Implementing Long-Acting Novel Antiretrovirals

Human Immunodeficiency Viruses Clinical Trial

— ILANA  

Official title:

Implementing Long-Acting Novel Antiretrovirals - the ILANA Study

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05294159
• Other study ID #: IMP 218081
• Status: Active, not recruiting
• Start date: July 19, 2022
• Est. completion date: June 2024

Study information

• Verified date: September 2023
• Source: Queen Mary University of London
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is a 12-month, dual arm, phase 4, open-label, multi-centre study examining the implementation of LA intra-muscular (IM) drugs in clinics and decentralised community-based settings in the UK.

Description:

Cabotegravir and Rilpivirine (CAB+RPV) LA, is recommended in European US and British guidelines as a treatment for HIV-1 that allows PWH to receive a two-monthly injectable treatment, rather than daily pills. Providing injectable therapy in a system designed to provide and manage patients on oral treatments poses logistical challenges namely how resources are used to accommodate patient preference within a constrained health economy with capacity limitations. Exploring the use of alternative settings for injection, including community-based settings to deliver CAB+RPV LA, has the potential to expand options and potentially improve clinic capacity. Many PWH report high levels of stigma when attending the HIV clinic which can affect engagement with care, so receiving care in a community setting may provide additional choices and the possibility of receiving treatment in a less medicalized setting. Implementation studies in Europe are also assessing this in their countries. The National Health Service (NHS) in the UK is a very specific health environment where people are entitled to treatment and care which is free at the point of delivery. Unlike other medical specialties where primary care physicians are responsible for prescribing treatment for chronic conditions, PWH are managed and receive their HIV treatment in HIV and sexual health clinics. For the circa 105K people with HIV in the UK, outcomes are excellent. More than 95% of those on treatment have undetectable viral loads. However, around 8100 people in the UK are not able to take oral ART successfully. US guidelines have specified that LA CAB+ RPV is particularly important for those who experience pill fatigue, stigma and have fears of inadvertent disclosure. This is highly relevant to the ethnically diverse population of people in the UK living with HIV, many of whom come from marginalized and minoritized communities in which stigma is rife and in whom the treatment outcomes are the poorest. Women, racially minoritized people and older people are chronically under-represented in HIV clinical trials which is why we have set recruitment caps to ensure we recruit 50% women, 50% ethnically diverse people and 30% over 50 years of age. This is to ensure that we go beyond lip-service and hold ourselves to account in designing our trials with peer researcher involvement from the outset and committing to include a more representative study population. We will achieve this by engaging actively with community organisations to ensure awareness of this implementation trials. The study will be conducted at six large clinic sites both in London and outside of London. In this pragmatic real-world trial, each site will identify the most workable option to deliver of CAB+RPV LA according to SmPC license in the community setting within their region or borough.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 114
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• = 18 years of age
• Documented HIV-1 infection
• Virologically suppressed (HIV-1 RNA <50 copies/ml) on a stable antiretroviral regimen
• Able and willing to complete informed consent prior to inclusion
• No hepatitis B
• In accordance with EU license and NICE guidance

Exclusion Criteria:

• Based on contraindication for CAB LA, RPV LA, in accordance with EU license and NICE guidance
• Prior virologic failure on substances of NNRTI or INI class
• Resistance mutations to any substance of the NNRTI or INI class
• Prior exposure to CAB + RPV LA

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• HIV Infections
• Human Immunodeficiency Viruses

Intervention

Other:
• The Feasibility of Intervention Measure (FIM) and Acceptability of Intervention Measure (AIM)
The Feasibility and Acceptability of Intervention Measure (FIM and AIM) are used to evaluate the feasibilit and acceptability of our implementation strategies. The FIM and AIM is a validated implementation outcome measure where higher scores indicate greater feasibility and acceptability

Locations

Country	Name	City	State
United Kingdom	Brighton and Sussex University Hospitals NHS Trust	Brighton
United Kingdom	Royal Liverpool University Hospital	Liverpool
United Kingdom	Blizard Institute	London
United Kingdom	Chelsea & Westminster NHS Foundation Trust	London
United Kingdom	Guys' and St Thomas' NHS Trust	London
United Kingdom	Royal Free Hospital NHS	London

Sponsors (7)

Lead Sponsor	Collaborator
Queen Mary University of London	Barts & The London NHS Trust, Brighton and Sussex University Hospitals NHS Trust, Chelsea and Westminster NHS Foundation Trust, Guy's and St Thomas' NHS Foundation Trust, Liverpool University Hospitals NHS Foundation Trust, Royal Free Hospital NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

