FOR NASDAQ Dec 9 1030 PM Phase 2 gMG Slides FINAL · Alternative Pathway Classical Pathway Lectin...
Transcript of FOR NASDAQ Dec 9 1030 PM Phase 2 gMG Slides FINAL · Alternative Pathway Classical Pathway Lectin...
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Zilucoplan in*Generalized*Myasthenia*GravisTop$line)Results)of)a)Phase)2)Study
December'10,'2018
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Topics
Introduction
Myasthenia1Gravis1Disease1Overview
Phase121Results
Closing1Remarks
Q&A
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Forward'Looking-Statements
This presentation contains "forward1looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including,
but not limited to, statements regarding the safety, efficacy, regulatory and clinical progress and therapeutic potential of our product
candidates, including zilucoplan SC, expectations surrounding plans to engage with regulatory agencies and timing thereof, plans and timing for
the presentation of clinical data, expectations surrounding the initiation of a Phase 3 clinical program evaluating zilucoplan SC for the treatment
of gMG and timing thereof, expectations surrounding the nomination of a new neurology indication for zilucoplan SC and timing thereof, our
market opportunities, the anticipated pricing of our product candidates, if approved, including zilucoplan SC, and management’s estimates
about the potential size and characteristics for the patient populations that our product candidates are targeting. All such forward1looking
statements are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could
cause actual results to differ materially and adversely from those set forth in or implied by such forward1looking statements. These risks and
uncertainties include the risks that Ra Pharma’s product candidates, including zilucoplan SC, will not successfully be developed or
commercialized; as well as the other factors discussed in the “Risk Factors” section in Ra Pharma’s most recently filed Annual Report on Form
101K, as well as other risks detailed in Ra Pharma’s subsequent filings with the Securities and Exchange Commission. There can be no assurance
that the actual results or developments anticipated by Ra Pharma will be realized or, even if substantially realized, that they will have the
expected consequences to, or effects on, Ra Pharma. Except as noted, information in this presentation is as of December 10, 2018, and Ra
Pharma undertakes no duty to update this information unless required by law.
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Topics
Introduction
Myasthenia1Gravis1Disease1Overview
Phase121Results
Closing1Remarks
Q&A
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Generalized*Myasthenia*Gravis*(gMG)*Is*a**Rare,*Debilitating,*C5;Mediated*Disease1
References:*1.*Howard*JF.*Lancet*Neurol.*2017;16(12):976A986.**2.*Gilhus*N,*N*Engl*J*Med*2016;375:2570A812015* 3. ContiAFine*BM.*J*Clin*Invest.*2006;*116(11):2843A2855.*4.*Wang*et*al.*BMC*Neurology.*2017;17:77A83.**5.*Renton*AE,*et*al.*JAMA*Neurol.*2015*Apr;72(4):396A404.**6.*Heatwole*C,*et*al.*J*Clin*Neuromuscul*Dis.*2011;*13(2):*85–94.*7.*MG*Cost*Calculator,*Data*on*File.**8.*Soliris®*[package*insert].*Alexion*Pharmaceuticals*Inc;*revised*10/2017.**9. Prime*Therapeutics.*AMCP*2018,*April*23A26,*Boston.
150;250/Million,*~60,000*(US),*~100,000*(EU),*~24,000*(JP)2
Autoantibodies*block*signals*from*nerves*to*muscles*and*complement*activation*destroys*the*neuromuscular*junction3
Acetylcholine*receptor*antibody*positive2
Serious*and*progressive! Significantly*impacts*quality*of*life1,2
