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Ionis Pharmaceuticals, Inc. logo

Ionis Pharmaceuticals, Inc.

IONS
NASDAQ: IONS Delayed
74.83USD 4.3%
As of 5 June 2026, Ionis Pharmaceuticals, Inc. has a market cap of $12.36B USD, ranking #1847 globally and #609 in the United States. It ranks #137 in the Healthcare sector, and #55 in the Drug Manufacturers - General industry.
Global Rank
1847
Country Rank
609
Sector Rank
137
Industry Rank
55
Key Stats
Market Cap
$12.36BUSD
Enterprise Value
$12.92BUSD
Revenue (TTM)
$1.06BUSD
EBITDA (TTM)
-$340.94MUSD
Net Income (TTM)
-$327.39MUSD
EBITDA Margin
-32%
Profit Margin
-31%
PS Ratio
11.6
PB Ratio
24.1
Company Profile
Country (HQ)
Sector
Healthcare
Industry
Drug Manufacturers - General
CEO
Brett Monia open_in_new
Employees
1,402
Founded
1989
IPO
17 May 1991
Website
ionis.com open_in_new
warningChart data may be delayed
1d 1w 1m 3m 6m 1y
4.3% -1.9% 3.7% -8.7% 1.7% 152%

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Markets

Exchange Ticker Price
NASDAQ
MIC: XNAS
PRIMARY
IONS
Ionis Pharmaceuticals Inc
ISIN: US4622221004
Shares Out.:
165.263M1 Shares Float: 162.055M2
TV:
SA:
YF:
GF:
NQ:
BA:
MS:
74.83 USD
London Stock Exchange
MIC: XLON
0JDI
Ionis Pharmaceuticals Inc
ISIN: US4622221004
TV:
SA:
YF:
GF:
BA:
MS:
72.55 USD
Borsa Italiana
MIC: XMIL
1IONS
Ionis Pharmaceuticals Inc
ISIN: US4622221004
TV:
SA:
YF:
GF:
BA:
MS:
64.84 EUR
Show all 5 markets
1Market cap is calculated using shares outstanding.
2Float shares are publicly tradable shares, excluding insider-held stock.

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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