A Study of HS135 for the Treatment of Pulmonary Arterial Hypertension in Adults
Phase 1b, Multicenter, Open-Label, Multiple Ascending Dose Study Assessing the Pharmacokinetics, Safety, Pharmacodynamics, and Efficacy of HS135 Added to Background Pulmonary Arterial Hypertension (PAH) Therapy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
HS135 is dosed subcutaneously
Site-501
Edmonton, Alberta, Canada
Site-202
Greifswald, Germany
Adverse Events (AEs)
Time frame: Up to 24 weeks
Change from Baseline in Physical Examination
Physical Examination will include the assessment of body systems.
Time frame: Up to 24 weeks
Change from Baseline in Clinical Laboratory Parameters
Time frame: Up to 24 weeks
Change from Baseline in Blood Pressure
Time frame: Up to 24 weeks
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