!~80%*progress*to*generalized*muscle*weakness4
! ~20%*experience*crisis5
Sporadic,*expensive,*and*often*non;specific!Cholinesterase*inhibitors,*corticosteroids,*ISTs,*thymectomy! IVIG,*PLEX*total*maintenance*costs*~$150,0006,7*per*year!Eculizumab*(Soliris®;*Alexion),*biAweekly*IV*therapy*approved*in*20178; ~$700,0009
Autoantibodies*and*complement;mediated*destruction*of*the*neuromuscular*junction*cause*pathology*in*gMG1,2
Signal*blocked
Signal*proceeds
Myasthenia*Gravis
NormalAcetylcholine*(ACh)
Acetylcholinereceptor*(AChR)
Muscle*cell
Autoantibody*that*binds*to*AChR
ComplementAmediated*MAC*assembly
Muscle*contracts
Destruction*of*membrane
FREQUENCY
CAUSE
DIAGNOSIS
TREATMENT
CONSEQUENCES
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Activated)by)non.self)cells Activated)by)antibody.antigen)complexes Activated)by)pathogen)surfaces
C5a
C3 C1q$$– C1r$$– C1s
C7,)C8,)C9
C5b6
Membrane)attack)complex)(MAC)
Binds&C5,&blocks&cleavageEculizumab$(IV)$
Zilucoplan$SCBinds&C5,&blocks&cleavage;Blocks&MAC&assembly
Proinflammatory&cytokine
Lectin$PathwayClassical$PathwayAlternative$Pathway
C5
C5b
C6
Factor D,)Factor)B
6
Zilucoplan:$A$Subcutaneously$SelfEadministered,$Macrocyclic$Peptide$Inhibitor$of$Complement$C5
aHUS/LN: Phase)1b positive
1
FactortargetedbyRaPharmaproductcandidates
Activatedbynon-selfcells Activatedbyantibody-antigencomplexes Activatedbypathogensurfaces
C5a
C3 C1q – C1r – C1s
C7,C8,C9
C5b6
MAC
BindsC5
FactorD,FactorB
eculizumab RA101495
Proinflammatorycytokine
BindsC5&C5b
LectinPathwayClassicalPathwayAlternativePathway
PNH:ruptureofRBC
gMG:destructionofneuromuscularjunction
LN:inflammationofkidneyglomerulus
C5
C2,C3,C4
C5b
C6
1
FactortargetedbyRaPharmaproductcandidates
Activatedbynon-selfcells Activatedbyantibody-antigencomplexes Activatedbypathogensurfaces
C5a
C3 C1q – C1r – C1s
C7,C8,C9
C5b6
MAC
BindsC5
FactorD,FactorB
eculizumab RA101495
Proinflammatorycytokine
BindsC5&C5b
LectinPathwayClassicalPathwayAlternativePathway
PNH:ruptureofRBC
gMG:destructionofneuromuscularjunction
LN:inflammationofkidneyglomerulus
C5
C2,C3,C4
C5b
C6
PNH: Phase 2 positive
gMG:$Phase)2)positive)
Neuropathies and$Myopathies: TBA
Multiple$Indications
15)amino.acid)cyclic)peptide)inhibitor)of)C5
Multiple(validated(indications,(pipeline1in1a1product(potential
PNH)– paroxysmal)nocturnal)hemoglobinuria;)gMG)– generalized)myasthenia)gravis;)aHUS)– atypical)hemolytic)uremic)syndrome;)LN)– lupus)nephritis
✅
✅
✅
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Topics
Introduction
Myasthenia1Gravis1Disease1Overview
Phase121Results
Closing1Remarks
Q&A
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Phase&2&Study&Targets&Broad&gMG&Patient&Population
Screening 1:1:1&Randomization 0.1&mg/kg&SC&+&Standard&of&Care LongFterm&Extension&(Active&Drug)
0.3&mg/kg&SC&+&Standard&of&Care
Placebo&+&Standard&of&Care
Main&Study&Period&(12&Weeks) Long&Term&Extension
Endpoints:
! Primary:&Change&in&QMG&score&from&baseline&to&week&12
! Key&Secondary: Change&in&MGHADL&score&from&baseline&to&week&12
! PreHspecified&significance&testing&at&1Hsided&alpha&of&0.1
Broad&Patient&Population:
! Generalized&MG&(Myasthenia&Gravis&Foundation&of&America&class&IIHIVa)
! AChRHantibody&positive
! Quantitative&Myasthenia&Gravis&(QMG)&score&of&≥&12
! Stable&doses&of&corticosteroids&and/or&immunosuppressants
! No&requirement&to&be&“refractory”&or&have&failed&multiple&prior&therapies
Randomized,&doubleHblind,&placeboHcontrolled,&multiHcenter&study&followed&by&an&openHlabel&longHterm&extension&(LTE)
Enrollment: 44&Patients&(vs.&target&of&36)
