Ionis Pharmaceuticals, Inc. (IONS)

NasdaqGS · Biotechnology

43.52
-0.87 (-1.96%)
Updated Nov 1, 12:48 AM ET
AI Rating
Sell
Overall Score
40
Trend
3
Momentum
66
Risk
64

Scores are generated from technical indicators for educational purposes and are not a recommendation to buy or sell.

Price history

Daily closes and volume
Oct 17, 2025 260 sessions Oct 29, 2026

AI Analysis

Ionis Pharmaceuticals, Inc. is trading at $43.57, down 1.86% on the session. The 50 day average sits at $49.32 and the 200 day at $66.96, which puts the stock in a downtrend. RSI is at 46.2, which reads as neutral, and MACD is bullish crossover. Volume is below average.

The nearest support is around $43.01 with resistance near $45.72, so that band frames the current range. Average daily movement is roughly $1.69, or about 3.9% of the share price, which is what any stop placement has to allow for. The overall health score of 40 out of 100 combines a trend score of 3, momentum of 66 and a risk score of 64.

Technical indicators

RSI (14)
46.2
neutral
MACD
-1.089
bullish crossover
SMA 20
43.86
SMA 50
49.32
SMA 200
66.96
downtrend
ATR (14)
1.69
avg daily range
Support
43.01
Resistance
45.72
Volume vs 20d
0.67x
below average
Volatility
37.1%
annualised
1 month
-0.58%
3 months
-14.26%

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.

Company website

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