References & Publications (3)

Damschroder LJ, Aron DC, Keith RE, Kirsh SR, Alexander JA, Lowery JC. Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science. Implement Sci. 2009 Aug 7;4:50. doi: 10.1186/ — View Citation

Proctor E, Silmere H, Raghavan R, Hovmand P, Aarons G, Bunger A, Griffey R, Hensley M. Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda. Adm Policy Ment Health. 2011 Mar;38(2):65-76. doi: 10.1007/s — View Citation

Weiner BJ, Lewis CC, Stanick C, Powell BJ, Dorsey CN, Clary AS, Boynton MH, Halko H. Psychometric assessment of three newly developed implementation outcome measures. Implement Sci. 2017 Aug 29;12(1):108. doi: 10.1186/s13012-017-0635-3. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Incidence of CAB and RPV LA related ADRs (adverse drug reactions) and all SAEs	To describe safety of CAB and RPV LA	12 months
Other	Proportion of participants who do not progress to injections/discontinuation during oral lead in	To describe safety of CAB and RPV LA	12 months
Other	Proportion of participants who discontinue CAB and RPV LA, for all cause, virological reasons or tolerability	To describe safety of CAB and RPV LA	12 months
Other	Proportion of participants who are virologically suppressed (plasma HIV-1 RNA VL<50 c/mL) at month 4 and 12 (with +/- 6-week window)	To describe effectiveness of CAB and RPV LA	12 months
Other	Proportion participants with VL = 50 c/mL at M4 and M12 (with a +/- 6-week window	To describe effectiveness of CAB and RPV LA	12 months
Primary	Proportion of participants that agree or completely agree (average score of 4 or higher) on the Feasibility of Intervention Measure (FIM) (a validated method)	To evaluate feasibility of CAB and RPV LA administration at clinics in England and community based settings by patients	12 months
Secondary	Proportion of care provider and nurse participants that agree or completely agree (average score of 4 or higher) on the FIM and via qualitative interviews	To evaluate feasibility of CAB and RPV LA administration at 6 English clinics and decentralised community settings by healthcare professionals (HCPs)	At Day 0, 4 Months and 12 Months
Secondary	Proportion of care provider and nurse participants that agree or completely agree (average score of 4 or higher) Acceptability of Intervention Measure (AIM) (a validated method)	To evaluate acceptability of CAB and RPV LA by participants and clinic staff	At Day 0, 4 Months and 12 Months
Secondary	Proportion of community site representatives that agree or completely agree (average score of 4 or higher) score of on the FIM and AIM with in-depth qualitative interviews with community site representative	To evaluate feasibility and acceptability of CAB and RPV LA by community site representatives	At 8 months and 12 months
Secondary	Proportion of injections occurring within target window from target date (± 7 days of target date)	To describe adherence to dosing window by clinicians	12 months
Secondary	Proportion of injections occurring after target window with/without use of oral ART	To describe adherence to dosing window by clinicians	12 months
Secondary	Incidence and extent of oral bridging use	To describe adherence to dosing window by clinicians	12 months
Secondary	Qualitative interviews with nurses to ascertain the utility of the Blueprints by Community Nurse or Clinic Nurse	To evaluate the utility of the Blueprints by Community Nurse or Clinic Nurse	12 months
Secondary	Questionnaire checklist of Blueprint activities documentation to ascertain adaptations to Blueprints	To evaluate the fidelity to Blueprint by Community Nurse or Clinic Nurse	12 months
Secondary	Qualitative interviews to ascertain the utility of Facilitation Calls to improve implementation from the HIV clinic staff, Community Nurses, Clinic Nurses	To evaluate the utility of Facilitation Calls to improve implementation from the HIV clinic staff, Community Nurses, Clinic Nurses	12 months
Secondary	HIV Treatment Satisfaction Questionnaire (HIVTSQs-12) (a validated questionnaire) to assess and ascertain the change in treatment satisfaction score over time and by setting	To describe the change in treatment satisfaction score over time and by setting	12 months
Secondary	Validated questionnaires to describe tolerability and acceptance of injections	To describe tolerability and acceptance of injections	12 Months
Secondary	Validated questionnaires and qualitative interviews to ascertain participants' overall treatment experience preference and medical need for long-acting therapy	To describe participants' overall treatment experience preference and medical need for long-acting therapy	12 Months
Secondary	Qualitative interviews to ascertain patient preference for setting they receive injections and the reasons for their choice	To describe patient preference for setting they receive injections and the reasons for their choice	12 Months