Company intelligence / Profile preview

Hynson, Westcott & Dunning

Baltimore, Maryland, United States
Ownership
Private
Development stage
Other
01

Overview

Lutrexin, a product for women's health indications, was withdrawn by FDA due to lack of adequate evidence for efficacy following the 1962 amendments requiring effectiveness as well as safety. The company challenged this withdrawal, resulting in a Supreme Court hearing on due process for regulatory drug approvals.

Therapeutic areas
Women's Health
Modalities
Small molecule
Industry
Pharma

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