Galderma, a global leader focused on meeting the world’s increasing skin health needs, announced today that results from the pivotal Phase 3 PERFECT 1 and PERFECT 2 clinical trials of once-daily trifarotene 50 µg/g cream in patients with moderate acne on the face and trunk were published online in the Journal of the American Academy of Dermatology.
FORT WORTH, Texas, /PRNewswire/ -- Galderma, a global leader focused on meeting the world’s increasing skin health needs, announced today that results from the pivotal Phase 3 PERFECT 1 and PERFECT 2 clinical trials of once-daily trifarotene 50 µg/g cream in patients with moderate acne on the face and trunk were published online in the Journal of the American Academy of Dermatology.1,2 Trifarotene, an investigational drug, is an innovative new molecule and a unique retinoid receptor agonist that selectively targets retinoic acid receptor gamma (RAR-γ).1 The publication, titled “Randomized Phase 3 Evaluation of Trifarotene 50 µg/g Cream Treatment of Moderate Facial and Truncal Acne,” can be accessed here. The two identical multicenter, randomized, 12-week clinical trials of more than 2,400 patients met all primary and secondary efficacy endpoints, including Investigator Global Assessment (IGA/facial acne), changes in inflammatory and non-inflammatory lesion counts and Physician Global Assessment (PGA/truncal acne).1,2 The majority of adverse events were local cutaneous irritation mainly during the first weeks of treatment, which improved thereafter.3 Data from the two trials were included in a New Drug Application (NDA) submitted to the U.S. Food and Drug Administration (FDA) for trifarotene for the treatment of facial and truncal acne. “Acne frequently affects both the face and trunk and can cause permanent scarring.4,5 Many patients with facial and truncal acne feel self-conscious and are often reluctant to engage with other people,” said Howard Marsh, M.D., Vice President of Medical Affairs at Galderma, USA.6,7 “Despite the negative outcomes experienced, truncal acne has been insufficiently studied.”4 “PERFECT 1 and PERFECT 2 are the first and only large-scale randomized trials to evaluate a topical retinoid for the treatment of both facial and truncal acne,” said Thibaud Portal, Vice President of Prescription, Strategy and Innovation Group at Galderma.1,2 “This underscores Galderma’s commitment to innovation, the dermatology community and patients, and we are excited about the potential of trifarotene and its novel features. We hope to bring this next-generation topical retinoid to patients suffering from acne as soon as possible.” About the PERFECT 1 and PERFECT 2 Study The three co-primary efficacy endpoints were IGA success rate on the face (clear/almost clear and at least a 2 grade improvement from baseline) at week 12, and absolute change from baseline in facial inflammatory and non-inflammatory lesion counts from baseline to week 12.3 The three secondary efficacy endpoints were Physician Global Assessment (PGA) success rate on the trunk (clear/almost clear and at least a 2 grade improvement from baseline) at week 12, and absolute change in truncal inflammatory and non-inflammatory lesion counts from baseline to week 12.3 Safety was assessed through recording of adverse events, local tolerability, vital signs and routine laboratory testing.3 About Trifarotene About Acne About Galderma Contacts: Sara Schwartz ____________________________ ©2019 Galderma Laboratories, L.P. All trademarks are the property of their respective owners. View original content to download multimedia:http://www.prnewswire.com/news-releases/galderma-announces-publication-of-pivotal-phase-3-perfect-1-and-perfect-2-clinical-trials-of-trifarotene-in-patients-with-moderate-facial-and-truncal-acne-in-the-journal-of-the-american-academy-of-dermatology-300804081.html SOURCE Galderma |