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Thanks for meeting us at the Canadian Breakpoint, a Canadian infectious disease podcast by infectious

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disease physicians.

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I'm Summer Stewart, here with Dr. Rupeena Purewal, pediatric infectious diseases specialist

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from Saskatoon.

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For this episode, we welcome Carly Pozniak, pharmacist with the Saskatoon Positive Living

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Program to review game changing novel HIV antiretroviral cabanouva.

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Welcome Dr. Purewal.

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All right, so welcome to another episode of our podcast the Canadian Breakpoint.

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Today we have a very special guest Carly Pozniak, is a pharmacist that's worked with Positive

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Living Program since 2017 here in Saskatoon, Saskatchewan.

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She is a part of an interdisciplinary team that provides care to people living with HIV

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and hepatitis C.

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Aside from providing care to her wonderful patients, she enjoys sharing her knowledge

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in this area by precepting pharmacy students and residents each year.

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She's also an active member of the Canadian HIV and viral hepatitis pharmacist network

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CHAP, which is a group of pharmacists that collaborate together on various projects and

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publications.

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She's currently serving on the executive team as the CHAP secretary.

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So today she's joining us to talk a little bit about a new novel way that patients can

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receive their antiretroviral therapy for HIV in the form of injectables.

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So I want to welcome Carly today.

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And I actually know Carly very well because we work together here in Saskatoon.

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So she's done a lot of work with pediatrics as well as adult HIV.

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So thanks Carly.

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Thank you for having me.

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Perfect.

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So I want to start off with, I think a lot of us clinicians aren't really aware of Cabinuva.

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So that's what we're talking about is our HIV injectable drug that was recently put

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on the market.

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So I think for kind of a broader range of knowledge, because most of clinicians, including

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myself, who is an infectious disease specialist, but don't haven't, I haven't dealt with Cabinuva

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much.

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So I think why don't we start off with just giving us a little bit of a background as

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in what is Cabinuva and when it was, when was it put on the market and some of the indications

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and contraindications that we should be aware of.

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For sure.

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So as you said before, it is a brand new delivery form that we can use for patients in antiretroviral

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therapy.

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It's given by intramuscular injection into the bed of regions.

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So there's one injection per bottle.

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So there's basically two shots.

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It contains two drugs in it.

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Traditionally, we've used three antiretrovirals in a regimen.

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This one has two.

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And one of the meds is called Cabotegra.

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It's an integrase inhibitor.

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It's the newest in that class.

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And then the other medication we've had around for a while, it's called Rilpivirin.

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And it's one of the non-nucleoside reverse trans-intra-base inhibitors.

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So with this injection, because it's given in the bed of region, it does have to be administered

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by a health care professional.

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So that can kind of limit, you know, patients can't just take this home at the moment and

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administer themselves.

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So it does, I guess, require a certain amount of coordination with a site that is able to

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provide it and administer it.

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It was, it first came out that it could be given every month.

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And then later on, they approved every two month administration as well.

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So I think this is a huge advance for antiretroviral therapy because we're starting to get into

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kind of more long acting formulations of just more options for patients to choose from.

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It's maybe like the daily grind of taking pills.

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You know, someone might want to look at this route.

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So yeah, so I think you touched on a really important topic there is, you know, I think

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the ease of taking injectables versus taking daily medications.

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And so I think that's probably what made me more excited about it because I know, and

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we'll probably talk a little bit about eligibility and I'm not sure how it is in the pediatric

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world yet, but you can probably give us some kind of information in regards to that, I'm

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sure today.

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But I think really looking at, you know, quality of care for patients, I think, you know, managing

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HIV patients myself, I find that compliance is sometimes an issue, especially in our teenager

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groups, right?

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And then, I mean, life gets hard, right?

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So with COVID, I mean, a lot of people can't even get access to care.

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And I know here in Saskatchewan, HIV has really skyrocketed in terms of our numbers in turn,

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like during the pandemic and whether that was, it's probably multifactorial, but I think

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it's something that drugs like this may help us curb that in the near future.

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So what are in terms of kind of, you mentioned the true drugs, why don't we talk a little

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bit about the indication for it?

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So what is like the ideal patient for this?

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And you can talk a little bit about eligibility, if that would, for us to clinicians to know

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kind of when to contact who.

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Great, who are we targeting here?

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Yeah, so presently, it's indicated for treating HIV one infection, and just in adults, though,

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ages 18 to 65.

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And I can talk a little bit more in a minute as well.

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They do have a trial ongoing in 12 to 18 year old patients.

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So I know as a pediatric infectious disease physician, probably very interested in that

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cohort.

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We can talk about that.

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Basically right now, it's sort of considered like a switch therapy.

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So the patients do have to be suppressed on antiretroviral therapy prior to initiating

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the injection.

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So we're looking for the patient to have less than 50 copies.

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In the trials that looked at this form of antiretroviral therapy, most patients were

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actually suppressed for six months or longer before they actually initiated the injectable.

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Not to say that you have to do that, I guess, in practice, but it does kind of promote a

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sense of that the patient is stable, getting their medications regularly, and can kind

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of commit to something like this as well.

