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Presentations of the preclinical results at the annual CCBIO Symposium

In collaboration with the University of Bergen, Norway, DCprime has established a preclinical mouse model to study DCP-001 vaccinations in monotherapy and in combination therapy settings. The collaboration is supported by the Horizon ...

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  • 14 May
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Presentation of the preclinical data at the annual CIMT meeting

At the 2019 CIMT Annual Meeting, preclinical study data have been presented, as DCprime was able to demonstrate that human antigen presenting cells (APCs) efficiently process DCP-001 through phagocytosis. These in vitro data suggest ...

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  • 21 Apr
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Approval ADVANCE-II study by Norwegian national authorities

On 29 January 2019 DCprime has received approval from the Norwegian Medicines Agency NoMa for the ADVANCE-II / DCOne-002 clinical study entitled ‘An international, multicenter, open-label study to evaluate the efficacy and safety of ...

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  • 29 Jan
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DCprime announces first patient dosed in phase 2 ADVANCE-II study with DCP-001 in patients with Acute Myeloid Leukemia

DCprime, participant of the EU sponsored Horizon2020 AML-VACCiN project, has announced that the first patient has been dosed with DCP-001 in a phase 2 study, called ADVANCE-II. Patients with Acute Myeloid Leukemia (AML) in complete ...

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  • 15 Nov
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Approval ADVANCE-II study by German national authorities

On 04 September 2018 DCprime has received approval from the German Paul-Ehrlich-Institute for the ADVANCE-II / DCOne-002 clinical study entitled ‘An international, multicenter, open-label study to evaluate the efficacy and safety of ...

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  • 05 Sep
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Clinical study data of DCP-001 in AML published in leading journal

DCprime announces that the results of the phase I study with its lead product DCP-001 in AML have been published in Cancer Immunology, Immunotherapy. This study was the starting point for the EU-funded AML-VACCiN project. The phase I ...

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  • 26 Jul
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Scientific report: AML-VACCiN achieves significant progress during first 18 months

In August 2017, the AML-VACCiN consortium delivered its scientific report over the first 18 months. We have made major progress for all the objectives that we set at the start of this ambitious project. In preparation of the clinical ...

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  • 30 Jan
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AML-VACCiN welcomes Accelovance as newest addition to its consortium

The AML-VACCiN team is excited to announce Accelovance as the latest member of its consortium. Accelovance is a clinical Contract Research Organization (CRO) which is specialized in early phase oncology trials (Phase I-II) and has been ...

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  • 30 Jan
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  • Recent Posts

    • AML-VACCiN promoted by the European Commission
    • Want to read more about the role of relapse vaccines in AML? Please read the article on this topic published in the November-December 2019 edition of MedNous
    • Third AML-VACCiN Consortium Meeting
    • Presentations of the preclinical results at the annual CCBIO Symposium
    • Presentation of the preclinical data at the annual CIMT meeting
  • PROJECT INFO

    This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 667713. The material presented and views expressed here are the responsibility of the author(s) only. The EU Commission takes no responsibility for any use made of the information set out.