March 15th 2024
A panel of experts discusses tailoring treatment to patient needs, supporting patients' mental health, and considering future directions.
Advances In: Integrating New Treatment Options into Management Plans for Patients with Moderate-to-Severe Atopic Dermatitis
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Medical Crossfire®: Maximizing Patient Outcomes in Shingles – Are You Leveraging Guideline Based Care?
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"REEL" Time Patient Counseling™: Integrating Biosimilars into the Clinical Conversation
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PER Skin Summit: Optimizing Diagnosis and Individualizing Management of Hidradenitis Suppurativa
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Community Practice Connections™: 19th Annual International Symposium on Melanoma and Other Cutaneous Malignancies®
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Expert Illustrations & Commentaries™: A Deeper Look at the Pathogenesis of Hidradenitis Suppurativa (HS)
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Cancer Summaries and Commentaries™: Clinical Updates in Melanoma from Philadelphia
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Expert Illustrations & Commentaries™: Picturing the Potential Role of OX40 and OX40L Inhibitors in Atopic Dermatitis
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FDA Accepts Accord BioPharma's BLA for Proposed Ustekinumab Biosimilar DMB-3115
January 4th 2024The BLA submission for DMB-3115 is rooted in phase III multi-regional clinical trials focusing on plaque psoriasis patients. The results demonstrated a high similarity between DMB-3115 and ustekinumab in terms of quality, safety, and efficacy.
CareFirst Files Lawsuit Against J&J Over Delay Tactics for Stelara Biosimilars
January 4th 2024While the first ustekinumab biosimilar, Wezlana, was approved in October 2023, a settlement with Johnson & Johnson (J&J) will keep it off the market until 2025, preventing competition, and causing purchasers to pay substantially more for the agent.