challenges in duchenne muscular dystrophy clinical trial design · 2019-06-29 · duchenne muscular...
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![Page 1: Challenges in Duchenne Muscular Dystrophy Clinical Trial Design · 2019-06-29 · Duchenne Muscular Dystrophy Clinical Trial Design Craig McDonald, MD Professor of PM&R and Pediatrics](https://reader034.vdocument.in/reader034/viewer/2022042803/5f4e7c78b6f9633f2c3bdb4c/html5/thumbnails/1.jpg)
Challenges in Duchenne Muscular Dystrophy Clinical Trial Design
Craig McDonald, MDProfessor of PM&R and Pediatrics University of California DavisSacramento, CAJune 27, 2019
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Disclosures
Consulting work on Duchenne muscular dystrophy clinical trials for:
• Santhera Pharmaceuticals**, CatabasisPharmaceuticals, Inc**, PTC Therapeutics**, Sarepta Therapeutics**, Prosensa, Pfizer, Eli Lilly**, Halo Therapeutics, Bristol Myers Squib, Novartis, Italfarmaco**, Astellas / Mitobridge, CarderoTherapeutics, Gilead, Capricor**
**Dr. McDonald has received research funding for the conduct of clinical trials.
3
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Clinical Experience with Eteplirsen (Dr. McDonald): Three Youngest Patients Treated for > 3 Years
7.5 yrs (Study 203) 8.5 yrs (Study 203) 10 yrs (Study 301)
How do we demonstrate safety and efficacy of a therapeutic in DMD?
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#PPMDConference
• Selection of responsive, reliable, meaningful endpoints varies with age and disease stage
• Variability (due to multiple issues)
• Maturation
• Required sample sizes for trials challenging in setting of a rare disease, competitive landscape and precision medicine approaches
Challenges in DMD Study Design
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#PPMDConference
• Need for enrichment of inclusion criteria or a primary analysis subgroup often based on factors making the selected subgroups more responsive to shorter duration treatment
• Desire for Extrapolation beyond the trial population is balanced by desire for inclusivity and need for broader safety database.
• Regulatory desire for placebo arms stands in contrast to community desire to minimize placebo exposure
Challenges in DMD Study Design
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0 5 10 15 20 25 30Years
Stages of DMD Disease Progression are captured with the use of multiple clinical endpoints
Loss of Ambulation
Death
Impaired ability toHop Run Jump Rise from Floor
Loss of Rise from
Floor
Loss of Stair Climb
Stages of DMD Disease Progression
Loss of Upper Limb Overhead reach
6
Late Ambulatory Stage (Rapid Functional decline)
Delayed & Impaired Acquisition of Milestones / Motor Skills
Early Ambulatory Stage (Modest functional decline)
Late Non-Ambulatory Stage
Early Non-Ambulatory Stage
Loss of Upper LimbHand to Mouth
Non-invasive Ventilation (Nocturnal)
Loss of Upper LimbDistal Hand
Non-invasive Ventilation (Diurnal)
AGE
BayleyNSAA
TFTs____________NSAA TFTs6MWT100 m. QMTNSAATFTs. 6MWT. PUL100 m. PFTs QMT
PFTsPUL
EK Scale. QMT
PFTsPUL
EK Scale
ExampleClinical Endpoints
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9 Year Old Boy: Baseline AssessmentRise From Floor 7 Sec; 6MWD 414 Meters
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Respiratory muscle weakness
Low lung volumes
Nocturnal hypoventilation
Poor airwayclearance
Loss of ambulation
Diurnalhypoventilation
Overhead motion
No overhead motion
Hand to mouth
No hand to mouth
Respiratory Lower extremityUpper extremity
Progressive loss of skeletal muscle fibers and muscle weakness in DMD leads to a sequential loss of function