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So in the beginning right now in Canada, in Europe, they've kind of taken the oral lead

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in phase out, they've taken that off the product monographs.

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You don't have to, there is evidence to skip that.

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But right now in Canada, there is an oral lead in phase with the oral form of Cabotrigavir

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and Rilpivirine that's given for four weeks.

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And the only purpose of doing that was to assess if there was any hypersensitivity reactions.

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And the EECS conference in the fall, they actually presented some information about

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that.

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And it has been found that there hasn't been any increase in hypersensitivity reactions.

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They've gone ahead, in your opinion, removed that, I guess you call restriction.

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But in Canada, if you're kind of going with the label, it's basically giving the oral

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form of Cabotigravir and Rilpivirine daily for four weeks.

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Now in some of our patients, we have considered going kind of off label, I guess you'd say,

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and if they're on a regimen, they're suppressed, just switching right from that to the injection.

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And the reason for that is one, you're getting extra kind of medication switches.

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So that kind of involves more follow up, more blood work, potentially more confusion for

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the patient.

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Rilpivirine orally does participate in a lot more drug interactions.

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So if anyone's on an antacid or something, an acid reducing medication, you can compromise

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Rilpivirine there.

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And again, for Rilpivirine, it is required to be taken with a meal.

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So for some of our patients in Saskatchewan, for example, who have food security issues,

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it's probably not a good approach to take for them to say you have to take this with

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a meal every time you take your oral meds.

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That's just not feasible for some of our patients.

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So there are a few, I guess, reasons why we might consider skipping that oral lead in

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phase if we're wanting to get someone going on the injectable.

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And I guess the perfect patient would probably be someone who's going to be able to commit

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to regular injection appointments and follow up and has kind of shown a track record of

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being stably suppressed.

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The biggest consideration, I guess, in that respect is that because this is an injectable

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medication, it has a really long PK tail on it.

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So once you have an injection of Capvenuba, it can actually last in your system for up

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to 12 months.

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So if someone gets an injection and then decides, no, I'm not going to go with this, they are

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committed to taking oral medications thereafter for at least 12 months regularly to prevent

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developing two class resistance with Capvenuba.

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So intergrazing inhibitors plus the non-new class could be completely wiped out potentially.

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So that's definitely a consideration that, you know, something to talk about with patients

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when considering this as an option, just making sure they're aware of kind of these ins and

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outs before they commit to it, I guess.

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And currently is this a monthly injection, right?

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It is monthly.

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They have approved in Canada to give it every two months.

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I would say for our patients, I lean more towards doing the monthly injections to begin

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with just so you can kind of build up that steady state.

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I think there'd be a little bit less risk of having any viral breakthrough.

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And then maybe after, you know, six months or so, you could, if the patient wants to

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go down every two months schedule, I'd probably consider it at that point.

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You know, you can, you know, if the patient is suppressed, you can go right to the every

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two months, you know, administration schedule.

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But I personally kind of like to stick with every month and, you know, see how that goes.

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No, that's for sure.

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And in terms of, I know you mentioned like some of the contraindications or some of the

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things that we should think about when we're putting these patients on medications.

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Are there any comorbidities, like if they have liver dysfunction or renal dysfunction,

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anything like that, that we should be aware of as clinicians?

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For sure.

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Yes.

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If anyone has a creatinine clearance of less than 30 mils a minute, or if they're on dialysis,

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or if they have liver failure, so if they're at the childhood C level, I wouldn't consider

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Cabinuga for those patients.

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Same with if they have a chronic hep B infection, Cabotricavir and Rilpivirine both don't provide

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any coverage for hep B. So you could have a flare.

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In the trials, they did have that as an exclusion criteria, but I think there was one or two

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that somehow they weren't aware that the patient had hep B and made it in there.

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They had a flare.

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So definitely making sure you're aware of their hep B status and looking at ahead of

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time and do you need to have tenofibir in their atrial regimen to help control that.

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In terms of other contraindications, there were some treatment failures in the trials.

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And this is people who have perfect adherence.

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They're in a study.

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We're not having missed appointments, that kind of thing.

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And it kind of varied from 1 to 1.7% of a failure rate in people who were taking it

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perfectly.

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And what they did find, they kind of looked into that a bit more to see, well, what was

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happening with those particular patients?

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Why was there a breakthrough?

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They found people that had played A or some type of A virus.

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That was a factor.

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Now, we don't have a lot of that in North America.

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That's probably a subtype you'd see more in Russia.

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So it's probably not something we'll run into kind of in our neck of the woods here.

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The other thing they found, if the patient had a BMI that was greater than 30, and then

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also if they had any resistance associated mutations, you know, that they tried to screen

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for that ahead of time, of course, but sometimes there's something that's lurking in the background.

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So it was kind of a combination of all three of those that seemed to predispose people

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to having confirmed neurologic failures on this.

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Now with the BMI alone, if that's the only factor in the mix, you know, that they're

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above 30, that didn't increase the risk of failure.

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So you can still consider patients with a BMI greater than 30 to be on this medication.

