Obesity evidence dossier

ARO-INHBE

The strategic read is add-on biology: if incretins reduce appetite and body weight, INHBE silencing may add a fat-distribution and liver-fat lever without leaning on gastrointestinal dose escalation alone.

Arrowhead PharmaceuticalsBody-composition watchlistSubcutaneous RNAi therapeutic under study
Weight loss score /100—
Comparison statusInputs not yet verified
EvidenceNot yet verified
Follow-up—

Total weight loss

Not reported

Phase 1/2a interim data

Placebo-adjusted

Not reported

Difference from placebo in the same study when reported.

Study context

INHBE / Activin E RNAi program/Adults with obesity with and without type 2 diabetes/Phase 1/2a; early dose-escalation cohorts/Week 12 to Week 24 interim body-composition and liver-fat follow-up.

Baseline: Obesity; some analyses enrich for baseline liver fat content and cardiometabolic risk

Ranked result & calculation

Trial inputs have not yet been verified for this scoring method.

Evidence

Benchmark read

Arrowhead reported ARO-INHBE reductions in visceral fat, total fat, and liver fat, including combination data with tirzepatide in patients with obesity and type 2 diabetes; a placebo-adjusted monotherapy visceral-fat result ~15.6% at Week 24 after two doses was reported in interim Phase 1/2a data.

Diabetes data

Combination data in people with type 2 diabetes should be compared within that harder-to-treat obesity phenotype, not directly against non-diabetic obesity trials.

Primary lens

Visceral fat + liver fat

Most relevant as a cardiometabolic add-on or MASH-adjacent obesity program, not as a pure appetite-suppression competitor.

Safety

Side effects and cautions

Discontinuation read

Early tolerability is encouraging but too immature for comparison with large incretin safety databases.

Common side effects

Arrowhead described early ARO-INHBE data as generally well tolerated, with mostly mild adverse events and no treatment-emergent adverse events leading to discontinuation in the January 2026 interim update.

Main cautions

Not approved; Phase 1/2a cohorts remain small. Liver-fat and visceral-fat signals need larger controlled trials and a clear regulatory endpoint strategy.

Upcoming catalyst

What to watch next

Phase 2 obesity and MASH designs, longer follow-up, and whether body-composition effects persist with infrequent dosing.

Linked clinical trials

Trials in the saddl3 obesity snapshot

Non-diabetic obesity studies are prioritized; diabetes and healthy-volunteer studies remain visible and labeled.

Back to obesity comparisonArrowhead, ARO-INHBE EASL 2026 updateBack to body composition