Strategies and Challenges in Human Clinical Trials Targeting Aging

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GLADSTONE INSTITUTE OF VIROLOGY AND IMMUNOLOGY Strategies and Challenges in Human Clinical Trials Targeting Aging John Newman, MD, PhD UCSF and Gladstone Institutes newman@ucsf.edu @GeriSciDoc

The Geroscience Hypothesis Targeting fundamental aging processes might delay, prevent, alleviate, or reverse a wide range of diseases and conditions for which age is the primary non-modifiable risk factor. 2

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Think Big Study Patients New Tools Easy Mode 5

Think big Do you want to lower cholesterol or do you want to change people s lives? 6 By Matt Yohe- Own work, CC BY-SA 3.0

Outcomes for aging interventions Age-related Diseases: T2DM, CAD, CKD, Alzheimer s, Parkinson s Physiological Age Age-related Changes: Muscle loss, kidney function Functional outcomes Geriatric syndromes Mortality 7

Scenarios for Clinical Trials of Aging 8

Scenarios for Clinical Trials of Aging Slow/prevent the progressive decline with age Long-term studies: years? Global outcomes representative of aging: Multimorbidity Geriatric syndromes Functional decline Multisystem effects 9

Scenarios for Clinical Trials of Aging Improve the response to a stressor May be short, with longer follow-up Intensity of stressor: Immunization Wound healing Surgery/Chemotherapy Planned vs. unplanned stressor Pre-, peri-, or post-stressor intervention Primary outcome related to the stressor, but global secondary outcomes 10

Think Big Study Patients New Tools Easy Mode 11

Don t Study Spherical Cows By Nepluno - Own work, CC BY-SA 4.0 12

Don t Study Spherical Cows By Nepluno - Own work, CC BY-SA 4.0 13

Study the patients you want to treat Embrace heterogeneity! Many elders are old Many elders are frail and/or have multiple chronic diseases Age-related diseases occur in the context of aging A real-life, non-spherical older adult who strongly values her independence Age-related diseases occur in the context of other age-related diseases 14

Population Selection Incidence of disease/condition Likelihood of poor outcome Room to benefit Susceptibility to harms?? Seek your balance Window of opportunity? Physiological age (age, frailty, multimorbidity...) 15

Samples, biomarkers, outcomes Mechanisms of aging Diseases Global outcomes ADLs IADLs Cognition Frailty Mobility 16

Outcomes How to measure aging? Accumulation of diseases, syndromes, conditions Decline in daily function: ADLs, IADLs, care settings Decline in physioloigcal function: gait speed, grip strength, etc. Healthspan trials: Broad aging outcomes, but could some of these be added on to a trial targeting one specific disease/condition? Resilience trials: Primary outcome is specific to stress, but should collect broad aging outcomes as well. Any trial involving older adults: Where appropriate, could expand utility and extend results by collecting outcomes and samples broadly relevant to aging - Longitudinal data collection as a salve for heterogeneity - Long-term, low-touch follow-up could be very informative - Development of validated biomarkers is an area for active investigation 17

Think Big Study Patients New Tools Easy Mode 18

New tools for you? Try me! 19

Interventions Dozens of drugs and other interventions are now known to extend healthspan and longevity in rodents. Several of these drugs are already FDA-approved and have human data suggestive of broad effects on aging. 20

Interventions Safety: New dugs, and many approved drugs, will require safety testing in the targeted population. No panaceas: Select drugs based on proposed mechanism. Not all drugs are likely to be helpful in all circumstances. Fit to study: Risk of adverse effects and intensity of therapy should be proportionate to the duration and outcomes of the study. Combinations: Multifactorial interventions may prove superior. Standard of care: Leverage existing programs to provide infrastructure as well as comparisons (e.g. ACE units, Prehab clinics). 21

Outcomes Regulatory agencies: Aging is not an FDA indication Registration indication is critical for new drugs, and preferable for repurposed drugs Geroscience hypothesis: drugs will affect multiple diseases/conditions The most impactful aspects of aging involve multiple pathophysiologies Solution: composite of existing outcomes, e.g. multiple diseaes Solution: Build evidence for adopting syndromes of aging as indications Multimorbidity, frailty, ADL/IADL functional decline, delirium immobility, cognitive decline, etc. 22

Think Big Study Patients New Tools Easy Mode 23

Easy Mode Clinical Trial Kit 24

Accelerating Progress Identifing new interventions: - systematic expert review of literature/libraries - standardized pre-clinical screening protocols - partnering with e.g. NCATS Drug Repurposing Program Shared library of templates: - trial designs, IND applications, IRB proposals, DSMB designs - all adpated to older adults and outcomes related to aging Standardized, modular outcome toolkit: - potentially applicable to ALL trials involving older adults - physiological, functional, molecular measures - natural history data needed! National geroscience biobank - diverse, uniquely enriched for multimorbidity, frailty, elderly - helpful to ALL investigators studying an age-related disease or a disease in older adults 25

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Thank you! newman@ucsf.edu @AgingSciDoc 27 Newman Keotgenic diet in Alzheimer s models 9/27/2016

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