To Get Full Access :

Daybue

Daybue is the first FDA-approved oral treatment for Rett syndrome in patients 2 years of age and older. It targets neurological function to address core symptoms of the disorder.

The information outlined in the molecule details section below would help you evaluate Para IV filing opportunities early to secure a first-to-file advantage.

Molecule Details :

  • Molecule Name :

    Trofinetide
  • Innovator :

    ACADIA PHARMACEUTICALS INC
  • Approval Date :

    10-Mar-23
  • NCE-1 Date :

    10-Mar-27
  • NCE Date :

    10-Mar-28
  • Dosage Form :

    Oral Solution
  • Strength :

    200mg/ml
  • Therapeutic Category :

    Neuroprotective
  • Revenue ($M) :

    348

Year-wise Projected Sales ($M) :

  • 2025 :

    389
  • 2026 :

    469
  • 2027 :

    536
  • 2028 :

    605
  • 2029 :

    658
  • 2030 :

    710
  • 2031 :

    763
Looking for this molecule for your next clinical research? Access regulatory-compliant comparators with assured timelines—delivered reliably through our global network.

Why Partner With Us

Login With

For full access Sign-up / Sign-in using below Methods:

By continuing, you agree to our Terms & Conditions and Privacy Policy. You can review them anytime.

Are you sure want to logout from NCE Grid?