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NCT02906124

Study to Evaluate the Safety of Repatha® in Pregnancy

Terminated Last updated 22 December 2020
What this trial tests

trial in Hypercholesterolaemia in 4 participants. Terminated before completion.

Timeline
12 January 2017
Primary endpoint
6 November 2020
6 November 2020

Quick facts

Lead sponsorAmgen
StatusTerminated
Study typeOBSERVATIONAL
Enrollment4
Start date12 January 2017
Primary completion6 November 2020
Estimated completion6 November 2020
Sites48 locations across Denmark, Italy, Netherlands, Slovakia, Greece, Belgium, Austria, Sweden

Conditions studied

Sponsor

Amgen — full company profile →

Who can join

Eligibility, female only, with Hypercholesterolaemia or Pregnancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate pregnancy and infant outcomes among females diagnosed with familial hypercholesterolaemia (FH), exposed to Repatha® during pregnancy. This includes follow-up of their infants to the age of 12 months

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Safety and Tolerability of PCSK9 Inhibitors: Current Insights.
    Kosmas CE, Skavdis A, Sourlas A, Papakonstantinou EJ, et al · · 2020 · cited 34× · PMID 33335431 · DOI 10.2147/cpaa.s288831

Verify or expand the search:

Other recruiting trials for Hypercholesterolaemia

Currently open trials in the same condition.

Other Amgen 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/NCT02906124.

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