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Mereo BioPharma plc (MREO) 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 $0.34, Mereo BioPharma plc (MREO) es una empresa del sector Healthcare valorada en 55M. La acción obtiene una puntuación de 58/100, una calificación moderada basada en 9 KPI cuantitativos.

Ultimo analisis: 15 mar 2026
Puntuación de IA de 58/100 Objetivo $0.83 (+145.9%) MCap 55M Vol 978K

Mereo BioPharma plc (MREO) Resumen de Asistencia Médica y Tuberías

CEODenise Vera Scots-Knight
Empleados36
Sede CentralLondon, GB
Año de la oferta pública inicial (OPI)2019
IndustriaBiotechnology

Mereo BioPharma Group plc, a UK-based biopharmaceutical firm, specializes in developing therapies for oncology and rare diseases. Its pipeline features clinical-stage assets like etigilimab and navicixizumab, positioning it within the competitive biotechnology landscape focused on unmet medical needs and strategic collaborations.

Procedencia de los datos | Datos financieros Análisis cuantitativo NASDAQ Análisis: 15 mar 2026

Tesis de Inversión

Mereo BioPharma presents a high-risk, high-reward investment profile due to its focus on clinical-stage assets targeting oncology and rare diseases. Key value drivers include the successful progression of etigilimab and navicixizumab through clinical trials, with potential market exclusivity upon approval. The company's collaboration with MD Anderson Cancer Center represents a potential catalyst for further development. However, the company's negative profit margin of -8301.5% and reliance on future clinical trial success pose significant risks. Successful Phase 2 trials for Acumapimod and Alvelestat could drive significant value. Investors should closely monitor clinical trial data and regulatory milestones.

Basado en las finanzas de FMP y el análisis cuantitativo

Puntos clave

  • Market capitalization of $0.06 billion, reflecting its position as a small-cap biopharmaceutical company.
  • P/E ratio of -1.49, indicating that the company is currently not profitable.
  • Gross margin of 19.1%, suggesting some efficiency in managing the cost of goods sold.
  • Beta of 0.33, indicating lower volatility compared to the overall market.
  • Profit Margin of -8301.5%, highlighting the company's significant losses.

Competidores y Pares

Fortalezas

  • Diverse pipeline of clinical-stage assets.
  • Focus on high-value therapeutic areas (oncology and rare diseases).
  • Strategic collaborations with leading research institutions.
  • Proprietary drug candidates with patent protection.

Debilidades

  • High cash burn rate and reliance on future funding.
  • Significant clinical trial risks and regulatory uncertainties.
  • Limited commercialization experience.
  • Negative profit margin.

Catalizadores

  • Upcoming: Interim data release from the Phase 1b clinical trial of etigilimab (OMP-313M32) in Q3 2026.
  • Upcoming: Initiation of Phase 2 clinical trials for Setrusumab (BPS-804) in Q4 2026.
  • Ongoing: Enrollment progress in the Phase II clinical trial of Acumapimod (BCT-197) for COPD.
  • Ongoing: Collaboration with The University of Texas MD Anderson Cancer Center to evaluate etigilimab.

Riesgos

  • Potential: Clinical trial failures for key product candidates.
  • Potential: Regulatory delays or rejection of marketing applications.
  • Ongoing: Competition from established pharmaceutical companies.
  • Ongoing: Dependence on future funding and potential dilution of existing shareholders.
  • Ongoing: Negative profit margin and high cash burn rate.

Oportunidades de crecimiento

  • Etigilimab (OMP-313M32) Development: The ongoing Phase 1b clinical trial of etigilimab for tumor treatment represents a significant growth opportunity. Success in this trial could lead to further clinical development and potential commercialization, addressing a substantial market in oncology. The timeline for potential market entry depends on clinical trial outcomes and regulatory approvals, but represents a multi-billion dollar market opportunity.
  • Navicixizumab (OMP-305B83) Advancement: Navicixizumab, having completed Phase 1b clinical trials for late-line ovarian cancer, offers a pathway to address unmet needs in ovarian cancer treatment. Further clinical development and potential regulatory approval could drive significant revenue. The ovarian cancer therapeutics market is projected to reach billions of dollars, offering substantial growth potential.
  • Acumapimod (BCT-197) for COPD: The Phase II clinical trials of Acumapimod for treating acute exacerbations of COPD present a valuable growth avenue. Successful trial results could lead to a novel treatment option for COPD, a prevalent respiratory disease. The COPD treatment market represents a multi-billion dollar opportunity, with a growing patient population.
  • Setrusumab (BPS-804) for Osteogenesis Imperfecta: The development of Setrusumab, a novel antibody for treating osteogenesis imperfecta, targets a rare disease with limited treatment options. Positive clinical trial outcomes and regulatory approval could establish Mereo as a key player in this niche market. The orphan drug market offers attractive pricing and regulatory incentives.
  • Alvelestat (MPH-966) for Alpha-1 Antitrypsin Deficiency: The Phase II clinical trial of Alvelestat for Alpha-1 antitrypsin deficiency provides another growth opportunity in the rare disease space. Successful development and commercialization could address a significant unmet need for patients with this genetic disorder. The market for Alpha-1 antitrypsin deficiency treatments is growing, driven by increased diagnosis and awareness.

