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CGRP Antibodies for Migraine Prevention – Part 2

Welcome to Part Two of our exploration into CGRP antibodies for migraine treatment. Today, we delve into crucial questions: do these antibodies really work, what are their side effects, and are they safe? We’ll provide an overview of the current research on CGRP antibodies without making direct comparisons between specific brands. Available treatments in Canada like Emgality, Aimovig, and Ajovy offer promising options, each with unique delivery methods and dosing schedules. Join us as we uncover the efficacy, safety, and considerations surrounding these innovative treatments. If you’re navigating migraine management, this video is your guide to understanding CGRP antibodies.

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0:00 [Music]
0:29 all right
0:31 so now we start our part two cgrp
0:34 antibodies
0:35 do they work and do they have side
0:37 effects and are they dangerous
0:39 right so this is a bit of an overview
0:42 of the research on cgrp antibodies
0:45 i will not make comparisons between
0:48 emmavig hov and galileo i’m just going
0:51 to give you
0:52 ballpark figures from science okay
0:56 what do we have in canada available at
0:58 present time
0:59 to treat migraine to prevent migraine
1:01 emmavig
1:02 m galilei ajovi v yupty
1:06 that’s the american name is likely to
1:08 come in canada in 2021 or 20
1:12 22. it’s going to be intravenous an
1:14 infusion
1:15 right the others come as
1:18 injectors or syringes and usually
1:21 there’s one dose
1:22 but there might be a loading dose and
1:24 there might be ways to
1:26 inject every three months or only every
1:28 month
1:29 um and you can just look at the cost the
1:33 light the line the last line
1:35 those are not cheap things because these
1:37 are new
1:39 antibodies bioengineered um
1:42 just for the record this goes up to
1:45 you know 500 so that would be something
1:47 like 10 to 10 12 000
1:49 per year many biological agents
1:53 antibodies for multiple sclerosis
1:56 crohn’s disease
1:57 arthritis are up to 50 000
2:00 dollars per year so these ones are
2:02 expensive but they’re not
2:04 that expensive for that type of
2:06 treatment
2:08 okay so how do they look like they do
2:11 they look like those are the boxes right
2:13 so you have the boxes with the injectors
2:16 and
2:16 gallery and angel and the emmavig sorry
2:19 come as self-injectors a bit like epipen
2:22 right and if you start these you will
2:25 learn
2:25 how to self-inject hov comes as a little
2:29 syringe
2:29 there’s pros and cons the injector you
2:32 just inject
2:33 the syringe you control it some people
2:35 like to control to inject slowly
2:38 others say i there’s no way i can
2:39 manipulate the syringe i’m going to have
2:41 the injector
2:42 others see the injector just is too fast
2:45 it hurts i prefer the syringe
2:47 it’s a matter of preference okay so will
2:50 they work
2:51 do they work for people who try them
2:54 maybe you have tried them already but
2:56 let’s have a look how do we look at
2:59 prevention success in migraine we look
3:02 at
3:02 decrease in headache days and decrease
3:05 in
3:05 acute medication intake so if you’re
3:08 taking
3:08 every month 12 trypton doses right
3:12 and then if you take something and you
3:14 go down to six trypton doses
3:16 that’s a fifty decrease and it’s a
3:19 success
3:20 depending on where you start different
3:23 responses
3:24 might be significant so let’s say you
3:27 have
3:27 10 migraine days per month and you have
3:30 50 percent better you have
3:32 four you go down to four you lose five
3:34 four days that’s great
3:35 but let’s say you have chronic and then
3:38 you have 22 days
3:40 to start with and then you have a 30
3:43 improvement so that’s still seven days
3:46 of improvement that’s actually um
3:50 significant it’s a whole week back so
3:52 that’s a problem with insurance
3:54 companies because
3:55 insurance companies based on research
3:58 they
3:58 ask for 50 response right so that’s one
4:02 of the issues we’ll discuss
4:03 later some people have super response
4:06 they are 75
4:08 better so if you start at 21 days it
4:10 means you’re down to
4:11 seven days you say 14 days that’s great
4:15 you may also see that okay you have less
4:18 attacks
4:19 maybe not that many less but they’re
4:21 less severe
