IPSEY News Alert Ipsen S.A. ADR (IPSEY) 12.3000 02/14/2015 2

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Ipsen S.A. ADR (IPSEY) 12.3000 $IPSEY

DBV Technologies Welcomes Dr. J-P Moreau to its Scientific Advisory Board
GlobeNewswire - Fri Feb 13, 12:46AM CST
DBV Technologies, (Euronext: DBV - ISIN: FR0010417345 - Nasdaq Stock Market: DBVT), a clinical-stage specialty biopharmaceutical company, announced today the appointment of Dr Jacques-Pierre Moreau to its Scientific Advisory Board. Dr. Moreau brings to DBV his unique expertise and knowledge across a wide range of disease areas and will contribute in defining aggressive approaches to potentially extend the use of epicutaneous immunotherapy (EPIT(R)) and Viaskin(R) technology to a wide range of therapeutic opportunities.
RDUS: 50.37 (+0.63), DBVT: 22.15 (-0.53)

Ipsen: Sales in the Fourth Quarter and Full Year 2014
Business Wire - Tue Feb 03, 1:30AM CST
--Specialty care sales up 9.9%(1) in 2014

Ipsen announces topline results of two double-blind phase III studies of Dysport(R) in lower limb spasticity in children and in adults
Business Wire - Tue Feb 03, 12:00AM CST
--Treatment with Dysport(R) at the dose of 1500U statistically significantly improved muscle tone (primary endpoint) in adult patients with lower limb spasticity

Dysport successful in two label expansion studies
Seeking Alpha - at Seeking Alpha - Mon Jan 26, 7:15AM CST


Ipsen Biopharmaceuticals to Present Further Data on Recently FDA-Approved Antitumor Therapy, Somatuline(R) Depot(R) (lanreotide), at Gastrointestinal Cancers Symposium
Business Wire - Tue Jan 13, 7:33AM CST
Ipsen Biopharmaceuticals Inc., an affiliate of Ipsen (Euronext:IPN; ADR:IPSEY) today announced three presentations of lanreotidedata to be shared at the 2015 Gastrointestinal Cancers Symposium, January 15-17, 2015 in San Francisco, CA. One oral and two poster presentations will explore the use of lanreotide in gastrointestinal and pancreatic neuroendocrine tumors (GEP-NETs), including sub analyses of the pivotal Phase III, multinational, randomized, double-blind clinical trial (CLARINET(R)).

FDA clears expanded label for Ipsen's Somatuline Depot
Seeking Alpha - at Seeking Alpha - Wed Dec 17, 6:56AM CST


Ipsen's Somatuline(R) Depot(R) is the First Therapy Approved by the FDA in the United States for the Treatment of Patients with Locally Advanced or Metastatic Gastroenteropancreatic Neuroendocrine Tumors
Business Wire - Tue Dec 16, 4:00PM CST
--US organization ready for launch in Q1 2015

Ipsen Announces the FDA Approval of Somatuline(R) Depot(R) (lanreotide) Injection for the Treatment of Gastroenteropancreatic Neuroendocrine Tumors
Business Wire - Tue Dec 16, 3:45PM CST
Ipsen Biopharmaceuticals, Inc., an affiliate of Ipsen (Euronext: IPN; ADR: IPSEY), today announced that Somatuline(R) Depot(R) (lanreotide) Injection 120 mg (referred to as Somatuline(R)) was approved by the U.S. Food and Drug Administration (FDA) for the treatment of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) in adult patients with unresectable, well or moderately differentiated, locally advanced or metastatic disease to improve progression-free survival (PFS).

Francois Garnier Appointed Executive Vice President, General Counsel of Ipsen
Business Wire - Tue Dec 16, 11:00AM CST
Regulatory News:

FDA clears expanded label for Novartis' Signifor
Seeking Alpha - at Seeking Alpha - Tue Dec 16, 6:10AM CST

NVS: 102.20 (-0.17)

Ipsen Announces That the International Breast Cancer Study Group (IBCSG) Presented Phase 3 Results Evaluating the Use of Ovarian Suppression to Adjuvant Treatment with Tamoxifen
Business Wire - Fri Dec 12, 12:00AM CST
--Ovarian suppression was obtained entirely by monthly injections of triptorelin over 5 years for 81% of patients

Ipsen Biopharmaceuticals, Inc. Announces FDA Acceptance of Filing for Dysport(R) (abobotulinumtoxinA) in the Treatment of Upper Limb Spasticity in Adult Patients
Business Wire - Mon Dec 01, 9:31AM CST
Ipsen Biopharmaceuticals, Inc., an affiliate of Ipsen (Euronext:IPN; ADR:IPSEY), today announced that the U.S. Food and Drug Administration (FDA) has accepted for review its supplemental Biologics License Application (sBLA) for Dysport(R) (abobotulinumtoxinA) for the treatment of upper limb spasticity in adult patients.

FDA agrees to review Ipsen Dysport label expansion application
Seeking Alpha - at Seeking Alpha - Fri Nov 28, 7:30AM CST


Ipsen Announces FDA Acceptance of Filing for Dysport(R) in the Treatment of Upper Limb Spasticity in Adult Patients
Business Wire - Fri Nov 28, 12:00AM CST
Regulatory News:

Ipsen Biopharmaceuticals, Inc. Announces IPSEN CARES(TM), An Enhanced Patient Support Program
Business Wire - Mon Nov 24, 9:42AM CST
Ipsen Biopharmaceuticals, Inc., an affiliate of Ipsen (Euronext: IPN; ADR: IPSEY) today announced the implementation of IPSEN CARES(TM) (Coverage, Access, Reimbursement, & Education Support). Ensuring patients, providers and caregivers have the resources needed to help access the Ipsen medications that are critical to managing their conditions, IPSEN CARES is staffed Monday to Friday by experts who can assist with a broad range of medical, educational, logistical and coverage information regarding Ipsen medicines, including Increlex(R) (mecasermin), Somatuline(R) Depot(R) (lanreotide), and Dysport(R) (abobotulinumtoxinA).

Lexicon Pharmaceuticals Fights On
Stephen Simpson, CFA - at Seeking Alpha - Fri Nov 21, 11:09AM CST

LXRX: 0.89 (unch)

Ipsen and CNRS Create the "Archi-Pex" Joint Research and Innovation Lab, in Collaboration with the University of Rennes 1 and CEA
Business Wire - Thu Nov 20, 11:00AM CST
--Five-year public-private research partnership, built on 15 years of collaboration

Ipsen and the Salk Institute renew their agreement for discovery research in medical sciences
Business Wire - Tue Nov 18, 12:00AM CST
--Ipsen to support innovative Salk investigations into biology for another three years

Ipsen Announces FDA Approval of a New Delivery Device for Somatuline(R) Depot(R) (lanreotide) Injection
Business Wire - Thu Nov 06, 9:06AM CST
Ipsen Biopharmaceuticals, Inc., an affiliate of Ipsen (Euronext: IPN; ADR: IPSEY), today announced that the U.S. Food and Drug Administration (FDA) has approved a new device to deliver Somatuline(R) Depot(R) (lanreotide). The device has an enhanced, prefilled, low-volume syringe that supports full-dose delivery with no reconstitution requirements.




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