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Genfit S.A. (GNFTF) Análisis de Acciones

Solo con fines informativos. No es asesoramiento financiero. Analysis by Sedat Aydin, Founder & Editor-in-Chief | AI-powered analysis. Data sourced from SEC filings and institutional-grade financial providers. Editorially reviewed. Not financial advice.

Cotizando a $, Genfit S.A. (GNFTF) es una empresa del sector Healthcare valorada en 0. Tiene una alta puntuación de convicción de 73/100 en factores fundamentales, técnicos y de sentimiento.

Ultimo analisis: 17 mar 2026
Puntuación de IA de 73/100

Genfit S.A. (GNFTF) Resumen de Asistencia Médica y Tuberías

CEOPascal Prigent
Empleados180
Sede CentralLoos, FR
Año de la oferta pública inicial (OPI)2014
IndustriaBiotechnology

Genfit S.A. is a biopharmaceutical company specializing in metabolic and liver disease treatments, including Elafibranor for primary biliary cholangitis. With diagnostic solutions like NIS4 technology and partnerships with Labcorp and Genoscience Pharma, Genfit navigates the competitive biotech landscape, focusing on unmet needs in liver-related conditions.

Procedencia de los datos | Datos financieros Análisis cuantitativo NASDAQ Análisis: 17 mar 2026

Tesis de Inversión

Genfit S.A. presents a focused investment opportunity within the biotechnology sector, driven by its pipeline of drug candidates targeting liver diseases. The Phase 3 clinical trial of Elafibranor for PBC represents a near-term catalyst, with potential for market approval and revenue generation. The development of NIS4 technology for NASH diagnosis offers a longer-term growth avenue, addressing the increasing prevalence of NASH globally. However, the company's negative profit margin of -85.9% and reliance on clinical trial outcomes pose significant risks. Successful commercialization of its products and strategic partnerships are crucial for achieving profitability and shareholder value. Investors should closely monitor clinical trial results, regulatory approvals, and competitive dynamics within the liver disease treatment market.

Basado en las finanzas de FMP y el análisis cuantitativo

Puntos clave

  • Market capitalization of $0.54 billion reflects investor valuation of Genfit's pipeline and potential.
  • A P/E ratio of -11.22 indicates that the company is currently unprofitable, typical for biotechnology firms in the development stage.
  • Gross margin of 93.1% suggests strong potential profitability upon successful commercialization of its products.
  • Beta of 1.19 indicates that the stock is slightly more volatile than the market, reflecting the inherent risks in biotechnology investments.
  • The company's focus on liver diseases addresses a significant unmet medical need, driving potential for future growth.

Competidores y Pares

Fortalezas

  • Proprietary drug candidates in clinical development.
  • Strong expertise in metabolic and liver diseases.
  • Strategic partnerships with leading companies.
  • Innovative diagnostic technologies.

Debilidades

  • High reliance on clinical trial outcomes.
  • Negative profitability.
  • Limited commercial infrastructure.
  • Dependence on partnerships for commercialization.

Catalizadores

  • Upcoming: Results from Phase 3 clinical trial of Elafibranor for PBC expected in late 2026 or early 2027.
  • Ongoing: Commercialization of NASHnext through partnership with Labcorp.
  • Upcoming: Potential regulatory approval of Elafibranor for PBC in late 2027, if Phase 3 results are positive.
  • Ongoing: Development of NIS4 technology for NASH diagnosis.
  • Upcoming: Advancement of GNS561 through Phase 1b/2 trial for CCA with potential data release in 2027.

Riesgos

  • Potential: Failure of Elafibranor in Phase 3 clinical trials.
  • Potential: Regulatory hurdles in obtaining approval for Elafibranor.
  • Ongoing: Competition from other companies developing treatments for liver diseases.
  • Ongoing: Dependence on partnerships for commercialization.
  • Potential: Patent expiration on key technologies.

