Trial Condition(s):

Primary pulmonary hypertension

Ventavis 20:PK compared with Ventavis 10 in healthy subjects

Bayer Identifier:

15762

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

2012-000119-10

Study Completed

Trial Purpose

Please see attached Study Results Summary below.

Inclusion Criteria
No Inclusion Criteria Available
Exclusion Criteria
No Exclusion Criteria Available

Trial Summary

Enrollment Goal
21
Trial Dates
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Phase
1
Could I receive a placebo?
No
Products
Ventavis (Iloprost, BAYQ6256)
Accepts Healthy Volunteers
N/A

Where to Participate

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Locations
Status
LocationsStatus
Locations

Bayer Pharma AG

Berlin, Germany, 13353

Status
Completed
 

For details, please refer to trial results

Additional Information