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Baseline(Characteristics(Confirm(Breadth(of(gMG(Study(PopulationVariable Placebo((n=15) Zilucoplan 0.1(mg/kg((n=15) Zilucoplan 0.3(mg/kg((n=14)
Age, mean years,(± SD) 48,(15.7) 46,(15.7) 55,(15.5)
Male,,n(%), 4,(27%) 7,(47%) 10,(71%)
Race,,n(%)• White• Asian• Black or,African,American
12,(80%)1,(7%)2,(13%)
13,(87%)0
2,(13%)
11,(79%)1,(7%)2,(14%)
MGFA,Class,at,Screening• II• III• IVa
7,(47%)8,(53%)
0
5,(33%)10,(67%)
0
5,(36%)5,(36%)4,(29%)
Duration,of,Disease, mean,years,(min,,max) 8.0,(0.1,,20.9) 8.7,(1.6,,24.1) 8.3,(0.5,,26.0)
Baseline,QMG,Score, mean (± SD) 18.7,(4.0) 18.7,(4.0) 19.1,(5.1)
Baseline,MGPADL,Score, mean (± SD) 8.8,(3.6) 6.9,(3.3) 7.6,(2.6)
Baseline,MG,Composite,Score, mean (± SD) 18.7,(5.7) 14.5,(6.3) 14.6,(6.3)
Baseline,MGQoL15r,Score, mean (± SD) 15.9,(7.4) 19.1,(5.0) 16.5,(7.3)
Prior,MG,Therapies (Standard,of,Care)• Pyridostigmine,,n(%)• Corticosteroids,,n(%)• Immunosuppressants,,n(%)
14,(93%)13,(87%)12,(80%)
15,(100%)13,(87%)12,(80%)
14,(100%)14,(100%)9,(64%)
Prior,IVIG,,n(%) 9,(60%) 8,(53%) 10,(71%)
Prior,Plasma,Exchange,,n(%) 7,,(47%) 9,(60%) 7,(50%)
Prior,Thymectomy,,n(%) 5,(33%) 8,(53%) 7,(50%)
Prior,MG,Crisis,Requiring,Intubation,,n(%) 3,(20%) 4,(27%) 2,(14%)
NonIRefractoryPatients(Included9%(no(prior(steroids25%(no(prior(ISTs39%(no(prior(IVIG48%(no(prior(PLEX(
High(Unmet(Medical(Need
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Primary'and'Key'Secondary'Endpoints'Met'with'0.3'mg/kg'Zilucoplan Dose:'Rapid,'Clinically'Meaningful,'and'Statistically'Significant'Reductions'in'QMG'and'MGGADL
Change'from'Baseline'in'QMG'
Pre&specified-significance-testing-at-1&sided-alpha-of-0.1-with-LOCF-ANCOVA-p-values-shown;-error-bars-denote-standard-errors-of least-squares-mean;-mITT
p=0.05p=0.04
G6.0
G3.2
G1.1
G3.4
!8
!6
!4
!2
0
S tu d y ,W e e k
Change,from,Baseline,(SEM)
P la c e b o0 .3 ,m g /k g ,Z ilu co p la n
0 1 2 4 8 12
!4
!2
0
S tu d y *W e e k
Change*from*Baseline*(SEM)
P la c e b o0 .3 *m g /k g *Z ilu co p la n
0 1 2 4 8 12
!8
!6
!4
!2
0
S tu d y ,W e e k
Change,from,Baseline,(SEM)
P la c e b o0 .3 ,m g /k g ,Z ilu co p la n
0 1 2 4 8 12
Change'from'Baseline'in'MGGADL
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Primary'and'Key'Secondary'Endpoints'Also'Met'with'0.1'mg/kg'Zilucoplan Dose
Pre%specified,significance,testing,at,1%sided,alpha,of,0.1,with,LOCF,ANCOVA,p,values,shown;,error,bars,denote,standard,errors,of least,squares,mean;,mITT
A5.5 A3.3
!8
!6
!4
!2
0
S tu d y ,W e e k
Change,from,Baseline,(SEM)
P la c e b o
0 .1 ,m g /k g ,Z ilu co p la n
0 1 2 4 8 12
!4
!2
0
S tu d y *W e e k
Change*from*Baseline*(SEM)
P la c e b o
0 .1 *m g /k g *Z ilu co p la n
0 1 2 4 8 12
!8
!6
!4
!2
0
S tu d y ,W e e k
Change,from,Baseline,(SEM)
P la c e b o
0 .1 ,m g /k g ,Z ilu co p la n
0 1 2 4 8 12
A3.2
A1.1
p=0.09p=0.05
Change'from'Baseline'in'QMG' Change'from'Baseline'in'MGAADL
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Pre$specified+Pooled+Analysis+of+Approval+Endpoint+(MG$ADL)+Satisfies+2$Sided+p<0.05+
LOCF'ANCOVA'2+sided'p'value'shown;'error'bars'denote'standard'errors'of'least'squares'mean;'mITT
*'Placebo+corrected'change'in'MG+ADL'at'26'weeks'in'REGAIN'study:'+1.9'LOCF'ANCOVA'p=0.039;'ref.'Howard'et'al'AANEM'2016
Zilucoplan in+Phase+2+met+approvable+endpoint+(MG$ADL)+at+12+weeks+with+similar+magnitude+and+statistical+
significance+as+eculizumab+in+Phase+3+REGAIN+study+at+26+weeks*
Change+from+Baseline+in+MG$ADL
$3.3
$1.1
p=0.047
!4
!2
0
S tu d y *W e e k
Change*from*Baseline*(SEM)
P la c e b o
P oo le d *A c tive
0 1 2 4 8 12
!4
!2
0
S tu d y *W e e k
