Use of a Novel SUBCUTaneous Preparation of Furosemide to Facilitate Early Supported Discharge of Patients With Heart Failure

Heart Failure Clinical Trial

— SUBCUT-HF II  

Official title:

Use of a Novel SUBCUTaneous Preparation of Furosemide to Facilitate Early Supported Discharge of Patients With Heart Failure: a Multicentre, Phase II, Randomised, Parallel Group, Active Comparator Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05419115
• Other study ID #: 2020-004833-19
• Status: Recruiting
• Phase: Phase 2
• Start date: November 17, 2022
• Est. completion date: August 30, 2024

Study information

• Verified date: April 2024
• Source: NHS Greater Glasgow and Clyde
• Contact: Mark Petrie, MBChB
• Phone: 0141 330 2427
• Email: mark.petrie[@]glasgow.ac.uk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate whether an early supported discharge strategy for patients admitted to hospital because of HF, using a pH neutral subcutaneous (SC) furosemide formulation (SQINFurosemide) at home (delivered by non-CE marked SQINInfusor), compared to a usual care strategy with intravenous (IV) furosemide in hospital, results in an increased number of days spent alive and out of hospital (DAOH) at 30 days.

Description:

HF is associated with frequent and lengthy hospitalisations. These hospitalisations are usually as a result of congestion, and the standard treatment of this is decongestion with intravenous (IV) diuretic (usually furosemide). This is usually delivered in a hospital setting. A new formulation of a pHneutral furosemide (SQIN-Furosemide) that can be delivered subcutaneously (SC) by a small patch pump (SQIN-Infusor) has been developed. Bioavailability of SQIN-Furosemide is similar to IV furosemide. This trial will test the efficacy and safety of novel SC furosemide 30mg/ml (SQIN-Furosemide), delivered in a home environment (compared to usual care strategy with IV furosemide delivered in secondary care) as part of a novel early supported discharge strategy in patients admitted to hospital with HF.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 550
• Est. completion date: August 30, 2024
• Est. primary completion date: May 28, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Written informed consent
• Male or female =18 years of age
• Meet European Society of Cardiology (ESC) criteria for diagnosis of HF1 o Elevated natriuretic peptide (BNP> 100 pg/mL or NTproBNP >300 pg/mL) o Signs and symptoms of HF o Echocardiographic structural or functional abnormality according to ESC guidelines (Appendix B)
• Have received IV diuretic for treatment of HF within preceding 24 hours
• Be less than 96 hours after admission to hospital
• Requiring IV diuretics for a minimum of 24 hours after screening
• Have an echocardiogram or other assessment of cardiac structure and function within preceding 12 months or at screening
• Have demonstrated an adequate diuresis with IV diuretic in the preceding 24 hours (defined as any weight loss or > 500 mLs negative fluid balance)
• Have a home environment that allows the patient to be able to mobilise within their residence and be able to pass urine into their toilet (unless catheterised)
• Able to operate (or has a caregiver who can operate) SQIN-Infusor (as assessed by training on a dummy device at screening)

Exclusion Criteria:

• Unable to consent due to significant cognitive impairment or lack of capacity
• Unable to operate SQIN-Infusor (or no caregiver who is able to operate the device)
• Geographical reasons preventing follow-up visits
• Pregnancy or breast-feeding
• Requiring treatment with IV furosemide >200 mg furosemide per day in the opinion of the treating physician
• Left sided valve disease with planned surgery or percutaneous intervention• Type 1 myocardial infarction during index hospitalisation (participants with type 2 myocardial infarction can be included)2
• Renal impairment, defined as estimated glomerular filtration rate (eGFR) < 20 mL/min/1.73 m 2 at screening
• Reasons (other than HF) which may prevent discharge from hospital, such as social circumstances or other significant medical condition (at investigator discretion)
• Women of childbearing potential
• Patient on active cardiac transplant waiting list
• Patient requiring on-going inotropic, vasopressor or intraaortic balloon pump support
• Potassium <3.0 mmol/L
• Potassium >6.0 mmol/L
• Sodium <125 mmol/L
• Any surgical or medical condition which, in the opinion of the investigator, may pose an undue risk to the subject, interfere with participation in the study or which may affect the integrity of the data

Related Conditions & MeSH terms

• Heart Failure

Intervention

Drug:
• SQIN-Furosemide
The investigational furosemide formulation (SQIN-Furosemide) is a Captisol®buffered solution of 80mg furosemide in 2.7 mL (30 mg/mL) at pH 7.4 (range: 7.0 to 7.8). SC infusion will be performed using the SQIN-Infusor which will deliver 2.7 mL of the SQIN-Furosemide formulation (80mg) over approximately 5 hours, using a biphasic delivery profile.

Device:
• SQIN-Infusor
The investigational device (SQIN-Infusor) is an on-body delivery system that consists of a RU, DU, plus a charger (Figure 2). For the purpose of SUBCUT-HF II trial, the RU will be used for multiple infusions for a single participant. The DU will be used only once per infusion and disposed of. The RU must be charged after each use and will not restart for the next infusion without charging. Charging takes up to 15 minutes. SQIN-Infusor is a bespoke system, adapted from the design of a SC insulin pump. The RU consists of the drive-unit, the controllers, the rechargeable battery, and the user interface.

Locations

Country	Name	City	State
United Kingdom	Glasgow Royal Infirmary	Glasgow	Scotland
United Kingdom	Queen Elizabeth University Hospital	Glasgow	Strathclyde

Sponsors (2)

Lead Sponsor	Collaborator
NHS Greater Glasgow and Clyde	University of Glasgow

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Days Alive Out of Hospital	Days spent alive and out of hospital (DAOH), from randomisation to 30 days.	30 days
Secondary	Length of index hospitalisation	Length of index hospitalisation	30 days
Secondary	Change in quality of life	Change in quality of life at 60 days (assessed by Kansas City Cardiomyopathy Questionnaire [KCCQ-12]) [0-100]	60 days
Secondary	Days Alive Out of Hospital	Days spent alive and out of hospital (DAOH), from randomisation to 60 days.	60 days
Secondary	Total number of HF hospitalisations at 60 days	Total number of HF hospitalisations at 60 days	60 days
Secondary	CV death or first HF hospitalisation at 60 days	CV death or first HF hospitalisation at 60 days	60 days
Secondary	CV mortality at 60 days	CV mortality at 60 days	60 days
Secondary	Safety as determined by treatment emergent adverse events (TEAEs) (including serious adverse events [SAEs]) and adverse drug events (ADEs) (including serious adverse drug events [SADEs])	Safety as determined by treatment emergent adverse events (TEAEs) (including serious adverse events [SAEs]) and adverse drug events (ADEs) (including serious adverse drug events [SADEs])	60 days
Secondary	Any device failures (e.g., adhesive failure and drug delivery failure)	Any device failures (e.g., adhesive failure and drug delivery failure)	60 days