
Ahead of Print: Inside the May 2026 Issue
Key Takeaways
- Next-generation oral TYK2 inhibitors (envudeucitinib, zasocitinib) and icotrokinra signal stronger oral performance in psoriasis, while effectiveness in biologic-experienced patients will determine algorithm placement.
- Long-term IL-17–pathway data in HS with bimekizumab and sonelokimab emphasize durability and depth, reinforcing early inflammatory control to avoid irreversible damage and reframing remission feasibility.
An early look at the finalized print issue—featuring key data, clinical takeaways, and expert insights before it reaches your mailbox.
“That first patient that I see… I hope I can draw things from this conference and have better outcomes.” — David Oberlin, MD, FAAD
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Before you dive in, don’t forget to
Psoriasis: A Quiet Shift With Major Implications
Oral therapies are drawing new attention—not just for convenience, but for performance. Data on next-generation TYK2 inhibitors, including envudeucitinib (ESK-001; Alumis) and zasocitinib (TAK-279; Takeda), suggest efficacy levels that begin to challenge long-standing assumptions about the oral–biologic divide. Meanwhile, novel approaches like icotrokinra (Icotyde; Johnson & Johnson) hint at alternative delivery strategies that could further expand patient choice.
📊 Quick Poll
In 12 months, where do you see high-efficacy orals fitting in PsO?
What remains unanswered, and explored in full in this issue, is how these agents will perform in biologic-experienced patients and where they will ultimately land in treatment algorithms.
Hidradenitis Suppurativa: Raising the Bar
HS management may be approaching its own turning point. Long-term and late-breaking data on IL-17–targeted therapies such as bimekizumab (Bimzelx; UCB) and sonelokimab (Moonlake) suggest not just improved response rates, but evolving expectations around durability and depth of response.
🧠 Clinical Note
Early signals point toward a shift from incremental improvement to more ambitious targets—but how far that shift will go remains an open question.
“If you don’t get inflammation under control early, damage becomes irreversible,” noted Kristian Reich, MD, PhD.
Whether remission becomes a realistic, sustained goal is a central theme explored in the full feature.
Atopic Dermatitis: Looking Upstream
New data on amlitelimab (Sanofi) introduce a different therapeutic angle—targeting earlier stages of immune activation. Early results suggest a balance of efficacy and extended dosing intervals that may appeal in real-world settings.
💊 Practice Watch
- Extended dosing intervals under investigation
- Potential implications for adherence and clinic flow
- Safety profile still under long-term evaluation
How this mechanism compares with existing systemic options—and where it may fit—remains to be seen.
Beyond the Core Diseases
Additional highlights from AAD 2026 point to continued expansion across dermatology:
- upadacitinib (Rinvoq; AbbVie) in vitiligo
- brepocitinib (Priovant Therapeutics) in dermatomyositis
- Emerging RNA-based therapies such as PH-762 (Phio Pharmaceuticals) in cutaneous oncology
🧩 Quick Check
When assessing high-risk nonmelanoma skin cancer, what matters most?
The Throughline
Across disease states, the direction is consistent: more options, higher expectations, and increasing emphasis on how therapies integrate into real-world care. As editor-in-chief Christopher Bunick, MD, PhD, highlights throughout this issue, the next phase in dermatology may be defined less by breakthrough efficacy and more by how seamlessly those advances translate into practice.
This preview only scratches the surface. In the full issue, we examine what these developments mean for sequencing, patient selection, and long-term management strategies.