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And does the BMI kind of, I'm just going back to thinking about like other injectables or

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anything like that when we talk about any injectable medications, does it relate to

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kind of the distribution, like the distribution of the drug?

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Is it a certain site that we're injecting that makes it difficult for those that have

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a BMI of greater than 30?

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I think something that can come into it a little bit, they presented in the fall that,

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you know, people with BMI greater than 30 recommend a longer needle.

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So it might be the fact that maybe it wasn't quite getting into the muscle in some of those

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folks too or not completely.

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So that's something we do recommend.

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It gets a two inch length of needle that they recommend you use.

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So with the Cabinuva package, there are needles and everything that come with it.

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But if you do need the longer length of needle, you'd have to get that ahead of time for the

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pain.

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So that's something that kind of came out with that.

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But yeah.

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All right.

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And I think, so I think I'm understanding a lot about the indications and the contribution

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and really like what an eligible patient is, even whether it was taking care of this patient

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in the community setting or in the hospital.

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Like obviously most of the HIV patients will be managed by subspecialists.

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So this obviously information is really, really good for us too.

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Obviously for me, a little premature because it hasn't been approved in the pediatric population

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yet, but definitely something to consider, especially when we're doing transition of

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care, right?

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So from transferring patients over to the adult side, something to consider.

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So whenever a new drug comes out, we always think about costs and that's an important

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thing.

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Is there a cost to the patient here?

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What type of coverage?

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And I guess like we'll probably know a little bit more about the Canadian healthcare system

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in terms of that.

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And probably if you can touch a little bit on that, that would be great.

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Yeah, for sure.

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Like you said, it's going to vary kind of where geographically the patient is located,

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but even in Canada from province to province, it can vary a little bit.

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But in Saskatchewan, for example, the provincial formulary did add it on and we do have universal

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antiretroviral drug coverage here.

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So that means any antiretroviral they add to our formulary, it'll be a hundred percent

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covered to the patient for the patient, no cost to the patient.

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The other, I guess, thing to consider too, anyone who has NHB coverage.

230
00:16:12,720 --> 00:16:14,880
So that's a federal program.

231
00:16:14,880 --> 00:16:20,200
So anyone who has treaty status and is eligible there for coverage, it's covered for them

232
00:16:20,200 --> 00:16:22,480
a hundred percent as well.

233
00:16:22,480 --> 00:16:26,880
So it kind of depends if the province, you know, the patient is living in has decided

234
00:16:26,880 --> 00:16:28,800
to add it onto the formulary.

235
00:16:28,800 --> 00:16:33,360
I know a few provinces in Canada have added it already, but there's still a few more that

236
00:16:33,360 --> 00:16:35,040
are probably considering it.

237
00:16:35,040 --> 00:16:42,520
I think most probably will end up adding it because it was, I guess, negotiated to be

238
00:16:42,520 --> 00:16:45,520
kind of a similar price to other regimens.

239
00:16:45,520 --> 00:16:51,120
So it's really not going to cost more than kind of our traditional regimens, which is

240
00:16:51,120 --> 00:16:52,120
good.

241
00:16:52,120 --> 00:16:55,400
You know, we don't have to feel bad about considering this as an option.

242
00:16:55,400 --> 00:17:00,200
It's not going to increase the cost of the health care system.

243
00:17:00,200 --> 00:17:06,320
I think it's probably around the $1,500 mark per month, kind of in that range, which is

244
00:17:06,320 --> 00:17:09,600
sort of what the other regimens cost.

245
00:17:09,600 --> 00:17:15,160
Some provincial formulars are able to negotiate a special price and so they might be able

246
00:17:15,160 --> 00:17:17,720
to get a better cost.

247
00:17:17,720 --> 00:17:19,240
So but that's confidential.

248
00:17:19,240 --> 00:17:22,040
I wouldn't be able to know what that price is.

249
00:17:22,040 --> 00:17:29,200
It's kind of a special agreement.

250
00:17:29,200 --> 00:17:38,880
In terms of so now, like obviously lots of physicians will see Cabanouva on like on somebody's

251
00:17:38,880 --> 00:17:43,480
PIP or, you know, documentation of their medication list.

252
00:17:43,480 --> 00:17:48,000
I guess for both like clinicians outside in the community, like family doctors, other

253
00:17:48,000 --> 00:17:51,720
pharmacists that may be working in the community that are not related to HIV.

254
00:17:51,720 --> 00:17:56,240
What are some of the things once the patient is on Cabanouva that we should all be looking

255
00:17:56,240 --> 00:17:57,920
for, like monitoring?

256
00:17:57,920 --> 00:18:02,240
Is there any kind of ongoing lab work or is that something that's done pretty much by

257
00:18:02,240 --> 00:18:06,400
the HIV team that's administering it?

258
00:18:06,400 --> 00:18:09,880
Maybe some touch on like some of the side effects that would be good because I think

259
00:18:09,880 --> 00:18:13,760
lots of questions will come around about on that as well.

260
00:18:13,760 --> 00:18:19,080
Yeah, generally the monitoring site, like the lab work should be done by whoever is

261
00:18:19,080 --> 00:18:21,920
prescribing this medication.

