CC-1 MT 100 MT 100 for the Acute Treatment of for the Acute Treatment of Migraine Migraine Peripheral & Central Nervous Peripheral & Central Nervous System Drugs Advisory Committee System Drugs Advisory Committee Rockville, MD Rockville, MD August 4, 2005 August 4, 2005 POZEN, Inc. POZEN, Inc. Chapel Hill, NC Chapel Hill, NC
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CC-1 MT 100 for the Acute Treatment of Migraine Peripheral & Central Nervous System Drugs Advisory Committee Rockville, MD August 4, 2005 POZEN, Inc. Chapel.
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MT 100MT 100for the Acute Treatment of Migrainefor the Acute Treatment of Migraine
Peripheral & Central Nervous System Peripheral & Central Nervous System Drugs Advisory CommitteeDrugs Advisory Committee
POZEN, Inc.POZEN, Inc.Chapel Hill, NCChapel Hill, NC
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Marshall Reese, PhDMarshall Reese, PhDExecutive Vice PresidentExecutive Vice President
Product DevelopmentProduct Development
POZEN, Inc.POZEN, Inc.Chapel Hill, NCChapel Hill, NC
MT 100MT 100for the Acute Treatment of Migrainefor the Acute Treatment of Migraine
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MT 100 Presentation OutlineMT 100 Presentation OutlineMarshall E. Reese, PhDMarshall E. Reese, PhDEVP Product Development, POZENEVP Product Development, POZEN
IntroductionIntroduction
A.H.V. Schapira, MD, DSc, FRCP, FMedSciA.H.V. Schapira, MD, DSc, FRCP, FMedSciProfessor and Chair, NeurologyProfessor and Chair, NeurologyRoyal Free and Univ. College Medical SchoolRoyal Free and Univ. College Medical School
Overview of Tardive Dyskinesia Overview of Tardive Dyskinesia Associated with Metoclopramide Associated with Metoclopramide UseUse
W. James Alexander, MD, MPH, FACPW. James Alexander, MD, MPH, FACPSVP Clinical DevelopmentSVP Clinical DevelopmentChief Medical Officer, POZENChief Medical Officer, POZEN
Review of MT 100 EfficacyReview of MT 100 Efficacy
David B. Matchar, MD, FACPDavid B. Matchar, MD, FACPProfessor of Medicine, Duke UniversityProfessor of Medicine, Duke UniversityDirector of Center for Clinical Health Director of Center for Clinical Health Policy ResearchPolicy Research
Potential Role of MT 100 in Potential Role of MT 100 in Migraine TherapyMigraine Therapy
Balancing Benefits and RisksBalancing Benefits and Risks
Stephen D. Silberstein, MD, FACPStephen D. Silberstein, MD, FACPDirector, Jefferson Headache CenterDirector, Jefferson Headache CenterDepartment of NeurologyDepartment of NeurologyPresident, American Headache SocietyPresident, American Headache Society
Clinical Considerations on Clinical Considerations on Migraine TreatmentsMigraine Treatments
Marshall E. Reese, PhDMarshall E. Reese, PhD SummarySummary
Does the potential risk of TD preclude the Does the potential risk of TD preclude the ultimate approval of MT 100, whether for all ultimate approval of MT 100, whether for all patients or for a readily identifiable group of patients or for a readily identifiable group of patients who receive maximum benefit from patients who receive maximum benefit from the product?the product?
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Schematic of MT 100 TabletSchematic of MT 100 Tablet
MT 100 Not Approvable IssuesMT 100 Not Approvable Issues
SafetySafety
– Tardive dyskinesiaTardive dyskinesia
– CarcinogenicityCarcinogenicity
Efficacy – according to FDA:Efficacy – according to FDA:
– Contribution of the metoclopramide component over Contribution of the metoclopramide component over naproxen sodium alone has not been establishednaproxen sodium alone has not been established 4-6% improvement over naproxen sodium not sufficient4-6% improvement over naproxen sodium not sufficient
– Efficacy of MT 100 over placebo for all migraine Efficacy of MT 100 over placebo for all migraine associated symptoms has not been established in associated symptoms has not been established in two controlled studiestwo controlled studies Pain, nausea, photophobia, phonophobiaPain, nausea, photophobia, phonophobia
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MT 100 and Tardive DyskinesiaMT 100 and Tardive Dyskinesia
Not Approvable Letter (NAL) states:Not Approvable Letter (NAL) states:
““The absence of any detected cases (among The absence of any detected cases (among 300 subjects) is consistent with a true rate of 300 subjects) is consistent with a true rate of TD of about 1%, an unacceptably high risk in TD of about 1%, an unacceptably high risk in the absence of any advantage of the product.”the absence of any advantage of the product.”
