Pharmaxis Ltd is an Australian pharmaceutical research company developing drugs for inflammatory and fibrotic diseases, with a focus on myelofibrosis. The company has a highly productive drug discovery engine built on its expertise in the chemistry of amine oxidase inhibitors, with drug candidates in clinical trials. Pharmaxis has also developed two respiratory products which are approved and supplied in global markets, generating ongoing revenue.
Pharmaxis is developing its drug PXS-5505 for the bone marrow cancer myelofibrosis which causes a build up of scar tissue that leads to loss of production of red and white blood cells and platelets. The US Food and Drug Administration has granted Orphan Drug Designation to PXS-5055 for the treatment of myelofibrosis and permission under an Investigational Drug Application (IND) to progress a phase 1c/2 clinical trial that is scheduled to begin recruitment in Q1 2021. PXS‐5505 is also being investigated as a potential treatment for other cancers such as liver and pancreatic cancer.
Other drug candidates being developed from Pharmaxis’ amine oxidase chemistry platform are targeting fibrotic diseases such as kidney fibrosis, NASH, pulmonary fibrosis and cardiac fibrosis; fibrotic scarring from burns and other trauma; and inflammatory diseases such as Duchenne Muscular Dystrophy.
Pharmaxis has developed two products from its proprietary spray drying technology that are manufactured and exported from its Sydney facility; Bronchitol® for cystic fibrosis, which is approved and marketed in Europe, Russia and Australia; and Aridol® for the assessment of asthma, which is approved and marketed in the United States, Europe, Australia and Asia.
Pharmaxis is listed on the Australian Securities Exchange (PXS). Its head office, manufacturing and research facilities are in Sydney, Australia.
Pharmaxis is developing its drug PXS-5505 for the bone marrow cancer myelofibrosis which causes a build up of scar tissue that leads to loss of production of red and white blood cells and platelets. The US Food and Drug Administration has granted Orphan Drug Designation to PXS-5055 for the treatment of myelofibrosis and permission under an Investigational Drug Application (IND) to progress a phase 1c/2 clinical trial that is scheduled to begin recruitment in Q1 2021. PXS‐5505 is also being investigated as a potential treatment for other cancers such as liver and pancreatic cancer.
Other drug candidates being developed from Pharmaxis’ amine oxidase chemistry platform are targeting fibrotic diseases such as kidney fibrosis, NASH, pulmonary fibrosis and cardiac fibrosis; fibrotic scarring from burns and other trauma; and inflammatory diseases such as Duchenne Muscular Dystrophy.
Pharmaxis has developed two products from its proprietary spray drying technology that are manufactured and exported from its Sydney facility; Bronchitol® for cystic fibrosis, which is approved and marketed in Europe, Russia and Australia; and Aridol® for the assessment of asthma, which is approved and marketed in the United States, Europe, Australia and Asia.
Pharmaxis is listed on the Australian Securities Exchange (PXS). Its head office, manufacturing and research facilities are in Sydney, Australia.
Location: Australia, New South Wales, Sydney
Employees: 51-200
Total raised: $4.9M
Founded date: 1998
Investors 3
Funding Rounds 1
| Date | Series | Amount | Investors |
| 16.08.2022 | - | $4.9M | - |
Mentions in press and media 13
| Date | Title | Description |
| 25.11.2021 | Pharmaxis : Security Purchase Plan | For personal use only PHARMAXIS LTD ABN 75 082 811 630 SHARE PURCHASE PLAN OFFER BOOKLET Thursday, 25 November 2021 Opening Date: Thursday, 25 November 2021 Closing Date: 5:00pm (Sydney, Australia time) on Wednesday, 15 December 2021 NOT FO... |
| 09.11.2021 | FDA Clears Pharmaxis Cancer Drug to Progress to Phase 2 Study in Liver Cancer | SYDNEY, Nov. 9, 2021 /PRNewswire/ -- Clinical stage drug development company Pharmaxis Ltd (ASX: PXS) today announced that an Investigational New Drug application (IND) for a trial of PXS-5505 in hepatocellular carcinoma (HCC) patients has ... |
| 09.11.2021 | FDA Clears Pharmaxis Cancer Drug to Progress to Phase 2 Study in Liver Cancer | SYDNEY, Nov. 9, 2021 /PRNewswire/ -- Clinical stage drug development company Pharmaxis Ltd (ASX: PXS) today announced that an Investigational New Drug application (IND) for a trial of PXS-5505 in hepatocellular carcinoma (HCC) patients has ... |
| 05.10.2021 | Pharmaxis Cleared To Progress To Phase 2 Bone Marrow Cancer Trial | SYDNEY, Oct. 5, 2021 /PRNewswire/ -- Clinical stage drug development company Pharmaxis Ltd (ASX: PXS) today announced further positive results of data analysis from a phase 1c clinical trial (MF-101) studying its drug PXS-5505 in patients w... |
| 05.10.2021 | Pharmaxis Cleared To Progress To Phase 2 Bone Marrow Cancer Trial | SYDNEY, Oct. 5, 2021 /PRNewswire/ -- Clinical stage drug development company Pharmaxis Ltd (ASX: PXS) today announced further positive results of data analysis from a phase 1c clinical trial (MF-101) studying its drug PXS-5505 in patients w... |
| 31.08.2021 | Pharmaxis Treatment to Prevent Wound and Burns Scars Clears Phase 1 Trial | Topical treatment safe and well tolerated in study of healthy volunteers Full inhibition of lysyl oxidase enzymes achieved in skin with minimal systemic exposure Collaboration with research team led by Professor Fiona Wood AM planning for t... |
| 05.08.2021 | Pharmaxis Cancer Drug Decreases Tumour Burden in Pre Clinical Liver Cancer Model | SYDNEY, Aug. 5, 2021 /PRNewswire/ -- Clinical stage drug development company Pharmaxis Ltd (ASX: PXS) today announced the first public presentation of data from a preclinical study of PXS-5505 in the liver cancer, cholangiocarcinoma (CCA) a... |
| 12.05.2021 | SYNAIRGEN PLC Preliminary results for the year ended 31 December 2020 | Press release Synairgen plc (‘Synairgen’ or the ‘Company’) Preliminary results for the year ended 31 December 2020 Significant progress continues towards a treatment for COVID-19 Southampton, UK – 12 May 2021: Synairgen plc (LSE: SNG), the ... |
| 18.12.2019 | Boehringer dumps its $250M NASH drug; Bavarian Nordic sells PRV for $95M; GBT inks deal with Syros, gets $150M loan | → Four years after Boehringer handed out a $250 million deal to get a NASH drug from Pharmaxis, they’re sweeping it out of the pipeline. The German pharma company noted today that the drug posed a threat of drug interactions,... |
| 18.12.2019 | Boehringer Ingelheim dumps NASH drug program amid concerns over drug interactions | Shares of Pharmaxis were down more than 40% on the Australian Stock Exchange when the market closed Wednesday. BI, based in Ingelheim am Rhein, Germany, is the largest privately owned drugmaker. “We are disappointed that BI 1467335 is not a... |
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