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A Feasibility Study to Collect Data in Patients With Haemophilia

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hemophilia

Treatments

Other: Laboratory variables

Study type

Observational

Funder types

Industry

Identifiers

NCT00798499
D0960M00006

Details and patient eligibility

About

The purpose of this study is to collect reference data in patients with haemophilia. The study will also collect and store blood samples for potential future exploratory research in the disease area.

Enrollment

50 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Provision of written informed consent
  • Patients with haemophilia, all severities
  • At least 18 years old.

Exclusion criteria

  • No exclusion criteria

Trial design

50 participants in 1 patient group

1
Description:
Laboratory variables
Treatment:
Other: Laboratory variables

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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