FSD201 (ultramicronized palmitoylethanolamide [ultramicronized PEA])

First hospitalised COVID-19 patient dosed in FSD201 treatment trial

17 December 2020 | By Hannah Balfour (European Pharmaceutical Review)

The study will evaluate whether FSD201 is safe and of benefit to hospitalised patients with COVID-19, in combination with standard of care.

doctors in Personal Protective Equipment (PPE) in the room of a hospitalised COVID-19 patient

news

FSD Pharma applies to FDA for trial testing FSD201 in COVID-19 patients

2 September 2020 | By Hannah Balfour (European Pharmaceutical Review)

The Investigational New Drug Application (IND) is for a Phase II trial evaluating the safety and efficacy of FSD201 (ultramicronized PEA) in hospitalised COVID-19 patients.

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FSD201 (ultramicronized palmitoylethanolamide [ultramicronized PEA])

First hospitalised COVID-19 patient dosed in FSD201 treatment trial

FSD Pharma applies to FDA for trial testing FSD201 in COVID-19 patients