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A Phase 1, Multi-center, Open-Label Dose Escalation Study of SYN004 in Patients With Solid Tumors to Evaluate the Safety, Immunogenicity and Pharmacokinetics of SYN004 Following Administration of Eight Intravenous Doses

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A Phase 1, Multi-center, Open-Label Dose Escalation Study of SYN004 in Patients With Solid Tumors to Evaluate the Safety, Immunogenicity and Pharmacokinetics of SYN004 Following Administration of Eight Intravenous Doses

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs SYN 004 Synermore Biologics (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors Synermore Biologics

    • Most Recent Events

    • 15 Nov 2018 Status changed from recruiting to completed.
    • 13 Aug 2018 Planned number of patients changed from 18 to 10.
    • 13 Aug 2018 Planned End Date changed from 1 Sep 2018 to 1 Nov 2018.

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