4:22 you don’t throw up anymore you don’t
4:24 have to go to the emergency
4:26 and you can troll control them with your
4:28 usual therapies
4:29 so this is how we evaluate response
4:33 to prevention um and that’s also all of
4:36 this
4:36 eventually leads to a better life for
4:38 you where you can
4:40 you know plan your party and attend the
4:42 event and
4:43 and and work and maybe uh you know train
4:46 or a glass of
4:47 a glass of wine and enjoy life right
4:51 all right so that’s an example with a
4:53 migraine tracker
4:54 um so the tracker i just showed like a
4:57 one monthly diary to show how it uh
4:59 looks like when you send to your doctor
5:02 um
5:03 here this person started with 18 days
5:06 and went back down to 11 days so that’s
5:08 a
5:08 40 response but also had less
5:12 severe days um and actually sorry had
5:15 more severe but had
5:16 less mild and moderate so that’s just an
5:19 example on how
5:20 a diary will help you to monitor your
5:22 success
5:24 okay graphs graphs are not always easy
5:27 to get but let’s let’s
5:28 let me walk through this you will see
5:31 here in the graphs in blue
5:33 that’s the placebo people who took a
5:36 sugar pill or a neutral injection during
5:38 a study
5:39 in red you have the active product in
5:42 this case
5:43 the oral medications aloe veille andra
5:46 propanol and on the right side you see
5:50 the tree antibodies so i put
5:53 little acronyms there but uh e and m is
5:56 emma vig
5:56 the middle one is m gallery and the last
5:59 one on the right side is
6:01 ajov right so this and the bar that you
6:04 see the little fine blue
6:06 line is fifty percent response so
6:08 everything that’s above that
6:10 is more than fifty percent response and
6:13 below that is forty percent
6:15 sorry forty percent of people or fifty
6:17 percent of people
6:18 so let’s look at our oral medications
6:20 that we had
6:21 so usually this 50 50 ballpark i talked
6:25 about
6:26 not everyone was reaching them right so
6:28 elleville and propanol
6:30 did not reach a really a 50 response and
6:33 trials topamax or to pyramid did but
6:35 overall the ballpark is 50.
6:37 if we look at the antibodies they do
6:40 better
6:41 they’re closer to 50 or above 50 even
6:44 for mgali
6:45 so they do reach this 50 bar of 50
6:49 improvement for episodic migraine so
6:52 episodic would be
6:54 a mean of 8 to 10 days per month of
6:56 migraine but less
6:58 than 15. okay but now if you’re here it
7:02 might be you have
7:03 chronic migraine which is the most
7:05 severe form
7:06 where you might have more than 15 20
7:09 days or
7:10 even every day a headache with some
7:13 migraines
7:14 patched over that and this is not a fun
7:16 way to live and that’s actually
7:17 one to two percent of canada canada’s
7:20 population and the world’s population so
7:23 you’re not alone in this okay so this is
7:26 the same graph
7:27 same concept blues placebo arranges the
7:30 actual treatment
7:31 and green is uh the great the gain the
7:33 difference between both
7:35 and you can see here that this is the
7:37 decrease in monthly days
7:39 so how many days do you gain and now we
7:42 compare
7:42 topermax and botox to the antibodies the
7:45 three of them
7:47 you can see that topamax and antibodies
7:49 gain approximately
7:51 six days better on amine botox fares a
7:54 bit better
7:54 with more than eight days that’s eight
7:57 days less
7:58 of migraine or headache so that’s great
8:00 remember
8:01 that this is the all the people so if
8:04 you remove the people who did not
8:06 improve
8:06 or if you look at people who did improve
8:08 a lot it means that you can
8:10 gain back like i said before 10 to 14 to
8:14 20 days
8:15 okay so if you’re a super responder so
8:18 what about people
8:19 with chronic migraine and bear with me
8:23 i have just two or three more slides
8:24 with graphs and then we’re back
8:27 to uh to no graphs um so
8:30 here are the results of chronic migraine
8:33 so chronic migraine if you want a 50
8:36 response
8:36 for topamax or botox that’s 30 to 46
8:40 people
8:41 percent of people will reach that three
8:43 to four over ten
8:44 okay antibodies it’s three to four over
8:47 ten it was very similar
8:49 right so there’s actually um we cannot
8:52 say that the antibodies are the silver
8:54 bullet they treat everyone their fifty
8:56 percent response rate
8:57 are similar to to pyramid and botox
