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NCT02953496

Safety/ Feasibility of Percutaneous Administration of Vonapanitase as Monotherapy for Peripheral Artery Disease (PAD) of the SFA and Popliteal Arteries

Withdrawn Phase 1 Last updated 2 May 2019
What this trial tests

Phase 1 trial testing vonapanitase in Peripheral Artery Disease. Withdrawn.

Timeline
Primary endpoint
30 April 2019
30 April 2019

Quick facts

Lead sponsorProteon Therapeutics
PhasePhase 1
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Primary completion30 April 2019
Estimated completion30 April 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Proteon Therapeutics — full company profile →

Who can join

Adults 18 to 100, any sex, with Peripheral Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The research study is designed to assess the technical feasibility and safety of percutaneous administration of vonapanitase to the superficial femoral or popliteal artery in patients with PAD.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Peripheral Artery Disease

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02953496.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing