Escalating Single Dose Study of Epsi- Gam in Healthy Normal Subjects
A Phase I, Randomized, Double-Blind, Placebo-Controlled, Escalating Single Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Epsi- Gam in Healthy, Cat-, Dust Mite-, or Bermuda Grass-Allergic Subjects
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Typ studie
Typ studie
Zápis (Aktuální)
Zápis
Fáze
Fáze
- Fáze 1
Kontakty a umístění
Studijní místa
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Queensland
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Brisbane, Queensland, Austrálie, 4006
- Q-Pharm
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-
Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Eligible subjects must meet all of the following inclusion criteria:
- Be informed of the nature of the study and provide written informed consent prior to undergoing screening procedures.
- Be a healthy male of any race or ethnicity, at least 18 years of age and no more than 65 years of age, inclusively, OR
- Be a healthy female of any race or ethnicity of non-childbearing potential, at least 18 years of age and no more than 65 years of age, inclusively, OR
- Be a healthy non-pregnant, non-lactating female of any race or ethnicity of childbearing potential, at least 18 years of age and no more than 65 years of age, inclusive, with a negative pregnancy test who agrees to use 2 medically acceptable forms of birth control from Screening through 57 days after receiving study drug.
- Have a Body Mass Index (BMI) within the range of 18.5 to 30.0 kg/m2.
- Have a history of allergic reactivity to cats, dust mite, or Bermuda grass as expressed by allergic symptoms including rhinitis.
- Standardized cat allergenic extract (10,000 BAU/mL, ALK- Abello), dust mite allergenic extract (10,000 AU/mL, ALK- Abello), dust mite allergenic extract (10,000 AU/mL, ALK- Abello), or Bermuda grass allergenic extract (10,000 BAU/mL, ALK- Abello) elicits a wheal at least 5 mm up to approximately 10-15 mm in diameter that exceeds two diluent controls by at least 4 mm.
- Have allergen-specific IgE for cat, dust mite, or Bermuda grass as measured by ImmunoCAP® with a Class rating of 1 or greater.
- Histamine reactivity of 3 mm or greater, with surrounding erythema, on testing using a standardized epicutaneous delivery device.
- Be able and willing to discontinue any first and second generation antihistamine use beginning at least 7 days prior to undergoing initial screening skin puncture tests and throughout study participation.
- Have baseline spirometry (FEV1, FVC, FEF 25%-75%) with FEV1 ≥ 80% predicted and other values within the normal range.
Exclusion Criteria:
Subjects who meet any of the following criteria must be excluded:
- Diluent control elicits a wheal ≥ 3 mm on testing.
- History of severe systemic allergic reactions to cats, dust mite, or Bermuda grass
- Clinical history of persistent asthma
- Dermatographism or any skin disorder (i.e., atopic dermatitis) that would make skin testing or proper interpretation impractical.
- Chronic urticaria.
- Underlying heart, liver, kidney, or lung disease or any other medical condition such that the subject would be at increased risk for a poor outcome should a generalized allergic or other reaction occur.
- Any abnormal laboratory value(s) considered to be clinically significant by the Investigator.
- Use of systemic corticosteroids within the past three months prior to initial screening.
- Use of topical corticosteroids on the area(s) to undergo skin tests within the past three weeks prior to initial screening.
- Use of systemic beta-blocking or ACE-inhibiting agents within the past three weeks prior to initial screening.
- Use of tricyclic antidepressants within the past three weeks prior to initial screening.
- Use of H2 antagonists within 24 hours prior to initial screening.
- Use of any agents known or likely to interact with adrenaline.
- Use of omalizumab (Xolair®) within the past six months prior to enrolment.
- Pregnant females as determined by a positive serum or urine hCG test.
- Lactating females.
- Participation in another experimental drug or device trial and receipt of an investigational product within the past 30 days, five half-lives or twice the duration of the biochemical effect of the investigational product (whichever is longer) prior to dosing in the present study.
- Any mental impairment as judged by the Investigator that would limit ability to comply with study requirements.
- History of infection with, or positive screen for, Hepatitis B (HBsAg, Hepatitis B Surface Antigen), Hepatitis C (HCVAb, Hepatitis C Antibody), or Human Immunodeficiency Virus (HIV 1 or 2).
- Positive urine screen for drugs of abuse. Positive ethanol breath test.
- Concurrent disease or condition, that, in the opinion of the Investigator, places the subject at high risk of poor treatment compliance or of not completing the study.
- Has smoked or consumed nicotine-containing products within past 3 months prior to receiving study drug or has a positive urine test for cotinine, and does not agree to refrain from smoking for the duration of the study.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Randomizované
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Čtyřnásobek
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
|---|---|
|
Experimentální: Kohorta 1
|
administered as a single intravenous infusion on Day 1, infused over 30 minutes
|
|
Experimentální: Kohorta 2
|
administered as a single intravenous infusion on Day 1 infused over 30 minutes
|
|
Experimentální: Kohorta 3
|
administered as a single intravenous infusion on Day 1 infused over 30 minutes
|
|
Experimentální: Kohorta 4
|
administered as a single intravenous infusion on Day 1 infused over 60 minutes
|
|
Experimentální: Kohorta 5
|
administered as a single intravenous infusion on Day 1 infused over 120 minutes
|
Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Safety and tolerability will be assessed by monitoring AEs (frequency and severity) and SAEs, vital signs, PFTs
Časové okno: From start of study drug administration through Day 57 (+/- 2 days)
|
ECGs, clinical laboratory values (including clinically significant changes from baseline) from blood and urine samples, performing physical examinations and pregnancy tests and reviewing concomitant medications.
|
From start of study drug administration through Day 57 (+/- 2 days)
|
Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Spolupracovníci
Spolupracovníci
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Začátek studia
Primární dokončení (Aktuální)
Primární dokončení
Dokončení studie (Aktuální)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další identifikační čísla studie
Další identifikační čísla studie
- TUN001-101
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