Oportunidades de crecimiento

  • Elafibranor for Primary Biliary Cholangitis (PBC): Elafibranor, currently in Phase 3 clinical trials, represents a significant growth opportunity for Genfit. If approved, Elafibranor could address a substantial unmet need in the treatment of PBC, a chronic liver disease. The PBC market is projected to grow, driven by increased awareness and improved diagnostic methods. Successful completion of Phase 3 trials and subsequent regulatory approval could lead to significant revenue generation for Genfit, potentially starting in late 2026 or early 2027.
  • NIS4 Technology for NASH Diagnosis: The development of NIS4 technology for the non-invasive diagnosis of NASH and fibrosis offers a compelling growth avenue. NASH is a rapidly growing liver disease, and early diagnosis is crucial for effective management. NIS4 aims to provide a convenient and accurate diagnostic tool, potentially capturing a significant share of the NASH diagnostics market. Commercialization of NIS4, potentially through partnerships, could contribute to Genfit's revenue growth starting in 2027.
  • GNS561 for Cholangiocarcinoma (CCA): Genfit's GNS561, currently in Phase 1b/2 trial for CCA, represents a longer-term growth opportunity. CCA is a rare but aggressive cancer of the bile ducts, with limited treatment options. Successful development and commercialization of GNS561 could address a critical unmet need and generate revenue for Genfit, although this is likely several years away, potentially 2029 or later.
  • Partnership with Labcorp for NASHnext: Genfit's licensing agreement with Labcorp for the commercialization of NASHnext provides a revenue stream and market access. NASHnext is a blood-based molecular diagnostic test for NASH. This partnership allows Genfit to leverage Labcorp's extensive network and expertise in diagnostics, accelerating the adoption of NASHnext and contributing to Genfit's financial performance. Revenue from this partnership is ongoing.
  • Expansion into New Therapeutic Areas: Genfit could explore expansion into new therapeutic areas within metabolic and liver diseases, leveraging its expertise and infrastructure. This could involve developing new drug candidates or acquiring existing assets. Expanding the pipeline would diversify Genfit's revenue streams and reduce its reliance on individual products. This is a longer-term strategy, potentially unfolding over the next 5-10 years.

Oportunidades

  • Growing market for NASH treatments and diagnostics.
  • Expansion into new therapeutic areas.
  • Potential for regulatory approval of Elafibranor.
  • Increased adoption of NIS4 technology.

Amenazas

  • Competition from other pharmaceutical and biotechnology companies.
  • Clinical trial failures.
  • Regulatory hurdles.
  • Patent expiration.

Ventajas competitivas

  • Proprietary drug candidates and diagnostic technologies protected by patents.
  • Expertise in metabolic and liver diseases.
  • Established partnerships with leading pharmaceutical and diagnostic companies.
  • Clinical trial data demonstrating the efficacy and safety of its products.

Acerca de GNFTF

Genfit S.A., established in 1999 and headquartered in Loos, France, is a biopharmaceutical company dedicated to discovering and developing innovative therapeutic and diagnostic solutions for metabolic and liver-related diseases. The company's primary focus is on addressing significant unmet medical needs in areas such as nonalcoholic steatohepatitis (NASH), primary biliary cholangitis (PBC), and cholangiocarcinoma (CCA). Genfit's lead product candidate, Elafibranor, is currently in Phase 3 clinical development for the treatment of PBC. Additionally, the company is developing NIS4 technology for the diagnosis of NASH and fibrosis, aiming to provide a non-invasive diagnostic tool for early detection and monitoring of disease progression. Genfit is also advancing GNS561, a drug candidate in Phase 1b/2 trial for CCA, and Nitazoxanide, in Phase 1 trial for acute-on-chronic liver failure. Genfit has established strategic collaborations, including a licensing agreement with Labcorp for the commercialization of NASHnext, a blood-based molecular diagnostic test, and with Genoscience Pharma for the development and commercialization of GNS561 for CCA. These partnerships underscore Genfit's commitment to expanding its reach and impact in the field of liver diseases.

Qué hacen

  • Discovers and develops drug candidates for metabolic diseases.
  • Focuses on treatments for liver-related diseases.
  • Develops diagnostic solutions for liver conditions.
  • Conducts clinical trials to evaluate the safety and efficacy of its drug candidates.
  • Seeks regulatory approval for its products from health authorities.
  • Commercializes its products through partnerships and direct sales.

Modelo de Negocio

  • Develops and patents novel drug candidates and diagnostic technologies.
  • Out-licenses or partners with other companies for commercialization.
  • Generates revenue through licensing fees, milestone payments, and royalties.
  • Potentially generates revenue through direct sales of diagnostic products.

