Peptide News Digest

#Arrowhead

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Clinical Trials · View digest

Arrowhead Plozasiran Phase 3 SHASTA-3 and SHASTA-4 12-Month Data at ESC 2026 Munich Show 79-81% Triglyceride Reduction and Pooled Reduction in Acute Pancreatitis Events

Arrowhead Pharmaceuticals (NASDAQ: ARWR) presented Sunday August 30, 2026 the full Phase 3 SHASTA-3 and SHASTA-4 12-month data of plozasiran (an RNAi therapeutic targeting APOC3, administered as quarterly subcutaneous injection) in adults with severe hypertriglyceridemia at the European Society of Cardiology Congress 2026 in Munich, Germany, in a Hot Line Late-Breaking Science session. SHASTA-3 and SHASTA-4 met their primary and all prespecified secondary endpoints with median triglyceride reductions from baseline of 79% and 81%, respectively, at Month 12 (p<0.0001 in both studies). More than 90% of plozasiran-treated patients achieved triglycerides below 500 mg/dL at Month 12, and more than half achieved TG below 150 mg/dL. In a prespecified pooled analysis, plozasiran significantly reduced acute pancreatitis events across the broad sHTG study population, with greater absolute benefit among higher-AP-risk patients. Three fatal events in the plozasiran arm (two cardiovascular deaths, one CMML death) were assessed as unrelated to study treatment. Arrowhead plans to file a supplemental NDA before end of 2026 for the broader sHTG population, building on the earlier familial chylomicronemia syndrome approval.

Clinical Trials · View digest

Arrowhead ARO-INHBE Plus Tirzepatide EASL 2026 Data Show Enhanced Visceral Fat and Liver Fat Reduction Versus Tirzepatide Alone

Arrowhead Pharmaceuticals (NASDAQ: ARWR) presented updated Phase 1/2a data on ARO-INHBE (an RNA interference therapeutic targeting Activin E) and ARO-ALK7 (RNAi targeting ALK7 receptor) at EASL 2026. Standalone data: ARO-INHBE monotherapy achieved mean visceral fat reduction of -9.9% at week 16 after a single dose and -15.6% placebo-adjusted after two doses at week 24, with a single dose increasing lean muscle tissue by 3.6%; ARO-ALK7 monotherapy achieved -14.1% placebo-adjusted visceral fat reduction at week 8 after a single dose. Combination data: ARO-INHBE plus low-dose tirzepatide (5 mg) enhanced reductions in visceral adipose tissue and liver fat content versus tirzepatide alone in participants with obesity with or without type 2 diabetes. Mean maximum Activin E reduction reached 85.3% at the 400 mg dose with persistent effect beyond 3 months. Additional 2026 readouts expected. The data extend the case for RNAi as a non-peptide, quarterly-dosed obesity add-on capable of shifting body composition rather than just body weight.