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Genfit S.A.

GNFT
EPA: GNFT Delayed
3.20EUR 0.8%
3.63 USD
As of 24 April 2025, Genfit S.A. has a market cap of $180.33M USD, ranking #17721 globally and #247 in France. It ranks #1767 in the Healthcare sector, and #500 in the Biotechnology industry.
Global Rank
17721
Country Rank
247
Sector Rank
1767
Industry Rank
500
Key Stats
Market Cap
$180.33MUSD
158.47M EUR
Enterprise Value
$186.57MUSD
164.63M EUR
Revenue (TTM)
$91.58MUSD
80.47M EUR
EBITDA (TTM)
$24.77MUSD
21.86M EUR
Net Income (TTM)
$25.34MUSD
22.27M EUR
EBITDA Margin
27%
Profit Margin
28%
PE Ratio
7.3
Company Profile
Country (HQ)
Sector
Healthcare
Industry
Biotechnology
CEO
M. Prigent open_in_new
Employees
159
Founded
1999
Website
genfit.com open_in_new
warningChart data may be delayed
1d 1w 1m 3m 6m 1y
0.8% -0.1% -5.7% -6.8% -41% -1.9%
Upcoming Earnings
Earnings Date
Thu, Apr 24 Today

Markets

Exchange Ticker Price
Euronext Paris
MIC: XPAR
PRIMARY
GNFT
Genfit SA
ISIN: FR0004163111
Shares Out.:
49.865M1 Shares Float: 43.858M2
TV:
SA:
YF:
GF:
BA:
MS:
3.20 EUR
London Stock Exchange
MIC: XLON
0QT6
Genfit SA
ISIN: FR0004163111
TV:
SA:
YF:
GF:
BA:
MS:
3.15 EUR
NASDAQ
MIC: XNAS
GNFT
Genfit SA ADR
ISIN: US3722791098
TV:
SA:
YF:
GF:
NQ:
BA:
MS:
3.64 USD
OTC Markets
MIC: OTCM
GNFTF
Genfit SA
ISIN: FR0004163111
TV:
SA:
YF:
GF:
BA:
MS:
3.54 USD
1Market cap is calculated using shares outstanding.
2Float shares are publicly tradable shares, excluding insider-held stock.

About Genfit S.A.

Genfit S.A., a late-stage biopharmaceutical company, discovers and develops drug candidates and diagnostic solutions for metabolic and liver-related diseases. The company develops Elafibranor, which is in Phase III clinical trial to treat patients with primary biliary cholangitis. It also engages in the development of NIS4 technology for the diagnosis of nonalcoholic steatohepatitis (NASH) and fibrosis; VS-01 for the treatment of Urea Cycle Disorder (UCD) and Organic Acidemia Disorder (OAD); GNS561, which is in Phase 1b/2a trial to treat patients with cholangiocarcinoma (CCA); VS-01-ACLF and Nitazoxanide (NTZ), which is in Phase 1 trial to treat acute-on-chronic liver failure, as well as VS-02-HE, which is in preclinical trial for the treatment of Reduction of Hyperammonemia and the Stabilization of Blood Ammonia; CML-022; SRT-015, an ASK1 inhibitor targets the inhibition of cellular apoptosis, inflammation, and fibrosis. The company has a licensing agreement with Labcorp for the commercialization of NASHnext, a blood-based molecular diagnostic test; and Genoscience Pharma to develop and commercialize the investigational treatment GNS561 for CCA. The company was incorporated in 1999 and is headquartered in Loos, France.

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