| September 2019 | Product Approval | Allergan received the US Food and Drug Administration (FDA) approval for the use of Juvéderm VOLUMA XC, a hyaluronic acid gel dermal filler, with a TSK STERiGLIDE cannula for cheek augmentation to correct age-related volume deficit in the middle part of the face in adults over the age of 21. |
| April 2019 | Launch | Allergan announced the launch of Juvéderm VOLUX in Monaco. It is HA-based, the innovative product used as facial filler for chin and jaw lines. |
| March 2019 | Acquisition | Allergan acquired Envy Medical, Inc., a privately held company with proprietary technology in skin resurfacing. The acquisition enhanced the former’s best-in-class medical aesthetics portfolio. |
| January 2019 | Expansion | Allergan announced the establishment of a research & development facility in the Kendall Square section of Cambridge, Massachusetts. Thus, through this, the company aims to expand its research facilities |
| September 2018 | Expansion | Allergan announced plans to open its first medical aesthetics innovation center in Chengdu, China. Through this, the company plans to expand its foothold in the Chinese market. |
| February 2017 | Acquisition | Allergan acquired LifeCell Corporation, a leading regenerative medicine company, thus expanding its product portfolio in the aesthetic and plastic surgery segment. |
| March 2017 | Product Approval | Allergan received the FDA approval for Juvéderm Vollure XC used to reduce facial wrinkles and folds in adults over the age of 21. |
| July 2017 | Clinical Trial Results Declaration | Allergan announced the results of a prespecified prospective pooled subgroup analysis from the two Phase 3 studies (IBS-3001 and IBS-3002), which evaluated the efficacy and safety of Viberzi to treat the irritable bowel syndrome with diarrhea (IBS-D), irrespective of the prior use of loperamide. |
| January 2017 | Agreement | Allergan entered into a license agreement with Assembly Biosciences, Inc. for the worldwide rights to Assembly’s microbiome gastrointestinal (GI) development activities. With this agreement, Allergen received the worldwide rights to preclinical compounds ABI_M201 and ABI-M301, as well as two additional compounds to be identified by Assembly for irritable bowel syndrome. |
| – | Agreement | Allergan and AbbVie Inc. entered into a definitive transaction agreement under which AbbVie Inc. acquired Allergan in a cash and stock transaction for a transaction equity value of approximately USD 63 billion. |
| – | Expansion | Allergan announced the establishment of a research & development facility in the Kendall Square section of Cambridge, Massachusetts. Thus, through this, the company aims to expand its research facilities. |
| – | Launch | Allergan launched Spotlyte, an innovative digital hub of curated content designed to create awareness about medical aesthetic treatments. |
| – | Agreement | Allergan acquired Bonti, Inc., a privately-held clinical-stage biotechnology company focused on the development and commercialization of novel, fast-acting neurotoxin programs for aesthetic and therapeutic applications. |
| – | Acquisition | Allergan acquired ZELTIQ Aesthetics, Inc., a medical technology company. The company comprises a proprietary controlled-cooling fat-reducing treatment, CoolSculpting. The acquisition of ZELTIQ Aesthetics cost an approximate of USD 2.4 billion. |
| November 2019 | Agreement | Allergan has teamed up with Exicure, a US-based clinical-stage biotechnology company, to discover treatments for hair loss disorders. Under this agreement, Exicure will receive USD 25 million from Allergan to apply Exicure’s spherical nucleic acid (SNA) technology for two collaborative programs. |
| June 2019 | Agreement | Allergan and AbbVie Inc. entered into a definitive transaction agreement under which AbbVie Inc. will acquire Allergan in a cash and stock transaction for a transaction equity value of approximately USD 63 billion. |
| January 2019 | Expansion | Allergan announced the establishment of a research & development facility in the Kendall Square section of Cambridge, Massachusetts. Through this, the company aims to expand its research facilities. |
| March 2019 | Product Approval | Allergan received the US Food and Drug Administration (FDA) approval for using hyaluronic acid gel filler product, named JUVÉDERM VOLUMA XC. This product will be used for cheek augmentation that will correct age-related volume deficit in the mid-face in adults aged over 21. |
| October 2018 | Product Approval | Allergan received approval by the US Food and Drug Administration (FDA) to treat the submandibular area through the CoolSculpting treatment. |
| June 2017 | Acquisition | Allergan acquired Keller Medical, Inc. With this acquisition, the company gained control over Keller’s product portfolio. |
| April 2017 | Acquisition | Allergan acquired Zeltiq Aesthetics, Inc. for USD 2,405.4 million to expand its product portfolio. Zeltiq is into development and commercialization of Coolsculpting products. |
| July 2016 | – | Chugai and Galderma Announce Global License Agreement for Nemolizumab (CIM331), Novel Biologic for Skin Diseases. The primary aim of this agreement is to improve atopic dermatitis by breaking the itch-scratch cycle which has great expectation for nemolizumab. |
| April 2016 | – | Galderma Announces U.S. Collaboration in Aesthetics with Mentor Worldwide, LLC by this Collaboration Mnetor and Galderma will provide huge products to healthcare professionals who have patients requiring products for facial injectable and breast enhancement. |
| January 2016 | – | Maruho and Galderma to Join Forces in a Strategic Alliance in Japan. One of the major reasons of this strategic alliance is that galderma will permit maruho to additionally promote their products in japan in the field of dermatology. |
| December 2015 | – | Galderma and ZELTIQ Announce U.S. Collaboration in Aesthetics. This collaboration between two of the fastest growing companies in aesthetics will provide healthcare professionals with beauty professionals and advanced technology for facial rejuvenation. |
| October 2019 | Product Approval | Allergan received approval for Botox by the US Food and Drug Administration (FDA) to treat the lower limb spasticity in pediatric patients of age group 2 to 17 |