LAD328 Phase 2 Proof-of-Concept Trial for Moderate-to-Severe Hidradenitis Suppurativa
Summary
The NIH ClinicalTrials.gov registry has published a new Phase 2 proof-of-concept study (NCT07547813) for LAD328 in adults with moderate-to-severe Hidradenitis Suppurativa. The study will evaluate LAD328 compared to placebo and assess safety, tolerability, pharmacokinetic, and immunogenicity parameters. The trial was registered with a start date of April 23, 2026, and lists LAD328 and placebo as the two interventions under investigation. Sponsors, clinical investigators, and patients interested in HS research can locate the study via its NCT identifier for further details.
“The main purpose of this study is to evaluate the effect of LAD328 compared to placebo in participants with moderate-to-severe Hidradenitis Suppurativa (HS), and to access the safety, tolerability, pharmacokinetic and immunogenicity in participants with moderate-to-severe HS.”
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What changed
The NIH ClinicalTrials.gov registry has added a new Phase 2 clinical trial registration for LAD328 (NCT07547813), a proof-of-concept study evaluating the investigational drug in adults with moderate-to-severe Hidradenitis Suppurativa. The study design includes LAD328 and placebo as interventions, with primary endpoints assessing comparative efficacy, safety, tolerability, pharmacokinetics, and immunogenicity. No enrollment count or specific completion date is listed in the registration record.
For pharmaceutical sponsors, clinical research organizations, and investigators active in inflammatory skin disease drug development, this registration signals the advancement of LAD328 into Phase 2 evaluation. Monitoring ClinicalTrials.gov for protocol details, enrollment status updates, and results postings will be relevant for competitive intelligence and patient-referral purposes.
Archived snapshot
Apr 24, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
A Proof-of-Concept Study of LAD328 in Adults With Hidradenitis Suppurativa
Phase 2 NCT07547813 Kind: PHASE2 Apr 23, 2026
Abstract
The main purpose of this study is to evaluate the effect of LAD328 compared to placebo in participants with moderate-to-severe Hidradenitis Suppurativa (HS), and to access the safety, tolerability, pharmacokinetic and immunogenicity in participants with moderate-to-severe HS.
Conditions: Hidradenitis Suppurativa
Interventions: LAD328, Placebo
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