Ionis Pharmaceuticals IONS

$43.54 -0.46 (-1.05%)

Valuation

Market cap
7,312,096,000
Revenue TTM
$943,710,000
Net income TTM
$-381,390,000
PE ratio
0.00
Forward PE
—
Profit margin
-40.41%
Debt to equity
0.00

Trading

Volume
2,312,000
Avg volume
3,289,102
Day's range
$43.24 – $44.17
Shares out
166,184,000
Stochastic %K
14%
Beta
0.38
Analysts
Strong Sell
Price target
$80.70

Price

Company profile

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-medi...

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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.

Industry
Biotechnology
Sector
Healthcare
Phone
760 931 9200
Website
https://www.ionis.com
Address
2855 Gazelle Court, Carlsbad, United States

Latest news

Stocktwits

Fingerlickengood Oct 2, 8:37 PM
$CDXS $IONS $ALNY Appears to have an interest as well. https://pmc.ncbi.nlm.nih.gov/articles/PMC8860597/
0 replies
Fingerlickengood Oct 2, 8:01 PM
$CDXS I see $IONS as the most likely 'unnamed' partner! https://pmc.ncbi.nlm.nih.gov/articles/PMC7038945/
0 replies
Fingerlickengood Oct 2, 7:50 PM
$CDXS As far as Im aware, $IONS is the only pharma company that optimizes its siRNA drug conjugates to maximize specific stereochemistry in order to increase potency. Ironically, Arthur Levin on Codexis' Strategic Advisory Board held senior drug development positions at Ionis. https://ionis.com/science-and-innovation/pipeline
1 replies
BiotechButterflies Oct 2, 6:48 PM
$IONS ... wow... retracing to a range that I was buying at back in 2025.... trimmed in the 70's so can rebuy soon and hold.... can these get cheaper?
0 replies
IR_propancbiopharma Oct 1, 7:36 PM
PRP’s path to the clinic is no longer just a development plan. The infrastructure behind it is taking shape. $PPCB has established key relationships supporting Phase 1b, including Avance Clinical for clinical delivery, a specialized CDMO for GMP manufacturing, and FyoniBio for PRP’s PK assay. Clinical development requires multiple pieces to come together. For PRP, those pieces are now being put in place. The foundation for the next stage is being built now. $IONS $BEAM
1 replies
Chinger18 Sep 30, 8:47 PM
$IONS wish we didn’t suck
0 replies
IR_propancbiopharma Sep 29, 3:18 PM
Preclinical evidence shows what a therapy may be capable of. Clinical evaluation begins to show how it performs in patients. Across biotech, that transition is critical—from RNA-targeted medicines at $IONS to gene-editing approaches at $CRSP. For $PPCB, February 2027 is targeted to mark that next step, with PRP’s Phase 1b First-In-Human study evaluating safety, tolerability, PK, PD and preliminary antitumor activity in up to 50 patients. Moving into the clinic begins a new stage for PRP, where clinical data can further define the program and shape the path ahead. Each milestone brings PRP one step closer to clinical evaluation.
0 replies
Tjcmd Sep 29, 4:17 AM
$IONS fyi…
0 replies