Marburg and Ravn viruses cause a disease that's very similar to the Ebola virus disease.
So, it's a multi-systemic, multi-organ failure, you do have hemorrhagic manifestations.
The case fatality rates are very high, just like Ebola.
In some of the outbreaks in central Africa, they've been up to 90% case fatality rates.
At this point there are no FDA approved therapeutics or vaccines for Marburg or Ravn virus.
So doctors typically treat patients that are infected with Marburg or Ravn virus through
palliative care.
Just like the Ebola patients in Emory where you'd be in a critical care unit and they
would be replacing electrolytes and replacing fluids, providing pain relief, that type of
thing.
Because during an outbreak scenario, when you have a patient come to your clinic or
to the treatment unit, you're not quite sure exactly where they are in their disease course.
They don't come to a hospital until they're at a very critical stage of illness.
So we would not begin treating an animal until it had signs of illness.
So we want to see how far into the disease course we can intervene and still save the
patient.
And in these studies we can test where that's at and know when the therapy is actually going
to be efficacious or not.
I think the benefit here is that this is a human, a fully human monoclonal antibody.
So, unlike a lot of the other therapies this is, there's a lot known about monoclonal antibody
therapy.
It's used for other infectious diseases, so safety would be one benefit.
And we had two groups of non-human primates, or actually three groups of non-human primates,
where one group received the antibody beginning four days after exposure to Marburg virus,
and they were completely protected.
A second group received the antibody five days after they were exposed to Marburg virus.
80% of those animals were protected.
And then the final group was treated with a monoclonal antibody five days after they
were infected with Ravn virus and they were completely protected.
The antibody that was employed in this particular project was made in plants.
So one of the things that we're looking at is seeing if we can manufacture this antibody
in mammalian.
And, so, basically it's a production issue so that we can do it cheaper and make more
of the antibody at a lower cost.
And, so if you do that, is the antibody still protective in primates?
So, that's one of the things that we're looking at.
The other thing that we're looking at is, again, is can we optimize this, can we develop
additional antibodies that maybe we can delay treatment even further and even closer to
the time of death and still protect humans or non-human primates?
So, we're following up on these results to see how much further can we push these out.
The antibody is not the only therapy that we have that work against Marburg and Ravn
viruses.
There are other ones that work very well and we're looking in to using these as combinations.
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