262
00:18:21,920 --> 00:18:28,600
So the first thing you'd want to do is confirm that the patient is actually virally suppressed.

263
00:18:28,600 --> 00:18:34,520
Then you can go ahead and start them on the oral lead-in phase if you like for four weeks.

264
00:18:34,520 --> 00:18:39,840
And then at the end of that point, you would want to do another check for suppression before

265
00:18:39,840 --> 00:18:43,880
initiating the injectable.

266
00:18:43,880 --> 00:18:49,920
And then from there, I'd say one month out from any kind of med change, including Cabanouva,

267
00:18:49,920 --> 00:18:53,680
we like to do a viral load and see where things are at.

268
00:18:53,680 --> 00:18:57,640
And then from there, it's basically like any other antiretroviral regimen, you can check

269
00:18:57,640 --> 00:19:04,440
every three to six months to see where the viral load is sitting.

270
00:19:04,440 --> 00:19:08,440
In terms of anything else specific to this medication, I'd probably make sure you're

271
00:19:08,440 --> 00:19:13,480
getting some LFTs done, checking their renal function just to make sure they're still kind

272
00:19:13,480 --> 00:19:20,080
of following in the range where you'd be able to use this medication.

273
00:19:20,080 --> 00:19:26,680
And other kind of lab work like CDC, stuff like that, kind of your usual HIV blood work

274
00:19:26,680 --> 00:19:27,680
that we would do.

275
00:19:27,680 --> 00:19:28,680
So that's nice.

276
00:19:28,680 --> 00:19:31,520
It doesn't kind of amount to kind of...

277
00:19:31,520 --> 00:19:34,880
In the beginning, there might be a little bit of extra blood work that happens, but

278
00:19:34,880 --> 00:19:40,000
after that, it should kind of follow the same course as other regimens.

279
00:19:40,000 --> 00:19:45,000
In terms of tolerability, most patients reported that it was really well tolerated.

280
00:19:45,000 --> 00:19:50,280
The single most high, like the highest side effect that people reported were injection

281
00:19:50,280 --> 00:19:52,800
site reactions.

282
00:19:52,800 --> 00:19:59,340
So which, you know, as could be expected with this, a bit of, you know, a swelling or soreness.

283
00:19:59,340 --> 00:20:05,580
And so I guess warning the patient about that ahead of time, because it's likely to happen.

284
00:20:05,580 --> 00:20:11,800
Other side effects that could occur, headache, nausea, you know, that sort of thing.

285
00:20:11,800 --> 00:20:16,840
But in general, I think most people tolerate quite well and most only reported the injection

286
00:20:16,840 --> 00:20:17,840
site reaction.

287
00:20:17,840 --> 00:20:19,520
So that's kind of a...

288
00:20:19,520 --> 00:20:21,680
That's nice to know that it is so well tolerated.

289
00:20:21,680 --> 00:20:24,200
So maybe if you have a patient that's...

290
00:20:24,200 --> 00:20:28,000
We have the odd person that even though we've got really well tolerated oral options, they

291
00:20:28,000 --> 00:20:32,320
have continuous nausea and they can't seem to tolerate an oral origin.

292
00:20:32,320 --> 00:20:36,800
And maybe, you know, if you can get them suppressed, maybe this is an option, you know, just totally

293
00:20:36,800 --> 00:20:39,480
bypassing the oral route.

294
00:20:39,480 --> 00:20:43,280
That might be something that, you know, they might get a lot of benefit from.

295
00:20:43,280 --> 00:20:44,280
Okay.

296
00:20:44,280 --> 00:20:46,080
That makes sense.

297
00:20:46,080 --> 00:20:52,320
And is there any absolute reason that there's a reaction or anything that was probably,

298
00:20:52,320 --> 00:20:55,800
I would say more probably in the clinical trials that they saw?

299
00:20:55,800 --> 00:21:01,240
I'm not sure how much post-marketing surveillance has been kind of reported for those kind of

300
00:21:01,240 --> 00:21:02,960
side effects yet.

301
00:21:02,960 --> 00:21:08,240
But is there like one of the main reasons where if I'm a clinician that's out in the

302
00:21:08,240 --> 00:21:13,320
community, I get a phone call, somebody's on Cabinuva and they have a reaction, I would

303
00:21:13,320 --> 00:21:15,200
probably tell them to go to the emergency department.

304
00:21:15,200 --> 00:21:19,920
But is there something that, you know, is life threatening or anything like that, that

305
00:21:19,920 --> 00:21:21,560
would be worrisome in this case?

306
00:21:21,560 --> 00:21:28,040
I'd say if you happen to have a patient that had the kind of acutely flare up, that would

307
00:21:28,040 --> 00:21:29,040
be a situation.

308
00:21:29,040 --> 00:21:36,360
If in your lab work you see that they have a detectable viral load, I'd probably jump

309
00:21:36,360 --> 00:21:40,240
on that and switch them to something else.

310
00:21:40,240 --> 00:21:46,960
Preferably before, you know, early on before more mutations can kind of develop.