No reports of TD during the 12 month No reports of TD during the 12 month safety studysafety study
– >1000 subjects treated for 3 months>1000 subjects treated for 3 months
– >600 subjects treated for 6 months>600 subjects treated for 6 months
– >300 subjects treated for 12 months>300 subjects treated for 12 months
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FDA Approved Labeling for Metoclopramide FDA Approved Labeling for Metoclopramide
TARDIVE DYSKINESIATARDIVE DYSKINESIA
““Both the risk of developing the syndrome Both the risk of developing the syndrome and the likelihood that it will become and the likelihood that it will become irreversible are believed to increase with the irreversible are believed to increase with the duration of treatment and the total cumulative duration of treatment and the total cumulative dose. Less commonly, the syndrome can dose. Less commonly, the syndrome can develop after relatively brief treatment periods develop after relatively brief treatment periods at low doses; in these cases, symptoms appear at low doses; in these cases, symptoms appear more likely to be reversible.”more likely to be reversible.”
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POZEN’s Position on TDPOZEN’s Position on TD
Therapeutic dose of metoclopramide hydrochloride in Therapeutic dose of metoclopramide hydrochloride in MT 100 is 16mg (equivalent to 13.5mg metoclopramide MT 100 is 16mg (equivalent to 13.5mg metoclopramide base)base)
Expected use of MT 100 approximately 4 times Expected use of MT 100 approximately 4 times per monthper month
Rare cases of TD in post-marketing surveillance Rare cases of TD in post-marketing surveillance databasesdatabases
No cases of TD from MT 100 clinical trial database No cases of TD from MT 100 clinical trial database
The available scientific evidence suggests that the risk The available scientific evidence suggests that the risk of TD associated with metoclopramide use is very low and of TD associated with metoclopramide use is very low and should be even lower with the episodic use of MT 100.should be even lower with the episodic use of MT 100.
““Two or more drugs may be combined in a single Two or more drugs may be combined in a single dosage form when each component makes a dosage form when each component makes a contribution to the claimed effects and the dosage contribution to the claimed effects and the dosage of each component (amount, frequency, duration) of each component (amount, frequency, duration) is such that the combination is safe and effective is such that the combination is safe and effective for a significant patient population requiring such for a significant patient population requiring such concurrent therapy as defined in the labeling for concurrent therapy as defined in the labeling for the drug.”the drug.”
Significant pain response at 24 hoursSignificant pain response at 24 hours
– 5 / 6 studies5 / 6 studies
Significant pain responses at 2 hoursSignificant pain responses at 2 hours
– 6 / 6 studies6 / 6 studies
Significant differences in secondary symptoms Significant differences in secondary symptoms at 2 hoursat 2 hours
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ConclusionConclusion
The potential risk of tardive dyskinesia should The potential risk of tardive dyskinesia should not preclude the approval of MT 100.not preclude the approval of MT 100.