9:00 some people are super responders to and
9:04 now you have the super response for all
9:06 antibodies
9:07 for episodic or chronic right so the
9:10 message here
9:11 is whatever you’ve tried okay and
9:14 whatever you’ve done before
9:15 to treat your migraine if you have the
9:18 software
9:18 the sensitivity if you’re determined to
9:20 respond to a cgrp antibody
9:23 it looks like you will and there’s
9:25 probably
9:26 three people over 10 and two people over
9:29 10
9:29 trying these drugs who will fall into
9:32 this super response category
9:34 where the the benefit will be very clear
9:37 so that’s what we hope
9:38 as clinicians that’s what you hope as a
9:40 patient
9:42 the super response so 3 over 10 if you
9:44 have episodic
9:45 2 over 10 if you are chronic
9:48 all right let’s take a little breath
9:51 there’s a lot of graphs
9:52 but i just wanted to show you what i
9:54 showed to actually your gps
9:57 this is what i show them right i’m
9:58 showing you the exact same stuff
10:00 right just to tell you what we saw in
10:03 the clinical trials about those
10:05 medications
10:07 another key question is how long should
10:10 you try them
10:11 because usually you take these injectors
10:14 and you inject yourself
10:15 every month but how many months in the
10:18 clinical trials
10:20 usually the response was seen sometimes
10:23 as early as the first month especially
10:25 for the super responders it’s like
10:27 boom you hit the right thing you get way
10:30 better
10:31 and then you’re very happy and then
10:33 usually it stays like that
10:35 but some people some people have more
10:38 severe chronic migraine
10:40 they may start from a very very deep and
10:42 tough place
10:43 and what we’ve seen as experts and we
10:46 talk among ourselves
10:47 what we’ve seen is that sometimes it
10:50 doesn’t work after one or two or three
10:52 months
10:53 sometimes you need four or five or
10:56 up to six months i would say after six
10:58 months if there’s no response whatsoever
11:01 it would be very surprising to see a
11:03 benefit from those antibodies
11:05 right so the message here is you might
11:08 get better
11:09 the first month right away but you might
11:13 need more time
11:14 than the three months that are you know
11:16 the the ballpark that they use in the
11:18 trials
11:19 is it going to last right are you still
11:22 going to be better a year later
11:24 in theory yes right so this is actually
11:27 data
11:27 from all the studies on emmavig hov and
11:31 uh and galilee showing that
11:33 three-quarters of people
11:35 that were chronic 15 plus just went down
11:39 to episodic and at one year they were
11:41 still there
11:42 so it means that somehow if you’re
11:44 chronic you have three quarter of a
11:46 chance to actually get back to episodic
11:49 doesn’t mean having no migraines but
11:51 being improved
11:52 okay so now let’s talk about
11:56 side effects because as a physician i do
11:59 prescribe
11:59 tons of pills and i know some of my
12:02 patients will get back to me
12:04 and say my god i tried this i was a
12:07 zombie
12:08 i gained weight i had a tremor i lost my
12:11 hair
12:12 uh i couldn’t think straight i had no
12:14 libido
12:15 my blood pressure went down i could not
12:17 train anymore
12:18 this is not good right that’s not what i
12:21 want for my patient
12:22 i want my patient to get better without
12:25 gaining weight or
12:27 fainting or being a zombie so side
12:30 effects
12:31 were a key problem with the drugs the
12:33 oral medications
12:34 and if you’ve tried them you might know
12:36 some of these side effects
12:39 so good news right so in the with the
12:42 actually i’ve showed you before
12:44 that the antibodies have similar
12:47 benefits a little bit better
12:49 right uh or close or a little bit less
12:51 than botox actually
12:53 but pretty close they don’t treat
12:55 everyone not everyone responds
12:57 but where they gain is that they are
12:59 better tolerated
13:01 so in clinical trials that means
13:04 thousands of patients total
13:06 less than two percent of people decided
13:08 to stop the drug
13:10 for side effects so that’s actually
13:12 pretty good because for oral medications
13:15 it’s five to ten percent so that means
13:18 that people said you know what maybe i
13:20 have a side effect but i’m gonna bear
13:21 with it
13:22 it’s not that bad it doesn’t mean there