311
00:21:46,960 --> 00:21:52,840
Yeah, like any kind of intolerable adverse reactions, it is nice to see in the study

312
00:21:52,840 --> 00:21:57,840
they presented in the fall that they really didn't find there to be many hypersensitivity

313
00:21:57,840 --> 00:22:01,080
reactions to this medication.

314
00:22:01,080 --> 00:22:06,360
And then I guess as well if the patient became pregnant, I'd probably consider, you know,

315
00:22:06,360 --> 00:22:09,400
switching them to a regimen that has more safety data behind it.

316
00:22:09,400 --> 00:22:16,240
Even though it does have kind of a long, you know, half-life in the body, I would swap

317
00:22:16,240 --> 00:22:21,320
them to something else just that has a little bit more to it.

318
00:22:21,320 --> 00:22:22,320
Yeah.

319
00:22:22,320 --> 00:22:23,320
Perfect.

320
00:22:23,320 --> 00:22:26,840
And then I just wanted to touch on the topic of the viral suppression that we're talking

321
00:22:26,840 --> 00:22:27,840
about.

322
00:22:27,840 --> 00:22:34,160
So I know when I was reviewing the monograph myself earlier this year, you know, there's

323
00:22:34,160 --> 00:22:39,080
a huge topic regarding, you know, what is suppressible viral load?

324
00:22:39,080 --> 00:22:40,800
So is it less than 50 copies?

325
00:22:40,800 --> 00:22:44,960
Am I looking at, is it, you know, viral load not detected?

326
00:22:44,960 --> 00:22:48,000
I guess just for more of my information.

327
00:22:48,000 --> 00:22:51,040
And if we don't have that clear cut data, that's completely fine too.

328
00:22:51,040 --> 00:22:52,040
Yeah.

329
00:22:52,040 --> 00:22:56,760
So in the trial, they put a fairly firm cut off of less than 50 copies.

330
00:22:56,760 --> 00:23:02,480
So if you were 50 copies or above, they consider that, you know, not to be suppressed in these

331
00:23:02,480 --> 00:23:04,920
particular trials.

332
00:23:04,920 --> 00:23:12,000
I know in other trials of antiretroviral therapy, sometimes they'll consider even up to 200

333
00:23:12,000 --> 00:23:18,440
to be suppressed, but for these, you know, trials, they put the cut off at 50.

334
00:23:18,440 --> 00:23:19,440
So.

335
00:23:19,440 --> 00:23:20,440
Okay.

336
00:23:20,440 --> 00:23:21,440
Okay.

337
00:23:21,440 --> 00:23:25,200
That's good for us to know because, and in terms of, I guess, getting those first initial

338
00:23:25,200 --> 00:23:28,800
kind of viral loads and then monitoring the viral loads, and you might've said this and

339
00:23:28,800 --> 00:23:35,280
I may have missed that was once you're on Kavanuvah, how frequently am I monitoring

340
00:23:35,280 --> 00:23:38,840
or how frequently are you guys monitoring the HIV viral load?

341
00:23:38,840 --> 00:23:39,840
Yeah.

342
00:23:39,840 --> 00:23:45,200
So we would do it one month post-starting, the Kavanuv injection.

343
00:23:45,200 --> 00:23:49,120
And then if that looks good, we would do it at the three months mark and then every three

344
00:23:49,120 --> 00:23:51,800
to six months kind of after that.

345
00:23:51,800 --> 00:23:52,800
Yeah.

346
00:23:52,800 --> 00:23:56,000
And if you've got someone who's really stable on it, especially when you're coming close

347
00:23:56,000 --> 00:23:59,680
to a year from starting them, I'd probably start doing it every six months.

348
00:23:59,680 --> 00:24:05,520
You know, eventually some people might even do it once a year kind of thing, but three

349
00:24:05,520 --> 00:24:08,400
to six months is probably generally what you're looking at.

350
00:24:08,400 --> 00:24:09,400
Okay.

351
00:24:09,400 --> 00:24:12,000
So I guess like knowing the half-life and knowing that it's in your system for that

352
00:24:12,000 --> 00:24:15,120
long kind of is reassuring too.

353
00:24:15,120 --> 00:24:20,320
So it actually, another kind of plus, I guess, side of this would be that you don't have

354
00:24:20,320 --> 00:24:24,920
to do frequent lab work because right now a lot in our, at least in the pediatric population,

355
00:24:24,920 --> 00:24:29,760
kind of roughly every four months, they're having to get pokes for blood work and doing

356
00:24:29,760 --> 00:24:37,960
that from when you're a baby till your adult age is going to be, it's a drawback for sure.

357
00:24:37,960 --> 00:24:40,680
So, okay.

358
00:24:40,680 --> 00:24:47,960
And then in terms of, so what's a clinic that can you give us some like clinical examples

359
00:24:47,960 --> 00:24:56,440
of patients, maybe even one example of a patient that you've managed obviously with confidentiality

360
00:24:56,440 --> 00:24:58,920
here taking that into consideration?

361
00:24:58,920 --> 00:25:06,240
Yes, actually that is, we recently started a patient in December on Kavanuba and it was

362
00:25:06,240 --> 00:25:08,920
because of confidentiality concerns.

