Our technology

There is unique potential of Radiopharmaceuticals in treating oncological diseases.
Learn more about our technologies below
Nano-mAbs is the invention of Dr Hong Hoi Ting, an internationally regarded radiopharmaceutical and nuclear medicine expert, formerly from the University of Oxford
  • Nano-mAbs is a novel radiopharmaceutical platform made using genetic engineered camelid derived single domain antibodies (sdAb) labelled with a radioisotope of therapeutic radiation
  • The product is paired with a diagnostic, using the same antibody vector but labelled with a lower radiation radioisotope for imaging
  • Initial targets are HER-2, TROP-2 and PD-L1



Good binding characteristics, highly specific and no off-target binding



Uptake of 99mTc-HER-2 was also observed in nodal and distant metastatic lesions in multiple pelvic bones and lungs of a HER2 IHC positive patient with excellent conspicuity to background.  Metastatic disease was confirmed with CT scan.


High PD-L1 expression within primary tumour and multiple metastases

Patient: Male, 75 years old, chest x-ray showed lung shadow. CT scan confirmed multiple lesions. Biopsy confirmed squamous cell carcinoma, a lower left lobe lung hilar tumour, 44 x 48 mm is size with multiple metastases, nodal and distant. 99mTc-NM-01 scan results had uptake in primary tumour and multiple metastatic lesions, a strong positive image. PD-L1 IHC likely understated PD-L1 expression for this patient, PD-L1 treatment prognosis for such a patient is expected to be favourable, though further investigation is required.☯

Pivalate is the invention of Professor Eric Aboagye of Imperial College London
  • Pivalate is an 18F-FPIA radiotracer, based on a short chain carbohydrate which utilises the early steps of fatty acid oxidation and is very stable
  • In comparison to the clinical standard in PET imaging, 18F-FDG in prostate and brain cancers, Pivalate showed superior imaging performance and was equally good for two breast cancer models
AVβ6 Integrin
AVβ6 is the invention of internationally regarded integrin expert Professor Johannes Notni, formerly at the Technical University of Munich and now Professor at Essen University
  • AVβ6 is a strong and selective ligand for a cell surface protein called αvβ6-integrin. As such, it can accumulate in tissue areas characterized by high αvβ6-integrin levels
  • There is compelling evidence that αvβ6-Integrin is found in many of the most challenging cancers, such as pancreatic carcinoma, cervical, head-and-neck and certain lung cancers
  • AVβ6 offers an unparalleled performance for radiolabelling with Gallium-68
  • AVβ6 is a highly promising clinical candidate for early detection of the aforementioned conditions by PET imaging
  • Radiopharm Theranositcs plans to design & synthesise a number of conjugates for a therapeutic approach and enter clinical trials at the earliest opportunity
European Journal of Nuclear Medicine and Molecular Imaging – Image of the Month
  • αvβ6-specific peptide
  • PET/CT image of primary tumour in pancreatic head
  • Pancreatic ductal carcinoma confirmed histologically
  • Prominent signals are observed only in kidneys and urinary bladder due to renal excretion
  • No relevant uptake is seen in lungs, stomach, liver and intestines
  • Potential applications for fibrosis, PDAC and other carcinomas (head-and-neck squamous cell, lung adenocarcinoma, colon, cervical, mammary)

Reference:- Quigley, Czech, Sendt, Notni 2021, “PET/CT imaging of pancreatic carcinoma targeting the “cancer integrin αvβ6″,European Journal of Nuclear Medicine and Molecular Imaging

PSA-mAb is the invention of Professor David Ulmert formerly of Memorial Sloan Kettering and now UCLA.
  • PSA-mAb is a proprietary humanised monoclonal antibody, capable of targeting free human prostate kallikrein (PSA) in prostate cancer cells and internalising payload
  • The antibody platform enables a radiotheranostic applicable therapy of prostatic cancer through radioimmunotherapy as well as diagnostics of advanced prostate cancer
  • 10 000-fold + higher expression of KLK3 (PSA) in prostate tissue, compared to other tissue
  • [225Ac]-PSA mAb results in curative treatment by sustained tumour regression and a significant increase in median survival time
  • Data demonstrates a stable humanised antibody, without signs of degradation and aggregation


Therapy sustained tumor regression and a significant increase in median survival time

While beta-emitting [90Y] PSA-mAb (labelled hu5A10 above) had a more immediate effect on tumour volume, treatment with [225Ac]PSA-mAb resulted in sustained tumour suppression and provided a significant increase in median survival time. The faster response time seen in Yttrium-90 treatment could be attributed to the difference between the chosen radionuclides in half-life and path length. demonstrates a stable humanised antibody, without signs of degradation and aggregation.

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