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A Post-Approval, Single-Arm Study of the SYNERGY Stent System in China

A prospective, observational, single-arm, open-label, multicenter, post-approval study. To compile real-world clinical outcomes data for the SYNERGYTM MONORAILTM Everolimus-Eluting ...

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DENEX Renal Denervation in Patients With Hypertension on no or 1-3 Antihypertens...

The objective of this study is to show that the safety and efficacy of renal denervation using DENEX, are superior...

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A Clinical Trial to Confirm Safety & Effectiveness of the SYNERGY 4.50 mm and 5....

EVOLVE 4.5/5.0 is a prospective, single-arm, multi-center observational (standard of care) trial intended to confirm the safety and effectiveness of...

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A Feasibility Study of the Millipede Transcatheter Annuloplasty Ring System in P...

To evaluate the feasibility and safety of the Millipede Transcatheter Annuloplasty Ring System (Millipede System) in patients with functional mitral...

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A Study Evaluating the Efficacy and Safety of Ralinepag to Improve Treatment Out...

Study ROR-PH-301, ADVANCE OUTCOMES, is designed to assess the efficacy and safety of ralinepag when added to pulmonary arterial hypertension...

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NAN-101 in Patients With Class III Heart Failure

This is a Phase 1, prospective, multi-center, open-label, sequential dose escalation study to explore the safety, feasibility, and efficacy of...

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Natural Killer Cell (CYNK-001) Infusions in Adults With Multiple Myeloma

This study will find the maximum tolerated dose of CYNK-001 which contain NK cells derived from human placental CD34+ cells...

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A Study of Ralinepag to Evaluate Effects on Exercise Capacity by CPET in Subject...

Study ROR-PH-302, ADVANCE CAPACITY, is designed to evaluate the effects of ralinepag therapy on exercise capacity as assessed by change...