Dermatology Advisor
DermatologyAdvisor.com serves as a valuable resource for dermatologists and healthcare professionals, delivering a wealth of practical information and tools to help them make informed decisions for their patients. The goal of Dermatology Advisor is to equip dermatologists and healthcare providers who treat skin and related conditions with up-to-date, relevant educational content that enhances their clinical practice and elevates patient care. The platform also offers practice management tools and continuing education programs, creating a comprehensive digital experience that tackles many challenges faced by dermatology professionals today.
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Articles
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5 days ago |
dermatologyadvisor.com | Jaymin Kang
The Food and Drug Administration (FDA) has approved a new presentation of Steqeyma® (ustekinumab-stba), a biosimilar to Stelara® (ustekinumab), for the treatment of pediatric patients aged 6 to 17 years, weighing less than 60kg, with plaque psoriasis or psoriatic arthritis.
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1 week ago |
dermatologyadvisor.com | Jessica Nye
Immunogenicity is more prevalent among individuals who receive subcutaneous (SC) infliximab vs intravenous (IV) infliximab with an immunomodulator combined, according to study results published in Clinical Gastroenterology and Hepatology. Data about whether IV combinatorial or IV infliximab monotherapy is associated with decreased risk for immunogenicity have been conflicting. In addition, an SC infliximab formulation is now available.
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1 week ago |
dermatologyadvisor.com | Jessica Nye
Higher concentrations of serum 25-hydroxyvitamin D (25[OH]D) are associated with decreased risk for cardiovascular disease (CVD) and mortality among individuals with psoriasis. These findings, from a cohort study, were published in the Journal of the American Academy of Dermatology. Individuals with psoriasis are at increased risk for vitamin D deficiency, CVD, and mortality.
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1 week ago |
dermatologyadvisor.com | Diana Ernst
The Prescription Drug User Fee Act (PDUFA) date refers to the deadline set by the US Food and Drug Administration (FDA) for reviewing a New Drug Application (NDA) or Biologics License Application (BLA) and making a final decision on marketing approval. The typical period for review is 10 months after the drug application has been accepted by the Agency. For drugs that have Priority Review, the review period is reduced to 6 months from the time of application acceptance.
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2 weeks ago |
dermatologyadvisor.com | Ron Goldberg
Better disease control and lower recurrence rates of seborrheic dermatitis (SD) are seen with higher doses vs lower doses of daily isotretinoin, according to study findings published in the Journal of the American Academy of Dermatology. As most first-line therapies for SD only provide temporary relief to patients, systemic therapies such as oral isotretinoin have emerged as a promising treatment option.
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