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Allarity Therapeutics Initiates Phase 2 Trial of IXEMPRA® in Europe for the Treatment of Metastatic Breast Cancer

Allarity Therapeutics Initiates Phase 2 Trial of IXEMPRA® in Europe for the Treatment of Metastatic Breast Cancer
Allarity Therapeutics A/S
Press release
Hørsholm, Denmark (4 March 2021) – Allarity Therapeutics A/S (“Allarity” or the “Company”) today announced that it has enrolled the first patient in its European Phase 2 clinical trial of IXEMPRA
® (ixabepilone) for the treatment of metastatic breast cancer.
The U.S. Food and Drug Administration (FDA) approved IXEMPRA
®, a microtubulin inhibitor, in 2007 for the treatment of metastatic breast cancer. Allarity holds exclusive European option rights to IXEMPRA
® from the pharmaceutical company R-Pharm U.S., LLC, which previously acquired global rights to the drug from Bristol-Myers Squibb (BMS). Allarity has previously developed and validated a Drug Response Predictor (DRP ....

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Embracer Group publishes Interim Report Q3, October-December 2020: Operational EBIT Increased 100% to SEK 603 Million

Embracer Group publishes Interim Report Q3, October-December 2020: Operational EBIT Increased 100% to SEK 603 Million
THIRD QUARTER, OCTOBER-DECEMBER 2020 (COMPARED TO OCTOBER-DECEMBER 2019)

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Allarity Therapeutics A/S: Allarity Therapeutics to test activity of its PARP inhibitor, stenoparib, as a potential therapy for new highly infectious Strain B.1.1.7 of Coronavirus

(2)
Press Release
Hørsholm, Denmark (26 January 2021) - Allarity Therapeutics A/S ( Allarity or the Company ) today announced plans to further test the antiviral activity of stenoparib, its PARP inhibitor, against SARS-CoV-2 lineage B.1.1.7, also known as Coronavirus Variant B117 (the British variant ), at the Pathogen and Microbiome Institute at Northern Arizona University (NAU).
The virus variant was labelled Variant of Concern 202012/01 by Public Health England (PHE), an agency of the UK Department of Health & Social Care, in a publication on 21 December 2020, after it was found to have spread rapidly within the UK, and the PHE assessed that this variant has a substantially increased transmissibility compared with other Coronavirus variants. This variant has also been identified in the U.S. in several states. ....

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Allarity Therapeutics to test activity of its PARP inhibitor, stenoparib, as a potential ...

Press release content from Globe Newswire. The AP news staff was not involved in its creation.
Allarity Therapeutics to test activity of its PARP inhibitor, stenoparib, as a potential .
Allarity Therapeutics A/SJanuary 26, 2021 GMT
Press Release
Hørsholm, Denmark (26 January 2021) – Allarity Therapeutics A/S (“Allarity” or the “Company”) today announced plans to further test the antiviral activity of stenoparib, its PARP inhibitor, against SARS-CoV-2 lineage B.1.1.7, also known as Coronavirus Variant B117 (the “British variant”), at the Pathogen and Microbiome Institute at Northern Arizona University (NAU).
The virus variant was labelled “Variant of Concern 202012/01” by Public Health England (PHE), an agency of the UK Department of Health & Social Care, in a publication on 21 December 2020, after it was found to have spread rapidly within the UK, and the PHE assessed that this variant has a substantially increased transmissibility compared ....

United States , United Kingdom , Northern Arizona University , Thomas Pedersen , Stever Carchedi , Paul Keim , Department Of Health , Microbiome Institute At Northern Arizona University , Centers For Disease , Biomedical Advanced Research , National Institutes Of Health , Carrotize Pr Communications , Human Services , Dana Farber Cancer Institute Boston , United Kingdom Department Of Health Social Care , Development Authority , Public Health England , Microbiome Institute , Allarity Therapeutics , United Kingdom Department , Social Care , Ribose Polymerase , Dana Farber Cancer Institute , Operation Warp Speed , Disease Control , National Institutes ,

2020 in Review: A Letter from Allarity's CEO

2020 in Review: A Letter from Allarity's CEO
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