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NCT02971930

Exit Interviews to Assess Impact of Infusion Frequency in Hemophilia A

Completed Last updated 1 February 2018
What this trial tests

trial testing BAY94-9027 in Hemophilia A in 30 participants. Completed in 15 December 2017.

Timeline
20 June 2017
Primary endpoint
26 November 2017
15 December 2017

Quick facts

Lead sponsorBayer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date20 June 2017
Primary completion26 November 2017
Estimated completion15 December 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

18 and older, any sex, with Hemophilia A. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is to generate qualitative data to evaluate the impact of frequency of FVIII infusions on patients' satisfaction with treatment and their quality of life.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of BAY94-9027

Trials testing the same drug.

Other recruiting trials for Hemophilia A

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02971930.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing