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NCT03320265

Phosphorylcholine PC-mAb Effects in Subjects With Elevated Lipoprotein a

Terminated Phase 2 Last updated 6 July 2018
What this trial tests

Phase 2 trial testing PC-mAb in Arterial Inflammation in 10 participants. Terminated before completion.

Timeline
11 October 2017
Primary endpoint
19 March 2018
3 July 2018

Quick facts

Lead sponsorAthera Biotechnologies AB
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment10
Start date11 October 2017
Primary completion19 March 2018
Estimated completion3 July 2018
Sites2 locations across Sweden, Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Athera Biotechnologies AB — full company profile →

Who can join

50 and older, any sex, with Arterial Inflammation or Cardiovascular Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Inflammation and abnormal amount of lipids in the blood are key factors for the development and progression of atherosclerosis (thickening of the artery wall) and cardiovascular disease. Lipoprotein (a) is a pro-inflammatory plasma lipoprotein that is believed to be a risk factor for cardiovascular diseases. Vascular inflammation generates a range of effects, including endothelial dysfunction and migration of white blood cells into the vessel wall, which results in increased risk of cardiovascular events. This study is designed to assess the effects of multiple monthly intravenous infusions with the fully human antibody called PC-mAb, in subjects with elevated lipoprotein (a).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Athera Biotechnologies AB trials

Trials by the same sponsor.

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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/NCT03320265.

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