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T 3011

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Drug Profile

T 3011

Alternative Names: B-015; MVR-T3011; MVR-T3011 IT; T-3 - ImmVira Pharma; T-3011

Latest Information Update: 19 Jul 2024

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At a glance

  • Originator Immvira Pharma
  • Developer Immvira Pharma; Shanghai Pharmaceuticals Holding
  • Class Antineoplastics; Gene therapies; Immunotherapies; Oncolytic viruses
  • Mechanism of Action Antibody-dependent cell cytotoxicity; Cell death stimulants; Immunologic cytotoxicity; Interleukin-12 expression stimulants; Programmed cell death 1 receptor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity No

Highest Development Phases

  • Phase II Breast cancer; Head and neck cancer; Malignant melanoma; Sarcoma
  • Phase I/II Non-small cell lung cancer; Solid tumours
  • Phase I Ascites; Bladder cancer; Colorectal cancer
  • No development reported Skin cancer

Most Recent Events

  • 31 May 2024 Updated efficacy and adverse events data from a phase I/IIa trial in Solid tumours presented at the 60th Annual Meeting of the American Society of Clinical Oncology (ASCO-2024)
  • 15 Mar 2024 T 3011 receives Fast Track Designation for Head and neck squamous cell cancer (Metastatic disease, Second-line therapy or greater) in USA (Intratumoural)
  • 29 Feb 2024 China Medical University and Immvira plans a phase I trial for Colorectal cancer (Monotherapy, Combination therapy, Second-line therapy or greater, Metastatic disease) in April 2024 (Intrahepatic) (NCT06283303)
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