13:24 were no side effects there were side
13:26 effects i’m gonna show you
13:27 but they were not severe enough for
13:29 people to leave the trial
13:31 so that’s actually encouraging okay what
13:33 are the side effects
13:35 injection side reactions so those drugs
13:38 may cause
13:38 redness swelling of the skin uh
13:42 it can happen it can get sometimes
13:45 pretty bad you know it looked it
13:46 swollen big and red discuss that with
13:49 your doctor
13:50 right if it happens sometimes it can be
13:52 managed
13:53 sometimes you have to stop um so that’s
13:56 something we can see and that’s
13:58 probably more than two percent of
14:00 patients probably around five
14:02 to ten percent constipation is common
14:05 in the studies we didn’t see it that
14:07 much but you know a lot of people
14:09 are taking illeville which is very
14:11 constipating some of them are taking
14:14 codeine or opioids very constipating uh
14:17 some people have constipation to start
14:18 with
14:19 so usually constipation is probably
14:22 probably one person over five for
14:25 emmavig
14:26 maybe a bit less with the two others
14:30 usually it’s mild to moderate and it can
14:32 be managed with
14:33 diet or laxatives or stuff but it is a
14:36 problem so if if you are
14:37 known to have severe constipation this
14:40 is this should be
14:41 discussed with your doctor allergy
14:44 may happen okay with these all of these
14:46 products
14:47 uh we call that hypersensitivity
14:50 reaction you know what
14:51 hives or a swelling of the of the the
14:53 throat that kind of thing
14:55 it may happen it is rare but it can
14:57 happen fatigue and muscle pains are
14:59 flu-like symptoms
15:00 right feeling feeling tired having pain
15:03 joint pains
15:04 um that has been reported and then some
15:07 people have reported a transient
15:09 increase in headache so that’s when we
15:12 see the most commonly
15:14 now if you go to social media and
15:18 support groups
15:19 you will see a bunch of other side
15:22 effects
15:23 right nightmares panic attacks sleep
15:26 issues
15:27 weight gain weight loss hair loss and
15:30 it’s a bit surprising to us
15:32 because when we um we discuss with the
15:35 big american clinics where they have
15:37 thousands of people they don’t see that
15:39 that often
15:41 so why is that well first it’s possible
15:44 that in real life
15:45 people are different than the people who
15:48 go to these studies
15:49 and maybe people have more problems more
15:51 medications you know
15:53 and they have more side effects so this
15:56 is not new
15:57 it’s it’s not new actually usually side
15:59 effects in real life
16:00 are always a bit more than in the
16:02 studies
16:03 so it might be that they’ve been
16:05 underestimated on the other side it’s
16:08 also possible to have what we call the
16:10 nocebo effect
16:12 some people take a sugar pill and they
16:15 have a benefit we call that placebo it’s
16:17 great
16:18 some people take a sugar pill and they
16:20 have side effects that’s kind of a dark
16:22 side of placebo
16:24 and it happens and we know because in
16:26 studies we give
16:27 tons of sugar pills to people and they
16:29 they still have side effects
16:31 and those are mediated by expectations
16:34 so they think they’re going to get bad
16:35 and they don’t get bad
16:37 it’s it’s exactly like placebo but
16:38 reverse um
16:40 and the other problem is that people who
16:42 do go to support groups
16:44 and those support groups are great
16:46 people do support each other it’s very
16:48 important
16:49 but those are usually not happy campers
16:51 they are not people
16:52 who are super responders because then if
16:55 you’re doing
16:56 so much better usually you stop going to
16:58 the support group
16:59 so it might be that in support groups
17:02 there’s a bit of an
17:03 over representation of people who have
17:06 side effects
17:06 just be careful with that if you go and
17:09 remember
17:10 that these medications are usually way
17:12 better tolerated
17:14 than the oral medications whatever
17:16 happens
17:17 if you have a reaction to a product any
17:20 product
17:21 always talk about about it with your
17:23 healthcare provider
17:25 okay are there people who cannot take
17:28 the cgrp antibodies
17:30 i didn’t mention it there because i
17:31 don’t do peeds but anyone below 18.
