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Previsión
El precio objetivo medio de los analistas es de 58,87 € (+155,51 %). La mediana es de 70,47 € (+205,86 %).
| Comprar |
19 |
| Mantener |
8 |
| Vender |
1 |
Noticias Ir al feed de noticias
Beam Therapeutics emphasizes leadership in base editing and shows positive BEAM‑302 data
Beam Therapeutics presented promising clinical data for the in‑vivo BEAM‑302 program in alpha‑1 antitrypsin deficiency at the Cantor conference, with the 60 mg dose reaching the protective threshold in all patients. The company reported $1.2 billion in cash with a financial runway to mid‑2029 and plans multiple launches, including Risto‑cel with a possible BLA filing and launch in the second half of 2027. Beam highlighted its integrated manufacturing infrastructure and an alleged lead of more than two years in base editing, but acknowledged safety monitoring (a transient grade‑3 liver enzyme increase) and intense competitive pressure. » Más en de.investing.com
Beam Therapeutics presents progress of base‑editing platform at Citigroup conference
Beam Therapeutics reported comprehensive advances across its base‑editing pipeline, including an expected BLA submission for Risto‑cel in sickle cell disease by the end of 2026 (possibly early 2027) and ongoing recruitment of the approval‑relevant cohort for BEAM‑302 (alpha‑1‑antitrypsin deficiency). An active IND is in place for BEAM‑304 (PKU) and patient screening is planned to start by the end of 2026; BEAM‑301 (GSD1a) could yield first human data in 2026. Management emphasized the platform‑based development approach, agreed regulatory collaboration with the FDA, and funding intended to support operations through mid‑2029. » Más en de.investing.com
Beam Therapeutics reports progress in base editing, alpha‑1 program shows durable effect
Beam Therapeutics presented clinical progress of its base‑editing platform at the Wells Fargo Healthcare Conference, notably with BEAM‑302 for alpha‑1 antitrypsin deficiency, which produced AAT levels above the protective threshold in all patients and durability beyond 18 months. Safety events were mostly limited to reversible liver enzyme elevations; there were no signs of liver injury or hospitalization. The company is advancing programs for sickle cell disease (Risto‑Cel, BLA plan by year‑end), PKU (BEAM‑304 IND cleared) and GSD1A, and expects multiple milestones in the next 12–18 months. A $500 million financing facility from Sixth Street is intended to support commercialization of the sickle cell therapy, while competition in the alpha‑1 field is increasing; Beam continues to see a multi‑year lead in base editing. » Más en de.investing.com
Dividendos históricos Dividendos
Todas las métricas de dividendos Todas las métricasDatos financieros de la empresa
| (EUR) | septiembre de 2026 | YoY |
|---|---|---|
| Ingresos | 271,04 mil | 96,72 % |
| Beneficio bruto | -124,77 M | 1609,76 % |
| Beneficio neto | -118,66 M | 23,53 % |
| EBITDA | -113,85 M | 24,67 % |
Datos fundamentales
| Métrica | Valor |
|---|---|
Capitalización bursátil | 2425,77 M € |
Número de acciones | 103,29 M |
Máximo/mínimo de 52 semanas | 34,13 € - 18,04 € |
| Dividendos | No |
Beta | 2,22 |
Ratio P/E | -26,33 |
Ratio PEG | -0,78 |
Ratio P/B | 2,89 |
Ratio P/S | 18,55 |
Perfil de la empresa
Beam Therapeutics Inc., una empresa de biotecnología, desarrolla medicamentos genéticos de precisión para pacientes que padecen enfermedades graves en Estados Unidos. La compañía desarrolla BEAM-101 para el tratamiento de la anemia falciforme y la beta talasemia; BEAM-102 para el tratamiento de la anemia falciforme; y BEAM-201, un receptor de antígeno quimérico de células T alogénico para el tratamiento de la leucemia linfoblástica aguda de células T recidivante/refractaria; y BEAM-301, un candidato de desarrollo dirigido al hígado para el tratamiento de pacientes con enfermedad por almacenamiento de glucógeno tipo Ia. También desarrolla terapias para la deficiencia de alfa-1 antitripsina; enfermedades oculares; y otros trastornos del hígado, los músculos y el sistema nervioso central. La compañía tiene una alianza con Boston Children's Hospital; un acuerdo de colaboración para investigación y ensayos clínicos con Magenta Therapeutics, Inc.; un acuerdo de licencia con Sana Biotechnology, Inc.; y una colaboración de investigación con el Institute of Molecular and Clinical Ophthalmology Basel. También tiene un acuerdo de colaboración para investigación con Pfizer Inc. y Apellis Pharmaceuticals, Inc.; y un acuerdo de colaboración y licencia con Verve Therapeutics, Inc. La compañía se constituyó en 2017 y tiene su sede en Cambridge, Massachusetts.
| Nombre | BEAM THERAPEUTICS DL-,01 |
| CEO | John Evans |
| Sede | Cambridge,
ma Estados Unidos |
| Sitio web | |
| Sector | Consumo básico |
| Industria | Productos alimenticios |
| Salida a bolsa | 06/02/2020 |
| Empleados | 540 |
Símbolos bursátiles
| Bolsa | Símbolo |
|---|---|
NASDAQ | BEAM |