Ionis Pharmaceuticals, Inc. (IONS) Stock

Healthcare · Biotechnology · Member of Other US Stocks

Ionis Pharmaceuticals, Inc. (IONS) closed at USD 42.70 on 2026-10-14, a change of -42 % over the past year, with a market capitalization of USD 7.33B.

Ionis Pharmaceuticals, Inc. recent closing prices

DateClose (USD)
2026-10-1442.70
2026-10-1342.38
2026-10-1243.67
2026-10-0945.28
2026-10-0843.30
2026-10-0744.16
2026-10-0644.00

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Ionis Pharmaceuticals, Inc. key figures

Previous close
USD 42.70 (2026-10-14)
1-year change
-42 %
Market cap
USD 7.33B
Enterprise value
USD 7.42B
P/E ratio (trailing)
-12.68
P/E ratio (forward)
-39.67
EPS (trailing)
-3.48
EPS (forward)
-1.11
PEG ratio
27.33
Price to book
16.62
Revenue growth
-40.7 %
Earnings growth
n/a
Dividend per share (trailing)
0.00
Short ratio
5.07
Employees
1,480
Analyst consensus (third-party)
buy

Source: Yahoo Finance via yfinance. Data may be delayed, incomplete or incorrect.

About Ionis Pharmaceuticals, Inc.

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.

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