AAAMS

JANUARY 21, 2025

Safe and Effective Procedures: Training ensures that your practitioners understand the proper techniques and safety protocols, minimizing risks and enhancing the quality of results. Enhanced Client Trust : Clients are more likely to choose a med spa where practitioners are certified, knowing their safety and satisfaction are prioritized.

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The Dermatology Digest

OCTOBER 16, 2024

_Ann Haas, MD, and Jerome Potozkin, MD, are being honored with the Patient Safety Hero Award for their efforts on behalf of the California Society of Dermatology and Dermatologic Surgery to protect physicians’ ability to mix and dilute drugs in-office. ASDSA is proud to name them as 2024 Patient Safety Hero Awardees.”

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Lipgloss and Aftershave

NOVEMBER 1, 2024

Active Ingredients in Pigmentation Therapy In-office treatments are complemented by topical agents that help maintain results and prevent new pigmentation. These are some topical agents to enhance in-office treatments, maintaining and prolonging results through consistent home care.

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The Dermatology Digest

APRIL 11, 2025

In the multicenter, open-label, 12-week, Phase 2 study evaluating the safety and efficacy of QTORIN rapamycin for microcystic LMs, 100% of participants were either “Very Much Improved (41.7%) or Much Improved (58.3%) as rated by the Clinician Global Impression of Change (CGI-C), a 7-point change scale conducted by live clinician assessment.

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The Dermatology Digest

MARCH 17, 2025

The overall safety profile of povorcitinib is consistent with previous data. No new safety signals were observed and both doses were well tolerated. Both studies include a 12-week double-blind, placebo-controlled treatment period, followed by a 42-week extension period and 30-day safety follow-up. 75mg: 40.6% 75mg: 42.3%

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The Dermatology Digest

JUNE 5, 2024

Check out TDD’s one-on-one interview with Iain Stuart, PhD , Chief Scientific Officer at Vyne Therapeutics. The randomized, double-blind, vehicle-controlled trial will evaluate the safety and efficacy of once-daily VYN201 topical gel in three dose cohorts (1%, 2% and 3% concentrations) compared to vehicle for 24 weeks.

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The Dermatology Digest

JANUARY 22, 2025

We are excited to partner with Revance to further clinical development of our unique program, using our Xyngari product for a needle-free, intradermal delivery of a botulinum toxin, like Daxxify, to the dermis, says Gerald Proehl, Chairman, President, and Chief Executive Officer of Dermata, in a news release.

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The Dermatology Digest

NOVEMBER 6, 2024

. “The new Translational Bridge Award addresses a critical gap in lupus research, enabling scientists to bring their most promising ideas closer to people living with lupus,” says Teodora Staeva, PhD, LRA Vice President and Chief Scientific Officer, in a news release.

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The Dermatology Digest

MARCH 5, 2025

This is a great milestone for our team, as we continue to examine the acne market, we believe there is still a high unmet need by patients for an acne product like XYNGARI, says Gerry Proehl, Dermatas Chairman, President, and Chief Executive Officer, in a news release.

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The Dermatology Digest

JANUARY 20, 2024

The study is designed to assess the safety, tolerability, and pharmacokinetics, of orally administered EVO756. The Phase 1 study is a randomized, double-blind, placebo-controlled single and multiple ascending dose (SAD and MAD) study in normal healthy adults and an open-label study in adults with CSU.

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The Dermatology Digest

JULY 16, 2024

Whether it’s your first visit to the city or an annual tradition, SHADES at Edge offers a fresh, imaginative way to take in the 360 views of our iconic skyline like never before,” says Francesca Merlino, Chief Commercial Officer at Hudson Yards Experiences, in a news release.

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The Dermatology Digest

MARCH 18, 2024

The Phase 3 clinical trials achieved all co-primary and secondary endpoints, and subjects completed the 16-week treatment with no significant safety issues.

