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FRNM

Freenome Inc

11,75 USD
-0,54
4,39 %
Zum Börsenschluss Aktualisiert 16. Okt., 16:00 EDT
Vor Börsenbeginn
Nachbörslich
11,89
+0,14
1,19 %
1 Tag
-4,39 %
5 Tage
-25,16 %
1 Monat
-20,23 %
3 Monate
-9,68 %
6 Monate
-9,68 %
Seit Jahresbeginn
-9,68 %
1 Jahr
-9,68 %
5 Jahre
-9,68 %
10 Jahre
-9,68 %
 

Profil: Freenome Inc is a development-stage, early cancer detection company developing blood-based screening tests leveraging a proprietary artificial intelligence/machine learning multiomics technology platform to transform multi-cancer and ultimately multi-disease detection. It is developing a range of blood-based cancer screening tests.

Nachrichten

Positiv
Neutral
Negativ
Stimmung 3 Monate
Positiv 40 %
Neutral 60 %
Negativ 0 %
Neutral
GlobeNewsWire
gestern
Freenome to Report Third Quarter 2026 Financial Results on November 10, 2026
BRISBANE, Calif., Oct. 15, 2026 (GLOBE NEWSWIRE) -- Freenome, Inc. (Nasdaq: FRNM), an early cancer detection company developing blood-based screening tests, today announced that the Company plans to release its financial results for the third quarter ended September 30, 2026, after the market close on Tuesday, November 10, 2026.
Freenome to Report Third Quarter 2026 Financial Results on November 10, 2026
Positiv
Seeking Alpha
vor 24 Tagen
Freenome: SimpleScreen CRC Unlocks A 50M Patient TAM, Bypassing Competition
Freenome is rated Buy, leveraging FDA-approved SimpleScreen CRC and a $410M cash reserve to target the vast unscreened colorectal market. FRNM's SimpleScreen CRC, now out-licensed to Abbott, offers a patient-friendly, blood-based alternative, with up to $700M in milestone payments and 10% royalties. Upcoming catalysts include the pivotal PROACT LUNG study for SimpleScreen Lung, which could validate the multiomics platform across multiple indications.
Freenome: SimpleScreen CRC Unlocks A 50M Patient TAM, Bypassing Competition
Neutral
GlobeNewsWire
vor 2 Monaten
FDA Grants Breakthrough Device Designation to Freenome's Blood-Based SimpleScreen™ Lung Cancer Screening Test
BRISBANE, Calif., Aug. 12, 2026 (GLOBE NEWSWIRE) -- Freenome, Inc. (Nasdaq: FRNM), an early cancer detection company developing blood-based screening tests, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation to SimpleScreen™ Lung, the company's investigational lung cancer screening test.
FDA Grants Breakthrough Device Designation to Freenome's Blood-Based SimpleScreen™ Lung Cancer Screening Test
Positiv
Reuters
vor 2 Monaten
FDA approves Freenome's blood test for colorectal cancer screening
The U.S. FDA has approved Freenome's blood-based colorectal cancer screening test for older adults, paving the way for partner Abbott ​to launch it in the U.S. this fall, ‌the companies said on Monday.
FDA approves Freenome's blood test for colorectal cancer screening
Neutral
GlobeNewsWire
vor 2 Monaten
FDA Approves Freenome's SimpleScreen™ CRC Blood-Based Screening Test; Abbott to Commercialize in the U.S.
– Approval expands colorectal cancer screening options for the up to 60 million Americans who are overdue for screening – – Medicare coverage and American Cancer Society guidance support broader access to blood-based colorectal cancer screening – BRISBANE, Calif. and ABBOTT PARK, Ill.
FDA Approves Freenome's SimpleScreen™ CRC Blood-Based Screening Test; Abbott to Commercialize in the U.S.
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