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Tuesday, June 28, 2022

3 Women's Health Stocks Are Soaring Following Roe v. Wade Ruling

Three days after the U.S. Supreme Court struck down Roe v. Wade in one of the most potentially impactful rulings of the last century, a handful of women's health stocks are on the move on Monday in response to the news.

Stocks On The Move: Evofem Biosciences Inc 

 shares ripped higher by more than 133% on Monday morning. Evofem's Phexxi vaginal gel is a contraceptive that can be applied zero to 60 minutes prior to each act of intercourse. Phexxis is a combination of lactic acid, citric acid and potassium bitartrate and is the first and only hormone-free, on-demand prescription contraceptive vaginal gel.

"When women are denied safe, legal abortion, the importance of access to FDA-approved contraception is greater than it has ever been," Evofem CEO Saundra Pelletier said in May.

Agile Therapeutics Inc 

 shares were up 15.1% on Monday morning. Agile is the maker of Twirla, a weekly contraceptive patch approved by the FDA in early 2020. Agile announced the commercial launch of Twirla in March and is targeting primarily 18- to 24-year-old women.

Dare Bioscience Inc 

 shares rallied 7.7% on Monday as well. Dare is a clinical-stage biopharmaceutical company focused on developing products for women’s health. Dare's Ovaprene is an investigational hormone-free monthly intravaginal contraceptive.

Benzinga's Take: It's unclear at this point how much of a sales boost contraceptives will get following the Roe v. Wade ruling and how much of Monday's trading action is simply volatility generated in relatively thinly traded stocks generated by the news headlines.

Regardless of your personal beliefs about Roe v. Wade, traders should tread cautiously in these birth control stocks.

https://www.benzinga.com/general/biotech/22/06/27865451/3-womens-health-stocks-are-soaring-following-roe-v-wade-ruling


Schrödinger's Initial-Stage Cancer Study Gains FDA Clearance

 Schrödinger Inc. 

 announced that the U.S. Food and Drug Administration (FDA) cleared its investigational new drug (IND) application for the drug candidate SGR-1505 in patients with relapsed or refractory B-cell lymphoma.

The Phase 1 clinical study will evaluate the safety, pharmacokinetics, pharmacodynamics of SGR-1505 in patients with relapsed or refractory B-cell lymphoma.

Karen Akinsanya, Ph.D., president of R&D, commented : “Based on the preclinical data for SGR-1505, we believe we have an opportunity to advance a potential best-in-class MALT1 inhibitor into the clinic, There is a significant medical need for patients with relapsed or refractory B-cell lymphoma who have exhausted currently approved treatment options.

The company is planning to initiate Phase 1 clinical study of SGR-1505 in the second half of 2022.

Further, an expansion cohort is planned to evaluate SGR-1505 in combination with other anti-cancer agents, such as BTK and BCL-2 inhibitors, in patients with specific B-cell malignancies.

https://www.benzinga.com/general/biotech/22/06/27883835/schr-dingers-initial-stage-cancer-study-gains-fda-clearance