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The Dermatology Digest

FEBRUARY 10, 2025

Proof-of-concept efficacy and safety data from a Phase 1b study of rezpegaldesleukin in AD patients were presented at the 2023 European Academy of Dermatology and Venereology Congress. Senior Vice President and Chief Research & Development Officer at Nektar, in a news release.

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The Dermatology Digest

MARCH 14, 2025

Novartis is the ideal partner to help us in this mission due to their unparalleled expertise in innovative medicines and their dedication to improving health outcomes,” adds Chief Medical Officer at the NFL, Dr. Allen Sills.

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The Dermatology Digest

JANUARY 29, 2024

The STudy of Roflumilast foam Applied Topically for the redUction of seborrheic derMatitis (STRATUM) was a parallel group, double-blind, vehicle-controlled study evaluating the safety and efficacy of Zoryve (roflumilast) foam, 0.3% Zoryve foam was well-tolerated with a favorable safety and tolerability profile.

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The Dermatology Digest

FEBRUARY 11, 2025

This is based on the continued emergence of bempikibart data in alopecia areata patients with longer-term follow-up from Part A of the SIGNAL-AA Phase 2a clinical trial, the robust pharmacologic data, and a well-tolerated safety profile,” says Jodie Morrison, Chief Executive Officer of Q32 Bio, in a news release.

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The Dermatology Digest

FEBRUARY 14, 2024

The prevalence of atopic dermatitis, an extremely burdensome skin condition, continues to grow, and there is an increasing need for new, long-term, treatment options, especially for children,” says Todd Zavodnick, Chief Executive Officer of Dermavant, in a news release.

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The Dermatology Digest

SEPTEMBER 20, 2024

Secondary efficacy objectives include progression-free survival, overall survival and local control up to twelve months after treatment, and the safety objective is the measurement of any related adverse events. Dr. Robert B.

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The Dermatology Digest

MAY 16, 2024

Sonelokimab in PsA For PsA, Phase 3 initiation is anticipated in Q4 2024 following the announcement in March 2024 of the full dataset from the global Phase 2 ARGO trial (M1095-PSA-201) evaluating the efficacy and safety of the Nanobody sonelokimab over 24 weeks in patients with active PsA.

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The Dermatology Digest

JANUARY 14, 2024

Zoryve foam was well-tolerated with a favorable safety and tolerability profile. As the first topical drug approved with a new mechanism of action for this condition in 20 years, foam represents an important advancement in treatment and addresses a truly significant need in this population.”

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The Dermatology Digest

FEBRUARY 26, 2024

“The favorable response from both the FDA and EMA aligns with the strengths we have consistently highlighted in our trial programs and outlines a clear regulatory path for sonelokimab in hidradenitis suppurativa” says Dr. Jorge Santos da Silva, Chief Executive Officer of MoonLake Immunotherapeutics, in a news release.“

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Natural Beauty Med Spa

JANUARY 4, 2025

Lets talk about why you can be confident in the safety of this treatment. CO2Lift treatment is a type of carboxytherapy, which has been around for years and has a sterling record of safety for patients of virtually all skin types. But did you know that CO2 can actually provide amazing results as part of a skincare treatment?

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North Dallas Dermatology Associates

NOVEMBER 1, 2023

One misconception is cosmetic procedures are the same everywhere, from a local spa to a board-certified physician’s office. Safety Concerns and Potential Adverse Effects Another crucial consideration in evaluating where to have your cosmetic procedure performed is the ability to manage potential adverse effects.

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Les Nouvelles Esthetics & Spa

JANUARY 31, 2024

An interview with Lauren Becotte Rampello Lauren Becotte Rampello is the Founder and Chief Creative Officer of Pure Glow, premium airbrush tanning that mimics the skin’s natural tan. We invest heavily in their training, focusing on the intricacies of our products and safety protocols. What is your plan for company growth?

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Natural Beauty Med Spa

APRIL 28, 2024

However, you might be reluctant to commit to it due to concerns about safety. Safety is of the utmost importance to us, and we take every reasonable precaution to protect our patients. If you would like to learn more about us and how we may be able to help you look and feel amazing, contact our Dearborn office at 312-981-1291.

