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)
Latest Information Update: 15 Nov 2021
At a glance
- Drugs Apixaban (Primary)
- Indications Deep vein thrombosis; Pulmonary embolism
- Focus Adverse reactions
- Sponsors Pfizer
- 09 Nov 2021 Status changed from not yet recruiting to withdrawn prior to enrolment due to company decision to not conduct study and was cancelled prior to any enrollment.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.