May 2nd 2024
This recap of skin cancer innovations accompanies the cover story of our May publication.
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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Hidradenitis Suppurativa (HS): Deepening Foundations of Knowledge in Disease Pathogenesis, Disease Severity Assessment, and Treatment Decision-Making
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FDA Approves Relatlimab Plus Nivolumab for Unresectable or Metastatic Melanoma
March 18th 2022The FDA has approved the fixed-dose combination of relatlimab plus nivolumab for the treatment of adult and pediatric patients who are 12 years of age or older and who have unresectable or metastatic melanoma.
Pembrolizumab Demonstrates Improvement in IIB, IIC Melanoma
March 7th 2022Merck announced that pembrolizumab led to significant improvement in distant metastasis-free survival (DMFS) compared to placebo as adjuvant therapy for patients with resected stage IIB and IIC melanoma in the phase 3 KEYNOTE-716 trial.
FDA Accepts IND for RM-1995 Photoimmunotherapy in Advanced Cutaneous or Head and Neck SCC
January 6th 2022The FDA has accepted an investigational new drug application for the photoimmunotherapy treatment, RM-1995, for patients with advanced cutaneous squamous cell carcinoma or head and neck squamous cell carcinoma.
Relatlimab/Nivolumab Application for Frontline Advanced Melanoma Validated by EMA
October 14th 2021The European Medicines Agency has validated its marketing authorization application for the fixed-dose combination of relatlimab and nivolumab in the frontline treatment of adult and pediatric patients with advanced melanoma.