Search This Blog

Sunday, August 22, 2021

Biotech week ahead, Aug. 23

 Biotech stocks swayed back and forth before ending the week lower. With earnings news dying down and an empty initial public offerings calendar, it was broader market cues, clinical readouts and regulatory actions that moved stocks during the week.

Virpax Pharmaceuticals, Inc.VRPX 9.7% was among the biggest gainers of the week following a positive regulatory communication regarding its MMS019.

Sesen Bio, Inc. SESN 9.91% extended its losses that were set in motion by an unexpected FDA rejection of its investigational bladder cancer drug Vicineum.

Eli Lilly and Company 

LLY 0.24% and partner Boehringer Ingelheim received Food and Drug Administration approval for Jardiance as a treatment option for a specific type of heart failure. The regulator also granted accelerated approval for GlaxoSmithKline's GSK 0.11% Jemperli for patients with previously treated, mismatch repair-deficient solid cancers. This is the second approval granted to the anti-PD-1 antibody treatment.

Among other key developments of the week was Lilly reorganizing its business with the objective of giving increased focus to its neuroscience business. Johnson & Johnson, Inc. JNJ 0.52% announced the transitioning of CEO Alex Gorsky to the role of executive chairman and the elevation of insider Joaquin Duato as CEO.

Here are the key catalytic events scheduled for the unfolding week.


Conferences

International Society for Experimental Hematology, ISEH, 2021 Virtual Scientific Meeting: Aug. 25-28

PDUFA Dates

The FDA is scheduled to rule on Axsome Therapeutics, Inc.'s AXSM 8.29% dextromethorphan-bupropion (AXS-05) as a treatment option for major depressive disorder. The PDUFA date is set for Sunday, Aug. 22. The prospect of approval coming through by the deadline is bleak, as the company indicated in its Aug. 9 earnings release that the FDA has identified deficiencies in the application.

Cara Therapeutics, Inc. CARA 10.39% and Vifor Pharma await an FDA nod for the new drug application for their Korsuva injection to treat moderate-to-severe pruritus in hemodialysis patients. The decision is due by Monday, Aug. 22.

Clinical Readouts

Aileron Therapeutics, Inc. ALRN 0.99% will present at the ISEH meeting. final data from the completed Phase 1b trial of ALRN-6924 in patients with small-cell lung cancer and initial findings from ongoing healthy volunteer Study of ALRN-6924.

Earnings

Ascendis Pharma A/S ASND 1.15% (Wednesday, after the close)

IPOs

IPO Quiet Period Expiry

https://www.benzinga.com/general/biotech/21/08/22598635/the-week-ahead-in-biotech-cara-fda-decision-ascendis-earnings-aileron-data-presentation-and-more

No comments:

Post a Comment

Note: Only a member of this blog may post a comment.