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Forum GENFIT
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GENFIT : Analyse de l AI sur Genfit

13 nov. 2024 13:10

Based on the financial information provided for GENFIT, let's analyze their earnings for 2023 and the first two quarters of 2024, as well as the perspectives for 2025.
2023 Full Year and Early 2024 Performance
Cash Position
At the end of 2023, GENFIT had €77.8 million in cash and cash equivalents1
3
. This decreased to €74.0 million by March 31, 20244
, and further to €61.6 million by June 30, 20241
2
. However, it's important to note that this figure excludes a significant milestone payment. Revenue

First half of 2024: €59.0 million in revenues, including a €48.7 million milestone payment invoiced in June 20241
2
.
First quarter of 2024: €1.1 million in revenues4
.
Full year 2023: Specific full-year revenue for 2023 is not provided, but we can infer it was lower than 2024 based on the quarterly comparisons.

Profitability
The company turned profitable in the first half of 2024, reporting a net profit of €30.3 million, compared to a net loss of €20.9 million in the first half of 20231
2
.
Key Developments

FDA Approval: Iqirvo® (elafibranor) received FDA approval in June 2024 for the treatment of Primary Biliary Cholangitis (PBC)1
.
European Progress: A positive opinion from the European Medicines Agency Committee was received in July 2024, with a final decision on marketing authorization expected in the second half of 20241
.
Milestone Payments: GENFIT received a €48.7 million milestone payment upon the first U.S. sale of Iqirvo®1
2
3
.

2025 Perspectives

Cash Runway: GENFIT expects its current cash position to fund operations until at least the start of the fourth quarter of 20253
.
Additional Milestone Payments: The company anticipates receiving approximately €26.5 million upon Iqirvo's pricing and reimbursement approval in three European countries1
.
Ongoing Research: GENFIT continues to invest in research and development, particularly in their ACLF franchise (VS-01, NTZ, SRT-015, CLM-022, and VS-02 HE) and GNS561 for cholangiocarcinoma3
.
Revenue Growth: With the commercial launch of Iqirvo®, GENFIT may see increased royalty revenues in 20253
.
Potential Profitability: Given the turnaround to profitability in the first half of 2024, GENFIT may be positioned for sustained profitability in 2025, depending on research expenses and milestone achievements.
Market Expansion: The potential European approval and launch of Iqirvo® could open new revenue streams1
.

In conclusion, GENFIT has shown significant financial improvement in 2024, driven by milestone payments and the approval of Iqirvo®. The outlook for 2025 appears positive, with potential for continued revenue growth and sustained profitability, supported by a strong cash position and anticipated milestone payments. However, ongoing research investments and market performance of Iqirvo® will be crucial factors in determining the company's financial trajectory.

2 réponses

  • 13 novembre 2024 13:19

    Based on the information provided, here are the perspectives for GENFIT regarding the treatment of Primary Sclerosing Cholangitis (PSC) with elafibranor:

    Ongoing Clinical Trial: GENFIT is currently conducting a study to assess the safety and effectiveness of elafibranor in adult participants with PSC1
    . This indicates that the company is actively pursuing the development of elafibranor for PSC treatment.
    Potential Expansion of Indications: Elafibranor has already received approval for Primary Biliary Cholangitis (PBC) in the US and EU3
    5
    . The ongoing research for PSC suggests GENFIT is aiming to expand the drug's indications, which could potentially increase its market reach and revenue potential.
    Mechanism of Action: Elafibranor is a dual peroxisome activated receptor (PPAR) alpha/delta agonist, which targets multiple cell types and biological processes involved in cholestatic liver diseases2
    . This mechanism could be beneficial for PSC patients, as it addresses cholestasis, bile toxicity, inflammation, and fibrosis.
    Potential First-in-Class Treatment: If successful, elafibranor could become a first-in-class treatment for PSC, as it has for PBC. This could give GENFIT a significant advantage in the market for rare liver diseases.
    Building on PBC Success: The positive results and regulatory approvals for elafibranor in PBC provide a strong foundation for its potential in PSC. The drug has demonstrated efficacy in improving liver function and reducing disease progression in PBC patients4
    , which could translate to benefits for PSC patients as well.
    Addressing an Unmet Need: PSC is a rare disease with limited treatment options. If elafibranor proves effective, it could address a significant unmet medical need, potentially leading to rapid adoption and favorable pricing.
    Potential for Additional Revenue Streams: Success in PSC would open up a new revenue stream for GENFIT, complementing the existing and potential future revenues from elafibranor's use in PBC.
    Long-term Growth Opportunity: The development of elafibranor for PSC represents a long-term growth opportunity for GENFIT, as clinical trials and potential regulatory approvals typically take several years.

    While these perspectives are promising, it's important to note that the success of elafibranor in PSC will depend on the results of the ongoing clinical trials. The outcomes of these studies will be crucial in determining the drug's efficacy and safety profile in PSC patients, and ultimately, its potential for regulatory approval and commercial success in this indication.


  • 13 novembre 2024 14:38

    Sur T3, Genfit a dépensé aux alentours de 13,3 M .
    Ce sont les PH3 qui sont vraiment coûteuses.
    Genfit n’en a pas en cours

    On peut douter qu’ils en mènent 3-4-5 de front.
    Sauf pipe-line PH2 avec des résultats exceptionnels.
    Genfit n’en est pas encore là.

    La trésorerie devrait s’allonger et durer plus que n’annoncent certains oiseaux


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