indwelling catheter into
the volunteer's median cubital vein in the forearm region. Blood samples will be taken 15
minutes prior to the dosing of the product (pre-dose sample) and 5, 10, 15, 20, 30, 45, 60
minutes, 1.5, 2, 3, 4, 6, 8, 10, 12, 14 and 24 hours post dosing. At each time point 9ml of
blood sample will be collected of which the first 1ml will be discarded and the remaining 8
ml will be stored in a vacutainer tube for plasma preparation and storage.
Inclusion Criteria:
1. Healthy male or female subjects aged 18 to 50 years (inclusive).
2. Females will be eligible only if they are currently non-lactating and demonstrate a
negative urine pregnancy test. Female subjects must be willing to use highly effective
methods of contraception throughout the study. A highly effective method of birth
control is defined as one which results in a low failure rate (i.e. less than 1% per
year) when used consistently and correctly e.g. no sexual intercourse, an intrauterine
device (IUD), using contraceptive foam AND a condom (double-barrier).
3. Body weight ranging from 50 to 100 kg, corresponding to a BMI of 18-29 kg/m2.
4. Non-smoker for at least 12 months prior to study screening and a maximum smoking
history of less than ten-pack years (i.e. the equivalent of one-pack per day for ten
years).
5. Healthy and free of significant abnormal findings as determined by medical history,
physical examination, vital signs, laboratory tests (including serum cortisol at
screening), complete blood count (CBC) with differential, urinalysis and basic
metabolic panel.
6. Ability to read, comprehend and sign the consent form.
7. Ability and willingness to comply with all study procedures, discontinue and/or
withhold medications as specified in the protocol, and attend scheduled study visits.
8. No history of respiratory disease.
9. Normal baseline spirometry as predicted for age, sex and height, including forced
expiratory volume in 1 second / forced vital capacity (FEV1/FVC) > 0.8.
10. Healthy and without any pre-existing medical conditions.
Exclusion Criteria:
1. Any history and/or conditions that might interfere with drug absorption, distribution,
metabolism or excretion of FP, e.g., pre-existing lung and liver disease.
2. Known or suspected sensitivity to Flonase (Fluticasone Propionate), Veramyst
(Fluticasone Furoate), or related compounds in that class.
3. Hypersensitivity to milk proteins or lactose (inactive ingredients in the
formulation).
4. Having a history and/or currently having the medical condition in the opinion of
medically accountable investigator and hence taking any medication for the following
(including but not limited to):
4.1 Significant cardiac, dermatologic, gastrointestinal, hepatic, renal,
hematological, neurological and psychiatric disease (determined by physical exam, CBC
with differential, urinalysis, basic metabolic panel and medical history).
4.2 Presence of glaucoma, cataracts, ocular herpes simplex or carcinoma (other than
basal cell).
4.3 Presence of tuberculosis and other respiratory diseases (including but not limited
to intermittent or persistent asthma, emphysema and chronic bronchitis); or
respiratory infection, common cold, sinusitis or ear infections.
5. Current use of hormone replacement therapy (HRT), hormonal contraceptives and/or
corticosteroid treatment within the last 2 months.
6. Smoker during the last 1 year prior to study screening (self-report).
7. Evidence of a positive pregnancy urine test for female volunteers or females who are
pregnant or breast-feeding or are likely to become pregnant during the trial. Women of
child-bearing potential may be included in the study if, in the opinion of the
investigator, they are taking adequate contraceptive precautions as described above.
8. Exposure to any investigational drug within 30 days of enrolment.
9. Subjects who are unable to demonstrate proper inhalation of the test products.
10. Subjects who have a history of anemia.
11. Exposure to any medication that alters CYP3A4 activity within last 2 weeks (e.g.:
azole antifungals, rifampin).
12. Nausea, vomiting or diarrhoea within 7 days of dosing.
13. Subjects who have donated 1 pint (450 mL) of blood or more within the previous 8 weeks
prior to study administration.
14. Any history or current drug or alcohol abuse, which would interfere with the subject's
completion of the study and with adherence to the protocol.
15. A subject will not be eligible for this study if he/she is an immediate family member
of the participating investigator, sub-investigator, study coordinator, or employee of
the participating investigator.
16. The subject is the student of the Principal Investigator (PI).
17. Lack of willingness to have personal study related data collected, archived and
transmitted according to the protocol.
We found this trial at
1
site
Gainesville, Florida 32610
(352) 392-3261
Principal Investigator: Juergen Bulitta, PhD
Phone: 352-273-7861
University of Florida The University of Florida (UF) is a major, public, comprehensive, land-grant, research...
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