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Another exciting advisor here is Alpha
Nooner.
Today, we're excited to be joined by Dr.
Dana Lambert,
who is the president and CEO of Endera
Pharmaceuticals.
We're going to spend some time today
talking about why cannabinoids might be
moving beyond dispensaries into areas like
infection control, recovery,
and next-generation healthcare
applications.
Should be a really interesting
conversation.
So if you're out there and joining us
and you have some questions,
put them in early so we can get
to them as we go along,
but should be a great conversation.
So with all that said,
thanks again for joining us, Dana.
Really appreciate it.
Thank you for having me.
Yeah.
So as I was talking to you early
before we went live,
kind of funny was reflecting we've had you
on before and it was exactly a year
ago.
So May twenty eight, twenty twenty five,
we had you on talking about the Indira
story.
A great episode.
I'll make sure I share it on social
afterwards so people can get that more
in-depth story of Indira.
But to start,
kind of can you tell us sort of
the high level story for Indira today for
people who are joining?
Yeah, absolutely.
So it's very exciting times for our
company moving forward.
We're actually advancing our lead
technology into clinical trials.
We're looking at applications in very
serious hospital infections and chronic
wounds.
So we're advancing into clinical trials
treating diabetic ulcer wounds and
non-healing surgical wounds.
So it's very busy times and also super
exciting.
Yeah,
really exciting and interesting work,
I think.
I feel like there's a kind of an
element where a lot of people will hear
cannabis or cannabis medicine and
cannabinoids and immediately think of
dispensaries and kind of more the consumer
product side of things.
You know,
how big is the opportunity in that sort
of wellness and like you're saying,
those antimicrobial sort of opportunities
becoming?
Well, I mean,
if we're just looking at our technology as
it stands,
we're looking at over forty billion in
addressable markets for applications and
hospital infection, chronic wounds,
many resistant infections.
I mean,
we can go into kind of the developments
and what our research shows a bit later
on, but it's a massive opportunity.
Diabetic ulcers alone
a seven billion dollar market,
only one FDA approved therapy.
And it has a black box warning for
increasing the risk of cancer.
So we're looking at a market that is
massively underserved and we believe that
our technology is a highly promising
candidate to help these people.
Yeah, it's fantastic.
I do think as we're seeing all this
momentum build around cannabis as
medicine, I think, again,
a lot of people are seeing it only
from one perspective.
And I think taking the Endera perspective
of how kind of widespread the applications
can be is really interesting and something
that people shouldn't overlook ultimately.
So I know we'll dig into kind of
some of the pipeline and some of the
studies that you guys have put out lately,
but did just want to talk about very
briefly, of course,
on the US side of the border,
we did see schedule three now for medical
cannabis, you know,
would love to hear one,
your kind of take on it.
And two,
does it have any impact in terms of,
you know,
how you're viewing the opportunity today?
Yeah, absolutely.
And I really applaud the US administration
for taking these steps.
I think it's been a long time coming.
I think a lot of people are highly
supportive of this.
It makes so much sense.
It's going to help the industry in so
many ways.
But what it really does, in my view,
is just validates this plant as a source
of healing and highlights that we really
need to be viewing this not as something
that has no medicinal value and is
potentially dangerous,
into something that can truly be a
therapeutic.
So really applaud what's happening in the
US.
It's fantastic.
It's a huge shift,
huge step in the right direction.
And I think if we touched on a
little bit
As we touched on a little bit before
the conversation,
if we could just contrast that with the
situation in Canada,
I personally think that it's important for
viewers to know the situation and kind of
the differences that are happening on both
sides of the border.
Yeah,
tell us about it a little bit more
in terms of that contrast,
because we were talking about it before,
but I think it's important for people to
understand and know.
Yeah.
So, I mean, as you know,
Andeera is headquartered in Vancouver,
Canada.
We're a fully registered Canadian-based
company.
However,
most of our key suppliers and research
contracts are based in the US.
