Starpharma DEP® docetaxel and gemcitabine combination trial commences

4 August 2020

Release date 30 July 2020

Starpharma today announced that it has commenced its DEP® docetaxel + gemcitabine combination study for patients with advanced cancers, including pancreatic cancer. Recruitment into the study has commenced at the Christie in the UK, with two further sites expected to open in the coming weeks.

This study will recruit an initial cohort of approximately 10-12 patients and will run in parallel with the phase 2 DEP® docetaxel trial. The study will explore the potential benefits of DEP® docetaxel in combination with gemcitabine (Gemzar®) and builds on the impressive performance of DEP® docetaxel combined with gemcitabine in a preclinical human pancreatic cancer model, as reported previously. In that study DEP® docetaxel in combination with gemcitabine resulted in complete tumour regression and 100% survival, significantly outperforming each standard treatment, gemcitabine and Abraxane® alone and in combination.

Pancreatic cancer is a leading cause of cancer deaths, with a one-year relative survival rate of 20%, and a five-year survival rate of only 7%. Gemcitabine is commonly used both alone and in combination with Abraxane® in pancreatic cancer as a first line treatment. Current therapeutic approaches for pancreatic cancer have significant bone marrow toxicities. An important feature of DEP® docetaxel is a significant reduction in bone marrow toxicity observed in both preclinical and clinical studies.

Gemzar® (gemcitabine) is one of the leading chemotherapeutics used to treat pancreatic cancer. It can be administered as a monotherapy or in combination with other therapies such as taxanes (e.g. Abraxane®). Annual sales of Abraxane® are approximately US$1.2 billion. Gemcitabine, which is now generic, had peak sales prior to patent expiry of US$1.7 billion.

Dr Jackie Fairley, Starpharma CEO, commented: “We have had enthusiastic feedback from clinicians for this combination given the bone marrow toxicities experienced with current pancreatic cancer therapies. Therefore, there is a significant unmet need in advanced pancreatic cancer and data from this study are expected to further enhance the commercial potential for DEP® docetaxel.”

This combination study will run in parallel with the phase 2 DEP® docetaxel trial program, which is currently recruiting at sites in the UK and continues to show encouraging efficacy signals including stable disease and substantial target tumour shrinkage in patients with cancers including lung, prostate, pancreatic, gastric and oesophageal.

Read the full media release. 


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