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Clinical Trials/JPRN-jRCT2080221493
JPRN-jRCT2080221493
Unknown
Phase 2

The clinical study to assess the efficacy, safety and pharmacokinetics of NS-304 in patients with pulmonary arterial hypertension (PAH)

IPPON SHINYAKU CO., LTD. / Actelion Pharmaceuticals Japan Ltd.0 sites30 target enrollmentJune 27, 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
IPPON SHINYAKU CO., LTD. / Actelion Pharmaceuticals Japan Ltd.
Enrollment
30
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 27, 2011
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
IPPON SHINYAKU CO., LTD. / Actelion Pharmaceuticals Japan Ltd.

Eligibility Criteria

Inclusion Criteria

  • Idiopathic pulmonary arterial hypertension (IPAH)
  • Heritable pulmonary arterial hypertension (HPAH)
  • Drug\- and Toxin\-induced pulmonary arterial hypertension
  • PAH associated with one of the following;
  • a) connective tissue disease
  • b) congenital heart disease (At least one year should be elapsed after pulmonary shunt at the time of each baseline measurement.)
  • c) HIV infection

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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