Atossa To Conduct Endoxifen Mid-Stage Study In Sweden

Atossa Therapeutics Inc ATOS has received approval from the Swedish Ethics Review Authority to begin a Phase 2 clinical study of oral Endoxifen to reduce mammographic breast density (MBD).
Atossa plans to start enrolling participants in Q4 of 2021.
The Karisma-Endoxifen study will enroll 240 healthy premenopausal women with increased breast density.
The study's primary objective is to determine the dose-response relationship of daily oral Endoxifen on MBD reduction.
Secondary endpoints for the trial include safety and tolerability.
The trial will be conducted in Stockholm, and participants will receive daily doses of oral Endoxifen or placebo for six months.
Price Action: ATOS stock is up 2.62% at $3.85 during the market session on the last check Thursday.