@DoctorBrad -
i really don’t think strategically dxb will look to fund another phase ii in dkd to reconfirm again what they already know - that dmx200 works well in sicker patients.
I believe they will aim to license it. Now it may actually be even more attractive to pharma since pharma will be able to get a way better deal considering the share price and the appropriate patient subgroup has now been defined (which is the achievement here that so many are overlooking). This greatly improves the odds for success in a future trial with appropriate inclusion criteria, derisking dmx200 for a pharma partner
future trial efforts led by dxb will be focused on the phase iii for FSGS to get the product to market
we already know patients with FSGS have higher proteinuria levels, so this is a very promising indication for dmx200
in this sense, nothing has really changed for dxb’s forward-looking plan. They were always going to look for a pharma deal for dkd after the phase ii readout and pursue FSGS phase iii internally
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