Argenx Halts Phase 3 Study in Rare Disease Following Futility Analysis

Argenx Halts Phase 3 Study in Rare Disease Following Futility Analysis

0Argenx SE(NASDAQ:ARGX) on Thursday delivered mixed clinical updates, announcing positive Phase 2 trial results for one experimental pipeline candidate alongside the failure of a Phase 3 study for another therapy.

In its first clinical readout since acquiring Forte Biosciences in August 2026, the immunology company reported positive Phase 2 topline data for FB102 in adults with celiac disease.

Celiac disease is a chronic autoimmune condition where eating gluten triggers an immune response that damages the lining of the small intestine, specifically destroying the tiny projections called villi that absorb nutrients.

The first-in-class CD122 inhibitor met its primary endpoint, showing a statistically significant change in the villus height-to-crypt depth ratio at day 78 compared to placebo in patients undergoing a gluten challenge.

The treatment also demonstrated consistent efficacy across secondary inflammatory, histologic, and clinical symptom measures.

Argenx observed no new safety signals and plans to present detailed findings at an upcoming medical meeting.

The drug also undergoes evaluation for vitiligo and alopecia areata.

Separately, Argenx announced it will discontinue its Phase 3 UNITY trial testing subcutaneous efgartigimod in moderate-to-severe Sjögren’s disease.

Sjögren’s disease is a chronic autoimmune disorder where the immune system mistakenly attacks the glands that make moisture, like tear and saliva glands.

An Independent Data Monitoring Committee recommended stopping the study for futility after an interim analysis indicated the trial could not meet its primary endpoint.

Although the treatment showed safety consistent with its established profile, the company will analyze the data following study closure to guide prospective research.

In May, the U.S. Food and Drug Administration (FDA) approved a label expansion for VYVGART (efgartigimod alfa-fcab) and VYVGART Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) for adult patients with generalized myasthenia gravis.

ARGX Price Action: Argenx shares were down 15.34% at $786.00 during premarket trading on Thursday, according to Benzinga Pro data.

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This article Argenx Halts Phase 3 Study in Rare Disease Following Futility Analysis originally appeared on Benzinga.com

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