Oportunidades

  • Successful clinical trial outcomes for lead product candidates.
  • Regulatory approvals and market exclusivity for novel therapies.
  • Expansion of pipeline through strategic acquisitions and licensing.
  • Partnerships with larger pharmaceutical companies for commercialization.

Amenazas

  • Competition from established pharmaceutical companies.
  • Clinical trial failures and regulatory setbacks.
  • Patent expirations and generic competition.
  • Economic downturn and reduced healthcare spending.

Ventajas competitivas

  • Proprietary drug candidates with patent protection.
  • Clinical-stage pipeline with potential for market exclusivity.
  • Strategic collaborations with leading research institutions.
  • Focus on rare diseases with limited treatment options.

Acerca de MREO

Mereo BioPharma Group plc, established in 2015 and headquartered in London, United Kingdom, is a biopharmaceutical company dedicated to the development and commercialization of innovative therapeutics, primarily targeting oncology and rare diseases. The company's strategy involves acquiring and advancing clinical-stage programs to address unmet medical needs. Its lead product candidate, etigilimab (OMP-313M32), an antibody T-cell immunoreceptor with Ig and ITIM domains, is currently in Phase 1b clinical trial for the treatment of tumors. Mereo's pipeline also includes Navicixizumab (OMP-305B83), which has completed Phase 1b clinical trials for the treatment of late-line ovarian cancer. Acumapimod (BCT-197), a p38 MAP kinase inhibitor, is in Phase II clinical trials for treating acute exacerbations of chronic obstructive pulmonary disease (COPD). Leflutrozole (BGS-649), an oral aromatase inhibitor, is being developed for the treatment of hypogonadotropic hypogonadism. Furthermore, Mereo is advancing rare disease product candidates, such as Setrusumab (BPS-804), a novel antibody for the treatment of osteogenesis imperfecta, and Alvelestat (MPH-966), an oral small molecule in Phase II clinical trial for Alpha-1 antitrypsin deficiency. The company collaborates with The University of Texas MD Anderson Cancer Center to evaluate etigilimab. Mereo BioPharma operates internationally, focusing on strategic partnerships and licensing agreements to enhance its portfolio and accelerate drug development.

Qué hacen

  • Develops therapeutics for oncology and rare diseases.
  • Advances clinical-stage programs through strategic acquisitions and licensing.
  • Focuses on unmet medical needs in specialized therapeutic areas.
  • Conducts clinical trials to evaluate the safety and efficacy of its product candidates.
  • Collaborates with research institutions and pharmaceutical companies.
  • Seeks regulatory approvals for its therapies in various markets.

Modelo de Negocio

  • Acquires and licenses clinical-stage assets.
  • Develops and conducts clinical trials for its product candidates.
  • Out-licenses or partners for commercialization of approved therapies.
  • Focuses on oncology and rare diseases with high unmet needs.

Contexto de la Industria

Mereo BioPharma operates within the competitive biotechnology industry, characterized by high R&D spending, lengthy clinical trials, and stringent regulatory approvals. The company focuses on oncology and rare diseases, aligning with the growing demand for targeted therapies and orphan drugs. The biotechnology sector is projected to grow, driven by technological advancements and an aging population. Competitors like ACIU and ALDX are also pursuing novel therapies, increasing the pressure on Mereo to achieve clinical and commercial success. Strategic collaborations and licensing agreements are crucial for navigating this landscape.

