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Phase 1 Completed N=91 Randomized Treatment

Clinical Study to Evaluate Z7200 Pharmacokinetics Profile

Source: ClinicalTrials.gov NCT02631941 ↗
Enrolled (actual)
91
Serious AEs
0.0%
Results posted
Jan 2022
Primary outcomePrimary: AUC0-last of Budesonide With and Without Charcoal Blockade — 1710; 1710; 1570; 1530 pg*h/mL — p=<0.001

Summary

Brief Summary: The primary objective was: * to assess the bioequivalence of a single dose (two inhalations) of the test product compared to the reference product, with and without charcoal blockade. The secondary objectives were: * to assess the pharmacokinetic profile of budesonide and formoterol in plasma after a single dose (two inhalations) of the test product and the reference product, with and without charcoal blockade. * to assess the safety and tolerability of the test product and the reference product, with and without charcoal blockade.

Outcome Measures

OutcomeResultp-value
PRIMARY
AUC0-last of Budesonide With and Without Charcoal Blockade
1710; 1710; 1570; 1530 <0.001 sig
PRIMARY
AUC0-last of Formoterol With and Without Charcoal Blockade
46.1; 52.6; 39.0; 42.8 0.002 sig
PRIMARY
Cmax of Budesonide With and Without Charcoal Blockade
1080; 686; 1110; 663 1.00
PRIMARY
Cmax of Formoterol With and Without Charcoal Blockade
10.1; 11.9; 10.3; 11.7 0.012 sig
SECONDARY
AUC0-30 of Budesonide With and Without Charcoal Blockade.
313; 238; 315; 237
SECONDARY
AUC0-30 of Formoterol With and Without Charcoal Blockade.
3.37; 3.88; 3.36; 3.76
SECONDARY
AUC0-∞ of Budesonide With and Without Charcoal Blockade
1820; 1830; 1670; 1640
SECONDARY
AUC0-∞ of Formoterol With and Without Charcoal Blockade
55.4; 63.0; 46.8; 53.7
SECONDARY
Tmax for Budesonide With and Without Charcoal Blockade
0.080; 0.250; 0.040; 0.250
SECONDARY
Tmax for Formoterol With and Without Charcoal Blockade
0.080; 0.080; 0.080; 0.080
SECONDARY
t1/2 for Budesonide With and Without Charcoal Blockade
3.21; 3.14; 3.23; 3.01
SECONDARY
t1/2 for Formoterol With and Without Charcoal Blockade
9.35; 9.28; 9.45; 9.08
SECONDARY
Change From Baseline in Forced Expiratory Volume in 1 Second (FEV1)
0.188; 0.170; 0.173; 0.153
SECONDARY
Change From Baseline in the Ratio of Forced Expiratory Volume in 1 Second to Forced Vital Capacity (FEV1/FVC)
3.94; 3.78; 3.75; 3.83
SECONDARY
Change From Baseline in Peak Expiratory Flow Rate (PEFR)
32.3; 22.4; 30.3; 19.3

Eligibility Criteria

Main Inclusion Criteria:

  • Male or female 18 to 45 years of age.
  • If female, is currently not pregnant/breast feeding/ or attempting to become pregnant has a negative serum pregnancy test, or is of non-childbearing potential or is of child-bearing potential, willing to commit to using a consistent and acceptable method of birth control or is of child-bearing potential and not sexually active
  • Body mass index (BMI) of 18.0 to 32.0 kg/m² inclusive and a body weight ≥50 kg.
  • 10 years or more past history of cigarette, <=5 pack year

Main Exclusion Criteria:

  • Forced Expiratory Volume in 1 sec (FEV1) value less than 80% of the predicted value and FEV1/FVC (Forced Vital Capacity) ratio <0.7.
  • History or current evidence of a clinically significant disease or disorder capable of altering the absorption, metabolism, distribution or elimination of drugs.
  • History or current evidence of a clinically significant disease including, but not limited to: cardiovascular, hepatic, renal, haematological, neuropsychological, endocrine, gastrointestinal or pulmonary.
  • Presence of glaucoma, cataracts, ocular herpes simplex, malignancy, regardless of the clinical significance or current stability of the disease.
  • positive tests for Human Immunodeficiency Virus (HIV), Hepatitis B and Hepatitis C.
  • Bacterial or viral infection of the upper respiratory tract (including the common cold and flu), sinus, or middle ear within 2 weeks of dosing.
  • Lower respiratory tract infection/pneumonia within the past 3 months.
  • Presence of any disease or condition or regular concomitant treatment (including vitamins and herbal products) known to interfere with the absorption, distribution, metabolism or excretion of drugs.
  • Screening haemoglobin value of less than 1g/dL above the Lower Limit of Normality
  • History of recurrent vasovagal collapses.
  • History of anaphylactic/anaphylactoid reactions.
  • History of seizures including febrile seizures excluding childhood febrile convulsions.
  • Unable to demonstrate proper inhalation techniques involved in using the delivery devices at screening.
  • Exposure to any investigational drug within 90 days of the Screening Visit.
  • Known or suspected hypersensitivity or idiosyncratic reaction to any steroid, any β2 agonist; allergy to milk protein.
  • Use of an inhaled corticosteroid within 30 days or systemic corticosteroid within 60 days of the Screening Visit.
  • Use of medications or herbal medicines that are strong cytochrome P450 3A4 (CYP3A4) inhibitors or inducers within 30 days prior to Screening Visit
  • Any clinically significant abnormal laboratory value or physical finding that may interfere with the interpretation of test results or cause a health risk for the subject if he/she participates in the study.
  • Use of caffeine containing beverages more than 5 cups/day.
  • Recent or current (suspected) drug abuse or positive result in the drugs abuse test.
  • Recent or current alcohol abuse (regular drinking more than 21 units per week for males and more than 14 units per week for females)
  • Predictable poor compliance, intolerance to charcoal solution, or inability to communicate well with the study centre personnel or inability to participate in all treatment periods.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02631941). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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