We do a lot of research and development
in Vancouver, in Canada,
with
leading universities and research
hospitals, University of BC,
Vancouver Coastal Health Research
Institute.
But the administrative burden for us being
able to do research has been, frankly,
it's been antagonistic to research.
And I think what a lot of people
believe when they think about Canada is
that we're ahead of the curve,
that we've adopted cannabis,
it's legal and very few restrictions or
issues.
Well, that's just not the case.
When it comes to consumer use,
medicinal use of cannabis,
it's readily available through licensed
dispensaries,
through Health Canada approved suppliers
and manufacturers,
and that really serves Canadians.
However,
If you should want to do research with
cannabinoids,
the amount of licensing and burden,
it's actually quite antagonistic.
You have to get a research license
approved.
You can't just say we're handling a
substance that falls into bucket or
schedule X.
Canada's established completely different
regulations for cannabis,
and that includes cannabinoids or pure
research compounds.
According to Canada,
that fits the definition of cannabis.
So we don't regulate it as a drug.
We regulate it as a plant.
And to do research,
you have to get a research license.
It can take months and you're not allowed
to just have have a site licensed.
You have to get a individual research
protocol approved.
So you have to get each experiment
essentially approved.
which can take months.
Then if you want to order cannabinoids to
do the research, import permits.
Our team has had to interface with
Canadian Border Services Agency and
scientifically justify why we're wanting
to order these compounds,
all the while
any Canadian is free to go into a
dispensary and buy highly concentrated
forms of THC, cannabis.
So to be frank,
I believe that the Canadian regulations
need a serious upgrade.
And I think they honestly should look to
the US when it comes to research.
Yeah,
so just a lot of red tape that
really slows things down and gums up the
work,
it seems like in terms of actually making
that research progress.
Do you think that because the US is
kind of turning on in this way that
that will influence Canada in terms of
easing those restrictions,
but easing sort of the red tape around,
you know, actually getting research done?
Or do you think that doesn't change?
Honestly,
I certainly hope that Canadian
administration just takes a step back and
looks at the impact that the current
regulations have on companies like Andeira
that are wanting to develop therapeutics
and legitimately need access to these
compounds to do research.
maybe just, you know,
remove a few layers of restriction would
be greatly appreciated.
Yeah, fair enough.
I do hope that's also sort of an
interesting learning lesson for new
markets that are coming online to,
you know, allow for research,
looking to Europe and other places.
Hopefully they are able to adopt.
It sounds like more of the U.S.
model than the Canadian model.
That's really interesting.
I think that's a perspective that people
don't really know much about, I think,
in general.
So really interesting.
All right.
Well,
then I'd love to cover kind of what
you guys have been working on.
I, you know,
one of the things that I think really
caught my attention was a relatively
recent peer reviewed paper that you guys
had come out with or study that you
guys had come out with.
You know,
what can you tell us about what that
was?
I think you released it late April,
I want to say.
What can you tell us about what that
is, the implications, the impact?
I'd love to hear about that more.
Yeah, absolutely.
So our paper on our technology, Sylvanex,
was published in the Oxford Journal of
Applied Microbiology,
one of the leading global journals in new
technologies in the antimicrobial space.
So what this did is it actually presented
our results and our findings on how this
triple combination,
including antimicrobial silver combined in
combination with CBC and CBG is number
one, synergistic, fully bactericidal.
prevents resistance.
It also reduces the toxicity of silver and
it boosts wound healing cells.
So there was a lot of data,
a lot of results.
We're very proud of it.
It's truly a landmark publication and
major validation for the technology.
It also demonstrates that this technology
can help with quite a number of different
applications throughout healthcare and
also more broadly in industrial uses.
And the reason I say that is because
this paper showed very clearly that
Silvan-X clears biofilms.
Now,
biofilms are essentially a slime that
infectious pathogens make to protect them
from being killed.
They don't just affect chronic wounds.
They're also leading to fouling on ships
in the US Navy, for example.
So any technology that has biofilm
clearing properties,
suddenly that opens up applications
within healthcare and outside of
healthcare.