1. Mayer OH, et al. US Neurology 2017;13:35–41; 2. Finder JD, et al. Am J Respir Crit Care Med;Article in Press 2017; 3. Finder JD, et al. Am J Respir Crit Care Med 2004;170:456-65; 4. Johnson JD and Theurer WM. Am Fam Physician 2014;89:359-66; 5. Humbertclaude V, et al. Eur J Paediatr Neurol 2012;16:149-60; 6. Mayer OH, et al. J Neuromuscul Dis 2017;4:189-98; 7. Bushby K, et al. Lancet Neurol 2010;9:177-89; 8. McDonald CM, et al. Neuromuscular Disorders 2016;26:473-80; 9. Brooke MH, et al. Neurology 1989;39475-481.8
Loss of Stand from supine
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1 2 3/4 5 6 7 8 9
Standfrom supine < 5 sec
Stand from supine 5-10 sec
Stand from supine > 10 sec or Lost Risefrom Floor
Lost4-StairClimb
Still Amb
Non-AmbFull Overhead reach
Lost Full Overhead Reach(Retains hand to mouth)
Lost Hand to Mouth(RetainsHand Function)
Lost Lost Hand Function(Brooke 6)
McDonald et al. Lancet, 2018
Milestones of Disease Progression and Health-related QoL (PODCI)
Clinical endpoints used in DMD capture how a patient “functions and feels.”
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0 1 2 3 4 5 6
No useful function of hands.
Can use hands to hold pen or pick up a coin ordrive a powered Chair
Can raise 1 or 2 hands to mouth but cannot raise a cup with a 200g weight in it to mouth
Can raise standardized plastic cup with 200g weight in it to mouth using both hands if necessary
Can raise both arms to shoulder height simultaneously w/ or w/o compensation
Can raise both arms simultaneously above head only by flexing the elbow
Can raise both arms simultaneously above head only by flexing the elbow
Performance of the Upper Limb (Entry Items)
Target Population
CeilingFloor
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050
100
150
FVC
% P
redi
cted
for A
ge
1 2 3 4 5 6
FVC % Predicted by Upper Extremity Grade
2345PUL EntryBrooke
McDonald, Henricson et al. CINRG DNHS
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#PPMDConference
• Gene Mutation• Genetic Modifiers (Sponsors do not want narrow label)• Baseline level of function impacts expected course of disease• Adherence to care standards; (e.g. differing steroid regiments)• Effort / motivation• Complexity of testing (ease of standardization important)• Maturity / developmental status / behavioral phenotype• Fatigue / time of day of testing• Responders / non-responders to a therapeutic agent evident• Duration of treatment can effect clinical response (e.g. dystrophin)
Sources of Variability:
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#PPMDConference
• Young DMD patients gain motor skills early on but at a reduced rate and acquired level versus typically developing children
– Greater improvements than expected needed to establish efficacy of a drug in the young
– Longer duration clinical trials often necessary with younger patients
• There are levels of skill acquisition that are highly unusual and persistent stable levels of function past specific ages are highly unusual
• Lung volumes increase with growth
• Need to normalize data for age / growth
Maturation
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NSAA Hop (Steroid Treated) NSAA Jump (Steroid Treated)
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Maturation, stability, and decline on hop and jump
• Maturation phase is similar across cluster classes • Proportion of patients who can hop and jump is highest in patients with milder trajectories • Decline phrase is separated by cluster class Muntoni et al. submitted
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RunRise from Floor
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Performance on rise from floor and run NSAA items by latent trajectory class
A
Proportion of patients with NSAA item score > 0
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CO-18
Complete Loss of Function on NSAA, 1 to 0 Change, Different from 2 to 1 Change
Stand from Supine NSAA: 1
Stand from Supine
NSAA: 0
McDonald et. al, The Lancet, 2018.
