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Clinical Trials/NCT02093923
NCT02093923
Completed
Phase 1

A Phase 1b, Double-Blind, Multiple Ascending Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DX-2930 in Hereditary Angioedema Subjects

Shire14 sites in 3 countries38 target enrollmentMay 14, 2014

Overview

Phase
Phase 1
Intervention
DX-2930
Conditions
Hereditary Angioedema (HAE)
Sponsor
Shire
Enrollment
38
Locations
14
Primary Endpoint
Number of Participants With Serious Adverse Events (SAE) and Treatment-Emergent Adverse Events (TEAE)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics (PK) profile of multiple subcutaneous administrations of DX-2930 across a range of doses in HAE participants.

Registry
clinicaltrials.gov
Start Date
May 14, 2014
End Date
May 18, 2015
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shire
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • At least 18 years of age at the time of screening
  • Documented diagnosis of HAE (Type I or II)
  • Experiencing ≥2 HAE attacks per year, with at least 1 attack in the past 6 months reported by the participant
  • Willing and able to read, understand, and sign an informed consent form
  • Females of childbearing potential must agree to be abstinent or else use acceptable forms of contraception throughout study
  • Males with female partners of childbearing potential must agree to be abstinent or use a medically acceptable form of contraception throughout study

Exclusion Criteria

  • Exposure to an investigational drug or device within 90 days prior to study
  • History of exposure within the past 5 years to a monoclonal antibody or recombinant protein bearing an Fc domain
  • Concomitant diagnosis of another form of chronic angioedema
  • Use of long-term prophylaxis for HAE within 90 days prior to study
  • Use of C1-INH that exceeds a total of 30 days within the past 90 days prior to study; any use of C1-INH within 7 days prior to study
  • Exposure to angiotensin-converting enzyme (ACE) inhibitors or any estrogen-containing medications with systemic absorption within 90 days prior to study
  • Exposure to androgens within 90 days prior to study
  • Presence of an indwelling catheter
  • Diagnosis of HIV
  • Active liver disease or liver function test abnormalities

Arms & Interventions

DX-2930, Cohort 1

Participants will receive 30 milligram (mg) dose of DX-2930 subcutaneous (SC) injection once and followed by the second dose after 2 week into the upper arm.

Intervention: DX-2930

DX-2930, Cohort 2

Participants will receive 100 mg dose of DX-2930 SC injection once and followed by the second dose after 2 week into the upper arm.

Intervention: DX-2930

DX-2930, Cohort 3

Participants will receive 300 mg dose of DX-2930 SC injection once and followed by the second dose after 2 week into the upper arm.

Intervention: DX-2930

DX-2930, Cohort 4

Participants will receive 400 mg dose of DX-2930 subcutaneous (SC) injection once and followed by the second dose after 2 week into the upper arm.

Intervention: DX-2930

Placebo

Participants will receive placebo matched to 30, 100, 300 and 400 mg dose of DX-2930 SC injection once and followed by the second dose after 2 week into the upper arm.

Intervention: Placebo

Outcomes

Primary Outcomes

Number of Participants With Serious Adverse Events (SAE) and Treatment-Emergent Adverse Events (TEAE)

Time Frame: From Day 1 up to final follow-up (Day 123)

A SAE was any adverse experience occurring at any dose that resulted in any of the following outcomes: Death, Life-threatening experience, required inpatient hospitalization or prolongation of existing hospitalization. Resulted in persistent or significant disability or incapacity. Was a congenital anomaly or birth defect. Was considered to be an important medical event. An AE was considered treatment-emergent if the onset time was after administration of study drug through the Day 120 post-dose final follow-up visit or, in the event that onset time preceded study drug administration, the AE increased in severity during the 120-day post-dose follow-up period.

Secondary Outcomes

  • Apparent Clearance (CL/F)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)
  • Terminal Elimination Half-Life (t1/2)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)
  • Time to Maximum Plasma Concentration (Tmax)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)
  • Area Under the Plasma Concentration-Time Curve (AUC)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)
  • Apparent Volume of Distribution (Vd/F)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)
  • Maximum Plasma Concentration (Cmax)(Days 1, 2, 4, 8, 15, 16, 18, 22, 29, 36, 50, 64, 92, and 120)

Study Sites (14)

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