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The Dermatology Digest

JULY 29, 2024

Key secondary endpoints will include PASI 90, PASI 100 and sPGA 0 measured at Weeks 16 and 24, and safety and tolerability. Patients completing Week 24 will have the opportunity to participate in a long-term extension (LTE) trial, ONWARD3, that will evaluate durability and maintenance of response and long-term safety.

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The Dermatology Digest

SEPTEMBER 12, 2024

“The positive pivotal data from this study reinforce the potential of Dupixent to offer a new treatment option for the many people suffering from chronic spontaneous urticaria who do not respond to standard-of-care antihistamines,” says Dietmar Berger, MD, PhD, Chief Medical Officer, Global Head of Development at Sanofi, in a news release.

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The Dermatology Digest

APRIL 18, 2024

The safety profile was similar across all three arms and overall, 88.9% of adverse events were rated as mild and no serious adverse events were identified. The study appears in the Aesthetic Surgery Journa l. “The The study appears in the Aesthetic Surgery Journa l.

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The Beauty Brains

MARCH 4, 2019

They also have advice from a body called the scientific committee for cosmetic safety or SCCS, which is composed largely of academics with an interest in medicine and general science. But the most significant way that cosmetic product safety is addressed is through the requirement for safety assessments. Smaller producers?

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The Dermatology Digest

JANUARY 5, 2024

“Verrica’s VP-315 program is designed to provide for the targeted delivery of an oncolytic peptide engineered to stimulate the patient’s immune system and destroy cancer cells,” says Ted White, Verrica’s President and Chief Executive Officer, in a news release.

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The Dermatology Digest

APRIL 9, 2025

This tip ensures a controlled treatment environment, increasing treatment efficacy and patient safety. Wang, MD, MBE, MBA, who is the Medical Director of Laser & Skin Surgery Center of Pennsylvania and Medical Research Director at the office of Roy Geronemus, MD.

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The Dermatology Digest

JUNE 10, 2024

With patients experiencing AK over larger surface areas, dermatologists are looking for ways to treat the entire affected area to help prevent further lesion progression,” saysKarl Ziegelbauer, Chief Scientific Officer at Almirall, in a news release.

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The Dermatology Digest

FEBRUARY 22, 2024

The primary endpoints of the study are the proportion of SK lesions with a Physician Lesion Assessment (PLA) score of clear (PLA=0) at last visit and the safety of SM-020 gel 1.0% CT-213 is a Phase 2b randomized, double-blind, vehicle-controlled clinical trial in 60 subjects with five to ten SK target lesions treated with SM-020 gel 1.0%

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The Dermatology Digest

FEBRUARY 22, 2024

The primary endpoints of the study are the proportion of SK lesions with a Physician Lesion Assessment (PLA) score of clear (PLA=0) at last visit and the safety of SM-020 gel 1.0% CT-213 is a Phase 2b randomized, double-blind, vehicle-controlled clinical trial in 60 subjects with five to ten SK target lesions treated with SM-020 gel 1.0%

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The Dermatology Digest

DECEMBER 14, 2023

Patients returned at week 16 to assess safety and evaluate maintenance response. Additionally, it can increase the time of use for biologics instead of switching between agents; therefore, decreasing overall healthcare costs and burden on patients and physician offices.” At week 12, patients stopped using the cream.

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The Dermatology Digest

APRIL 17, 2024

The randomized, double-blind, placebo-controlled, parallel group Phase 2 study is evaluating the efficacy and safety profile of multiple dose regimens of barzolvolimab in patients with CIndU who remain symptomatic despite antihistamine therapy, to determine the optimal dosing strategy.

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The Dermatology Digest

APRIL 23, 2024

The CRL did not identify any deficiencies related to the clinical efficacy or clinical safety data in the BLA, and the FDA did not request any new clinical trials or clinical data to support the approval of pz-cel. The BLA for pz-cel was accepted for filing and granted priority review designation by the FDA in November 2023.

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