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Probability of NSAA items to shift up or down over 1 year
0 0.1 0.2 0.3 0.4 0.5 0.6
head
stand
stand1R
sit.to.stand
descendL
climbL
run
heels
hopLPatients < 7 years of age
Shift upShift down On most NSAA items, young
patients are more likely to gain function than to lose it
The probability of patients to decline in their ability to hop
and to jump is the same as the probability of improvement
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In older patients, shifting down is more likely than shifting up
However, some patients continue to gain function after the age of 7,
especially on run, walk and stand
0 0.1 0.2 0.3 0.4 0.5 0.6
head
stand
stand1R
sit.to.stand
descendL
climbL
run
heels
hopL7-12 years
shift upshift down
Probability of NSAA items to shift up or down over 1 year
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Mean of individual patient fitted curves with higher and lower quartiles
Muntoni et al, WMS, 2018Signorovitch et al, ISPOR, 2018
NSAA Score at
mean peak
AGE (years)
50% of mean peak NSAA
27
23
3030
20
10
1086 12 1614
6.8
7.85.9
Age at mean peak NSAA score
Upper quartile
Lower quartile
NSAA
Scor
e
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10 meter walk /run (velocity – meters / sec)Prosensa / Biomarin Natural History data (cTap)
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Stand from Supine5th %tile to 95th %tile (CINRG)
0.5
1
Time t
o stan
d fro
m su
pine v
elocit
y (ris
es/s)
4 5 6 7 8 9 10 11 12 13 14 15Age (years)
Control DMD
Lines represent linear model accounting for repeated measuresDots represent collected or imputed data values
TTSTAND velocity over time in DMD and control participants
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X0
24
68
Time t
o run
/walk
10m
veloc
ity (m
/s)
4 5 6 7 8 9 10 11 12 13 14 15Age (years)
Control DMD
Lines represent linear model accounting for repeated measurmentsDots represent collected or imputed data values
TTRW velocity over time in DMD and control participants
5th %tile to 95th %tile (CINRG)
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Median Absolute FVC (Liters) by Age and GC use. Peak in median FVC is shown and
the point at which the median absolute FVC value drops below 1 liter.
McDonald et al. Neuromuscular Disorders, 2018
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Clinical thresholds of respiratory function can guide patient management
26 1. Mayer OH et al. US Neurology 2017;13:35-41; 2. Bushby K, et al. Lancet Neurol 2010;9:177-89; 3. Birnkrant DJ, et al. Lancet Neurol 2018;17:347-61. 4. Sawnani, H. et al. J Pediatr 2015;166:640-5.
5 10 20 25 3015Age (years)
Resp
irato
ry fu
nctio
n te
st
100
80
60
40
0
50
30
Daily in-exsufflator / airway clearanceNight time ventilation
Mouthpiece ventilation
Raised volume Rx in-exsufflator
Continuous ventilation
For every 10% reduction in FVC, odds of hypoventilation increase by 20%
n = 334
Change in PEF%p and FVC%p with age
PEF%pFVC%p
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Decline in respiratory function correlates to risk of hospitalization due to respiratory events
Data from CINRG-DNHS.Mayer OH, et al. US Neurology 2017;13:35-41.
PEF%p at the time of event
Trend test: p < 0.001
0.02
0.2
0.180.160.140.120.1
0.060.04
0
0.08
<30
Rate
of h
ospi
taliz
atio
ns /
yea
r
≥50 -<80
≥40 -<50
≥30 -<40
FVC%p at the time of event
Trend test: p < 0.001
0.02
0.2
0.180.160.140.120.1
0.060.04
0
0.08
<30
Rate
of h
ospi
taliz
atio
ns /
yea
r
≥50 -<80
≥40 -<50
≥30 -<40
n = 247 n = 230
27
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#PPMDConference
• Stage of disease, choice of primary endpoint, expected disease progression and anticipated effect of treatment (improvement vs. slowing rate of decline) all impact sample size for trial
• Symptomatic treatment versus disease-modifying approach (both likely on top of standard of care)
• Landscape increasingly competitive
• World-wide reach of trials creates challenges with standard of care
Required sample sizes can can be challenging for trials
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#PPMDConference
• Should be enriched for the primary analysis subgroup; not for inclusion / exclusion criteria
• Frustrating for families/patients when inclusion criteria are not met
• Companies becoming more flexible and inclusive
• Should not negatively impact broad labels for drugs (FDA and EMA not the same in this regard)
Need for Enrichment (for those patients predicted to be responsive over a specific time frame)
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#PPMDConference
Regulatory Approaches to Extrapolation of Trial Results• Steroids preserve ambulatory, upper limb and pulmonary
function (proof of concept regarding “extrapolation” of treatment effects)
• FDA more flexible regarding extrapolation than EMA
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#PPMDConference
• Smaller placebo arms enriched (validated) by natural history data will make prospective natural history data collection critical
• Platform trial designs may allow the sharing of placebo data and 2:1 or 3:1 randomization
• Lead-in natural history data collection could bolster the evidence for drug effectiveness
Community desire to minimize placebo exposure is being considered by FDA and EMA
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#PPMDConference
• Confirmatory trials using manufactured / future commercial product were necessary for AAV gene therapy in SMA
• Clinical data will be required to establish that increased levels of microdystrophin expression are reasonably likely to predict benefit
• Natural history data will be critical to contextualize trial results
• Durability of clinically meaningful clinical results will be important for continued marketing authorization and third party payor reimbursement
Accelerated approval for AAV-microdystrophin gene replacement treatments
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Distance in the Community by Activity Monitoring (Ages 4-6)
Distance (m/day) at range of step-rates (1-79 steps/min) for ambulatory DMD boys 4-6 years (n=7, sample size=87 days) versus TDY 4-6 years (n=7, sample size = 41days) over 24 hours (1440 mins).
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Distance in the Community by Activity Monitoring (Ages 7-9)
Distance (m/day) at range of step-rates (1-79 steps/min) for ambulatory DMD boys 4-6 years (n=7, sample size=87 days) versus TDY 4-6 years (n=7, sample size = 41days) over 24 hours (1440 mins).
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Distance in the Community by Activity Monitoring (Ages 10-12)
Distance (m/day) at range of step-rates (1-79 steps/min) for ambulatory DMD boys 4-6 years (n=7, sample size=87 days) versus TDY 4-6 years (n=7, sample size = 41days) over 24 hours (1440 mins).
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Height-adjusted distance over 24 hoursshows disease progression in DMD
• Height-adjusted distance ambulated becomes significantly reduced in DMD with disease progression from age 4-6 to 7-9 to 10-12 using both Chi-square and Hotelling’s T2 test.
• The pattern of loss of function in DMD shows that differences between 4-6 and 7-9 year old groups are more readily apparent at high step rates (>60 SPM).
• Measureable differences between 7-9 and 10-12 year age groups are best seen at household (20-40 SPM) step rates.• Differences between 4-6 and 10-12 year age groups are seen at all step rates.
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#PPMDConference
• Trial design driven by therapeutic mechanism, stage of disease and anticipated benefit (improvement, stabilization or slowing of rate of decline)
• Maturational issues growth / addressed by normative data for age / height• Need for placebo-controlled design can be mitigated by:
– Natural history enrichment of Placebo groups– Off treatment lead-in (patient serves as own control)– Platform designs
• Variability of gene mutation, genetic modifiers, and progression rate• Consistent standard of care provided • Impact of floor, ceiling on progression rate
Things to Consider
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#PPMDConference
• Wearables – Real world community data– Objective– Part of precision health trend– Reduces burden of travel for clinical efficacy assessments
• Innovative composite endpoints• Platform trials• Biomarkers in addition to dystrophin will expand eligibility for trials, and reduce
timeframe for efficacy read-out
Future Directions: Opportunities to improve
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Thank you!
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Questions?