FDA grants emergency authorization to two blood purification systems [MarketWatch]
Marker Therapeutics, Inc. (MRKR)
Last marker therapeutics, inc. earnings: 11/12 04:01 pm
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Source: MarketWatch
The Food and Drug Administration (FDA) on Friday issued emergency use authorizations to blood purification devices manufactured by Terumo Corp. and Marker Therapeutics Inc. in response to the COVID-19 pandemic. Terumo is a Japanese medical device maker. Marker is a clinical-stage immuno-oncology company based in Houston. An EUA does not mean that that the device has been approved by the FDA; it is an authorization granted during an emergency when there are no other treatment options available. The regulator said that the devices can be used for adult patients with COVID-19 who are being cared for in the intensive care unit and have confirmed or imminent respiratory failure to reduce the amount of cytokines in those patients. Some severely ill COVID-19 patients have had "cytokine storms" that can lead to organ failure and death. Year-to-date, Terumo's stock is down 3.9%, while shares of Marker have dropped 39.2%. The S&P 500 has dropped 13.6% since the beginning of 2020.
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News
- Marker Therapeutics Reports Third Quarter 2024 Financial Results and Provides Business Updates [Yahoo! Finance]Yahoo! Finance
- Marker Therapeutics Reports Third Quarter 2024 Financial Results and Provides Business UpdatesGlobeNewswire
- Marker Therapeutics, Inc. (NASDAQ: MRKR) had its price target raised by analysts at LADENBURG THALM/SH SH from $11.00 to $19.00. They now have a "buy" rating on the stock.MarketBeat
MRKR
Analyst Actions
- 10/21/24 - Ladenburg Thalmann
MRKR
Sec Filings
- 11/14/24 - Form 8-K
- 11/14/24 - Form 10-Q
- MRKR's page on the SEC website