Mallick Rajiv, Carlton Rashad
CSL Behring, King of Prussia, PA, 19406, USA.
Cencora, 1 West First Avenue, Conshohocken, PA, 19428, USA.
Pharmacoecon Open. 2025 Sep 18. doi: 10.1007/s41669-025-00594-y.
Primary immune deficiency (PID) comprises over 400 inborn errors of immunity. Immune globulin replacement therapy (IGRT) is the standard of care for many PID subtypes. Intravenous immunoglobulin (IVIG) is the historic standard of care, but subcutaneous immunoglobulin (SCIG) offers several advantages for IGRT. Further, a novel pre-filled syringe (PFS) drug packaging form of SCIG is expected to facilitate more efficient patient infusions.
The aim of this study was to quantify the projected budget impact associated with adding the IgPro20 PFS as an SCIG drug packaging option to a health plan formulary for the treatment of PID.
A budget impact model (BIM) was developed across the United States (US) integrated delivery networks (IDNs)' perspective over a 3-year time horizon to quantify the projected budget impact of adding the IgPro20 PFS as an SCIG packaging option for the treatment of PID. Model comparators included six IVIGs and seven SCIGs. A one-way sensitivity analysis was conducted to assess the impact of model parameters on the budget impact. Scenario analyses of alternative market share shifts and pricing were conducted to test the robustness of the model results.
From the perspective of an IDN with 25 million members, the average annual expected cost per PID patient was US$73,343 for IgPro20 vials w/pump, US$60,892 for IgPro20 PFS w/pump, US$72,179 for IVIG, and US$96,581 for other SCIGs. Assuming market share uptake of 6.0% in the first year for IgPro20 PFS w/pump, rising to 8.4% by year 3, and offset by corresponding proportionate reductions in shares of the non-PFS SCIG IgPro20 vials w/pump only, the expected incremental budget impact over the 3-year horizon was savings of US$10.5 million.
This BIM demonstrates that uptake of subcutaneous IgPro20 PFS is expected to be associated with substantial savings for a US IDN, including drug cost savings if offset by reduced non-PFS SCIG-packaging use.
原发性免疫缺陷(PID)包括400多种先天性免疫缺陷病。免疫球蛋白替代疗法(IGRT)是许多PID亚型的标准治疗方法。静脉注射免疫球蛋白(IVIG)是传统的标准治疗方法,但皮下注射免疫球蛋白(SCIG)在IGRT方面具有多个优势。此外,一种新型的预填充注射器(PFS)形式的SCIG药物包装有望使患者输注更加高效。
本研究的目的是量化将IgPro20 PFS作为SCIG药物包装选项添加到健康计划处方中用于治疗PID所带来的预计预算影响。
从美国综合医疗服务网络(IDN)的角度,在3年的时间范围内建立了一个预算影响模型(BIM),以量化将IgPro20 PFS作为SCIG包装选项用于治疗PID的预计预算影响。模型比较对象包括六种IVIG和七种SCIG。进行了单向敏感性分析,以评估模型参数对预算影响的作用。对替代市场份额转移和定价进行了情景分析,以检验模型结果的稳健性。
从一个拥有2500万成员的IDN的角度来看,使用带泵的IgPro20小瓶时,每位PID患者的年均预期成本为73343美元;使用带泵的IgPro20 PFS时为60892美元;IVIG为72179美元;其他SCIG为96581美元。假设带泵的IgPro20 PFS在第一年的市场份额占有率为6.0%,到第3年升至8.4%,并由仅带泵的非PFS SCIG IgPro20小瓶的相应比例份额减少来抵消,那么在3年时间范围内预计的增量预算影响为节省1050万美元。
该BIM表明,皮下注射IgPro20 PFS的采用预计会为美国的IDN带来大量节省,包括如果因减少非PFS SCIG包装的使用而抵消的药物成本节省。