Clientes Clave

  • Patients suffering from cancer and rare diseases.
  • Healthcare providers prescribing therapies.
  • Pharmaceutical companies partnering for commercialization.
  • Research institutions collaborating on drug development.
Confianza de la IA: 81% Actualizado: 15 mar 2026

Finanzas

Gráfico e información

Precio de la acción de Mereo BioPharma plc (MREO): $0.34 (-0.01, -3.12%)

Últimas noticias

Consenso de analistas

Calificación de Consenso

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

Objetivos de Precios

Objetivo de consenso: $0.83

MoonshotScore

58/100

¿Qué significa esta puntuación?

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

Último análisis de Mereo BioPharma plc

Liderazgo: Denise Vera Scots-Knight

CEO

Denise Vera Scots-Knight serves as the Chief Executive Officer of Mereo BioPharma Group plc. Her background includes extensive experience in the pharmaceutical and biotechnology industries. She has held various leadership positions in companies focused on drug development and commercialization. Her expertise spans strategic planning, business development, and clinical operations. She is responsible for guiding Mereo's strategic direction and overseeing its clinical programs.

Historial: Under Denise Vera Scots-Knight's leadership, Mereo BioPharma has focused on advancing its clinical-stage pipeline and securing strategic collaborations. Key milestones include the progression of etigilimab and navicixizumab through clinical trials. Her tenure has been marked by efforts to strengthen the company's financial position and expand its portfolio of rare disease and oncology assets.

Información de ADR de Mereo BioPharma plc Patrocinado

An American Depositary Receipt (ADR) is a certificate representing shares of a foreign company trading on U.S. stock exchanges. MREO, as an ADR, allows U.S. investors to invest in Mereo BioPharma Group plc, a UK-based company, without the complexities of cross-border transactions. The ADR is denominated in U.S. dollars and trades during U.S. market hours.

  • Ticker del mercado local: London Stock Exchange, United Kingdom
  • Nivel de ADR: 2
  • Ratio de ADR: 1:1
Riesgo cambiario: As an ADR, MREO is subject to currency risk. Fluctuations in the exchange rate between the British pound (GBP) and the U.S. dollar (USD) can impact the value of the ADR. A strengthening pound relative to the dollar could increase the ADR's value, while a weakening pound could decrease it. Investors may want to evaluate this currency exposure when evaluating MREO.
Implicaciones fiscales: Dividends paid on MREO ADRs may be subject to foreign dividend withholding tax by the United Kingdom. The standard withholding tax rate may be reduced under tax treaties between the U.S. and the UK. U.S. investors may be able to claim a foreign tax credit on their U.S. tax return for the amount of foreign tax withheld.
Horario de negociación: The London Stock Exchange (LSE) operates from 8:00 AM to 4:30 PM GMT. U.S. markets (e.g., NASDAQ) typically operate from 9:30 AM to 4:00 PM EST. This results in an overlap in trading hours, but U.S. investors may experience limited trading activity on MREO ADRs outside of the U.S. market hours.

Lo Que los Inversores Preguntan Sobre Mereo BioPharma plc (MREO)

¿Cuáles son los factores clave para evaluar MREO?

Mereo BioPharma plc (MREO) actualmente tiene una puntuación IA de 58/100, indicando puntuación moderada. Los analistas apuntan a $0.83 (+146% desde $0.34). Fortaleza clave: Diverse pipeline of clinical-stage assets.. Riesgo principal a monitorear: Potential: Clinical trial failures for key product candidates.. Esto no es asesoramiento financiero.

¿Qué es el MoonshotScore de MREO?

MREO actualmente puntúa 58/100 (Grado C) en el MoonshotScore, lo que sugiere calificación moderada. 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 MREO?

Los precios de MREO 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 MREO?

Los analistas han establecido un precio objetivo de consenso de $0.83 para MREO, representando un potencial alcista del 146% desde el precio actual de $0.34. La cobertura incluye calificaciones de compra, mantener y venta, estimaciones de ganancias y recientes mejoras o rebajas. Consulte la sección de Consenso de Analistas en esta página.

¿Cuáles son los riesgos de invertir en MREO?

Las categorías de riesgo para MREO 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: Clinical trial failures for key product candidates.. 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 MREO?

La relación P/E para MREO 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 MREO sobrevalorada o infravalorada?

Determinar si Mereo BioPharma plc (MREO) está sobrevalorada o infravalorada requiere examinar múltiples métricas. Objetivo de analistas $0.83 (+146% desde el precio actual). 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 MREO?

Mereo BioPharma plc (MREO) 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 as of 2026-03-15.
  • Clinical trial outcomes are inherently uncertain.
  • Financial projections are subject to change.
Fuentes de datos

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