Pelacarsen Roll-over Extension Program

Novartis Pharmaceuticals

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Brief summary

This non-randomized, rollover extension study will provide post-trial access to pelacarsen (TQJ230) to participants who have successfully completed either of the double-blind parent studies (CTQJ230A12303 or CTQJ230A12304). Study has been terminated by sponsor following the outcome of the Lp(a)HORIZON study (NCT04023552), which did not meet its primary endpoint.

Source: ClinicalTrials.gov (U.S. National Library of Medicine), data processed 2026-10-29T09:00:05; modifications: selected fields only; whitespace normalized; brief summary truncated to 2,000 characters. Not a U.S. Government endorsement.

Trial details

status
ACTIVE_NOT_RECRUITING
phase
PHASE3
study type
INTERVENTIONAL
enrollment
599
sponsor
Novartis Pharmaceuticals
conditions
Atherosclerotic Cardiovascular Disease
interventions
DRUG: Pelacarsen (TQJ230)
start date
2025-05-19
start date type
ACTUAL
primary completion date
2030-12-08
has results
false
data source
ClinicalTrials.gov
data processed
2026-10-29T09:00:05
modifications
selected fields only; whitespace normalized; brief summary truncated to 2,000 characters

Record

Archive ID
nct:NCT06875973
Published
Mar 14, 2025
Updated
Oct 14, 2026
Venue
ClinicalTrials.gov
ClinicalTrials.gov
NCT06875973
Categories
Atherosclerotic Cardiovascular Disease
License
ClinicalTrials.gov terms (attribution, processing date, modifications noted)
Provenance
clinicaltrials

Topics