$ARWR

ARROWHEAD PHARMACEUTICALS, INC.

alphai earnings readFiscal 2026 third quarter · AUG 4Arrowhead Pharmaceuticals Reports Fiscal 2026 Third Quarter ResultsVerdict: mixed

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Arrowhead (ARWR) Reported a 78% Lower Pancreatitis Event Rate With Plozasiran. Does the Absolute Benefit Support a Broader Label?

Arrowhead Pharmaceuticals (ARWR) reported Phase 3 trial results for plozasiran, showing 79-81% triglyceride reductions vs. 27% for placebo. Pooled analysis indicated a 78% reduction in pancreatitis events, but absolute risk reduction was 4.1%. ARWR plans to submit a broader-label application by 2026. Plozasiran is FDA-approved for familial chylomicronemia syndrome. The company aims to expand its use to severe hypertriglyceridemia. Triglyceride reductions were consistent, with 91-93% of treated p

ARWR Reiterated by HC Wainwright & Co. -- Price Target Maintaine

HC Wainwright & Co. maintained a 'Buy' rating for Arrowhead Pharmaceuticals (ARWR) with a $120.00 price target. The stock is currently trading at $82.39, which is 52.3% above its GF Value™ of $54.09. The company has a GF Score™ of 49/100, indicating moderate performance. Insiders have sold $1,186,600 worth of shares in the last three months. Arrowhead focuses on RNAi therapies for genetic diseases.

Plozasiran durably cuts triglycerides, pancreatitis risk in severe hypertriglyceridemia

Plozasiran, an FDA-approved drug by Arrowhead, reduced triglycerides by up to 81% in severe hypertriglyceridemia patients and prevented pancreatitis. Two trials, SHASTA-3 and SHASTA-4, showed sustained reductions and favorable safety profiles. Gerald F. Watts, a cardiometabolic medicine professor, highlighted the therapy's potential impact on clinical practice. The drug is not yet approved for severe hypertriglyceridemia.

ARWR sentiment & insider activity

Over the past 7 days, alphai's AI scored 2 news stories mentioning ARWR (ARROWHEAD PHARMACEUTICALS, INC.). Coverage has skewed bullish: 1 bullish, 1 neutral, and 0 bearish.

Recent ARWR coverage spans technology, financial news and insider activity.

In the last 30 days, ARWR insiders filed 2 SEC Form 4 transactions — no purchases and 2 sales ($1.2M). The most active reporter was OLUKOTUN ADEOYE Y with 1 filing.

What's driving ARWR

alphai scores every news story that mentions ARWR with an AI model for sentiment and relevance, and aggregates insider trades from ARROWHEAD PHARMACEUTICALS, INC.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $ARWR

Score
$ARWRHighAI 9/10

Arrowhead (ARWR) Reported a 78% Lower Pancreatitis Event Rate With Plozasiran. Does the Absolute Benefit Support a Broader Label?

Arrowhead Pharmaceuticals (ARWR) reported Phase 3 trial results for plozasiran, showing 79-81% triglyceride reductions vs. 27% for placebo. Pooled analysis indicated a 78% reduction in pancreatitis events, but absolute risk reduction was 4.1%. ARWR plans to submit a broader-label application by 2026. Plozasiran is FDA-approved for familial chylomicronemia syndrome. The company aims to expand its use to severe hypertriglyceridemia. Triglyceride reductions were consistent, with 91-93% of treated p

ARWR Reiterated by HC Wainwright & Co. -- Price Target Maintaine

HC Wainwright & Co. maintained a 'Buy' rating for Arrowhead Pharmaceuticals (ARWR) with a $120.00 price target. The stock is currently trading at $82.39, which is 52.3% above its GF Value™ of $54.09. The company has a GF Score™ of 49/100, indicating moderate performance. Insiders have sold $1,186,600 worth of shares in the last three months. Arrowhead focuses on RNAi therapies for genetic diseases.

$ARWRMedAI 8/10

Plozasiran durably cuts triglycerides, pancreatitis risk in severe hypertriglyceridemia

Plozasiran, an FDA-approved drug by Arrowhead, reduced triglycerides by up to 81% in severe hypertriglyceridemia patients and prevented pancreatitis. Two trials, SHASTA-3 and SHASTA-4, showed sustained reductions and favorable safety profiles. Gerald F. Watts, a cardiometabolic medicine professor, highlighted the therapy's potential impact on clinical practice. The drug is not yet approved for severe hypertriglyceridemia.

$ARWRHighAI 8/10

Arrowhead’s new Redemplo findings in severe hypertriglyceridemia have analysts split

Arrowhead Pharmaceuticals presented late-stage trial results for plozasiran (Redemplo) in severe hypertriglyceridemia, showing favorable safety and efficacy. Analysts are divided: Stifel highlights its safety and dosing advantages over Ionis' Tryngolza, while BMO favors Tryngolza due to glycemic control concerns. Arrowhead plans an FDA submission for expanded use later this year.

$ARWRHighAI 8/10

Arrowhead Pharmaceuticals, Inc.: Arrowhead Pharmaceuticals Presents Phase 3 SHASTA-3 and SHASTA-4 Data Demonstrating Plozasiran Reduced Acute Pancreatitis Events in Patients with Severe Hypertriglycer

Arrowhead Pharmaceuticals presented Phase 3 data showing plozasiran reduced triglycerides by 79-81% and acute pancreatitis events by 78% in severe hypertriglyceridemia patients. Over 90% of patients achieved TG levels below 500 mg/dL. The company plans to file an FDA application by year-end 2026, utilizing a Priority Review Voucher. Plozasiran demonstrated a favorable safety profile.

$ARWRLow

Arrowhead Pharmaceuticals (ARWR) Advances REDEMPLO Launch, Is The Stock Still Undervalued?

Arrowhead Pharmaceuticals (ARWR) gained attention after its plozasiran therapy was listed in the Lauer-Taxe database following European marketing authorization. The company's stock has seen significant gains, with a 30-day return of 24.79% and a year-to-date return of 31.89%. Analysts debate its valuation, with some arguing it is undervalued at $89.41, while others point to its high P/S multiple and ongoing losses.

$ARWRMedAI 8/10

People Living with Familial Chylomicronaemia Syndrome (FCS) in Germany Have Access to REDEMPLO® (plozasiran) as a New Treatment Option to Reduce Triglycerides

Arrowhead Pharmaceuticals (NASDAQ: ARWR) said the European Commission approved REDEMPLO (plozasiran) in June 2026, and it is now listed in Germany’s Lauer-Taxe database for prescribing and reimbursement. REDEMPLO is used with diet for adult FCS patients, with dosing as a subcutaneous injection every three months. Phase 3 PALISADE showed significant fasting triglyceride reductions at Month 10 versus placebo; common adverse reactions included hyperglycaemia and headache.

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