Fidia S.p.A. (BIT: FDA)
Market Cap | 1.27M |
Revenue (ttm) | 29.17M |
Net Income (ttm) | -6.44M |
Shares Out | 31.09M |
EPS (ttm) | -0.44 |
PE Ratio | n/a |
Forward PE | n/a |
Dividend | n/a |
Ex-Dividend Date | n/a |
Volume | 3,705,120 |
Open | 0.0438 |
Previous Close | 0.0438 |
Day's Range | 0.0400 - 0.0448 |
52-Week Range | 0.0398 - 1.1100 |
Beta | 0.07 |
Analysts | n/a |
Price Target | n/a |
Earnings Date | Mar 17, 2025 |
About Fidia
Fidia S.p.A., together with its subsidiaries, designs, manufactures, and sells high speed milling systems, numerical controls, milling heads, and software systems. Its accessories comprise HMS, a device for measuring and compensating geometric error on continuous or indexed bi-rotary heads and roto-tilting tables; TMSC, a device to measure length and diameter of the tool, as well as to check the shape; K5 tracer, a solution to perform continuous scanning of 3D surfaces; pushbutton panels; XPower digital drives for axis and spindle movement; and... [Read more]
Financial Performance
Financial StatementsNews
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FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea in Adults with Obesity
FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea in Adults with Obesity
FDA approves weight loss drug Zepbound for sleep apnea
Zepbound, Eli Lilly’s weight loss drug, can now be used to treat obstructive sleep apnea in adults with obesity, the FDA said.
FDA approves Eli Lilly's weight loss drug Zepbound for sleep apnea, expanding use in U.S.
The agency's decision expands the use of Zepbound and could potentially pave the way for Eli Lilly to gain broader insurance coverage for the treatment.
FDA approves Zepbound® (tirzepatide) as the first and only prescription medicine for moderate-to-severe obstructive sleep apnea in adults with obesity
Averaging up to 20% of weight loss, adults taking Zepbound had at least 25 fewer breathing interruptions each hour as they slept Up to 50% of adults taking Zepbound no longer had symptoms associated w...
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Pfizer Inc (PFE) Gains FDA Approval for New Colorectal Cancer Treatment
Pfizer Inc (PFE) Gains FDA Approval for New Colorectal Cancer Treatment
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On Thursday, the FDA granted full approval to Humacyte, Inc.’s (NASDAQ: HUMA) Symvess (acellular tissue-engineered vessel-tyod) use in adults as a vascular conduit for extremity arterial injury when ...
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