Author Interviews, Dermatology / 09.07.2020

MedicalResearch.com Interview with:   Julie C. Harper, MD Clinical Associate Professor of Dermatology University of Alabama-Birmingham MedicalResearch.com: What is the background for this study? How common is rosacea? What are the clinical manifestations of facial rosacea or psoriasis? 
    • In 2018, the initial Beyond the Visible report provided new insights into rosacea and the psychosocial burden associated with invisible symptoms. These insights further highlighted how little is really known of the burden faced by those suffering from facial skin diseases. In this new 2020 report, Beyond the Visible: rosacea and psoriasis of the face, we explored new dimensions of the burden faced by both rosacea and psoriasis of the face patients to learn from patients’ experiences and behaviors to better inform treatment based on the comparisons and contrasts. The survey spanned six countries, 300 rosacea patients and 318 psoriasis of the face patients to answer three questions:
      • What is the burden faced by patients with psoriasis of the face and of rosacea?
      • How does the burden faced by rosacea patients differ from patients with psoriasis of the face?
      • What can we learn to help both patients and doctors to achieve the best possible outcomes for their patients?
    • Rosacea is more common than people might initially assume. There are an estimated 16 million Americans with rosacea, building up to 415 million rosacea sufferers worldwide.
    • Rosacea is commonly characterized by persistent redness and facial flushing, inflammatory lesions which may resemble acne-like bumps, visible blood vessels, and skin thickening. However, it’s important to note that rosacea symptoms vary person to person. Psoriasis of the face symptoms present themselves as red, scaly lesions that are usually along the forehead, hairline and ears. Moreover, psoriasis is known to be associated with itching, while rosacea sufferers have reported burning and stinging.
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Author Interviews, Dermatology / 21.05.2020

MedicalResearch.com Interview with: Dr. Melanie D. Palm, MD, MBA Board-certified dermatologist and cosmetic surgeon San Diego, CA Clinical investigator in the Restylane Kysse phase 3 Galaderma trial Dr. Palm discusses the recent announcement that the FDA has approved Restylane® Kysse for lip augmentation and the correction of upper perioral rhytids (wrinkles)  in adults over the age of 21.   MedicalResearch.com: What is the background for this announcement?
    • Restylane® Kysse has been approved and used in Europe and Canada for several years. It is now the first FDA-approved hyaluronic acid (HA) lip filler in the U.S. formulated with XpresHAn Technology™ (pronounced ex-'spre-shan’) for smooth, natural-looking results.
    • It is FDA-approved for use not only in the lip but for improvement of upper lip lines.
    • Restylane Kysse is the third product (following Restylane Defyne and Restylane Refyne) in the Restylane family of fillers to use XpresHAn Technology™ which allows for a gel that integrates into the skin for natural expression in motion
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Author Interviews, Dermatology, Pharmaceutical Companies / 05.03.2019

MedicalResearch.com Interview with: Dr. James Q. Del Rosso, D.O., FAOCD, Dermatologist Research Director and Principal Investigator Del Rosso Dermatology Research Center, Las Vegas, NV Galderma Consultant MedicalResearch.com: What is the background for this study? What are the main findings?
  • The ANSWER study, a 12-week, randomized, multicenter, Phase 4, Phase 3b in Canada and Europe clinical trial, is the first study of its kind to compare the efficacy and safety of combination therapy with Oracea® (doxycycline, USP) 40 mg Capsules + Soolantra® (ivermectin) Cream, 1% versus Soolantra® (ivermectin) Cream, 1% monotherapy in 273 adults with severe papulopustular rosacea (IGA 4) at clinical trial sites in the United States, Canada and Europe (Czech Republic, Poland, Hungary and Germany).
  • Results showed the combination therapy with Oracea Capsules + Soolantra Cream was well tolerated and effective with a faster onset of action than Soolantra Cream given as monotherapy. Key highlights of the study include:
  • The mean reduction in percentage of inflammatory lesions from baseline to Week 12 was significant with combination therapy compared to monotherapy (80.29% vs. 73.56%, respectively; p=0.032).
  • 5 times as many patients taking combination therapy achieved 100% clearance of inflammatory lesions by Week 12 compared with monotherapy (17.8% vs. 7.2%, respectively; p=0.006).
  • Over 2 times as many patients taking combination therapy achieved 100% clear (IGA 0) by Week 12 compared with monotherapy (11.9% vs. 5.1%, respectively; p=0.043).
  • Combination therapy was generally well tolerated and no discontinuation of treatments due to side effects.
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