The first patient has been dosed in the UK as part of a collaborative trial between Sosei Group and Cancer Research UK. Image credit: SDI Productions / Getty Images

Sosei Group and Cancer Research UK have announced the first patient has been dosed in a Phase I/IIa clinical trial of pipeline drug HTL0039732 for advanced solid tumors.

The trial (NCT05944237) will evaluate Sosei’s oral small-molecule cancer immunotherapy drug HTL0039732. Cancer Research UK and Sosei Heptares signed an agreement in July 2022 to allow Cancer Research UK’s Centre for Drug Development (CDD) to sponsor, design and execute the trial.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

The Phase I trial will define the toxicity, tolerability and pharmacokinetics of HTL0039732, identify the recommended dose for Phase II studies, and assess the antitumor activity as a monotherapy and combination therapy with the PD-L1 inhibitor atezolizumab. Phase IIa of the trial will expand the optimal combination dose in up to four cohorts in specified cancer indications.

First patients dosed in the UK

Patient recruitment has been initiated at Cambridge University Hospitals and Guy’s and St Thomas’ NHS Foundation Trusts in the UK. More sites will open across the Experimental Cancer Medicine Centre (ECMC) network.

The UK Medicines and Healthcare products Regulatory Agency (MHRA) has granted HTL0039732 an Innovation Passport, the first step in its Innovative and Licensing Access Pathway (ILAP), which aims to improve patient access to new medicines by reducing the time to market.

See Also:

The MHRA grants Innovation Passports to medicines that treat life-threatening or seriously debilitating conditions, and where there is a significant patient or public health need.

How HTL0039732 works

HTL-0039732 acts as an EP4 antagonist. Targeting EP4 blocks the effects of PGE2 and increases the ability of the immune system to detect and control cancer cells. This makes HTL0039732 a potential candidate to treat patients with cancers that generally do not respond well to current immunotherapies.

The drug candidate is under development for the treatment of various cancers, including mesothelioma, sarcoma and pheochromocytoma.

CDD director Dr Nigel Blackburn said: “We are delighted to have reached this next significant milestone in our partnership with Sosei Heptares. The fact that immunotherapy works for some patients but not others means we desperately need more trials like this to open up potentially life-saving treatment options to more people.”