17:34 so any kid or teen that’s that’s like
17:37 that there are trials
17:39 in children and teenagers but they’re
17:41 not there yet so health canada does not
17:43 allow cgrp antibodies for young people
17:47 apart in this study cgrp
17:50 does play a role in pregnancy if you are
17:52 planning
17:53 a pregnancy or if you are pregnant you
17:55 should not be taking these meds
17:58 and because the entire body stay in your
18:00 system for quite a bit
18:01 you should probably stop taking
18:03 antibodies four to five
18:06 months before even starting conceiving
18:08 okay so this
18:09 is really something you have to think
18:11 about if you’re a woman
18:12 and if you’re talking or thinking about
18:15 having a child
18:16 breastfeeding it’s a matter of caution
18:20 so usually we do not recommend to take
18:22 those drugs during breastfeeding
18:24 discuss with your doctor cgrp plays a
18:27 role
18:28 in our vascular bodies and vascular
18:30 system blood pressure you know the heart
18:32 the kidney the brain
18:34 so at present time there’s no formal
18:36 contraindication
18:38 in kind of the label of health canada
18:40 but many of us experts
18:42 we will be cautious if we have patients
18:45 who have a lot of vascular
18:46 issues you know uncontrolled diabetes
18:49 hypertension
18:50 recent heart problems that kind of thing
18:52 it’s caution
18:54 discuss this with your physician because
18:55 there’s no official rule
18:57 but you may hear about it if you suffer
18:59 from a lot of vascular troubles
19:01 severe constipation i talked about it
19:04 and in the studies
19:05 usually the studies have not included
19:07 above 65 apart from some studies within
19:10 galilee
19:11 so this also you may be declined by
19:13 insurance companies for that reason so
19:15 discuss with your physician and i have
19:17 to underline that
19:18 because i’m actually telling you a lot
19:20 of medical stuff here
19:22 and i my my goal is to help you but uh i
19:25 have
19:26 also have to just be careful uh not to
19:29 give you you know the holy bible uh
19:31 thing and maybe it wasn’t clear
19:33 uh and maybe uh maybe i didn’t think
19:36 about your particular case discuss with
19:38 your doctor
19:39 whatever medical treatment you’re doing
19:42 okay so
19:42 the big question before we discuss
19:45 coverage
19:46 is is there one best
19:49 antibody the answer is no they haven’t
19:52 been compared to one another
19:54 the all the studies actually showed very
19:57 similar results so it’s the same thing
19:59 as the whole headache medicine mojo
20:03 or rule which is one size does not fit
20:07 all
20:07 so you may have to try one and then
20:10 another who knows
20:11 so let me show you because maybe you
20:14 you’ve tried one and you want to try
20:15 another
20:16 let me show you data that’s that’s done
20:19 by a guy i know dr larry robbins
20:22 in the states in chicago um and he has a
20:25 big clinic
20:25 so he recorded the patients that he
20:28 switched
20:29 and who started with let’s say emmavig
20:32 was the first to market
20:33 switched to him galilee or jovi and then
20:36 he actually looked at if people were
20:38 switching
20:39 because they did not respond because
20:42 they had side effects
20:43 or or because the insurance was not
20:46 covering anymore and they wanted to
20:48 switch to have some financial support
20:51 from a new antibody so as you can see if
20:54 you switch for
20:55 financial reason which is the fourth
20:58 column financial
20:59 well you have a good chance of
21:01 responding you know 50 to 60 percent
21:03 chance of response and those were very
21:06 tough patients so it’s a 30
21:08 response another 50. so if you switch
21:11 because
21:11 your company your insurance is not
21:13 covering you have and you responded to
21:15 the entire body
21:16 of course you have a good chance of
21:18 responding to another
21:20 if you switch because the first one
21:22 didn’t work
21:23 then you have a lower chance but you
21:25 still have a chance probably around 20
21:27 if we just look roughly maybe
