Chat IA
Loading data for IONS — first visit, this takes a few seconds.

Ionis Pharmaceuticals, Inc.

IONS · NasdaqGS · USD

46.53 -0.22 (-0.47%)

Al cierre: Sep 17, 2026, 3:59 PM

Volumen
83.2K

Ionis Pharmaceuticals, Inc. (IONS): cotización, análisis y datos

Valor intrínseco

Cargando valor intrínseco…

Pronóstico del analista

Previsiones bursátiles →

Previsión de analistas no disponible

Objetivo a 12 meses · n/a analistas

Consenso de analistas: n/a

Intervalo:1D
Cargando velas y señales…

Desempeño financiero

Ver finanzas →

Cargando...

Últimos resultados

ReportadoVs. estimaciónCambio interanual
Ingresos$267.9Mn/a-40.73%
EPS-$0.42+$0.46-149.41%

Próximos resultados

antes de que se abra el mercado.

Estimar · Actualizar →

Ver detalles de resultados →

Métricas

Precio de compra
42.98
Beneficio neto (TTM)
-565M
0.42
-3.48
n/a
-40.37
P/B (TTM)
16.91
P/S (TTM)
8.54
Fecha de resultados
Nov 4, 2026
Precio de venta
49.87
Volumen
83,187
Volumen medio (20D)
3,466,856
Abierto
46.66
Anterior Cerrar
46.75
Rango del día
46.20 - 46.75
Rango de 52 semanas
44.66 - 86.74
Fecha ex dividendo
n/a

Acerca de Ionis Pharmaceuticals, Inc.

Ver perfil →
Ionis Pharmaceuticals, Inc., a commercial-stage biotechnology company, provides RNA-targeted medicines in the United States. The company offers TRYNGOLZA reduces triglyceride levels in adults with familial chylomicronemia syndrome (FCS) and acute pancreatitis; DAWNZERA for prophylaxis to prevent attacks of hereditary angioedema in adults; WAINUA for the treatment of the polyneuropathy of hereditary transthyretin-medicated amyloidosis (ATTRv-PN) in adults; and SPINRAZA for pediatric and adult patients with spinal muscular atrophy (SMA). It also provides QALSODY for the treatment of Amyotrophic Lateral Sclerosis (ALS); TEGSEDI for the treatment of ATTRv-PN in adults; and WAYLIVRA for treatment for FCS and familial partial lipodystrophy. It also develops products under Phase 3 clinical trials, such as Olezarsen for patients with hypertriglyceridemia (SHTG) and cardiovascular disease (CVD); and Zilganerse, a potential treatment for people with genetically confirmed Alexander disease, as well as ION582 which is in Phase 3 clinical trial for the potential treatment of AS, a rare genetic neurological disease. In addition, the company develops Eplontersen to degrade mutant and wild-type TTR mRNA through binding to the TTR mRNA; Pelacarsen to inhibit the production of apolipoprotein(a) in the liver to offer a direct approach for reducing lipoprotein(a); Bepirovirsen to inhibit the production of viral proteins associated with hepatitis B virus; Sefaxersen to reduce the production of complement factor B and lower activation of the alternative complement pathway; and Ulefnersen to reduce the production of the fused in sarcoma, as well as other mid-stage pipeline investigational medicines. It has a strategic collaboration with Biogen for the treatment of neurological disorders; and collaboration and license agreement with GSK, AstraZeneca, Novartis, and Roche, as well as with Metagenomi. The company was incorporated in 1989 and is headquartered in Carlsbad, California. Biotechnology · Healthcare

Ionis Pharmaceuticals, Inc., a commercial-stage biotechnology company, provides RNA-targeted medicines in the United States. The company offers TRYNGOLZA reduces triglyceride levels in adults with familial chylomicronemia syndrome (FCS) and acute pancreatitis; DAWNZERA for prophylaxis to prevent attacks of hereditary angioedema in adults; WAINUA for the treatment of the polyneuropathy of hereditary transthyretin-medicated amyloidosis (ATTRv-PN) in adults; and SPINRAZA for pediatric and adult patients with spinal muscular atrophy (SMA). It also provides QALSODY for the treatment of Amyotrophic Lateral Sclerosis (ALS); TEGSEDI for the treatment of ATTRv-PN in adults; and WAYLIVRA for treatment for FCS and familial partial lipodystrophy. It also develops products under Phase 3 clinical trials, such as Olezarsen for patients with hypertriglyceridemia (SHTG) and cardiovascular disease (CVD); and Zilganerse, a potential treatment for people with genetically confirmed Alexander disease, as well as ION582 which is in Phase 3 clinical trial for the potential treatment of AS, a rare genetic neurological disease. In addition, the company develops Eplontersen to degrade mutant and wild-type TTR mRNA through binding to the TTR mRNA; Pelacarsen to inhibit the production of apolipoprotein(a) in the liver to offer a direct approach for reducing lipoprotein(a); Bepirovirsen to inhibit the production of viral proteins associated with hepatitis B virus; Sefaxersen to reduce the production of complement factor B and lower activation of the alternative complement pathway; and Ulefnersen to reduce the production of the fused in sarcoma, as well as other mid-stage pipeline investigational medicines. It has a strategic collaboration with Biogen for the treatment of neurological disorders; and collaboration and license agreement with GSK, AstraZeneca, Novartis, and Roche, as well as with Metagenomi. The company was incorporated in 1989 and is headquartered in Carlsbad, California.

Industria Biotechnology
Sector Healthcare
IPO Fecha May 17, 1991
Empleados 1,480
Bolsa de Valores NasdaqGS
Símbolo bursátil IONS