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Escalating Single Dose Study of Epsi- Gam in Healthy Normal Subjects

15 juin 2016 mis à jour par: Tunitas Therapeutics, Inc.

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

This is a single-center, randomized, double-blind, placebo-controlled, single-dose, dose- escalation study in otherwise healthy cat-, dust mite-, or Bermuda grass-allergic male and female subjects. There will be five dosing cohorts (0.1, 0.3, 1.0, 3.0 and 10.0 mg/kg), with eight subjects in each cohort, randomized to either epsi-gam (6 subjects) or placebo (2 subjects) for a total of 40 subjects. The first cohort will receive the starting dose of 0.1 mg/kg epsi-gam or placebo and subsequent cohorts will be recruited sequentially to receive escalating doses of epsi-gam or placebo.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

5

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Queensland
      • Brisbane, Queensland, Australie, 4006
        • Q-Pharm

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Eligible subjects must meet all of the following inclusion criteria:

  1. Be informed of the nature of the study and provide written informed consent prior to undergoing screening procedures.
  2. 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
  3. 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
  4. 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.
  5. Have a Body Mass Index (BMI) within the range of 18.5 to 30.0 kg/m2.
  6. Have a history of allergic reactivity to cats, dust mite, or Bermuda grass as expressed by allergic symptoms including rhinitis.
  7. 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.
  8. Have allergen-specific IgE for cat, dust mite, or Bermuda grass as measured by ImmunoCAP® with a Class rating of 1 or greater.
  9. Histamine reactivity of 3 mm or greater, with surrounding erythema, on testing using a standardized epicutaneous delivery device.
  10. 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.
  11. 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:

  1. Diluent control elicits a wheal ≥ 3 mm on testing.
  2. History of severe systemic allergic reactions to cats, dust mite, or Bermuda grass
  3. Clinical history of persistent asthma
  4. Dermatographism or any skin disorder (i.e., atopic dermatitis) that would make skin testing or proper interpretation impractical.
  5. Chronic urticaria.
  6. 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.
  7. Any abnormal laboratory value(s) considered to be clinically significant by the Investigator.
  8. Use of systemic corticosteroids within the past three months prior to initial screening.
  9. Use of topical corticosteroids on the area(s) to undergo skin tests within the past three weeks prior to initial screening.
  10. Use of systemic beta-blocking or ACE-inhibiting agents within the past three weeks prior to initial screening.
  11. Use of tricyclic antidepressants within the past three weeks prior to initial screening.
  12. Use of H2 antagonists within 24 hours prior to initial screening.
  13. Use of any agents known or likely to interact with adrenaline.
  14. Use of omalizumab (Xolair®) within the past six months prior to enrolment.
  15. Pregnant females as determined by a positive serum or urine hCG test.
  16. Lactating females.
  17. 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.
  18. Any mental impairment as judged by the Investigator that would limit ability to comply with study requirements.
  19. 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).
  20. Positive urine screen for drugs of abuse. Positive ethanol breath test.
  21. 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.
  22. 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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Cohorte 1
administered as a single intravenous infusion on Day 1, infused over 30 minutes
Expérimental: Cohorte 2
administered as a single intravenous infusion on Day 1 infused over 30 minutes
Expérimental: Cohorte 3
administered as a single intravenous infusion on Day 1 infused over 30 minutes
Expérimental: Cohorte 4
administered as a single intravenous infusion on Day 1 infused over 60 minutes
Expérimental: Cohorte 5
administered as a single intravenous infusion on Day 1 infused over 120 minutes

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Safety and tolerability will be assessed by monitoring AEs (frequency and severity) and SAEs, vital signs, PFTs
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 août 2015

Achèvement primaire (Réel)

1 mai 2016

Achèvement de l'étude (Réel)

1 mai 2016

Dates d'inscription aux études

Première soumission

2 septembre 2015

Première soumission répondant aux critères de contrôle qualité

23 septembre 2015

Première publication (Estimation)

24 septembre 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

17 juin 2016

Dernière mise à jour soumise répondant aux critères de contrôle qualité

15 juin 2016

Dernière vérification

1 juin 2016

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • TUN001-101

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

Essais cliniques sur Allergie et immunologie

Essais cliniques sur 0.1 mg/kg epsi-gam or placebo (6:2)

3
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