Apr 10, 2019

Allergan Earns 2019 ENERGY STAR® Partner of the Year - Sustained Excellence Award for the Sixth Consecutive Year

DUBLIN, April 10, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN), a leading global pharmaceutical company, today announced that it has received the 2019 ENERGY STAR® Partner of the Year Sustained Excellence Award for its continued leadership in energy management and efficiency. The U.S. Environmental Protection Agency award recognizes Allergan as an ENERGY STAR® partner that has demonstrated exemplary commitment to energy leadership year over year. Allergan has a long history of promoting environmental responsibility within its global operations including through reducing greenhouse gas emissions and increasing use of renewable energy.
Apr 09, 2019

Allergan to Report First Quarter 2019 Financial Results and Host Conference Call and Webcast

DUBLIN, April 9, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN) today announced it will release first quarter 2019 financial results on Tuesday, May 7, 2019, prior to the open of U.S. Financial Markets. Allergan will host a conference call and webcast at 8:30 a.m. Eastern Time on Tuesday, May 7, 2019 to discuss its financial results. The dial-in number to access the call is U.S./Canada (877) 251-7980, International (706) 643-1573, and the conference ID is 7466378.
Apr 08, 2019

Allergan 360° Aesthetics Report™ Reveals Evolving Beauty Perceptions And Diverse Priorities Around The World

DUBLIN, April 8, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN) today released the results of their first-of-its-kind worldwide medical aesthetics study, titled the Allergan 360° Aesthetics Report, exploring the mindset and motivations of aesthetically conscious consumers across a variety of ages, races, cultures and genders, as well as the physicians who treat them.  
Apr 02, 2019

Allergan and Molecular Partners Announce Topline Safety Results from MAPLE study of Abicipar pegol

DUBLIN, April 2, 2019 /PRNewswire/ -- Allergan plc, (NYSE: AGN), a leading global pharmaceutical company and Molecular Partners (SIX: MOLN), a clinical-stage biotechnology company developing a new class of drugs known as DARPin® therapies, today announced topline safety results from MAPLE, a 28 week open-label study which enrolled 123 age-related Neovascular Macular Degeneration (nAMD) patients and evaluated the safety of abicipar produced via a modified manufacturing process. In this single arm study, treatment naïve or prior anti-VEGF treated patients received three monthly 2mg abicipar injections followed by 2mg injections every 8 weeks for up to a total of five injections through week 28.
Mar 26, 2019

Allergan Acquires Envy Medical, Inc., Adding Skin Resurfacing Dermalinfusion System to Best-in-Class Medical Aesthetics Portfolio

DUBLIN, March 26, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN), a leading global pharmaceutical company, today announced it has completed the acquisition of Envy Medical, Inc., a privately held company with proprietary technology in skin resurfacing. The acquisition enhances Allergan's best-in-class Medical Aesthetics portfolio with the addition of Envy's Dermalinfusion, a non-surgical, non-invasive skin resurfacing system for the face and body. Offered in physician's offices, medical spas and luxury spas, Dermalinfusion is the only treatment that simultaneously exfoliates, extracts and infuses the skin with professional strength serums, using medical grade diamond treatment tips. Each serum is specifically formulated to help treat a variety of skin concerns across all skin types.
Mar 21, 2019

CoolSculpting® and Sonja Morgan Talk Bikini Denial Just In Time For Summer

DUBLIN, March 21, 2019 /PRNewswire-PRWeb/ -- CoolSculpting, owned by Allergan plc, is partnering once again with television personality on Bravo's "The Real Housewives of New York City", philanthropist and fashion lifestyle entrepreneur Sonja Morgan to help women prepare for warmer weather and banish their Bikini Denial this summer.
Mar 20, 2019

CoolSculpting® and Sonja Morgan Partner to Talk Bikini Denial

DUBLIN, March 20, 2019 /PRNewswire/ -- Television personality on Bravo's "The Real Housewives of New York City", philanthropist, fashion lifestyle entrepreneur and mom, Sonja Morgan, continues her partnership with CoolSculpting, owned by Allergan plc, to talk about "Bikini Denial." Bikini Denial identifies the feeling that many woman get when realizing that swimsuit season has snuck up on her and she is not prepared to bare it all at the beach or pool until she frees herself of stubborn fat. According to a recent survey, the most common area women feel self-conscious about is their belly1. CoolSculpting is FDA-cleared to reduce fat in the abdomen area, along with eight other areas of the body, and can target that unwanted fat without surgery and little to no downtime.
Mar 18, 2019

Allergan Announces FDA Approval of AVYCAZ® (ceftazidime and avibactam) for Pediatric Patients

DUBLIN, March 18, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN) today announced that the U.S. Food and Drug Administration (FDA) has approved the company's supplemental New Drug Application (sNDA) for AVYCAZ® (ceftazidime and avibactam), expanding the label to include pediatric patients 3 months and older for the treatment of complicated intra-abdominal infections (cIAI) in combination with metronidazole and complicated urinary tract infections (cUTI). This is the first FDA approval of a pediatric indication for cUTI and cIAI in more than a decade.
Mar 14, 2019

Allergan to Present New Data - "Extended Duration of Intraocular Pressure (IOP) Control with Intracameral Bimatoprost Sustained-Release (SR) Implant" -- Highlighting Clinical Advances at the American Glaucoma Society Annual Meeting

DUBLIN, March 14, 2019 /PRNewswire/ -- Allergan plc, (NYSE: AGN), a leading global pharmaceutical company with more than 70 years of heritage in eye care, will present new data including a late-breaking abstract for Bimatoprost SR at the Annual Meeting of the American Glaucoma Society (AGS) to be held in San Francisco, California. The late-breaking abstract, to be presented for the first time during a podium session on Saturday, March 16th, is the initial treatment duration analysis of Phase 3 clinical data for Bimatoprost SR, a first-in-class sustained-release, biodegradable implant being evaluated for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Topline Phase 3 efficacy and safety results from the ongoing studies will also be presented at a congress later this year. Allergan anticipates submitting a New Drug Application (NDA) to the FDA in the second half of 2019.

Mar 11, 2019

Allergan Announces FDA Acceptance of New Drug Application for Ubrogepant for the Acute Treatment of Migraine

DUBLIN, March 11, 2019 /PRNewswire/ -- Allergan plc (NYSE: AGN) today announced that the U.S. Food and Drug Administration (FDA) has accepted the company's New Drug Application (NDA) for ubrogepant for the acute treatment of migraine in adults. The NDA filing is based on the successful completion of four clinical trials – two pivotal studies, ACHIEVE I and ACHIEVE II, which demonstrated the efficacy, safety and tolerability of ubrogepant, as well as two additional safety studies. A 10-month review period has been assigned with the Prescription Drug User Fee Act (PDUFA) in the fourth quarter of 2019.