363
00:25:08,920 --> 00:25:13,480
So she was newly diagnosed really at this point.

364
00:25:13,480 --> 00:25:18,040
I don't know if she ever will be, but at this point isn't really wanting to share this information

365
00:25:18,040 --> 00:25:19,040
with others.

366
00:25:19,040 --> 00:25:21,600
She does live with other people in her house.

367
00:25:21,600 --> 00:25:27,280
So her concern was that she has a lot of oral and territorial sitting around that someone

368
00:25:27,280 --> 00:25:31,320
might see it, Google the name of it and find out kind of what's going on.

369
00:25:31,320 --> 00:25:39,560
So she was quite interested in trying this out because she's so concerned and even in

370
00:25:39,560 --> 00:25:43,680
the workplace, she was worried about people finding out there as well.

371
00:25:43,680 --> 00:25:50,440
So for her, I think it's been a really good switch.

372
00:25:50,440 --> 00:25:54,760
And she was also a little bit concerned about forgetting to take her pills every day.

373
00:25:54,760 --> 00:25:59,800
She did really well in the first bit and she got suppressed very quickly, but I think long

374
00:25:59,800 --> 00:26:04,200
term she was thinking day to day super busy with other things.

375
00:26:04,200 --> 00:26:05,640
She could have some misses.

376
00:26:05,640 --> 00:26:12,520
So she kind of wanted a less, I guess, involved kind of regimen and just get the shots once

377
00:26:12,520 --> 00:26:19,040
a month and forget about it until the next appointment.

378
00:26:19,040 --> 00:26:24,880
So basically kind of the ideal or the most eligible patient is that someone who is virally

379
00:26:24,880 --> 00:26:31,480
suppressed, obviously for many years would be preferable, right, because then you know,

380
00:26:31,480 --> 00:26:37,000
probably somebody who doesn't have too many comorbidities in terms of like the renal dysfunction

381
00:26:37,000 --> 00:26:39,480
that we talked about.

382
00:26:39,480 --> 00:26:45,280
And then the ideal patient in a lot of our clinics would be the ones that we worry about

383
00:26:45,280 --> 00:26:47,240
noncompliance and that type of thing.

384
00:26:47,240 --> 00:26:53,320
So obviously more of a structured setting, they would get the injectable and then be

385
00:26:53,320 --> 00:26:57,480
able to live their day to day life and don't really want to do blood work frequently and

386
00:26:57,480 --> 00:26:58,480
all that.

387
00:26:58,480 --> 00:27:04,800
So that's kind of what I'm understanding, which is a huge already like significant advantages,

388
00:27:04,800 --> 00:27:05,800
right?

389
00:27:05,800 --> 00:27:12,040
So especially dealing with chronic conditions like HIV, like we're aware of their people,

390
00:27:12,040 --> 00:27:13,040
it's tough.

391
00:27:13,040 --> 00:27:17,240
Like you don't have the ability to, as much as you want to live like your normal life,

392
00:27:17,240 --> 00:27:22,560
I think HIV medications have revolutionized that over the years and we're grateful for

393
00:27:22,560 --> 00:27:23,560
that.

394
00:27:23,560 --> 00:27:30,360
But definitely, if we can get towards, you know, even decreasing all of those drawbacks

395
00:27:30,360 --> 00:27:33,400
of taking medications, blood work, etc.

396
00:27:33,400 --> 00:27:35,040
I think we're winning.

397
00:27:35,040 --> 00:27:40,480
So that's a yeah, moving towards improving, you know, just quality of life.

398
00:27:40,480 --> 00:27:44,800
Thank you so much on, you know, taking pills every day.

399
00:27:44,800 --> 00:27:51,560
I know some practitioners, the tendency with this injectable form is to think of some of

400
00:27:51,560 --> 00:27:55,120
their patients that they've been struggling with adherence, they're thinking, okay, if

401
00:27:55,120 --> 00:27:58,400
we can get them on this, you know, then we can keep them suppressed because they only

402
00:27:58,400 --> 00:28:01,920
have to come in once a month to get the injection.

403
00:28:01,920 --> 00:28:07,920
But I would definitely say to caution around around that idea, just because, you know,

404
00:28:07,920 --> 00:28:12,600
they are going to have to be suppressed before you can actually even start the injection.

405
00:28:12,600 --> 00:28:17,400
And then you do have to be able to get a hold of the patient, they have to be reachable.

406
00:28:17,400 --> 00:28:23,640
So that involves, you know, having some, you know, access to a phone or a computer or something.

407
00:28:23,640 --> 00:28:26,200
So that you can follow up with the patient.

408
00:28:26,200 --> 00:28:30,720
And the real risk is if they aren't coming to their appointments, you kind of have a

409
00:28:30,720 --> 00:28:35,960
seven day window where you can get the injection from your cancer, January 10, as your treatment

410
00:28:35,960 --> 00:28:41,640
date, you know, every month on the 10th, you're supposed to come in for your, your injection

411
00:28:41,640 --> 00:28:42,640
appointment.

412
00:28:42,640 --> 00:28:47,920
And then you have a bit of a seven day window to work with that you can still get the injection.