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Review of MT 100 EfficacyReview of MT 100 Efficacy
W. James Alexander, MD, MPH, FACPW. James Alexander, MD, MPH, FACP
Senior Vice President, Clinical DevelopmentSenior Vice President, Clinical DevelopmentChief Medical OfficerChief Medical Officer
POZEN, Inc.POZEN, Inc.Chapel Hill, NCChapel Hill, NC
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Presentation OutlinePresentation Outline
Results of the MT 100 Phase 3 controlled trials Results of the MT 100 Phase 3 controlled trials for migraine endpointsfor migraine endpoints
– MT 100 vs. placebo or metoclopramide as MT 100 vs. placebo or metoclopramide as pseudo-placebopseudo-placebo
Results of the MT 100 Phase 3 component-Results of the MT 100 Phase 3 component-controlled (factorial) trialscontrolled (factorial) trials
– MT 100 vs. naproxen sodium vs. metoclopramideMT 100 vs. naproxen sodium vs. metoclopramide
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Results of the MT 100 Phase 3 Controlled Results of the MT 100 Phase 3 Controlled Trials for Migraine EndpointsTrials for Migraine Endpoints
*Primary endpoint. *Primary endpoint. ††Not powered to detect a difference.Not powered to detect a difference.
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Results of the MT 100 Phase 3 Factorial Results of the MT 100 Phase 3 Factorial Trials- MT100-301 and MT100-304Trials- MT100-301 and MT100-304
Randomized, double-blind, parallel-group, Randomized, double-blind, parallel-group, multicenter, single-attack studies conducted multicenter, single-attack studies conducted in US evaluating (2:2:1):in US evaluating (2:2:1):– MT 100MT 100
– Naproxen sodium 500mgNaproxen sodium 500mg
– Metoclopramide 16mgMetoclopramide 16mg
Treatment of moderate or severe migraine Treatment of moderate or severe migraine attack; symptom assessments at baseline attack; symptom assessments at baseline and hourly for 24 hours post-doseand hourly for 24 hours post-dose
Use of rescue medication permitted after Use of rescue medication permitted after 2 hours2 hours
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Pain Assessments for MT 100Pain Assessments for MT 100
How many subjects respondHow many subjects respond Incorporates 2-hour response rate, remedication and Incorporates 2-hour response rate, remedication and
How many subjects respondHow many subjects respond Evaluates pain response at only one point in time Evaluates pain response at only one point in time
– PID, SPID, and TOTPAR scoresPID, SPID, and TOTPAR scores How much relief is obtainedHow much relief is obtained Accepted general analgesic endpoints per FDAAccepted general analgesic endpoints per FDA
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Sustained Pain Response at 24 Hours – Sustained Pain Response at 24 Hours – ITT PopulationITT Population
MT 100 (n=1459)
Naproxen sodium (n=1492)
Metoclopramide (n=743)
**
Pe
rce
nt
Re
spo
nd
ers
Pe
rce
nt
Re
spo
nd
ers
3228
19
**POZENPOZEN p p = 0.03 = 0.03*FDA *FDA pp = 0.06 = 0.06
**36
30
20
0
10
20
30
40
50
60
MT100-301 MT100-304
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Mean SPID Scores at 24 Hours in Studies Mean SPID Scores at 24 Hours in Studies MT100-301 and MT100-304 – ITT PopulationMT100-301 and MT100-304 – ITT Population
Me
an
SP
ID S
core
Me
an
SP
ID S
core
pp = 0.046 = 0.046pp = 0.002 = 0.002
27.227.226.026.0
23.723.7 22.922.9
17.817.8 17.317.3
0
10
20
30
40
MT100-301 MT100-304
MT 100 (n=1031)
Naproxen sodium (n=1057)
Metoclopramide (n=528)
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Mean TOTPAR Scores at 24 Hours in Studies Mean TOTPAR Scores at 24 Hours in Studies MT100-301 and MT100-304 – ITT PopulationMT100-301 and MT100-304 – ITT Population
pp = 0.042 = 0.042
pp = 0.033 = 0.033
41.6
45.9
38.340.3
34.730.7
Me
an
TO
TP
AR
Sc
ore
Me
an
TO
TP
AR
Sc
ore
0
10
20
30
40
50
60
MT100-301 MT100-304
MT 100 (n=1031)
Naproxen sodium (n=1057)
Metoclopramide (n=528)
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Pre-Planned Subgroup Analyses in AllPre-Planned Subgroup Analyses in AllPhase 3 StudiesPhase 3 Studies
AgeAge
Gender Gender
Presence or absence of nausea with attackPresence or absence of nausea with attack
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Sustained Pain Response at 24 Hours in Sustained Pain Response at 24 Hours in Attacks Without Nausea Attacks Without Nausea
