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Danny Rischin

Danny Rischin

Verified

Associate Editor, Journal of Global Oncology

Melbourne

Doesn’t Cover

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Journalist Type

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Seniority Positions

Industries

Medium Formats

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Content

Total articles 22

  • "High Response Rate With Extended Dosing of Cemiplimab in Advanced Cuta" by Danny Rischin, Brett G M Hughes et al.

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer| Texas Medical Center@ BACKGROUND: Cemiplimab (LibtayoMETHODS: In this open-label, phase II trial (ClinicalTrials.gov identifier NCT02760498), the cohort of patients ≥18 years old with advanced CSCC received cemiplimab 600 mg intravenously Q4W for up to 48 weeks. Tumor measurements were recorded every 8 weeks. The primary endpoint was objective response rate by independent central review. RESULTS: Sixty-three patients with advanced CSCC were treated with cemiplimab.

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer · Texas Medical Center

    Jun. 05, 2024

  • High response rate with extended dosing of cemiplimab in advanced cutaneous squamous cell carcinoma

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer| bmj.com@ Clinical/translational cancer immunotherapy High response rate with extended dosing of cemiplimab in advanced cutaneous squamous cell carcinoma Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer · bmj.com

    Mar. 01, 2024

  • "High Response Rate With Extended Dosing of Cemiplimab in Advanced Cuta" by Danny Rischin, Brett G M Hughes et al.

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer| Texas Medical Center@ BACKGROUND: Cemiplimab (LibtayoMETHODS: In this open-label, phase II trial (ClinicalTrials.gov identifier NCT02760498), the cohort of patients ≥18 years old with advanced CSCC received cemiplimab 600 mg intravenously Q4W for up to 48 weeks. Tumor measurements were recorded every 8 weeks. The primary endpoint was objective response rate by independent central review. RESULTS: Sixty-three patients with advanced CSCC were treated with cemiplimab.

    By Danny Rischin, Nicole Basset-Seguin, Dirk Schadendorf, Samantha Bowyer · Texas Medical Center

    Jun. 05, 2024

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Company Info

Journal of Global Oncology

Melbourne, Victoria, Australia

+61 3 8559 5000