413
00:28:47,920 --> 00:28:52,840
If they go outside of that, though, then you're starting to risk, you know, that two class

414
00:28:52,840 --> 00:28:58,440
resistance I talked about earlier, which can really limit your options, still have some

415
00:28:58,440 --> 00:29:03,920
NRTIs to work with and the protease inhibitors, but you know, who wants to be on a protease

416
00:29:03,920 --> 00:29:04,920
inhibitor anymore?

417
00:29:04,920 --> 00:29:06,920
You don't have to be.

418
00:29:06,920 --> 00:29:07,920
Exactly, right?

419
00:29:07,920 --> 00:29:08,920
Yeah.

420
00:29:08,920 --> 00:29:12,920
And you don't want to lose that integrase inhibitor class.

421
00:29:12,920 --> 00:29:14,360
So I mean, you know that those drugs are great.

422
00:29:14,360 --> 00:29:16,920
So yeah, yeah, yeah, that's fair.

423
00:29:16,920 --> 00:29:17,920
Okay.

424
00:29:17,920 --> 00:29:24,560
And then in terms of, I guess, if there's any like kind of other clinical evidence that

425
00:29:24,560 --> 00:29:29,760
you want to share with us today, that's, that would be helpful to anything that, you know,

426
00:29:29,760 --> 00:29:31,560
we didn't touch on today.

427
00:29:31,560 --> 00:29:32,560
Yeah.

428
00:29:32,560 --> 00:29:39,280
I'd say there is one trial going on called the MoCA trial, and that is in the 12 to 18

429
00:29:39,280 --> 00:29:47,120
year old cohort, and it's going to be presented at the IAS conference in July this year.

430
00:29:47,120 --> 00:29:51,120
And there's going to be a special PEDS workshop that they're going to be presenting this and

431
00:29:51,120 --> 00:29:56,400
mostly I think the information they'll be sharing is around the PK data, the safety and

432
00:29:56,400 --> 00:29:57,960
the acceptability results.

433
00:29:57,960 --> 00:30:04,680
So I think that's definitely something that we'll be looking forward to seeing because

434
00:30:04,680 --> 00:30:10,160
it seems to be we're always kind of limited in our options for our pediatric population.

435
00:30:10,160 --> 00:30:16,440
So any kind of new things that kind of come along that might be options are welcome, I

436
00:30:16,440 --> 00:30:17,440
think.

437
00:30:17,440 --> 00:30:18,440
So yeah,

438
00:30:18,440 --> 00:30:19,440
so that's exciting.

439
00:30:19,440 --> 00:30:26,320
I'm really, really excited to see where Cabanuba is going to take us, especially with HIV care

440
00:30:26,320 --> 00:30:28,480
here in Saskatchewan.

441
00:30:28,480 --> 00:30:34,880
I think it's something that is important because we know that we we've had an increase in number

442
00:30:34,880 --> 00:30:41,280
of our cases, compliance, definitely because we have a lot of remote rural areas.

443
00:30:41,280 --> 00:30:44,820
So access to health care is a challenge.

444
00:30:44,820 --> 00:30:48,520
So I guess the last kind of thing I want to touch on is it might be different in different

445
00:30:48,520 --> 00:30:54,720
centers, but here in Saskatchewan, which you're probably more familiar with is, if is this

446
00:30:54,720 --> 00:30:56,640
something that can be done at different sites?

447
00:30:56,640 --> 00:31:01,800
So like is Regina and Saskatoon doing kind of the injectables or is it something the

448
00:31:01,800 --> 00:31:05,400
patient has to be referred to the ID group here in Saskatoon?

449
00:31:05,400 --> 00:31:10,200
Yeah, so the Regina ID group is using it there.

450
00:31:10,200 --> 00:31:15,040
And I think they have a pharmacy that they have a bit of a relationship set up with who

451
00:31:15,040 --> 00:31:21,680
is kind of trained about this medication and monitoring it and administering and everything

452
00:31:21,680 --> 00:31:22,680
like that.

453
00:31:22,680 --> 00:31:28,000
So they kind of set up there in Saskatoon that we just recently set up with a community

454
00:31:28,000 --> 00:31:33,640
pharmacy that will kind of offer patients, you know, if you technically in Saskatchewan

455
00:31:33,640 --> 00:31:36,680
you can go anywhere to receive your antiretrovirals.

456
00:31:36,680 --> 00:31:41,640
But the fact is that this medication is a bit different and whoever is kind of involved

457
00:31:41,640 --> 00:31:46,760
in the administration of it is going to have to kind of have a special know how, you know,

458
00:31:46,760 --> 00:31:48,060
to get it to the patient.

459
00:31:48,060 --> 00:31:54,880
So we're kind of working on increasing locations that patients can access this.

460
00:31:54,880 --> 00:32:01,320
We have, you know, started patients off with a first dose with our clinic staff.

461
00:32:01,320 --> 00:32:05,120
But like you said, we're facing, you know, ever increasing numbers.

462
00:32:05,120 --> 00:32:08,760
We don't have enough staff to kind of deal with the present situation.