21:30 around 25 30 percent chance so you’re
21:32 still still worth trying
21:33 right and if you switch because you have
21:36 side effects it’s a bit similar
21:38 and that seems to be the case for
21:39 switching between hov and gallery
21:42 aimovig so is we need more data
21:46 but i think this is important for those
21:47 of you thinking about switching an
21:50 antibody to another part three
21:53 welcome to part three cgrp antibodies
21:56 coverage
21:57 and access um so
22:01 we have said and we have discussed
22:03 together
22:04 that first cgrp antibodies are
22:07 a groundbreaking new scientific thing in
22:10 migraine world
22:11 because for the first time we target
22:14 something we know
22:15 that plays a role in migraine that’s new
22:17 so scientifically it’s great
22:19 we know that all the studies on cgrp
22:22 antibodies
22:23 have shown effectiveness not for
22:25 everyone
22:26 so maybe 50 percent of people with
22:28 episodic migraine
22:30 40 of people with chronic migraine will
22:33 improve
22:34 by half or more and there’s maybe 25 30
22:38 percent chance of being a super
22:39 responder
22:40 which is great still 40 to 50 to 60
22:44 percent of people
22:45 will not respond to those drugs and it’s
22:47 okay i mean it’s
22:48 science is still evolving there might be
22:50 other targets other things
22:52 um they are well tolerated for a
22:55 majority of people
22:56 and they are safe to use over years up
22:59 to five years we have data for mlv
23:01 so that’s what we have that’s what we
23:04 are so now
23:06 will my insurance cover them all right
23:10 so this is this is where we entered a
23:13 world of coverage in canada
23:15 and you have to remember and i didn’t
23:17 know you know we don’t
23:18 learn that stuff in medical school
23:20 because medical school is about medicine
23:23 it’s not about
23:23 insurance companies but soon enough when
23:26 you’re a doctor
23:27 you discover that you have to deal with
23:29 insurance companies if you want to help
23:31 people
23:32 so in canada there’s between 50 and 60
23:36 of people who are insured by private
23:38 payers
23:39 sun life ssq manulife blue cross green
23:42 shield
23:43 name it one thing i learned and it’s
23:45 very crucial
23:46 is that you cannot just say sun life
23:49 covers ambiality
23:50 or ssu covers hov
23:53 they have plans and the plans can be the
23:56 super you know
23:57 top vip plan or it can be the little
24:00 plan
24:01 for you know a smaller employer for
24:03 example you can’t
24:05 ever be sure that your private insurer
24:08 will cover uh these medications
24:12 in the public side public is complicated
24:14 because
24:15 it’s like first we have different public
24:17 system in all different provinces
24:20 and so what usually happens is that
24:23 the drug is examined by something called
24:26 catis which which is the canadian agency
24:29 for drug
24:30 technologies and health and they look at
24:34 the results you know what i’ve just
24:35 shown you
24:36 and they look at the cost and then they
24:38 say okay
24:39 is this a good product that we want in
24:41 canada so first health canada
24:43 sorry first half canada says the product
24:46 works and it’s safe
24:48 then cadet says okay is this something
24:50 that we
24:51 public covers or insurers should cover
24:54 should pay for
24:55 and then there’s something called the
24:57 pcpa which is a pharmacological alliance
25:00 of canada or something like that
25:02 and they do negotiations about the cost
25:05 right they don’t have that in the states
25:07 and that’s probably why the states is
25:09 paying
25:10 humongous costs for their meds right
25:14 so that’s overall a good system and
25:16 sometimes the private payers
25:18 listen to what’s or look at what’s going
25:20 on in the public world
25:22 and they kind of adapt to it okay
25:26 so um which is done by novartis
25:29 emmavig has been evaluated by calif
25:33 and they have had a positive
25:35 recommendation okay so that’s very good
25:38 because if it was declined and they said