So as a company,
we're strictly focused on advancing
SylvanX for healthcare applications,
diabetic ulcer wounds,
as well as surgical wounds.
But we are actively talking with other
organizations around the world
that are going, hey,
can we use this to prevent mold or
fouling on plants, on cannabis crops?
Can we use this for applications XYZ?
So we are actively looking at partnerships
and uses for the technology that are
non-competitive and outside the scope of
our therapeutic development.
Really interesting.
So diverse applications there.
Out of curiosity,
I feel like when we talked about SylvanX
last year,
I feel like a lot of it was
focused on the application,
obviously on the medical side of things
and how impactful that can be.
When did the industrial kind of story or
opportunity, I guess,
kind of come to light or how did
you guys open that up?
I'd love to know.
In December.
Okay, very recently, okay.
Very recently, McKinsey,
one of our primary research sites based at
the Vancouver Coastal Health Research
Institute,
one of the leading labs in the field,
got very clear definitive data showing
that Silvan-X actually clears biofilms and
not just one type of biofilm,
we show that it clears biofilms from the
two major and most problematic bacterial
causes of biofilms.
So the data are not subtle.
We compared the effect head to head with
existing antimicrobials that do have some
ability to clear biofilms.
We showed Silvan-X blew that out of the
water, essentially.
So extremely exciting.
So antimicrobial silver on its own has
sort of mediocre to very low ability to
clear biofilms.
On the other hand,
in synergistic triple combination,
as Sylvanex,
huge biofilm clearing properties.
We're talking MRSA biofilms being cleared
by over a ninety percent,
which is almost unheard of.
Really interesting.
I can't wait till we talk in about
a year and there's another application
that you guys can open up for SylvanX.
Really interesting.
All right, well then,
so for people who are following the story
and kind of the work you're doing,
which again seems to be expanding
constantly, which is great, you know,
what should people be keeping an eye on
when it comes to Indira?
You know,
what has you most excited about kind of
in the coming months?
Yeah, so for us as a company,
we're actually about to undergo one of the
strongest periods of growth that companies
in our sector tend to see,
which is transitioning from preclinical
development into clinical stage
development.
So we are advancing Silvanex into two
clinical trials.
So these are not just phase one trials
that are, you know,
applying the drug and looking at safety.
These are phase one to a trials where
we will be evaluating safety,
tolerability,
and efficacy in diabetic ulcers and
surgical wounds.
So we're extremely excited about that.
Really interesting.
Oh, go ahead.
Sorry.
The other thing I just want to add
that has me most excited is that,
and what I think is really important for
viewers to understand is that Silvinex is
not just an antimicrobial.
Our data shows that it reduces the chronic
inflammation and stimulates wound healing.
And as far as existing therapies go,
there's essentially nothing available that
can do this.
Diabetics and chronic wound sufferers need
something that can clear biofilms and
stimulate their wounds to heal.
Our data and other independent published
data shows that the ingredients in
Silvanex, specifically CBC and CBG,
do just that.
So we're extremely excited to record
safety and efficacy in the clinic.
Yeah,
I think really interesting and very
excited to see kind of what comes next
for the Endera story.
I think there's a lot of focus,
of course, for cannabis broadly, you know,
really having,
picking up some momentum kind of probably
across categories,
whether you're even looking at adult use,
but obviously in medical,
but then I think this specific form of
kind of
uh medical applications um really really
interesting or industrial applications
which is um you know really fascinating
excited to see kind of where the story
goes for people who want to kind of
get a better sense of you know uh
updates follow along with the story where
would you point them um go to our
website andira.ca you can also follow us
on linkedin and twitter
That's fantastic.
All right.
Well,
then thanks so much for taking the time,
Dr. Dana.
Really appreciate it.
It's a really interesting story and
looking forward to hopefully next year
having you tune in and let us know
what the next updates are because it's a
very exciting story.
Thank you so much, Mackenzie.
Thanks so much, everyone.
We'll catch you next time.
Thanks.
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