A Comparison of Pegfilgrastim (Neulasta®) Application Via Manual Injection Versus Injection Via an On-body Injector Regarding Patient Preference and Health Economics
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- iOMEDICO AG
- 入组人数
- 404
- 试验地点
- 49
- 主要终点
- Patient preference for type of pegfilgrastim application assessed via project specific survey answered after 4 applications.
研究概览
简要总结
The study aims to compare two application forms (pre-filled syringe and On-body injector) of the same active drug (pegfilgrastim) in adult patients under chemotherapy regarding patient preference and health economics. Chemotherapy will be supported with pegfilgrastim for four subsequent chemotherapy cycles using alternating application forms.
详细描述
Neutropenia is one of the most common side effects of myelosuppressive chemotherapy. Febrile neutropenia and infectious complications are associated with chemotherapy dose delays and reductions and an increased risk of hospitalization. Prophylaxis with recombinant G-CSFs reduces the incidence, severity and duration of CIN and the risk of developing FN. Pegfilgrastim is available for over 10 years and is specified in the SmPC to be applied at least 24 hours after cytotoxic chemotherapy. For this application patients often have to return to their physician one day after chemotherapy treatment for the sole purpose of receiving pegfilgrastim subcutaneous (s.c.) injection. For different reasons, some of the patients requiring pegfilgrastim may not be able to return at this day and thus may not receive pegfilgrastim in accordance with the SmPC. The On-body injector for pegfilgrastim provides an option for patients not to return to the clinic/medical office the day after chemotherapy for their pegfilgrastim injection. The kit includes a single-use prefilled syringe co-packed with the On-body injector for pegfilgrastim. The On-body injector is applied to the patient's skin at the day of chemotherapy treatment and it automatically delivers pegfilgrastim approximately 27 h after the On-body injector was applied to the patient's skin.
Patient-reported outcomes on preference for either application form can help to guide physicians' treatment choice, particularly in terms of application of the same active substance, in this study pegfilgrastim.
This study aims to compare the two application forms of pegfilgrastim (pegfilgrastim pre-filled syringe vs. On-body injector for pegfilgrastim) with regard to patient preference and health economy. A trial design with randomization of patients to receive the two application forms of pegfilgrastim in an alternating sequence for 4 cycles starting with either On-body injector for pegfilgrastim (Arm A) or pegfilgrastim pre-filled syringe (Arm B) was chosen. In this way, all patients will receive both application forms in order to be able to decide for their individual preference. Four cycles (that means each patient will receive each application form of pegfilgrastim twice) should be a sufficient number for the patient to make a decision. This design with two treatment arms serves to exclude a systematic bias that might be generated when starting with the same application form for all patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with early breast cancer planned to receive 3 weekly or dose-dense anthracycline/cyclophosphamide combination or 3 weekly taxane containing chemotherapy regimen or patients with NHL planned to receive R-CHOP-14 or R-CHOP-21 immunochemotherapy as 1st-line treatment with the indication for G-CSF prophylaxis with pegfilgrastim for the prevention of FN and reduction in CIN duration. Patients have to be included before start of their (immuno-) chemotherapy.
- •ECOG (Eastern Cooperative Oncology Group) performance status 0, 1 or 2
- •Life expectancy > 3 months
- •Absolute neutrophil count ≥ 1.5 x 109/L
- •Ability to read and understand German
- •Signed informed consent
排除标准
- •Hypersensitivity to the active substance or to any of the excipients
- •Subject is currently enrolled or has not yet completed at least 30 days since ending other investigational device or drug trial(s) or is receiving investigational agent(s)
- •Active infection or any serious underlying medical condition, which would impair the ability of the patient to receive protocol treatment
- •Prior bone marrow or stem cell transplantion
- •Subject of child-bearing potential is evidently pregnant (e.g. positive HCG (Human Chorionic Gonadotropin) test) or is breast feeding
- •Subject is not using adequate contraceptive precautions.
- •Other conditions which, in the opinion of the investigator, make participation in an investigational trial of this nature a poor risk
- •Concerns for subject's compliance with the protocol procedures
结局指标
主要结局
Patient preference for type of pegfilgrastim application assessed via project specific survey answered after 4 applications.
时间窗: 4 cycles of chemotherapy, i.e. 8 to 12 weeks (depending on chemotherapeutic regimen)
Percentage of patients favoring pegfilgrastim application via On-body injector. Patients are answering the questionnaire after 4 applications of pegfilgrastim in total, with On-body injector and pre-filled syringes used in alternating sequence (each type of application administered two times in total).
次要结局
- Patient preference for pegfilgrastim application assessed via project specific survey answered at time of enrollment(at enrollment)
- Preference of investigators for either type of pegfilgrastim application at study start und at end of study assessed via project specific investigator survey(from first enrollment to end of study of last patient at a site (= end of cycle 4 of last patient, expected to be latest 2.5 years after study start))
- Impact of type of pegfilgrastim application on daily life of the patient assessed by direct questioning using project specific patient survey.(4 cycles of chemotherapy, i.e. 8 to 12 weeks (depending on chemotherapeutic regimen))
- Time point of pegfilgrastim application within a chemotherapy cycle(4 cycles of chemotherapy, i.e. 8 to 12 weeks (depending on chemotherapeutic regimen))
- Percentage of nurses favoring pegfilgrastim application via On-body injector at study start and at end of study as stated via a project specific nurse survey(from first enrollment to end of study of last patient at a site (= end of cycle 4 of last patient, expected to be latest 2.5 years after study start))
- Cost factors for the health care system for both types of application of pegfilgrastim(4 cycles of chemotherapy, i.e. 8 to 12 weeks (depending on chemotherapeutic regimen))