463
00:32:08,760 --> 00:32:12,960
So to add in something like this probably wouldn't be feasible for us.

464
00:32:12,960 --> 00:32:19,380
So I know a lot of other centers in Canada are kind of facing the same situation.

465
00:32:19,380 --> 00:32:22,480
So with the CHAP group it's kind of been a hot topic.

466
00:32:22,480 --> 00:32:27,200
People are asking how are you rolling this out and what are you guys doing?

467
00:32:27,200 --> 00:32:32,000
And it sounds like a lot of people are looking to community programs.

468
00:32:32,000 --> 00:32:36,520
Some places have infusion clinics and so people who have, you know, RA and they're getting

469
00:32:36,520 --> 00:32:42,240
those TNEP inhibitors, they're kind of approaching those places too because they kind of have

470
00:32:42,240 --> 00:32:46,160
beds and things set up for administering medication there.

471
00:32:46,160 --> 00:32:48,360
So those are some places.

472
00:32:48,360 --> 00:32:54,080
I know in Toronto they've got a very special program where they offer the service to actually

473
00:32:54,080 --> 00:32:57,200
come to the patient's home and administer the injection.

474
00:32:57,200 --> 00:32:59,000
So that's a pretty cool idea.

475
00:32:59,000 --> 00:33:03,760
Obviously you have to have the resources there to do that.

476
00:33:03,760 --> 00:33:06,720
That would be the ideal, you know, bring it right to the patient.

477
00:33:06,720 --> 00:33:11,400
But, you know, so that's kind of how we're planning to roll it out, just kind of connecting

478
00:33:11,400 --> 00:33:17,960
with some community partners and making sure that they're kind of up to speed on this medication

479
00:33:17,960 --> 00:33:23,040
and how to obtain it and lots of things.

480
00:33:23,040 --> 00:33:24,520
So lots of new exciting things.

481
00:33:24,520 --> 00:33:32,240
I think Cabinuba and, you know, since it's been on the market and coming into formulary,

482
00:33:32,240 --> 00:33:37,240
something that we'll probably see more, become more familiar with over the next few years

483
00:33:37,240 --> 00:33:38,240
here.

484
00:33:38,240 --> 00:33:43,240
I think the underlying thing for, you know, because we have a vast audience across North

485
00:33:43,240 --> 00:33:48,240
America, but especially across Canada, I would say, you know, if there is a patient that

486
00:33:48,240 --> 00:33:52,940
is eligible, kind of what we talked about today, reaching out to the infectious disease

487
00:33:52,940 --> 00:34:00,080
group in that center, discussing with specific HIV pharmacists in that center would be a

488
00:34:00,080 --> 00:34:05,240
good approach, initial approach to see if they can get some more information if that

489
00:34:05,240 --> 00:34:08,880
patient is eligible and that type of thing.

490
00:34:08,880 --> 00:34:13,440
So I think that gives me a lot of information for sure.

491
00:34:13,440 --> 00:34:18,040
I think I learned a lot during this episode and I really want to thank you, Carly, for

492
00:34:18,040 --> 00:34:22,120
taking the time out today to come on the podcast.

493
00:34:22,120 --> 00:34:32,320
It's an initiative that we started to help clinicians, pharmacists, family doctors, pediatricians,

494
00:34:32,320 --> 00:34:38,240
disease specialists, microbiologists to really just bring out hot topics like Kabanuva because

495
00:34:38,240 --> 00:34:42,240
a lot of us don't have the time to sit and, you know, discuss all of these things with

496
00:34:42,240 --> 00:34:48,360
our pharmacists who are super educated on this topic compared to a lot of us.

497
00:34:48,360 --> 00:34:54,800
And so I think, you know, bringing it all together in one episode here was something

498
00:34:54,800 --> 00:34:58,380
that I was looking forward to doing and I think you did a fantastic job.

499
00:34:58,380 --> 00:35:07,000
So thank you so much for educating us today and we'll definitely all be in touch with

500
00:35:07,000 --> 00:35:14,440
you for sure regarding future updates on this and maybe in the next few months to years

501
00:35:14,440 --> 00:35:21,880
we can kind of see what other case studies, case series or RCTs that come out of using

502
00:35:21,880 --> 00:35:22,880
Kabanuva.

503
00:35:22,880 --> 00:35:23,880
For sure.

504
00:35:23,880 --> 00:35:24,880
Yeah, thanks for having me.

505
00:35:24,880 --> 00:35:29,320
I'm always happy to share info on new things that are coming out in this area.

506
00:35:29,320 --> 00:35:31,320
So that's great.

507
00:35:31,320 --> 00:35:32,320
Thanks.

508
00:35:32,320 --> 00:35:36,820
A special thanks to Carly for joining us and thank you Dr. Pirawel.

509
00:35:36,820 --> 00:35:43,600
Follow us on Twitter at CA Breakpoint and email us at thecanadianbreakpoint at gmail.com

510
00:35:43,600 --> 00:35:47,900
to suggest infectious disease topics or discussions you'd like to hear.

511
00:35:47,900 --> 00:35:55,320
We look forward to seeing you again at the Canadian Breakpoint.

