Logo

Sedor's Sesquient Receives the US FDA's Approval for Status Epilepticus

Share this

Sedor's Sesquient Receives the US FDA's Approval for Status Epilepticus

  • The US FDA has approved Sesquient (fosphenytoin sodium for injection) for the treatment of status epilepticus in adult and pediatric patients
  • Sedor is actively in discussions to license the rights to Sesquient for NA- EU- and other territories- except for the People’s Republic of China- where it has already been licensed
  • Sesquient is the first and only FDA-approved room temperature stable fosphenytoin and can help HCPs to treat status epilepticus patients and reduce hospital costs associated with this condition

 ­ Ref: BusinessWire  | Image: Twitter

Click here to­ read the full press release 

Senior Editor

This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions