To Get Full Access :

Veozah

Veozah is the first FDA‑approved non‑hormonal oral neurokinin 3 (NK3) receptor antagonist for moderate to severe vasomotor symptoms (hot flashes and night sweats) due to menopause. It blocks neurokinin B activity in the hypothalamus to regulate body temperature without estrogen .

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 :

    Fezolinetant
  • Innovator :

    ASTELLAS PHARMA US INC
  • Approval Date :

    12-May-23
  • NCE-1 Date :

    12-May-27
  • NCE Date :

    12-May-28
  • Dosage Form :

    Tablet
  • Strength :

    45MG
  • Therapeutic Category :

    Anti-Menopausal
  • Revenue ($M) :

    222

Year-wise Projected Sales ($M) :

  • 2025 :

    331
  • 2026 :

    446
  • 2027 :

    578
  • 2028 :

    707
  • 2029 :

    836
  • 2030 :

    953
  • 2031 :

    1,053
Looking for this molecule for your next clinical research? Access regulatory-compliant comparators with assured timelines—delivered reliably through our global network.

Why Choose Spring Bio Solution?

Supported 1000+ Clinical Trials globally

Provides services across regulatory, legal & clinical research

Unmatched intelligence on batches, expiry, spacing, and historical data from innovators

Integrated CRO Services as part of our offerings

Insights on global pricing for smarter clinical trial supply decisions 


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?