25:41 no
25:41 public’s not going to cover then that
25:44 would have been the end of it or
25:46 a very bad place but now it’s covered
25:48 i’ll show you the criteria in just one
25:50 sec
25:51 um and overall in canada there’s zero to
25:54 ten percent of people depending of
25:56 province
25:57 that have to pay out of pocket and if
26:00 you don’t have any coverage
26:01 there’s no you have to pay that’s just
26:03 that’s just we’ve we’ve had some
26:05 comments from people
26:06 on groups or on our facebook i don’t
26:09 have coverage what do i do
26:11 well that’s that’s really too bad but
26:13 you may actually consider
26:14 trying to get coverage because it’s a
26:16 it’s a difficult situation
26:19 all right so let’s let’s look at the
26:20 criteria okay
26:22 so if you have private coverage and
26:24 those are criteria
26:26 that the private the private people
26:28 insurance companies
26:30 they decide based on their own analysis
26:33 of the drug so usually basic things
26:37 for private is that you have to have
26:39 eight or more days of migraine per month
26:42 to start with in canada health canada
26:45 just approved in galilee
26:47 jovi and emovig for four days of
26:50 migraine per month and plus okay so
26:53 medically wise
26:54 you could have it if you have four more
26:56 but private insurance and public
26:58 actually said well
26:59 four per month is it’s not worth the
27:01 cost
27:02 so we won’t cover it with eight plus
27:05 and you have to have tried or and failed
27:09 or not tolerated at least two and
27:11 sometimes three
27:13 okay so that’s for private so usually if
27:15 you have private your dog will say great
27:18 let’s start
27:18 this and this entire body i’m gonna fill
27:21 this form
27:22 and prove that you have eight days and
27:24 then you’ve tried one two three
27:26 and then you’re good to go for public
27:29 payers so public payers at present time
27:31 um cadif only evaluated emmavig right
27:35 so m gallery uh was with it was not
27:38 submitted to cadiz so we don’t know
27:39 what’s going to happen there
27:40 and hov has been presented to cadiz but
27:44 is on hold at present time we’ll see
27:45 what will happen
27:46 but let’s look at the criteria for
27:48 emmavig that
27:49 has been recommended first there’s no 8
27:52 plus you need to have
27:54 chronic 15 days of headache or migraine
27:59 you need to have failed or not tolerated
28:03 or have a contraindication to two
28:06 or three previous trials
28:09 um and then here’s a little
28:12 weird thing if you have failed
28:15 four or more and then there’s
28:18 for no efficacy then you cannot have
28:21 emmavig
28:23 so it puts you in a weird place right
28:24 because what if you failed not enough
28:27 you cannot have it
28:28 if you fail too much you cannot have it
28:30 so i’ll tell you the little
28:32 trick here and you may share that with
28:34 your doctor
28:35 the two or three previous trials can be
28:38 for efficacy
28:39 or side effects or contraindications
28:42 but the failures are only for failures
28:45 no efficacy
28:46 so it means in theory you can have tried
28:50 five drugs but two you had side effects
28:53 and you’re good to go all right so this
28:56 is a little little twist but i think
28:57 it’s useful
28:58 um and then they also will ask for your
29:01 number of days per month they may
29:03 ask for specific questionnaires which we
29:05 have in the app
29:07 and then they will recommend for six
29:10 months
29:10 okay patient support programs
29:13 if you have been on so those are support
29:16 programs that the companies
29:18 the pharma companies so this is um
29:20 novartis uh eli lilly and teva
29:23 they support to the to offer a bridge or
29:26 financial support they pay for the drug
29:29 virtually when you start it
29:31 um so emma vig their support this part
29:33 of terminated in september
29:35 lily is still ongoing um and teva just
29:38 started
29:39 but for pride people with private
29:41 coverage only they’re not going to
29:43 bridge people
29:44 with public coverage which is really
