RE: RE: Patent news7 Jun 2021 16:58
It shouldn't be too much of an issue, the recent FDA 503a bulks list was related to compounding drugs, so the ability for compounding pharmacies to use tranilast to create patient specific mixes.
Whilst tranilast itself doesn't have FDA approval, although it does have Orphan designation for maligant glioma, and also orphan status in the EU, which ever company licenses from NFX will be undergoing the usual 3 phase trials anyway. Just as they would if this was a brand new drug.