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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04336449
Other study ID # 18899A
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date April 1, 2020
Est. completion date August 13, 2020

Study information

Verified date August 2020
Source H. Lundbeck A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate how eptinezumab enters, moves through and exits the body. Safety and tolerability will also be investigated.


Description:

The study will consist of 18 healthy Japanese subjects, divided into two single dose cohorts with 9 subjects in each cohort.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date August 13, 2020
Est. primary completion date August 13, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 55 Years
Eligibility Inclusion Criteria:

- Healthy Japanese subjects with a BMI of = 18.5 and = 25 kg/m2

Other in- and exclusion criteria may apply

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Eptinezumab
Eptinezumab - single intravenous infusion
Placebo
Placebo - single intravenous infusion

Locations

Country Name City State
Japan P-One Clinic Tokyo

Sponsors (1)

Lead Sponsor Collaborator
H. Lundbeck A/S

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cmax eptinezumab maximal observed plasma concentration From dosing to week 12
Primary AUC(0-t) eptinezumab area under the plasma concentration-time curve from zero to time t From dosing to week 12
Primary AUC(0-inf) eptinezumab area under the plasma concentration-time curve from zero to infinity From dosing to week 12
Primary Systemic Clearance of eptinezumab From dosing to week 12
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