29:46 unfortunate but
29:47 that’s the the decision um the patient
29:50 support programs will assist you
29:52 in uh with coverage criteria and
29:55 negotiations
29:56 i’ll tell you how they do that they will
29:58 support you with injections and
30:00 questions
30:01 and then they will they may provide a
30:03 copay so let’s say your insurance
30:05 company says
30:06 are we going to pay 80 they might
30:08 provide a copay of 20
30:10 so you don’t pay anything which is great
30:12 and that can be on the long term
30:14 so those are the patient support
30:16 programs and your doctor
30:18 has to fill a form to register you to
30:21 these
30:22 right and then your doctor will have to
30:24 probably deal
30:26 with the insurance companies to tell
30:28 them
30:29 this patient needs this drug this
30:30 patient has triso and so this patient is
30:32 disabled
30:34 and please do provide and pay and cover
30:37 so i i just have to say here just please
30:40 remember that your doctor we are doing
30:43 this we want to help
30:45 it takes tons of our time um and we’re
30:47 doing this because insurance companies
30:49 ask us and the pharma industry ask
30:51 us um but this is this is really a part
30:54 that takes a lot of time
30:56 and hopefully somehow we’ll find ways to
30:58 do this
30:59 faster and better for you guys but this
31:01 is something that is a burden
31:03 on us and we really wish that it was
31:06 more simple for
31:07 everyone sick right so what are we doing
31:10 and we’re about to
31:12 finish before i take questions um
31:15 migraine canada is working for access to
31:19 therapy
31:21 that’s one of our goal you know we want
31:23 to raise awareness we want to bring some
31:25 support
31:26 medical information but we are also
31:28 working on
31:29 access to care and this is a bit what we
31:31 call advocacy and it’s going to be a
31:33 topic of
31:34 dr lena uh in november for on our next
31:37 webinar
31:38 so we did participate and you did
31:41 guys you did fill surveys and you
31:44 participated
31:45 to the catholic and ils process ines is
31:47 the the cadif of quebec
31:49 okay that’s a group of people who look
31:51 at drugs and they decide if public
31:53 coverage is going to
31:54 cover or not um we did send letter to
31:57 caliph
31:58 we did send letters to health ministries
32:01 to start telling them that those are
32:02 important medications for people with
32:04 migraine
32:06 we are in the process of sending letters
32:08 and formation to major private payers to
32:11 try to
32:12 negotiate what are we defending well
32:15 we’re defending you know we want we want
32:18 people to be able to try those
32:20 medications
32:21 and if they’re responders that’s great
32:23 so we want public coverage
32:25 we want less restrictions so more people
32:28 can try
32:28 we would like to have more flexibility
32:30 in the definition of response
32:32 not ask for a 50 response or more you
32:35 know and chronic should be 30 percent
32:38 and we also ask for the difficult
32:40 situation of combination with botox
32:42 where most of insurance companies refuse
32:45 to cover for that but for some of you
32:47 some of you with you know deep chronic
32:49 migraine botox with an antibody is the
32:52 key
32:53 so we will need your voice stay tuned uh
32:56 now i’ve covered everything i hope
33:00 you enjoyed it and now i’m going to um
33:03 just underline that access to migraine
33:06 care
33:07 it’s a teamwork and it’s you it’s your
33:10 physician
33:11 it’s your network it may be your
33:13 employer and migraine canada
33:15 wants to help and wants to be there
33:17 we’re growing we’re young
33:18 but please please please um share about
33:21 what we’re doing if you believe in this
33:23 cause
33:24 um and help us to grow because the
33:27 bigger we are
33:28 the stronger we’ll be and believe me
33:30 with four million people with migraine
33:32 in the country
33:33 um we should be able to make a
33:36 difference
33:40 [Music]

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