38 37
29 27
1916
pp < 0.01 < 0.01 pp < 0.01 < 0.01
MT 100 (n=229; 335)
Naproxen sodium (n=232; 356)
Metoclopramide (n=110; 162)
0
10
20
30
40
50
60
MT100-301 MT100-304
Pe
rce
nt
Re
spo
nd
ers
Pe
rce
nt
Re
spo
nd
ers
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Mean SPID Scores at 24 Hours in Attacks Mean SPID Scores at 24 Hours in Attacks Without NauseaWithout Nausea
pp = 0.042 = 0.042 pp = 0.009 = 0.009
28 27
23 22
1816
MT 100 (n=229; 335)
Naproxen sodium (n=232; 356)
Metoclopramide (n=110; 162)
MT100-301 MT100-3040
10
20
30
40M
ea
n S
PID
Sco
reM
ea
n S
PID
Sco
re
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00
1010
2020
3030
4040
5050
Only MT 100 Provides Better Sustained Pain Response Only MT 100 Provides Better Sustained Pain Response in Attacks Without Nausea – MT 100 Phase 3 Studiesin Attacks Without Nausea – MT 100 Phase 3 Studies
p p = 0.727= 0.727
PlaceboPlacebo
p p = 0.356= 0.356
MetoclopramideMetoclopramide
p p = 0.001= 0.001
MT 100MT 100
p p = 0.454= 0.454
NaproxenNaproxensodiumsodium
Pe
rce
nt
Re
spo
nd
ers
Pe
rce
nt
Re
spo
nd
ers
Without NauseaWithout Nausea With NauseaWith Nausea
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Unique Contribution of MetoclopramideUnique Contribution of Metoclopramide
Enhances the rate of absorption of naproxenEnhances the rate of absorption of naproxen
Better pain relief in the overall treatment Better pain relief in the overall treatment populationpopulation
Maximum benefit in attacks without nauseaMaximum benefit in attacks without nausea
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Summary – Results of Factorial Studies – Summary – Results of Factorial Studies – MT 100 vs. Naproxen sodiumMT 100 vs. Naproxen sodium
MT 100 is an effective migraine treatment MT 100 is an effective migraine treatment
MT 100 provides absolute 4 to 6% improvements in MT 100 provides absolute 4 to 6% improvements in sustained pain response over naproxen sodium sustained pain response over naproxen sodium
MT 100 provides absolute 9 to 10% improvements in MT 100 provides absolute 9 to 10% improvements in sustained pain response over naproxen sodium in sustained pain response over naproxen sodium in migraine attacks without nauseamigraine attacks without nausea
Secondary endpoints confirm superiority of MT 100 Secondary endpoints confirm superiority of MT 100 over naproxen sodiumover naproxen sodium
The contribution of metoclopramide to the primary The contribution of metoclopramide to the primary endpoint of sustained pain response is demonstrated endpoint of sustained pain response is demonstrated in two studiesin two studies
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Potential Role of MT 100 in Potential Role of MT 100 in Migraine Therapy - Migraine Therapy -
Balancing Benefits and RisksBalancing Benefits and Risks
David B. Matchar, MD, FACPDavid B. Matchar, MD, FACP
Professor of MedicineProfessor of MedicineDuke University School of MedicineDuke University School of Medicine
Director, Duke Center for Clinical Health Policy ResearchDirector, Duke Center for Clinical Health Policy ResearchDurham, NCDurham, NC
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Presentation OutlinePresentation Outline
Perspectives on:Perspectives on:
– Clinical burden of migraine Clinical burden of migraine
– Efficacy in clinical trialsEfficacy in clinical trials
– Available oral treatmentsAvailable oral treatments
Balancing benefits and risks in Balancing benefits and risks in migraine treatmentmigraine treatment
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Any 2 of the following Any 2 of the following characteristics:characteristics:
Unilateral locationUnilateral location
Pulsating qualityPulsating quality
Moderate or severe Moderate or severe pain intensitypain intensity
Worsened by movementWorsened by movement
Migraine is an episodic headache lasting 4-72 hrs with:Migraine is an episodic headache lasting 4-72 hrs with:
+
International Headache Society – International Headache Society – Criteria for MigraineCriteria for Migraine
At least 1 of the At least 1 of the following:following:
Photophobia and Photophobia and phonophobiaphonophobia
Nausea and/or Nausea and/or vomitingvomiting
Headache Classification Committee of the IHS. Headache Classification Committee of the IHS. Cephalalgia.Cephalalgia. 2004;24(suppl 1). 2004;24(suppl 1).
