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Zealand hosts conference call on March 15 at 4 pm CET to present 2016 full-year results
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Zealand reports Q4 2016 Lyxumia® royalty revenue
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Notice of the date of Zealand's Annual General Meeting 2017 and of deadline for proposals for the agenda
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Patient recruitment completed for phase II trial with glepaglutide for treatment of short bowel syndrome
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EU approval of Suliqua(TM) triggers USD 10 million milestone payment to Zealand
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Zealand reports that Sanofi announces Soliqua(TM) 100/33 now available in the U.S
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Financial calendar for 2017
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Zealand initiates Phase IIa clinical trial with dasiglucagon in a dual-hormone artificial pancreas system from Beta Bionics
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The U.S. FDA approves Soliqua(TM) 100/33 for the treatment of adults with type 2 diabetes
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CHMP issues positive opinion recommending Suliqua(TM) (iGlarLixi) for approval in the EU
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Zealand presents at three international biotech/healthcare investor conferences in November and December 2016
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Zealand interim report for the first nine months of 2016 (unaudited)
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Notice of Zealand's interim report for the first nine months of 2016 and invitation to conference call
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Zealand sponsored educational symposium highlights the need for better medical treatment of short bowel syndrome
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Zealand's interim report for the first half of 2016 (unaudited)
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Helsinn Announces Top-Line Results of its Phase IIb Trial With Elsiglutide for the Prevention of Chemotherapy-induced Diarrhea in Colorectal Cancer Patients
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Zealand announces that Sanofi has submitted LixiLan for regulatory review in the US, triggering a USD 20 million milestone payment
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Zealand to present at 34th Annual J.P. Morgan Healthcare Conference on 14 January 2016
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Zealand presented on its dual acting peptides at the New York Academy of Sciences' meeting GLP-1 Treatment for Diabetes and Beyond
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Zealand strengthens its Senior Management team with the appointment of Carlos de Sousa as Chief Business Officer
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Zealand interim report for the first nine months of 2015 (un-audited): Financial results on target with significant pipeline progress
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Zealand is ready to take next steps in a diligent growth strategy for accelerated value creation: From peptide to patient
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Zealand reports Lyxumia(r) royalty revenue for Q3 2015 and that Sanofi confirms expected next steps in the US regulatory process
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Zealand to host Capital Markets Days in New York City and Copenhagen in November
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Zealand meets development milestone in collaboration with Boehringer Ingelheim
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Zealand informs that Sanofi's New Drug Application for lixisenatide (Lyxumia(R)) has been accepted for review by the FDA
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Zealand advances its proprietary, long-acting GLP-2 analogue, ZP1848, into clinical Phase II development for the treatment of Short Bowel Syndrome
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Zealand presents new preclinical data on its novel GIP peptide therapeutic, ZP-I-98, at the 51st EASD Annual Meeting
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Sanofi has announced the successful completion of LixiLan-L, the second pivotal Phase III trial with LixiLan to demonstrate positive results
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Major shareholder announcement
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Lixisenatide (Lyxumia(R)) royalty revenue increased in Q2 2015 as Sanofi confirms the submission of a NDA in the US
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CORRECTION: Sanofi has announced that the first LixiLan Phase III trial, LixiLan-O, met primary study endpoint
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Sanofi has announced that the first LixiLan Phase III trial, LixiLan-O, met primary study endpoint
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Phase I trial results for Zealand's glucagon analogue, ZP4207 support its further development as a ready-to-use rescue treatment for severe hypoglycemia in diabetes patients on insulin therapy
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Major Shareholder Announcement
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Zealand informs of updates given by Sanofi on Lyxumia(r) and LixiLan on an IR Thematic Conference Call on Diabetes
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Zealand informs that data presented from the ELIXA study establish Lyxumia(r) as the first GLP-1 receptor agonist with cardiovascular safety proven in a long-term outcome trial
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Presentations on two novel Zealand preclinical peptide therapeutics as possible approaches for the treatment of Type 2 diabetes and obesity at the American Diabetes Association's (ADA) 74th Scien
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Zealand announces that Sanofi has informed of results from GetGoal Duo-2, showing advantages of Lyxumia(r) versus rapid-acting insulin as add-on to Lantus(r) for the treatment of Type 2 diabetes
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Zealand Increases the Share Capital After Exercise of Employee Warrants and Announces an Amendment to Its Articles of Association
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New data on lixisenatide (Lyxumia(r)) including ELIXA results on LixiLan, and on novel Zealand peptide therapeutics, to be presented at the American Diabetes Association's (ADA) 75th Scientific S
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Zealand Presents to Investors at Four Conferences in June 2015
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Zealand Interim Report for Q1 2015 (unaudited) Increase in royalty revenue and progression of the development pipeline
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Zealand starts clinical development of a multiple-dose version of its stable glucagon analogue, ZP4207
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Zealand gives three presentations at the American TIDES 2015 conference - including as keynote speaker
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Zealand reports Lyxumia(r) royalty revenue for Q1 2015
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Zealand Announces Organizational and Management Changes
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Zealand announces that Sanofi has published top-line results from the ELIXA cardiovascular safety outcomes study of Lyxumia(r) (lix-isenatide)
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Zealand announces Full Year results in line with guidance and publication of the Annual Report for 2014

