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FDA imposes clinical hold on REGENXBIO gene therapies after tumor case
The FDA has imposed a clinical hold on REGENXBIO’s development programs RGX-111 and RGX-121 after an intraventricular CNS tumor was discovered in a five-year study participant four years after receiving RGX-111. Initial genetic analyses showed an AAV integration event and overexpression of the proto-oncogene PLAG1, but a causal link to the therapy has not yet been confirmed. The affected participant is asymptomatic and, according to the treating physician, is showing positive developmental progress; no tumors have been reported in other participants so far. REGENXBIO is awaiting the full FDA letter; the stock had fallen earlier, but analysts remain largely positive. » Más en de.investing.com
Datos financieros de la empresa
| (EUR) | 2024 | |
|---|---|---|
| Ingresos | 119,09 mil | 72,83 % |
| Beneficio bruto | -445,45 mil | 1,47 % |
| Beneficio neto | -3,42 M | 21,36 % |
| EBITDA | -1,32 M | 52,83 % |
Datos fundamentales
| Métrica | Valor |
|---|---|
Capitalización bursátil | 34,08 mil € |
Número de acciones | 395,98 M |
Máximo/mínimo de 52 semanas | 0,86 € - 0,0000861 € |
| Dividendos | No |
Beta | 0,17 |
Ratio P/E | -0,01 |
Ratio PEG | 0,00 |
Ratio P/B | 0,01 |
Ratio P/S | 0,31 |
Perfil de la empresa
| Nombre | Regenx Tech Aktie |
| CEO | Donald Edward Weatherbee |
| Empleados | 4 |
Descubrir activos
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