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Migraine is NOT a Homogeneous Disease Migraine is NOT a Homogeneous Disease
Pain is nearly always presentPain is nearly always present
However –However – Presence of associated symptoms variesPresence of associated symptoms varies– Phonophobia or photophobiaPhonophobia or photophobia
80% report either symptom in more than half of attacks80% report either symptom in more than half of attacks11
67% have photophobia and 44% have phonophobia in 67% have photophobia and 44% have phonophobia in all attacksall attacks22
– NauseaNausea Only 38% reported nausea or vomiting in more than Only 38% reported nausea or vomiting in more than
half of attackshalf of attacks11
Only 32% reported nausea in all attacksOnly 32% reported nausea in all attacks22
11Morillo LE, et al. Morillo LE, et al. Headache.Headache. 2005;45:118-126. 2005;45:118-126.22Silberstein SD. Silberstein SD. Headache.Headache. 1995;35:387-396. 1995;35:387-396.
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Migraine Therapy – The Unmet NeedMigraine Therapy – The Unmet Need
53% of people with migraine attacks described 53% of people with migraine attacks described disability or need for bed restdisability or need for bed rest
Migraine sufferers are often not satisfied with Migraine sufferers are often not satisfied with their treatmenttheir treatment
– Don’t get effective care in early visitsDon’t get effective care in early visits
– Don’t like how medication makes them feelDon’t like how medication makes them feel Groggy, chest symptoms, washed out, and so onGroggy, chest symptoms, washed out, and so on
– Medications are too expensiveMedications are too expensive
Lipton RB, et al. Lipton RB, et al. Post Graduate Medicine.Post Graduate Medicine. 2001;109:38-45. 2001;109:38-45.
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What do patients want? Pain ReliefWhat do patients want? Pain Relief
In a survey of persons with migraine, the most In a survey of persons with migraine, the most desirable outcomes of acute migraine therapy desirable outcomes of acute migraine therapy included:included:
– Rapid onset of pain relief Rapid onset of pain relief
– Freedom from painFreedom from pain
– No recurrence of painNo recurrence of pain
Lipton RB, et al. Lipton RB, et al. HeadacheHeadache. 2001;41:638-645.. 2001;41:638-645.
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The “Standard” Migraine Pain OrdinalThe “Standard” Migraine Pain OrdinalRating System Used In Clinical TrialsRating System Used In Clinical Trials
““Pain Response”Pain Response”
33SevereSevere PainPain
22ModerateModerate
PainPain
11Mild Mild PainPain
00NoneNone
(Pain Free)(Pain Free)
Treatment CriteriaTreatment Criteria
““Pain Response Rate” = The proportion of Pain Response Rate” = The proportion of subjects who achieve mild or pain free status subjects who achieve mild or pain free status 2 hours after dosing when pain was either 2 hours after dosing when pain was either moderate or severe at baseline. No rescue moderate or severe at baseline. No rescue medications allowed.medications allowed.
