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临床试验/NCT05848206
NCT05848206已完成不适用

Impact of Formulary Coverage of Entresto (Sacubitril/Valsartan) on Prescription Abandonment/Rejection and Subsequent Treatment and Economic Outcomes in Chronic Heart Failure Patients in the U.S.

Novartis Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 251,831 人开始时间: 2022年3月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
251,831
试验地点
1
主要终点
Percentage of patients who had abandoned (not accepted) SAC/VAL prescriptions

研究概览

简要总结

This was a retrospective cohort study utilizing IQVIA open-source pharmacy and medical claims data among patients with a sacubitril/valsartan (SAC/VAL) prescription transaction.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary IQVIA Longitudinal Access and Adjudication Data (LAAD) Cohort (for primary objective)
  • Patients with ≥1 transaction for SAC/VAL in LAAD between 01 January 2017 and 30 November 2019 (index period). Date of the 1st SAC/VAL prescription transaction during this period was the index date.
  • Patients from the Novartis-provided list of 21 plans and formularies of interest (mapping to LAAD data was based data elements such as plan name, payer name, and pharmacy benefit manager [PBM] name) as of the index date.
  • Patients aged ≥18 years on the index date.
  • Patients with 12-months of data visibility pre-index.
  • Patients with 3-months of data visibility post-index (to allow for final adjudication/abandonment status confirmation).
  • For comorbidity data only:
  • Patients with linkage of LAAD FIA to LAAD Dx by patient ID.
  • Patients with ≥2 non-ancillary medical claims ≥30 days apart within the 12 months pre-index period.
  • Secondary LAAD Cohort (for secondary objective)
  • Among patients from the Primary LAAD Cohort remaining in Step 6, patients who abandoned their 1st SAC/VAL prescription or did not receive SAC/VAL due to claim rejection in LAAD between 01 January 2017 and 28 February 2019 (index period). Date of the 1st abandoned/rejected SAC/VAL prescription transaction during this period is the index date.
  • Patients aged ≥18 years on the index date.
  • Patients with 12-months of data visibility pre-index.
  • Patients with 12-months of data visibility post-index.
  • For comorbidity data only:
  • Patients with linkage of LAAD FIA to LAAD Dx by patient ID.
  • Patients with ≥2 non-ancillary medical claims ≥30 days apart within the 12 months pre-index period.

排除标准

  • Patients with a SAC/VAL transaction during the 12-month pre-index period.
  • Patients with data quality issues (e.g., missing gender).

结局指标

主要结局

Percentage of patients who had abandoned (not accepted) SAC/VAL prescriptions

时间窗: Up to 3 months

Percentage of patients who had SAC/VAL prescriptions filled

时间窗: Up to 3 months

Percentage of patients who had SAC/VAL prescriptions rejected by an insurance payer

时间窗: Up to 3 months

次要结局

  • Time to first angiotensin-converting enzyme inhibitor (ACEi), angiotensin II receptor blockers (ARB), or angiotensin-receptor neprilysin inhibitors (ARNI, i.e., SAC/VAL) in the follow-up period(Up to 12 months)
  • Percentage of patients who had a disruption in the use of ACEi/ARB/ARNI in the follow-up period(Up to 12 months)
  • Percentage of patients who utilized a heart failure-related treatment in the follow-up period(Up to 12 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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