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American Heart Association

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Final ID: Mo3132

A 3-Year, Pre-Trial, Real-world Data Analysis of Patients Enrolled in VICTORION-INITIATE: Insights Using Tokenization

Abstract Body (Do not enter title and authors here): Background: VICTORION-INITIATE (NCT04929249) showed significantly greater LDL-C lowering in patients (pts) with ASCVD with an inclisiran first (IF) strategy (adding inclisiran immediately on failure to achieve LDL-C <70 mg/dL on maximally tolerated statin therapy) vs usual care (UC). Tokenization can be leveraged to link clinical trial data to pt-level real-world data (RWD) to provide a comprehensive overview of the pt journey pre- and post-trial and enhance understanding of clinical trial and long-term pt outcomes.

Aim: To utilize tokenization and linked RWD to characterize the pt journey pre-VICTORION-INITIATE enrollment.

Methods: Eligible pts from VICTORION-INITIATE were deidentified and tokenized with unique IDs, allowing linking to RWD (EMR, claims, hospital, and lab records) to follow the pt journey in the 3-year pre-trial and 2-year post-trial periods. Here we present demographics, clinical characteristics, and lipid-lowering therapy (LLT) use of pts with linked pre-trial RWD.

Results: Of 450 pts randomized, 383 (85.1%) were linked with pre-trial RWD (IF arm, n=193; UC arm, n=190); 26.9% were female, first available recorded mean (SD) age was 64 (9.36) years. Among the 74.2% (n=284) of pts with linked, pre-trial, lipid test RWD, mean (SD) earliest and latest LDL-C values were 100.1 mg/dL (35.70) and 99.3 mg/dL (30.06), respectively, for pts in the IF arm vs 97.3 mg/dL (40.43) and 97.8 mg/dL (27.60) for pts in the UC arm (Table). Overall, in the pre-trial period, LLT was dispensed/prescribed to 66.1% of pts, statins to 64.5%, ezetimibe to 4.4%, and PCSK9i to 4.4%. Of pts with ≥1 recorded ASCVD events in the pre-trial period (n=141), 53.2% and 68.8% had available LLT dispensing/prescription records pre- and post-event, respectively.

Conclusions: In the 3 years pre-VICTORION-INITIATE, mean LDL-C levels were above recommended goals, non-statin LLT prescription was infrequent, and ~31% of pts with ≥1 recorded ASCVD event had no evidence of post-event LLT use, highlighting a need for more aggressive LDL-C management. Full data visibility for each pt is a limitation of this approach. Tokenization post-trial will allow for long-term evaluation of LLT practices.
  • Rodriguez, Fatima  ( Stanford University School of Medicine , Stanford , California , United States )
  • Cosmatos, Irene  ( United BioSource Corporation , Blue Bell , Pennsylvania , United States )
  • Desai, Nihar  ( Yale School of Medicine , New Haven , Connecticut , United States )
  • Wright, R  ( Mayo Clinic , Rochester , Minnesota , United States )
  • Ross, Elsie  ( University of California San Diego Health , San Diego , California , United States )
  • Ali, Yousuf  ( Novartis Pharmaceutical Corporation , East Hanover , New Jersey , United States )
  • Kumar, Biswajit  ( Novartis Pharmaceutical Corporation , East Hanover , New Jersey , United States )
  • Han, Guangyang  ( Novartis Pharmaceutical Corporation , East Hanover , New Jersey , United States )
  • Cai, Beilei  ( Novartis Pharmaceutical Corporation , East Hanover , New Jersey , United States )
  • Abbas, Cheryl  ( Novartis Pharmaceutical Corporation , East Hanover , New Jersey , United States )
  • Ryan, Amy  ( United BioSource Corporation , Blue Bell , Pennsylvania , United States )
  • Author Disclosures:
    Fatima Rodriguez: DO have relevant financial relationships ; Consultant:HealthPals:Active (exists now) ; Consultant:iRhythm:Active (exists now) ; Consultant:HeartFlow:Active (exists now) ; Consultant:Arrowhead Pharmaceuticals:Active (exists now) ; Consultant:Edwards:Past (completed) ; Consultant:Inclusive Health:Active (exists now) ; Consultant:Kento Health:Active (exists now) ; Consultant:Movano Health:Active (exists now) ; Consultant:Esperion Therapeutics:Past (completed) ; Consultant:NovoNordisk:Active (exists now) ; Consultant:Novartis:Active (exists now) | irene cosmatos: DO NOT have relevant financial relationships | Nihar Desai: DO have relevant financial relationships ; Researcher:Amgen:Active (exists now) ; Consultant:CSL Behring:Past (completed) ; Researcher:Vifor:Active (exists now) ; Consultant:SC Pharmaceuticals:Past (completed) ; Consultant:Novartis:Active (exists now) ; Consultant:Merck:Active (exists now) ; Researcher:Cytokinetics:Active (exists now) ; Consultant:Bristol Myers Squibb:Past (completed) ; Consultant:Boehringer Ingelheim:Active (exists now) ; Consultant:Bayer:Active (exists now) ; Researcher:Astra Zeneca:Active (exists now) | R Wright: DO have relevant financial relationships ; Consultant:Novartis:Active (exists now) | Elsie Ross: DO have relevant financial relationships ; Consultant:Novartis:Active (exists now) ; Research Funding (PI or named investigator):Doris Duke Foundation:Active (exists now) ; Research Funding (PI or named investigator):National Institutes of Health:Active (exists now) ; Speaker:Cook Medical:Active (exists now) | Yousuf Ali: DO NOT have relevant financial relationships | Biswajit Kumar: DO NOT have relevant financial relationships | Guangyang Han: DO have relevant financial relationships ; Employee:Novartis Pharmaceuticals:Active (exists now) | Beilei Cai: DO have relevant financial relationships ; Employee:Novartis:Active (exists now) | Cheryl Abbas: No Answer | Amy Ryan: No Answer
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

A Grab Bag of Novel Diabetes, Obesity and Lipid Lowering Therapies

Monday, 11/18/2024 , 01:30PM - 02:30PM

Abstract Poster Session

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