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Pain Endpoints Used In Migraine Clinical Trials – Pain Endpoints Used In Migraine Clinical Trials – Value to the PatientValue to the Patient
GoodGood– Pain relief at 2 hoursPain relief at 2 hours
(traditionally used as the regulatory endpoint)(traditionally used as the regulatory endpoint) Moderate or severe pain becomes mild to noneModerate or severe pain becomes mild to none
BetterBetter– Sustained pain response at 24 hoursSustained pain response at 24 hours
Mild or no pain at 2 hoursMild or no pain at 2 hours No relapse to moderate or severe painNo relapse to moderate or severe pain No use of rescue medicationsNo use of rescue medications
BestBest– Sustained pain-free at 24 hoursSustained pain-free at 24 hours
No pain at 2 hoursNo pain at 2 hours No relapse to mild, moderate, or severe painNo relapse to mild, moderate, or severe pain No use of rescue medicationNo use of rescue medication
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The “Typical” Associated Symptom Rating The “Typical” Associated Symptom Rating System Used In Migraine Clinical TrialsSystem Used In Migraine Clinical Trials
Photophobia (baseline incidence usually ~80%)Photophobia (baseline incidence usually ~80%)
Phonophobia (baseline incidence usually ~80%)Phonophobia (baseline incidence usually ~80%)
Nausea (baseline incidence usually 40% to 70%)Nausea (baseline incidence usually 40% to 70%)
Symptoms recorded as present or absentSymptoms recorded as present or absent
Efficacy = Significantly lower proportion of Efficacy = Significantly lower proportion of subjects with symptoms at 2 hourssubjects with symptoms at 2 hours
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Oral Pharmacologic Therapy for Migraine: Oral Pharmacologic Therapy for Migraine: Products with FDA Approved “Migraine” IndicationProducts with FDA Approved “Migraine” Indication
Migraine Therapy – Real WorldMigraine Therapy – Real World
Half of patients often delay treatment with Half of patients often delay treatment with prescribed medicationsprescribed medications11
– 69% want to wait and see if the headache 69% want to wait and see if the headache is really a migraineis really a migraine
– 47% only want to take their medication 47% only want to take their medication if the attack is severeif the attack is severe
79% of sufferers showed an interest in trying 79% of sufferers showed an interest in trying a novel product with similar efficacy but fewer a novel product with similar efficacy but fewer adverse effects than existing migraine adverse effects than existing migraine medicationsmedications22
11Foley KA, et al. Foley KA, et al. HeadacheHeadache. 2005;45:538-45.. 2005;45:538-45.22Gallagher RM, Kunkel R. Gallagher RM, Kunkel R. HeadacheHeadache. 2003;43:36-43.. 2003;43:36-43.
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Most Bothersome Adverse EffectsMost Bothersome Adverse Effects
– Unable to function (11%)Unable to function (11%)
– Dizziness (8%)Dizziness (8%)
Gallagher RM, Kunkel R. Gallagher RM, Kunkel R. HeadacheHeadache. 2003;43:36-43.. 2003;43:36-43.
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Balancing Benefits and RisksBalancing Benefits and Risks
Migraine lends itself to tailoring therapyMigraine lends itself to tailoring therapy
– Multiple (episodic) attacks over many yearsMultiple (episodic) attacks over many years
– Immediate feedback on efficacy of acute treatmentImmediate feedback on efficacy of acute treatment
Tailoring is aimed at maximizing the chance Tailoring is aimed at maximizing the chance that the therapy will work for a given attackthat the therapy will work for a given attack
Consequently, the benefit-to-risk margin Consequently, the benefit-to-risk margin continues to improve for an individual patient continues to improve for an individual patient over timeover time
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Benefit to RiskRatio
Benefit to RiskRatio
AcceptableAcceptable
MaximalMaximal
All patients treatedAll patients treated
Some don’t respondSome don’t respond
ConsistentConsistentrespondersresponders
Tailoring of Therapy – Tailoring of Therapy – “Filter of Clinical Experience”“Filter of Clinical Experience”
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MT 100 in the Clinical MixMT 100 in the Clinical Mix
OTC/OTC/NSAIDNSAID TriptanTriptanMT 100MT 100
Treatment OptionsTreatment Options
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Summary Summary
Role for a new migraine drug?Role for a new migraine drug?
– Migraine is a common disorder; patients have Migraine is a common disorder; patients have significant unmet needs; available orals are limitedsignificant unmet needs; available orals are limited
Meaning of clinical trial differences to patients?Meaning of clinical trial differences to patients?
– The primary objective of acute migraine therapy is The primary objective of acute migraine therapy is rapid and sustained pain relief rapid and sustained pain relief
Meaning of benefit to risk in clinical practice?Meaning of benefit to risk in clinical practice?
