ARQT Arcutis Biotherapeutics

Courtney Barton Joins Arcutis as Chief Compliance Officer and Chief of Staff

Courtney Barton Joins Arcutis as Chief Compliance Officer and Chief of Staff

WESTLAKE VILLAGE, Calif., Feb. 18, 2021 (GLOBE NEWSWIRE) -- . (Nasdaq: ARQT), a late-stage biopharmaceutical company focused on developing and commercializing treatments for unmet needs in immune-mediated dermatological diseases and conditions, or immuno-dermatology, today announced that Courtney Barton has joined the company as Chief Compliance Officer and Chief of Staff. Ms. Barton will also serve as the company’s Chief Privacy Officer.

"Courtney’s extensive corporate and healthcare compliance background and proven track record of leadership make her the right leader to assume this important role within our company," said , Arcutis’ General Counsel. "Arcutis is committed to conducting our business with the highest level of integrity and in full compliance with the laws and regulations that govern our operations. Courtney is an accomplished compliance and data privacy leader with extensive global experience in pharmaceutical and medical device industries and a proven track record of success, and I am confident that she will be successful in leading our comprehensive companywide compliance program, in addition to her role as our Chief of Staff."

“I am incredibly excited to be joining Arcutis at this pivotal time in the company’s evolution and applaud Arcutis’ continued investment in compliance and data privacy,” said Ms. Barton. “Arcutis is progressing on its bold strategy to become the preeminent innovation-driven medical dermatology company. I look forward to leading our comprehensive compliance program and acting as Chief of Staff as the company continues its impressive growth trajectory.”

Ms. Barton brings over 17 years of corporate and healthcare compliance experience to Arcutis' growing team. Prior to joining Arcutis, Ms. Barton served as Vice President, Commercial Excellence & Chief Compliance Officer at Cipla Therapeutics, a division of Cipla, USA. Ms. Barton has broad, global compliance and ethics expertise, having begun her compliance and ethics career at Winn-Dixie Stores, Incorporated before transitioning to roles in the pharmaceutical and medical device sector with Bausch + Lomb, Allergan, KYTHERA, Anacor and MannKind Corporation. She has also held positions with Merrill Lynch and Janus, including an appointment overseas. A graduate of Syracuse University, Ms. Barton holds Bachelor’s degrees in Political Science and International Relations, both magna cum laude, and is a Certified Compliance and Ethics Professional (CCEP) and Certified Information Privacy Professional (CIPP US/E).

About Arcutis - Bioscience, applied to the skin.

Arcutis Biotherapeutics, Inc. (Nasdaq: ARQT) is a late-stage biopharmaceutical company focused on developing and commercializing treatments for unmet needs in immune-mediated dermatological diseases and conditions, or immuno-dermatology. The company is leveraging recent advances in immunology and inflammation to develop differentiated therapies against biologically validated targets to solve persistent treatment challenges in serious diseases of the skin. Arcutis’ robust includes four novel drug candidates currently in development for a range of inflammatory dermatological conditions. The company’s lead product candidate, topical roflumilast, has the potential to revitalize the standard of care for plaque psoriasis, atopic dermatitis, scalp psoriasis, and seborrheic dermatitis. For more information, visit or follow the company on and .

Forward Looking Statements

This press release contains "forward-looking" statements, including, among others, statements regarding the potential for Arcutis to become the preeminent innovation-driven medical dermatology company. These statements involve substantial known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements and you should not place undue reliance on our forward-looking statements. Risks and uncertainties that may cause our actual results to differ include risks inherent in the clinical development process and regulatory approval process, the timing of regulatory filings, and our ability to defend our intellectual property. For a further description of the risks and uncertainties applicable to our business, see the "Risk Factors" section of our Form 10-K filed with U.S. Securities and Exchange Commission (SEC) on February 16, 2021, as well as any subsequent filings with the SEC. We undertake no obligation to revise or update information herein to reflect events or circumstances in the future, even if new information becomes available.

Investors and Media:

Heather Rowe Armstrong

Vice President, Investor Relations & Corporate Communications



805-418-5006, Ext. 740



EN
18/02/2021

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Arcutis Biotherapeutics

 PRESS RELEASE

Arcutis Biotherapeutics Reports Inducement Grants Under Nasdaq Listing...

Arcutis Biotherapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) WESTLAKE VILLAGE, Calif., Sept. 05, 2025 (GLOBE NEWSWIRE) --  (Nasdaq: ARQT), a commercial-stage biopharmaceutical company focused on developing meaningful innovations in immuno-dermatology, today reported the grant of an aggregate of 35,500 restricted stock units of Arcutis’ common stock to four newly hired employees. These awards were approved by the Compensation Committee of Arcutis’ Board of Directors and granted under the Arcutis Biotherapeutics, Inc. 2022 Inducement Plan, with a grant date of Sept...

 PRESS RELEASE

Arcutis Submits Supplemental New Drug Application for ZORYVE® (roflumi...

Arcutis Submits Supplemental New Drug Application for ZORYVE® (roflumilast) Cream 0.3% to Expand Indication for Treatment of Plaque Psoriasis in Children Ages 2 to 5 If approved, ZORYVE cream would be the first and only topical PDE4 inhibitor indicated for plaque psoriasis in children as young as 2, offering patients and caregivers an important alternative to topical steroids and vitamin-D analogsZORYVE cream is uniquely formulated to be effective, safe, and well tolerated for all areas of the body, including sensitive areas such as intertriginous skin, where plaque psoriasis often presents...

 PRESS RELEASE

Arcutis to Present at Upcoming Investor Conferences

Arcutis to Present at Upcoming Investor Conferences WESTLAKE VILLAGE, Calif., Aug. 19, 2025 (GLOBE NEWSWIRE) --  (Nasdaq: ARQT), a commercial-stage biopharmaceutical company focused on developing meaningful innovations in immuno-dermatology, today announced that Arcutis management will participate in three upcoming investor conferences. Details for the company’s participation are as follows: Citi’s 2025 Biopharma Back to School Conference, September 2-3, 2025 Fireside Chat Date: Wednesday, September 3, 2025 Fireside Chat Time: 9:45 am EDT  Morgan Stanley’s 23rd Annual Global Healthcare Co...

 PRESS RELEASE

Arcutis Biotherapeutics Reports Inducement Grants Under Nasdaq Listing...

Arcutis Biotherapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) WESTLAKE VILLAGE, Calif., Aug. 08, 2025 (GLOBE NEWSWIRE) --  (Nasdaq: ARQT), a commercial-stage biopharmaceutical company focused on developing meaningful innovations in immuno-dermatology, today reported the grant of an aggregate of 21,000 restricted stock units of Arcutis’ common stock to three newly hired employees. These awards were approved by the Compensation Committee of Arcutis’ Board of Directors and granted under the Arcutis Biotherapeutics, Inc. 2022 Inducement Plan, with a grant date of Augu...

 PRESS RELEASE

Arcutis Announces Second Quarter 2025 Financial Results and Provides B...

Arcutis Announces Second Quarter 2025 Financial Results and Provides Business Update Q2 2025 net product revenue for ZORYVE® (roflumilast) was $81.5 million, a 164% increase compared to Q2 of 2024, and a 28% increase compared to Q1 of 2025, driven by strong portfolio demand growthZORYVE foam 0.3% received U.S. Food and Drug Administration (FDA) approval for the treatment of plaque psoriasis of the scalp and body in adults and adolescents 12 years of age and olderInitiated INTEGUMENT-INFANT study to evaluate the safety and efficacy of ZORYVE cream 0.05% in infants with atopic dermatitis ages...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch