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Clinical Trial · NCT04391244
Investigating National Solutions for Personalised Iodine-131 Radiation Exposure - Measuring Absorbed Dose to Tumour and Organs at Risk Following Routine Iodine Ablation Therapy
Overview
Investigating National Solutions for Personalised Iodine-131 Radiation Exposure - Measuring Absorbed Dose to Tumour and Organs at Risk Following Routine Iodine Ablation Therapy
Sponsor
Royal Marsden NHS Foundation Trust
Phase
N/A
Contacts
Yvonne Fox-Miller
yvonne.fox-miller@rmh.nhs.uk
020 86613760
Jan Taprogge
jan.taprogge@icr.ac.uk
020 8661 3086
ClinicalTrials.gov
NCT04391244Drug / Compound
Isotope(s):
IODINE-131
Radioisotope: I-131
Theranostic Role: Therapeutic Agent & SPECT Imaging
T1/2 (Half-Life): 8 Days
Decay Mode: BETA, GAMMA
Energy: βeta max 0.6 MeV Gamma 364 keV
Range: In Tissue: 0.8 -2.1 mm
Decay Daughters: Xe131
Status: FDA Approval: 1951-First FDA Approved Radiopharmaceutical), AZEDRA® (2018)
Target(s):
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