– Migraine treatment lends itself to tailoring; patients Migraine treatment lends itself to tailoring; patients don’t take drugs that don’t work don’t take drugs that don’t work in practice, in practice, benefit to risk can be optimizedbenefit to risk can be optimized
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Clinical Considerations on Clinical Considerations on Migraine TreatmentsMigraine Treatments
Stephen D. Silberstein, MD, FACPStephen D. Silberstein, MD, FACP
Director, Jefferson Headache CenterDirector, Jefferson Headache CenterDepartment of NeurologyDepartment of Neurology
Thomas Jefferson UniversityThomas Jefferson UniversityPhiladelphia, PAPhiladelphia, PA
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Clinical ConsiderationsClinical Considerations
Rationale for Use of MetoclopramideRationale for Use of Metoclopramide
Migraine Attacks Without NauseaMigraine Attacks Without Nausea
A.A. Headache present on Headache present on 15 d/mo fulfilling 15 d/mo fulfilling criteria B and Ccriteria B and C
B.B. Regular overuse for >3 mo of acute medicationRegular overuse for >3 mo of acute medication
C.C. Headache has developed or markedly Headache has developed or markedly worsened during overuseworsened during overuse
D.D. Headache resolves/reverts to previous pattern Headache resolves/reverts to previous pattern within 2 mo after discontinuing overusewithin 2 mo after discontinuing overuse
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ICHD-2: MOH (8.2) ICHD-2: MOH (8.2)
Ergot, triptan, Ergot, triptan, opioid, or butalbital analgesicsopioid, or butalbital analgesics
TakenTaken on a regular basis on a regular basis 10 days/month 10 days/month
High ProbabilityHigh Probability OpioidsOpioids ErgotamineErgotamine ButalbitalButalbital CaffeineCaffeine
Low ProbabilityLow Probability ASA/APAPASA/APAP TriptansTriptans
High ProbabilityHigh Probability OpioidsOpioids ErgotamineErgotamine ButalbitalButalbital CaffeineCaffeine
Low ProbabilityLow Probability ASA/APAPASA/APAP TriptansTriptans
UnlikelyUnlikely
NSAIDsNSAIDs
DHEDHE
NeurolepticsNeuroleptics
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MT 100 Migraine TherapyMT 100 Migraine Therapy
Primary therapy when simple analgesics failPrimary therapy when simple analgesics fail
Triptans contraindicated, failed or overusedTriptans contraindicated, failed or overused
Unlikely to produce MOHUnlikely to produce MOH
Fills the gap between simple analgesics and Fills the gap between simple analgesics and triptans that are now being filled by opioidstriptans that are now being filled by opioids
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““Migraine is one of Migraine is one of the 4 most disabling the 4 most disabling disorders known to disorders known to mankind”mankind”
-World Health -World Health OrganizationOrganization
““Migraine is one of Migraine is one of the 4 most disabling the 4 most disabling disorders known to disorders known to mankind”mankind”
-World Health -World Health OrganizationOrganization
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MT 100MT 100for the Acute Treatment of Migrainefor the Acute Treatment of Migraine
Peripheral & Central Nervous System Peripheral & Central Nervous System Drugs Advisory CommitteeDrugs Advisory Committee
POZEN, Inc.POZEN, Inc.Chapel Hill, NCChapel Hill, NC
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Oral Metoclopramide in Migraine Oral Metoclopramide in Migraine
Tfelt-Hansen, Olesen J. Effervescent metoclopramide and asprin Tfelt-Hansen, Olesen J. Effervescent metoclopramide and asprin (Migravess) versus effervescent aspirin or placebo for migraine (Migravess) versus effervescent aspirin or placebo for migraine attacks: a double-blind study. attacks: a double-blind study. CephalalgiaCephalalgia. 1984; 4:107-11.. 1984; 4:107-11.
Pharmacokinetics of Naproxen With Various Doses of Pharmacokinetics of Naproxen With Various Doses of Metoclopramide in VolunteersMetoclopramide in VolunteersPOZEN Studies MT100-101 and MT100-102 POZEN Studies MT100-101 and MT100-102