US-based company Bellicum Pharmaceuticals has entered into a research agreement with Leiden University Medical Centre (LUMC) in the Netherlands, to discover and validate natural high-affinity T-cell receptor (TCR) product candidates targeting a wide range of cancers.

Built on a previous agreement with LUMC, the new partnership has provided Bellicum with global rights to TCR product candidates that target solid tumours expressing preferentially-expressed antigen in melanoma (PRAME) and other antigens.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

Bellicum Pharmaceuticals president and chief executive officer Tom Farrell said: "We are enthusiastic about the potential of TCRs that incorporate our switch technology to produce a targeted, potent and controlled attack on certain cancers.

"Dr Mirjam Heemskerk and her group from the Department of Hematology of the LUMC have made significant breakthroughs in the development of natural high-affinity TCRs, and we look forward to their continued discoveries as we prepare to launch clinical studies this year of our first TCR, BPX-701, under our current licence from Leiden."

"We are enthusiastic about the potential of TCRs that incorporate our switch technology to produce a targeted, potent and controlled attack on certain cancers."

As part of the agreement, Bellicum will provide financial assistance to the university over a term of three years in exchange for the exclusive rights to license any high-affinity TCRs discovered under the deal.

T-cell receptors are engineered T-cells that become activated while in the presence of the cancer cells containing a target antigen.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

Bellicum’s first TCR product candidaten, known as BPX-701 targeting PRAME, is expected to enter Phase I/II clinical trials in the middle of this year in order to treat patients suffering from refractory acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).

BPX-701 was licensed from Leiden last year and implements the biopharmaceutical company’s proprietary safety mechanism CaspaCIDe, in order to ensure enhanced control over the cells.

Pharmaceutical Technology Excellence Awards - Nominations Closed

Nominations are now closed for the Pharmaceutical Technology Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact.

Excellence in Action
Awarded the 2025 Pharmaceutical Technology Excellence Award for Business Expansion in Integrated Manufacturing, Upperton Pharma Solutions is rapidly expanding its UK GMP and sterile manufacturing footprint. Find out how Upperton’s integrated CDMO model helps pharma companies move from early development to clinical and niche commercial supply with fewer handovers and faster timelines.

Discover the Impact