Oslo, Norway

Cuthbertson
Radiopharm
Consulting

Opening Scandinavia to the next generation of targeted radiopharmaceuticals.

About the consultancy → Get in touch

86

Publications

1,993+

Citations

25+

Years Experience

About

Alan S. Cuthbertson is one of Europe's most experienced radiopharmaceutical scientists — a consultant, advisor, and scientist with more than 25 years at the forefront of radiopharmaceutical sciences.

After completing his PhD in Organic Chemistry at the University of Edinburgh, Alan built his career across the leading institutions shaping the field — including GE Healthcare, Algeta, and Bayer — working across radiopharmaceutical science in molecular imaging and targeted radiotherapy.

At Bayer AS in Oslo, he served as Head of R&D for targeted alpha radiotherapy, building the chelation chemistry, conjugation platform, and preclinical evaluation framework that underpins Bayer's clinical-stage targeted alpha-particle therapy pipeline. His work spans the full arc of radiopharmaceutical discovery: from novel octadentate HOPO chelator synthesis to biodistribution, dosimetry, and IND-enabling packages across prostate, breast, and mesothelioma indications.

Now operating independently, Cuthbertson Radiopharm Consulting works with pharmaceutical and biotech organisations, as well as academic institutes, seeking rigorous scientific expertise at the intersection of chemistry, oncology, and nuclear medicine — with a particular focus on advancing access to targeted radiotherapeutics across the Scandinavian market.

Alan S. Cuthbertson

Alan S. Cuthbertson
PhD Organic Chemistry, University of Edinburgh

Areas of Expertise

01

Targeted Alpha Therapy

Strategic and scientific advisory on TAT platform development, mechanism of action, and clinical positioning across oncology indications.

02

Radiometal Chelation Chemistry

Design, synthesis, and characterisation of chelators for Th-227, Ac-225, Pb-212, and other therapeutic radiometals — including novel HOPO scaffolds.

03

Preclinical Programme Design

Experimental design for biodistribution, efficacy, tolerability, and dosimetry studies in xenograft and syngeneic models.

04

Due Diligence & Expert Review

In-depth technical assessment of radiopharmaceutical assets for investors, acquirers, and licensing partners. Written reports and expert testimony available.

05

Combination Therapy Frameworks

Scientific rationale and study design for RLT combinations with PARP inhibitors, DNA damage response agents, chemotherapy, and anti-angiogenics.

Services

Scientific Advisory

Ongoing advisory relationships with biotech and pharmaceutical companies developing targeted radiotherapeutics. Structured as a monthly retainer with a defined scope: scientific board participation, programme review, and strategic guidance on platform development.

Project-Based Consulting

Defined-scope engagements for specific technical challenges: chelator selection and optimisation, preclinical study design, CMC/IND chemistry sections, or combination therapy rationale and experimental design. Typically two to twelve weeks in duration.

Due Diligence & Expert Review

Technical assessment of radiopharmaceutical assets for investment, acquisition, or licensing decisions. Includes written reports and, where required, expert testimony. Suitable for venture capital, private equity, and corporate development teams.

Contact

Enquiries for consulting engagements, advisory roles, and expert review are welcome.

Location Oslo, Norway
Profiles