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API (Commercialized)GMP/DMFWomen's Health

Fezolinetant

Moderate-to-severe vasomotor symptoms (hot flashes) of menopause

CAS No.
1629229-37-3
Indication Class
Urology / Women's Health
Patent Expiry
To be assessed
Therapeutic Area
Women's Health
Target / Mechanism
TACR3
Labeled Purity
99%+
Registration Readiness
GMP/DMF
Commercialization Tier
API (Commercialized)
Linked Intermediates
6 key intermediates available
First NK3 AntagonistNon-hormonal TherapyMenopause Segment

Key Intermediates for This API

Order: listed intermediates that accept enquiries first; fragments shared across several APIs rank higher

Listing Logic · Why It's Worth Listing

The first approved non-hormonal therapy for menopausal hot flashes, with broad scope to replace hormone therapy, a large and long-unmet patient population.

Demand

Women's Health · Marketed; available for immediate sourcing

Compliance

GMP/DMF-ready; supports regulatory filing and audit in target markets

Supply

6 key intermediates available; scale-up and cost control manageable

Product Description

Fezolinetant is the first FDA-approved medication in a new class of drugs for treating moderate to severe vasomotor symptoms (hot flashes and night sweats) associated with menopause. It represents a significant advancement as a non-hormonal treatment option for women seeking relief from these common and often disruptive symptoms.

Supply source: Unibest · Fezolinetant, sourced, vetted and delivered by Unibest. Therapeutic area, indication and listing rationale are qualitative summaries based on public drug knowledge for business reference; actual registration availability and quality specifications are subject to DMF/GMP documentation and the technical agreement confirmed at order.