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

NCT02559258 | Terminated Phase 1

• 1 other identifier: TUN001-101
• Study Type: interventional
• Target: 5
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Allergy and Immunology

Outcome Measures

Primary Outcomes (1)

• Safety and tolerability will be assessed by monitoring AEs (frequency and severity) and SAEs, vital signs, PFTs

  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)

Study Arms (5)

Cohort 1

EXPERIMENTAL

Drug: 0.1 mg/kg epsi-gam or placebo (6:2)

Cohort 2

EXPERIMENTAL

Drug: 0.3 mg/kg epsi-gam or placebo (6:2)

Cohort 3

EXPERIMENTAL

Drug: 1.0 mg/kg epsi-gam or placebo (6:2)

Cohort 4

EXPERIMENTAL

Drug: 3 mg/kg epsi-gam or placebo (6:2)

Cohort 5

EXPERIMENTAL

Drug: 10 mg/kg epsi-gam or placebo (6:2)

Interventions

0.1 mg/kg epsi-gam or placebo (6:2) DRUG

administered as a single intravenous infusion on Day 1, infused over 30 minutes

Cohort 1

0.3 mg/kg epsi-gam or placebo (6:2) DRUG

administered as a single intravenous infusion on Day 1 infused over 30 minutes

Cohort 2

10 mg/kg epsi-gam or placebo (6:2) DRUG

administered as a single intravenous infusion on Day 1 infused over 120 minutes

Cohort 5

3 mg/kg epsi-gam or placebo (6:2) DRUG

administered as a single intravenous infusion on Day 1 infused over 60 minutes

Cohort 4

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Tunitas Therapeutics, Inc.: lead
• Tunitas Therapeutics Australia Pty Ltd: collaborator

Study Sites (1)

Q-Pharm

Brisbane, Queensland, 4006, Australia

Location

MeSH Terms

Conditions

Hypersensitivity

Condition Hierarchy (Ancestors)

Immune System Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 2, 2015
• First Posted: September 24, 2015
• Study Start: August 1, 2015
• Primary Completion: May 1, 2016
• Study Completion: May 1, 2016
• Last Updated: June 17, 2016

Record last verified: 2016-06

Locations

AU (1)