The shareholders of SynAct Pharma AB, Reg. No. 559058-4826, are hereby invited to attend the extraordinary shareholders’ meeting to be held at the premises of Setterwalls Advokatbyrå AB at Stortorget 23...
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Press releases
October 2020
Shareholders together representing more than 20 per cent of the shares and votes in the company has announced that they propose Uli Hacksell to be elected as new board member of SynAct Pharma. For this...
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SynAct Pharma AB (publ) today announced that it has terminated its agreement with Sedemera Fondkommission to act as the company’s liquidity provider.
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SynAct Pharma AB ("SynAct") today announced that dosing of the leading candidate drug AP1189 was successfully completed in the second cohort (100 mg dose level) in part 1 of the company’s Phase IIa st...
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September 2020
SynAct Pharma AB ("SynAct Pharma") today announced the initiation of a Phase II clinical study to evaluate the safety and efficacy of the company’s lead candidate drug AP1189 in adults diagnosed with C...
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SynAct Pharma AB ("SynAct") today announces that recruitment to the second cohort in part 1 of the company’s Phase IIa study in patients with Rheumatoid Arthritis (RA) with high disease activity has be...
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SynAct Pharma AB ("SynAct Pharma") hereby informs that the company has terminated the agreement with Redeye relating to the coverage of the company. For further information, please contact: Jeppe Øvlesen ...
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August 2020
SynAct Pharma AB ("SynAct Pharma") hereby announces that the company together with Prof Mauro Teixeira, MD, PhD, Universidade Federal de Minas, Belo Horizonte, Brazil and Prof Mauro Perretti, PhD William...
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July 2020
On Wednesday, July 22, 2020, the exercise period for SynAct Pharma AB's (“SynAct” or “the Company”) warrants of series TO 2 (“TO 2”) ended. A total of 4,839,860 warrants of series TO 2 were exercised, ...
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SynAct Pharma AB ("SynAct") today announces that the company is making progress in the second and final dose level (100 mg) in part 1 in patients with a Rheumatoid Arthritis with high disease activity...
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June 2020
SynAct Pharma AB ("SynAct" or "The Company") today announces that the exercise period for warrants of series TO 2 ("TO 2") will start on 1 July 2020. The exercise period runs from 1 July to 22 July 2020....
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SynAct Pharma AB ("SynAct") today announced that the company has initiated a Phase II clinical study with the AP1189 compound in idiopathic membranous nephropathy patients with Nephrotic Syndrome.
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SynAct Pharma AB ("SynAct") today announces that the company's Board of Directors and management have agreed to subscribe for 100 percent of the Board of Directors and management's total holding of warrants...
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SynAct Pharma AB ("SynAct") today announced that the Danish Medical Agency has approved the company’s clinical trial application (CTA) for a Phase IIa study in idiopathic membranous nephropathy patients w...
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May 2020
SynAct Pharma AB (“SynAct”) today announces that the company has filed an international patent application under the Patent Coordination Treaty (PCT), to cover combination treatment with the company’s lead ...
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SynAct Pharma AB (”SynAct”) meddelar härmed att alla personer i styrelse och ledning i bolaget har ingått avtal om en förlängning av lock-up om tolv månader. Totalt motsvarar lock-up-avtalen minimum 25 proce...
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· The first of two tested doses (50 mg) identified to be safe and well-tolerated.
· The blinded review revealed that patients in the study form two groups based on changes in their clinical disease a...
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April 2020
SynAct Pharma AB ("SynAct") hereby announces that the company has filed a patent application to the European Patent Office (EPO) covering the use of AP1189 for the treatment of COVID-19 infection, including...
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March 2020
SynAct Pharma AB ("SynAct") today announced that the company has submitted a clinical trial application (CTA) to the Danish Medicines Agency to initiate a Phase IIa study with its lead candidate drug AP1189...
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SynAct Pharma AB ("SynAct") today announced that the company investigates the possibility of developing its clinical anti-inflammatory lead candidate drug AP1189 as an additional therapy in hospitalized...
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