Change*from*Baseline*(SEM)
P la c e b o
Z ilu co p lan *P oo led
0 1 2 4 8 12
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Responder)Analysis:)Robust)and)Meaningful)Improvements)over)Placebo
QMG MG=ADL
Zilucoplan arm)favored)overall)and)in)patients)exhibiting)largest)point)
improvements)
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Patients(Can(Achieve(Minimal(Symptom(Expression(by(Week(12
*Vissing)J,)Jacob)S,)Fujita)K,)et)al.)Minimal)Symptom)Expression)with)Eculizumab)in)Myasthenia)Gravis.))AANEM)2018
0 .1 $m g /kg $Zi lu co p la nW e e k $12
1200 $m gEcu l iz um a bW e e k $26
0 .3 $m g /kg $Zi lu co p la nW e e k $12
0
5
1 0
1 5
2 0
2 5
P la c e b o <C o r r e c t e d $R a t e s
Percent$of$$Patients$(%)
23%(of(patients((placeboAcorrected)(achieved(MSE(in(12(weeks(in(0.3(mg/kg(zilucoplan arm
Minimal(symptom(expression((MSE)(=((Achieving(MGAADL(score(of(0(or(1
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Safety'and'Tolerability'Profile'Supports'Continued'Development
Placebo(n=15)
Zilucoplan 0.1'mg/kg'(n=15)
Zilucoplan 0.3'mg/kg'(n=14)
Patients'requiring rescue'with'IVIG'or'PLEX 3'(20%) 1'(7%) 0'(0%)Patients*with*adverse*events*(AEs) 12 15 12
Patients*with*related*AEs 3 8 3
Patients*with*serious*AEs 3 0 5
Patients*with*related*serious*AEs 0 0 0
Patients*with*most*common related*AEs:
Nausea 0 2 2
Injection*site*bruising 1 2 0
Injection*site*scab 0 3 0
Contusion 0 1 1
Headache 1 4 2
Patients*with*injection*site*reactions 3 4 3
• No*meningococcal*infections
• Profile*consistent*with*Ph1*and*Ph2*PNH*studies
MedDRA*Version*20.0*Adverse*Event*Preferred*Terms;*injection*site*reactions*defined*as*pain,*tenderness,*erythema,*or*induration
• All*44*subjects*completed*12Qweek*study;*No*early*withdrawals
• 43/44*subjects*(98%)*entered*longQterm*extension
No'patients'required'rescue'in'0.3'mg/kg'zilucoplan arm
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! Positive*Phase*2*study*in*broad*gMG*population*(not*restricted*to*“refractory”)
! Primary*and*key*secondary*endpoints*met*with*clinically*meaningful*and*statistically*
significant*reductions*in*QMG*and*MGCADL*in*both*0.3*mg/kg*and*0.1*mg/kg*dose*
groups
! Magnitude*and*speed*of*effect,*no*rescue*therapy*required,*and*higher*rate*of*
minimal*symptom*expression*all*favor*0.3*mg/kg*dose*over*0.1*mg/kg*dose*for*Phase*3
! Favorable*safety*and*tolerability*profile*with*no*early*withdrawals*in*the*study;*Safety*
and*PK/PD*profile*consistent*with*Phase*1*healthy*volunteer*and*Phase*2*PNH*studies
! EndCofCPhase*2*meetings*with*FDA*and*other*regulatory*agencies*planned*for*1H19*to*
confirm*Phase*3*design
! Expanded*dataset,*including*pharmacodynamics*and*extension*data,*planned*for*1H19
Zilucoplan*in*gMG:*Phase*2*Top5line*Data*Summary
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Topics
Introduction
Myasthenia2Gravis2Disease2Overview
Phase222Results
Closing2Remarks
Q&A
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Zilucoplan:+A+Convenient+Complement+Inhibitor+for+a+Broad+gMG Population
Zilucoplan
1Soliris(QMG,(ADL(at(12wk(estimated((Ref.(Howard(et(al. Lancet 2017)2Soliris(QMG,(ADL(improvement(at(26wks((Ref.(Howard(et(al.(Lancet 2017)3Soliris(Highlights(of(Prescribing(Information;(http://alexion.com/Documents/Soliris_USPI.aspx
~0.5+mL+(3+kDa)SC+daily+selfJadmin+
120(mL((140(kDa)(
Intravenous(infusion(
every(14(daysADL
QMG
~U1.7
≥7 34%
≥6 39%
ADL
QMG J2.8
@(12wks
@+12wks
@(26wks
@+12wks
(U3*)
≥7 43%
≥6 36%
18
QMG,+ADLMean+δ vs+Placebo1 %+Improvement2
*At(26wks
C5(mAb
C5+Cyclic+Peptide
(U1.9*)
Eculizumab3
UncontrolledMG
(~30k)
Refractory(MG
(~3U5k)
5J8+sec.+
45(min.
