Drug intelligence / Profile preview

RAD202

Development stage
Phase 1
Lead developer
Radiopharm Theranostics, Ltd
Modality
Alpha Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Beta Emitters → Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Small Molecules, Nanobodies (VHH) → Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

RAD202 is a proprietary single-domain antibody (nanobody) radiopharmaceutical developed for the treatment of HER2-expressing solid tumors. It specifically targets the Human Epidermal growth factor Receptor 2 (HER2), which is overexpressed in breast cancer and several other solid tumors. The drug is designed as a therapeutic radiopharmaceutical by conjugating the nanobody to radioisotopes such as Lutetium-177 (for therapy) or Technetium-99m/Gallium-68 (for imaging). This enables targeted delivery of ionizing radiation to tumor cells while minimizing exposure to healthy tissue. Preclinical and early clinical data have demonstrated favorable biodistribution, high tumor uptake, significant inhibition of tumor growth in HER2-positive xenograft models, and prolonged survival with fractionated dosing regimens. A Phase 1 first-in-human trial evaluating safety and preliminary efficacy in advanced HER2-positive cancers is ongoing[1][4][5][6][7].

Other names
Lu-177 RAD202Lu177 RAD202Lu 177 RAD202
02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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