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 Provides a Clinical Update on MT-601 in Patients with Lymphoma [Yahoo! Finance]Yahoo! Finance
- Marker Therapeutics Announces $16.1 Million Private Placement [Yahoo! Finance]Yahoo! Finance
- Marker Therapeutics Announces $16.1 Million Private PlacementGlobeNewswire
- Marker Therapeutics Provides a Clinical Update on MT-601 in Patients with LymphomaGlobeNewswire
- Marker Therapeutics Awarded $9.5 Million Grant from the Cancer Prevention & Research Institute of Texas (CPRIT) to Support the Investigation of MT-601 in Patients with Pancreatic Cancer [Yahoo! Finance]Yahoo! Finance
MRKR
Analyst Actions
- 10/21/24 - Ladenburg Thalmann
MRKR
Sec Filings
- 12/26/24 - Form 4
- 12/23/24 - Form 4
- 12/23/24 - Form 8-K
- MRKR's page on the SEC website