Contexto de la Industria

Genfit S.A. operates within the competitive biotechnology industry, focusing on the development of treatments and diagnostics for liver diseases. The NASH market, in particular, is experiencing significant growth due to the increasing prevalence of obesity and related metabolic disorders. Key competitors include BRIBF, BXPHF, IPHYF, JWCTF, and MLLCF, each pursuing different approaches to address liver diseases. Genfit's strategic partnerships and focus on innovative diagnostic solutions position it to capture a share of this expanding market, estimated to reach billions of dollars in the coming years.

Clientes Clave

  • Patients suffering from metabolic and liver diseases.
  • Physicians who treat patients with these conditions.
  • Diagnostic laboratories that use Genfit's diagnostic products.
  • Pharmaceutical companies that partner with Genfit for drug development and commercialization.
Confianza de la IA: 81% Actualizado: 17 mar 2026

Finanzas

Gráfico e información

Precio de la acción de Genfit S.A. (GNFTF): Price data unavailable

Últimas noticias

Consenso de analistas

Calificación de Consenso

Recomendaciones agregadas de Compra/Mantener/Vender de Benzinga, Yahoo Finance y Finnhub para GNFTF.

Objetivos de Precios

Análisis del precio objetivo de Wall Street para GNFTF.

MoonshotScore

73/100

¿Qué significa esta puntuación?

El MoonshotScore califica el potencial de crecimiento de GNFTF en una escala de 0 a 100 en múltiples factores, incluyendo innovación, disrupción del mercado, salud financiera e impulso.

Liderazgo: Pascal Prigent

Chief Executive Officer

Pascal Prigent serves as the Chief Executive Officer of Genfit S.A., bringing extensive experience in the pharmaceutical and biotechnology industries. His career spans various leadership roles, including positions in sales, marketing, and business development. He has a proven track record of driving growth and innovation in the healthcare sector. Prigent's expertise encompasses strategic planning, product development, and commercialization, making him well-suited to lead Genfit in its mission to develop treatments for metabolic and liver diseases. His leadership is focused on advancing the company's pipeline and expanding its market presence.

Historial: Under Pascal Prigent's leadership, Genfit has focused on advancing its clinical pipeline, particularly Elafibranor for PBC. He has overseen strategic partnerships aimed at expanding the company's reach and commercial capabilities. Key milestones include the progression of Elafibranor through Phase 3 clinical trials and the development of innovative diagnostic solutions. Prigent's tenure has been marked by a commitment to addressing unmet medical needs in liver diseases and driving shareholder value.

Información del mercado OTC de GNFTF

The OTC Other tier represents the lowest tier of the OTC market, indicating that Genfit S.A. (GNFTF) may not meet the minimum financial or disclosure requirements of higher tiers like OTCQX or OTCQB. Companies in this tier may have limited financial reporting, potentially increasing investment risk. Unlike companies listed on major exchanges like the NYSE or NASDAQ, OTC Other companies face fewer regulatory requirements, resulting in less transparency for investors. This tier is often associated with speculative investments and requires careful due diligence.

  • Nivel OTC: OTC Other
  • Estado de divulgación: Unknown
Liquidez: Liquidity for GNFTF on the OTC market is likely limited, potentially resulting in wider bid-ask spreads and increased trading costs. Lower trading volumes can make it difficult to buy or sell shares quickly without significantly impacting the price. Investors should be aware of the potential for price volatility and consider using limit orders to manage their risk. The limited liquidity of OTC stocks can pose challenges for institutional investors.
Factores de riesgo OTC:
  • Limited financial disclosure increases information asymmetry.
  • Lower liquidity can lead to price volatility and difficulty in trading shares.
  • The OTC Other tier carries a higher risk of fraud or mismanagement.
  • Fewer regulatory requirements provide less investor protection.
  • Potential for delisting or suspension of trading.
Lista de verificación de diligencia debida:
  • Verify the company's financial statements and SEC filings (if any).
  • Research the company's management team and their track record.
  • Assess the company's business model and competitive landscape.
  • Evaluate the company's legal and regulatory compliance.
  • Check for any red flags, such as pending lawsuits or regulatory investigations.
  • Monitor trading volume and price volatility.
  • Consult with a financial advisor.
Señales de legitimidad:
  • The company has a well-defined business model and a clear focus on liver diseases.
  • Genfit has established partnerships with reputable companies like Labcorp and Genoscience Pharma.
  • The company's lead product candidate, Elafibranor, is in Phase 3 clinical trials.
  • Genfit has a team of experienced scientists and executives.
  • The company has a history of innovation in the field of liver diseases.

