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  • A phase I clinical trial to ev...
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A phase I clinical trial to evaluate the pharmacokinetics, toxicity and dosimetry of 111-indium-labeled human epidermal growth factor in patients with metastatic breast cancer

A phase I clinical trial to evaluate the pharmacokinetics, toxicity and dosimetry of 111-indium-labeled human epidermal growth factor in patients with metastatic breast cancer

Bibliográfalaš dieđut
Váldodahkkit: Vallis, K, Reilley, R, Scollard, D, Petronis, J, Caldwell, C, Hendler, A, Lockwood, G, Oza, A
Materiálatiipa: Conference item
Almmustuhtton: 2005
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Geahča maid

  • Phase I trial to evaluate the tumor and normal tissue uptake, radiation dosimetry and safety of (111)In-DTPA-human epidermal growth factor in patients with metastatic EGFR-positive breast cancer.
    Dahkki: Vallis, K, et al.
    Almmustuhtton: (2014)
  • Preclinical pharmacokinetic, biodistribution, toxicology, and dosimetry studies of 111In-DTPA-human epidermal growth factor: an auger electron-emitting radiotherapeutic agent for epidermal growth factor receptor-positive breast cancer.
    Dahkki: Reilly, R, et al.
    Almmustuhtton: (2006)
  • A phase I trial of In-111-human epidermal growth factor in patients with metastatic EGFR-positive breast cancer
    Dahkki: Vallis, K, et al.
    Almmustuhtton: (2008)
  • A kit formulated under good manufacturing practices for labeling human epidermal growth factor with 111In for radiotherapeutic applications.
    Dahkki: Reilly, R, et al.
    Almmustuhtton: (2004)
  • Amplified delivery of indium-111 to EGFR-positive human breast cancer cells.
    Dahkki: Wang, J, et al.
    Almmustuhtton: (2001)

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