Yeah, I’d say the zaltenibart trial, which is one that will come out in suboptimal responders and despite the fact that we have proximals now, I think this every eight week treatment is a very attractive one. And then there’s another compound that’s called KP104, that’s basically a combination of a C5 inhibitor and factor H. So you have proximal and terminal inhibition at the same time...
Yeah, I’d say the zaltenibart trial, which is one that will come out in suboptimal responders and despite the fact that we have proximals now, I think this every eight week treatment is a very attractive one. And then there’s another compound that’s called KP104, that’s basically a combination of a C5 inhibitor and factor H. So you have proximal and terminal inhibition at the same time. It’s a Chinese product that so far only has been shown the proof-of-concept in naive patients but there’s trials going to come out with this product. And I think that’s a very attractive idea because we’re all wondering whether or not proximal or terminal would be the best. In this case you would have both at once and you would have with your factor H that is activated at the level where a complement is activated you would have it specifically working at the site of action and so I think that totally makes sense.
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