Acciones de Genfit S.A.: Preguntas Clave Respondidas

¿Cuáles son los factores clave para evaluar GNFTF?

Genfit S.A. (GNFTF) actualmente tiene una puntuación IA de 73/100, indicando puntuación alta. Fortaleza clave: Proprietary drug candidates in clinical development.. Riesgo principal a monitorear: Potential: Failure of Elafibranor in Phase 3 clinical trials.. Esto no es asesoramiento financiero.

¿Qué es el MoonshotScore de GNFTF?

GNFTF actualmente puntúa 73/100 (Grado A) en el MoonshotScore, lo que sugiere calificación alta. La puntuación evalúa el potencial de crecimiento, la salud financiera, el impulso del mercado y los factores de riesgo en 9 KPIs cuantitativos. Se recalcula diariamente con los últimos datos del mercado. Esta puntuación es solo informativa.

¿Con qué frecuencia se actualizan los datos de GNFTF?

Los precios de GNFTF se actualizan en tiempo real durante el horario del mercado estadounidense (9:30-16:00 ET, días laborables). Los fundamentales se actualizan después de los informes trimestrales o anuales. Las calificaciones de analistas y las perspectivas de IA se actualizan diariamente. Las noticias se agregan continuamente de fuentes financieras.

¿Qué dicen los analistas sobre GNFTF?

La cobertura de analistas para GNFTF incluye calificaciones de consenso (compra, mantener, venta), objetivos de precio a 12 meses y estimaciones de ganancias de las principales firmas de investigación. Consulte la sección de Consenso de Analistas en esta página.

¿Cuáles son los riesgos de invertir en GNFTF?

Las categorías de riesgo para GNFTF incluyen riesgo de mercado, riesgo específico de la empresa (gestión, competencia), riesgo financiero (deuda, consumo de efectivo) y riesgo macroeconómico (tasas, inflación). Un riesgo clave identificado: Potential: Failure of Elafibranor in Phase 3 clinical trials.. Un beta superior a 1,0 indica mayor volatilidad que el S&P 500. Revise la sección de Factores de Riesgo en esta página. Todas las inversiones conllevan riesgo de pérdida.

¿Cuál es la relación P/E de GNFTF?

La relación P/E para GNFTF compara el precio actual de la acción con sus ganancias por acción. Un P/E más alto puede indicar expectativas de crecimiento, mientras que un P/E más bajo puede sugerir valor. Consulte la pestaña de Financieros para métricas actuales.

¿Está GNFTF sobrevalorada o infravalorada?

Determinar si Genfit S.A. (GNFTF) está sobrevalorada o infravalorada requiere examinar múltiples métricas. Compare los ratios de valoración (P/E, P/S, EV/EBITDA) con pares del sector. Esto no es asesoramiento financiero.

¿Cuál es el rendimiento por dividendo de GNFTF?

Genfit S.A. (GNFTF) actualmente no paga un dividendo regular, o los datos de rendimiento no están disponibles. Consulte la pestaña de Financieros para información actual.

Descargo de responsabilidad: Este contenido es solo para fines informativos y no constituye asesoramiento de inversión. Siempre haga su propia investigación y consulte a un asesor financiero.

Recursos Oficiales

Análisis actualizado el Puntuación de IA actualizada diariamente
Fuentes de Datos y Metodología
Datos de mercado proporcionados por Financial Modeling Prep y Yahoo Finance. Análisis de IA por algoritmos propietarios de Stock Expert AI. Indicadores técnicos mediante cálculos estándar de la industria. Última actualización: .

Datos proporcionados solo con fines informativos.

Notas de análisis
  • Information is based on available data and may be subject to change.
  • AI analysis is pending and may provide further insights.
  • OTC market data may be less reliable than exchange-listed data.
Fuentes de datos

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