Simplify and standardise clinical trial outcome measures, including steroid-sparing as an outcome.
Develop data sharing approaches related to biomarkers, clinical data and lab samples.
Propel quality of life-driven studies (eg, fatigue).
Increase participant representativeness in clinical trials (e.g., minority, paediatric and cutaneous lupus erythematosus).
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Define the lupus spectrum.
Perform longitudinal studies of prognostic and diagnostic biomarkers.
Drive clinical and lab-based measures for individualised treatments.
Identify and support development of treatment adherence strategies that work for lupus and communicate them to patients and providers.
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Build the case for World Health Organisation (WHO) prioritisation of lupus.
Develop standardised and specialised, expert-driven care pathways.
Drive telehealth advances and reimbursement, and build on current infrastructures.
Explore broader partnering.
Leverage social media.
Develop evidence base for interventions, including standardised endpoints/outcomes.
Provide payor education and establish alignment.
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