Study to See if Platelet Transfusion Stop or Lessen the Effect of the Drug on Platelets
Completed · Phase 1
Conditions studied: Inhibition on Platelet Aggregation
In brief
Study to see if platelet transfusion stop or lessen the effect of the drug on platelets
Key facts
- Study ID
- NCT01744288
- Run by
- AstraZeneca
- People needed
- 258
- Starts
- 2012-12-01
- Expected to finish
- 2014-04-01
- Last updated by the study team
- 2014-04-24
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Provision of signed and dated, written informed consent prior to any study specific procedures
- Healthy male and/or female volunteers aged 18 to 50 years, inclusive, with suitable veins for cannulation or repeated venipuncture. (Healthy as determined by medical history and physical examination, laboratory parameters, electrocardiogram (ECG) perform
- Have a body mass index (BMI) between 18 and 35 kg/m2 (inclusive) and weigh at least 50 kg and no more than 120 kg
You may not qualify if…
- ADP induced platelet aggregation <60% prior to platelet apheresis
- History of peptic ulcer disease Healthy volunteers with a propensity to bleed (eg, due to recent trauma, recent surgery, active or recent gastrointestinal bleeding or moderate hepatic impairment)
- Any clinically significant illness, medical/surgical procedure or trauma within 4 weeks of the first administration of the investigational product
- Current smokers, those who have smoked or used nicotine products within the previous 3 months and those who tested positive for cotinine at screening or at admission to the study center
Where it is running
- Research Site — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
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