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A PHASE IV NON-INTERVENTIONAL STUDY. REGISTRY OF ADVERSE EVENTS (AES)/SUSPECTED ADVERSE DRUG REACTIONS (SADRS) OF ADULT PATIENTS UNDER TREATMENT OF DEEP VEIN THROMBOSIS (DVT) AND PULMONARY EMBOLISM (PE); PREVENTION OF RECURRENT DVT AND PE WITH ELICUIS REGISTERED (APIXABAN)

Trial Profile

A PHASE IV NON-INTERVENTIONAL STUDY. REGISTRY OF ADVERSE EVENTS (AES)/SUSPECTED ADVERSE DRUG REACTIONS (SADRS) OF ADULT PATIENTS UNDER TREATMENT OF DEEP VEIN THROMBOSIS (DVT) AND PULMONARY EMBOLISM (PE); PREVENTION OF RECURRENT DVT AND PE WITH ELICUIS REGISTERED (APIXABAN)

Status: Withdrawn prior to enrolment
Phase of Trial: Phase IV

Latest Information Update: 15 Nov 2021

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At a glance

  • Drugs Apixaban (Primary)
  • Indications Deep vein thrombosis; Pulmonary embolism
  • Focus Adverse reactions
  • Sponsors Pfizer
  • Most Recent Events

    • 09 Nov 2021 Status changed from not yet recruiting to withdrawn prior to enrolment due to company decision to not conduct study and was cancelled prior to any enrollment.
    • 29 Mar 2021 Planned End Date changed from 28 Feb 2023 to 23 Aug 2023.
    • 29 Mar 2021 Planned primary completion date changed from 30 Aug 2022 to 23 Aug 2023.

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