By Matteo Castia

 

Futura Medical PLC said Monday that the Food and Drug Administration has agreed to the design of the non-clinical human factor study on the group's MED3000 treatment for erectile dysfunction.

The U.K. pharmaceutical developer, which focuses on sexual health and pain relief, said the study will test the ability of subjects to self-diagnose their erectile dysfunction, correctly select the product based on label information and test their ability to correctly use the product without supervision of a doctor.

The company said it aims to launch the product on the market during 2022 and that manufacturing scale-up and capacity to meet projected demand is progressing well.

 

Write to Matteo Castia at matteo.castia@dowjones.com

 

(END) Dow Jones Newswires

July 19, 2021 02:43 ET (06:43 GMT)

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