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NASDAQ · GNFT

Genfit S.A.

Healthcare · Biotechnology

$8.95

Up+$0.35 (+4.07%)

Updated Aug 28, 2026, 5:18 PM

SID Score

3.9/10

Composite research score

Smart Money

Institutional and insider signal

Market cap
283.59M
P/E ratio
-6.54
Dividend yield
0.00%
52-week range
$2.55 – $5.21
Volume
56.95K
Avg. volume
9.4K

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Overview

Company profile and research snapshot.

Company profile

Genfit S.A., a biopharmaceutical company, discovers and develops drug candidates and diagnostic solutions for metabolic and liver-related diseases. The company's products include Elafibranor, which is in Phase 3 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; GNS561, which is in Phase 1b/2 trial to treat patients with cholangiocarcinoma (CCA); and Nitazoxanide, which is in Phase 1 trial to treat acute-on-chronic liver failure. The company has a licensing agreement with Labcorp for the commercialization of NASHnext, a blood-based molecular diagnostic test; and with Genoscience Pharma to develop and commercialize the investigational treatment GNS561 for CCA. Genfit S.A. was incorporated in 1999 and is headquartered in Loos, France.

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Analyst outlook

Consensus and target data currently published for this company.

Consensus
Average target
$13.00
Implied upside
Analysts
GNFT recent ratings
DateFirmRatingTarget
Jul 2, 2026ODDO BHFBuy
Jun 28, 2026PORTZAMPARC BNP PARIBASBuy
Jun 17, 2026ESN/CIC MARKET SOLUTIONSBuy
Mar 15, 2026LEERINK PARTNERSOutperform
Feb 27, 2026ODDO BHFBuy
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globenewswire.com · Dec 10, 2025

GENFIT : GNS561 montre une activité antitumorale prometteuse en combinaison thérapeutique

Données préliminaires très encourageantes de l'étude de Phase 1b en cours évaluant le médicament expérimental GNS561 associé à un inhibiteur de MEK (MEKi) dans le cholangiocarcinome (CCA) avec mutation KRAS, positionnant cette combinaison innovante comme une nouvelle approche thérapeutique potentielle pour les cancers difficiles à traiter: Pas de toxicité dose-limitante observée à ce jour, permettant la poursuite du recrutement d'une troisième cohorte de patientsLa combinaison GNS561MEKi a démontré une stabilisation de la maladie chez tous les patients évaluables, avec des signes de réduction tumorale dans un sous-groupe de patients, justifiant la poursuite de l'investigationDoses recommandées pour la Phase 2 attendues au premier semestre 2026 Lille (France), Cambridge (Massachusetts, United States), Zurich (Switzerland), le 10 décembre 2025 - GENFIT (Euronext: GNFT), société biopharmaceutique engagée dans l'amélioration de la vie des patients atteints de maladies rares du foie pouvant engager le pronostic vital, annonce aujourd'hui des données préliminaires de Phase 1b encourageantes issues de son essai clinique évaluant GNS561 en combinaison dans le CCA.

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