Phase I Study on Rivaroxaban Granules for Oral Suspension Formulation in Children

• Children with an age ≥2 months and weight between 3 and \<12 kg, who have completed anticoagulant treatment at least 10 days prior to the planned study drug administration.

  • Gestational age at birth of at least 37 weeks
  • Oral feeding/ nasogastric/ gastric feeding for at least 10 days
• Normal PT and aPTT within 10 days prior to planned study drug administration
• Written informed consent provided and, if applicable, child assent provided

Exclusion Criteria:

• Active bleeding or high risk for bleeding, contraindicating anticoagulant therapy
• Planned invasive procedures, including removal of central lines, within 24 hours before and after single dose intake
• An estimate glomerular filtration rate (eGFR) \< 30 mL/min/1.73m2

• Hepatic disease which is associated either with:

  • coagulopathy leading to a clinically relevant bleeding risk, or alanine aminotransferase (ALT) > 5x upper level of normal (ULN), or
  • total bilirubin > 2x ULN with direct bilirubin > 20% of the total.
• Platelet count \< 50 x 10\^9/L
• Hypertension (defined as systolic and/or diastolic blood pressure >95th percentile for age)
• Concomitant use of strong inhibitors of both CYP3A4 and P-glycoprotein, e.g., all human immunodeficiency virus protease inhibitors and the following azoleantimycotic agents: ketoconazole, itraconazole, voriconazole, and posaconazole, if used systemically (fluconazole is allowed)
• Concomitant use of strong inducers of CYP3A4, e.g., rifampicin, rifabutin, phenobarbital, phenytoin and carbamazepine
• Inability to cooperate with the study procedures
• Hypersensitivity to rivaroxaban
• Participation in a study with an investigational drug other than rivaroxaban or a medical device within 30 days prior to treatment
• History of gastrointestinal disease or surgery associated with impaired absorption