Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of Recombinant Human C1 Esterase Inhibitor in Healthy Adult Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Hereditary Angioedema (HAE)
In brief
This trial is looking to gain information about the safety and tolerability of an investigational treatment (SHP623) in healthy adult volunteers. This study will also collect pharmacokinetic data (how the body absorbs and breaks down the study drug).
Key facts
- Study ID
- NCT02663687
- Run by
- Shire
- People needed
- 48
- Starts
- 2016-02-19
- Expected to finish
- 2016-12-05
- Last updated by the study team
- 2021-06-03
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must be considered healthy. Healthy status is defined by absence of evidence of any active or chronic disease
- Male, or non-pregnant, non-lactating female, who agrees to comply with any applicable contraceptive requirements of the protocol, or females of non-child-bearing potential.
- Body mass index between 18.0 and 30.0 kg/m2 inclusive with a body weight >50 kg (110 lbs.). This inclusion criterion will be assessed only at the first screening visit.
- Hemoglobin ≥12.0g/ld.
You may not qualify if…
- Have a history of allergic reaction to C1 INH products (e.g. C1 Inhibitor [Human], Berinert [C1 Estrace Inhibitor (Human)] and C1 estrace [recombinant]
- Known history of alcohol or other substance abuse within the last year.
- Donation of blood or blood products within 60 days prior to receiving investigational product.
- Current use of any medication except hormonal replacement therapy, hormonal contraceptives and occasional use of any over-the-counter non-steroidal anti-inflammatory drug (NSAID) or acetaminophen.
- Have a history of hypercoagulability or other predisposition to thrombotic events.
Where it is running
- Clinical Pharmacology of Miami — Miami, Florida, United States
Full record on ClinicalTrials.gov
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