Administration Tx+Time Population Mechanism
J2.3
~U2.5
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Market'Opportunity:'Extend'Complement'Inhibition'to'More'Patients
SteroidsAcetylcholinesterase0
Inhibitor
Immunosuppressive0
Therapies
IVIG/PLEX
(Crises0or0Chronic)
Target'Complement=Mediated'Damage'Earlier(~50%'of0MG0patients0are0uncontrolled)
Data'source:'IQVIA'market'projections'(93%'retail,'1.5B'LRx'&'Dx'claims,'CDM'~350'hospitals,'PharMetrics'health'plan'150M'pts)Jan020160– Dec020170selection0period0(patients0with0at0least010MG0diagnosis0claim0ICDN100G70.000or0G70.01);050years0history0for0treatment0and0procedures0(starting0Jan02013)
Applied0best0practice0eligibility0controls0and0apply0appropriate0preNscreener/endNtreater0rules
Used0Rx/Dx0intersection0to0project0Rx0and0officeNbased0treatments,0and0projected0hospital0utilization0of0relevant0therapies0(ie. IVIG,0PLEX)0using0CDM0
Segment0size0projected0with0Pharmetrics0Plus0data,0therapy0usage0does0not0use0Pharmetrics0Plus;0therapy0analysis0on0steroid0dosage0used0to0allocate0patients0on0high0dose0steroid0to0uncontrolled
US0Prevalence:0~2000per0million0(~60K0pts)0
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REGAIN'Population'(Eculizumab)
Zilucoplan Phase'2'Population
Opportunity'to'Treat'~30K'Patients'(U.S.'Only)'with'AChR+'gMG
<10K'pts'~'15%>20K'pts'~'35%
MG0
Diagnosis
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Zilucoplan:+Designed+for+Everyday+Complement+Control
Positioned+for+Earlier+Use:+Targets*complement1mediated*damage*at*all*stages*of*treatment*paradigm
Convenient:+518*sec*push,*~0.5*mL,*room*temperature;*Experience*comparable*to*daily*insulin*injection
Easy+to+Use:+BD*UltraSafe*Plus™*PFS*with*>13,000*doses*administered*in*zilucoplan clinical*trials;*
91%+of*gMG*patients*interested*in*daily*self1administered*SC*complement*inhibitor1
Accessible:+Pricing*expected*to*enable*broader*access;*Non1refractory and*refractory*patients
Efficacious:+Rapid*and*meaningful*reductions*in*QMG*&*MG1ADL*with*high*proportion*of*patients*
achieving*MSE;*Favorable*safety*and*tolerability
1Data*on*file:*market*research*with*MGFA*(n=372)
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Array%of%C5%Inhibitor%Assets%Provides%an%Opportunity%to%Build%a%Transformative%Franchise%in%Neurology%
Zilucoplan%QD
Zilucoplan%XR
Oral%Small%Molecule%C5%Inhibitor
Neuromuscular
Neurodegenerative
Neuropathies/Myopathies
SC%once%daily,%small%peptide%inhibitor,%designed%to%inhibit%C5%systemically%and%locally
Added%convenience%of%SC%once%weekly
Highly%potent,%orally%available
C5%LifecycleNeurology%Disease%TargetsSystemic%&%Local%C5
Potential%of%a%Peptide%Inhibitor%in%TissueNBased%C5%diseases%and%a%FirstNinNClass%Oral%Small%Molecule 21
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Topics
Introduction
Myasthenia1Gravis1Disease1Overview
Phase121Results
Closing1Remarks
Q&A
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For$information,$please$contact:David$LubnerEVP,%Chief%Financial%Officer,%Ra%Pharmaceuticals,%Inc.
Natalie'WildenradtInvestor%Relations,%Argot%Partners