PGD2 receptor

The patient is taking part in a phase 1/2a trial with the immunotherapy drug HTL0039732 for advanced solid tumors. Sosei Heptares’ drug works by blocking signalling through a specific type of prostaglandin receptor – the E2 (PGE2)-type prostanoid receptor 4 (EP4). Sosei Group Corporation, the world-leader in GPCR-focused structure-based drug design (SBDD) and development, and Cancer Research UK, the world’s largest independent funder of cancer research have been working together on the trial evaluating Sosei Heptares’ orally available small molecule cancer immunotherapy drug HTL0039732 for advanced solid tumors. HTL0039732 works by blocking signalling through a specific type of prostaglandin receptor, the prostaglandin E2 (PGE2)-type prostanoid receptor 4 (EP4). In cancer, PGE2 acts in the tumor microenvironment to trigger cancer cells to evade the immune system. Targeting EP4 to block the effects of PGE2 increases the ability of the immune system to detect and control cancer cells and makes HTL0039732 a potential candidate to treat patients with cancers that generally do not respond well to current immunotherapies. Cancers not responding to current immunotherapies These include microsatellite stable colorectal, gastroesophageal, head and neck, and castrate-resistant prostate cancer. Positive results from the trial will bring effective treatment closer to these underserved patient populations. Approximately 80–85% of colorectal cancer patients are classified as ‘microsatellite stable’ (MSS), which means they have low instability in short, repeated sequences of DNA in their tumours, known as microsatellites. MSS tumours often exist in an environment that suppresses the immune system and do not respond well to immunotherapies. googletag.cmd.push(function () { googletag.display('text-ad1'); }); Matt Barnes, president of Heptares Therapeutics and head of UK R&D, said: “We are very pleased to be collaborating with Cancer Research UK to advance HTL0039732 into clinical development. This novel oral small molecule drug candidate was rationally designed using our SBDD platform and has the potential to become a best-in-class approach to enhance the efficacy of immunotherapies used to treat many cancer patients.” Cancer Research UK’s Centre for Drug Development (CDD) is sponsoring, designing and conducting the trial with three main objectives: to define the toxicity, tolerability and pharmacokinetics of HTL0039732, to identify the recommended dose for phase 2 studies, and to assess its antitumor activity as a monotherapy and in combination with the PD-L1 inhibitor atezolizumab. 'Desperately need more trials like this' Nigel Blackburn, director of Cancer Research UK’s CDD, 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.” Phase 2a of the trial will expand the optimal combination dose in up to four cohorts in specified cancer indications. Sosei Heptares holds a license to the results generated under the trial to continue the clinical development and commercialization of HTL0039732. Chief investigator Bristi Basu, University of Cambridge, and co-chief investigator Debashis Sarker, King’s College London, are leading the trial. Patient recruitment has been initiated in the UK at Cambridge University Hospitals and Guy’s and St Thomas’ NHS Foundation Trusts, with additional sites across the Experimental Cancer Medicine Centre (ECMC) network to open soon. Immnosuppresive environment Dr. Bristi Basu, University of Cambridge, said: “We are excited to be opening a new UK clinical trial using HTL0039732 to target a protein called EP4, a member of the prostaglandin receptor family that has been implicated in creating the immunosuppressive environment which promotes tumor growth in multiple cancer types. “By studying HTL0039732 alone and in combination with immunotherapy, we aim to understand more about how to optimize modulation of the immune system to fight cancers. We hope that this EP4-targeting approach will deliver a promising route to improving treatment options for patients with a broad range of cancers.” 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. 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.

HTL0039732 is a novel EP4 antagonist designed by Sosei Heptares with potential to treat a wide range of cancers in combination with other immunotherapies Tokyo, Japan, London and Cambridge, UK, 10 August2023 – Sosei Group Corporation (“the Company”; TSE: 4565), the world-leader in GPCR-focused structure-based drug design (SBDD) and development, and Cancer Research UK, the world’s largest independent funder of cancer research, today announce that the first patient has been dosed in a Phase I/IIa clinical trial evaluating Sosei Heptares’ orally available small molecule cancer immunotherapy drug HTL0039732 for advanced solid tumors. HTL0039732 works by blocking signalling through a specific type of prostaglandin receptor, the prostaglandin E2 (PGE2)-type prostanoid receptor 4 (EP4). In cancer, PGE2 acts in the tumor microenvironment to trigger cancer cells to evade the immune system. Targeting EP4 to block the effects of PGE2 increases the ability of the immune system to detect and control cancer cells and makes HTL0039732 a potential candidate to treat patients with cancers that generally do not respond well to current immunotherapies, such as microsatellite stable* colorectal, gastroesophageal, head and neck, and castrate-resistant prostate cancer. Positive results from the trial will bring effective treatment closer to these underserved patient populations. Cancer Research UK’s Centre for Drug Development (CDD) is sponsoring, designing and conducting the Phase I/IIa trial with three main objectives: to define the toxicity, tolerability and pharmacokinetics of HTL0039732, to identify the recommended dose for Phase II studies, and to assess its antitumor activity as a monotherapy and in combination 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. Sosei Heptares holds a license to the results generated under the trial to continue the clinical development and commercialization of HTL0039732. Chief Investigator Dr. Bristi Basu, University of Cambridge, and Co-Chief Investigator Dr. Debashis Sarker, King’s College London, are leading the trial. Patient recruitment has been initiated in the UK at Cambridge University Hospitals and Guy’s and St Thomas’ NHS Foundation Trusts, with additional sites across the Experimental Cancer Medicine Centre (ECMC) network to open soon. Please refer here for more details on this trial. Matt Barnes, President of Heptares Therapeutics and Head of UK R&D,said: “We are very pleased to be collaborating with Cancer Research UK to advance HTL0039732 into clinical development. This novel oral small molecule drug candidate was rationally designed using our SBDD platform and has the potential to become a best-in-class approach to enhance the efficacy of immunotherapies used to treat many cancer patients.” Dr.BristiBasu, University of Cambridge, said: “We are excited to be opening a new UK clinical trial using HTL0039732 to target a protein called EP4, a member of the prostaglandin receptor family that has been implicated in creating the immunosuppressive environment which promotes tumor growth in multiple cancer types. By studying HTL0039732 alone and in combination with immunotherapy, we aim to understand more about how to optimize modulation of the immune system to fight cancers. We hope that this EP4-targeting approach will deliver a promising route to improving treatment options for patients with a broad range of cancers.” Dr. Nigel Blackburn, Director of Cancer Research UK’s CDD,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.” 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. 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. -ENDS- Notes to editors *Approximately 80–85% of colorectal cancer patients are classified as ‘microsatellite stable’ (MSS), which means they have low instability in short, repeated sequences of DNA in their tumours, known as microsatellites. MSS tumours often exist in an environment that suppresses the immune system and do not respond well to immunotherapies. About the agreement between Cancer Research UK and Sosei Heptares Cancer Research UK and Sosei Heptares signed a Clinical Trial and Licence Agreement in July 2022 to allow Cancer Research UK’s Centre for Drug Development (CDD) to sponsor, design and execute a first-in-human Phase I/IIa clinical trial of HTL0039732. Sosei Heptares was responsible for enabling activities and other pre-clinical studies before the trial began and holds a license to the results generated to continue the clinical development and commercialization of the drug. The CDD was responsible for obtaining the Clinical Trial Authorisation. About Cancer Research UK’s Centre for Drug Development Cancer Research UK has an impressive record of developing novel treatments for cancer. The Cancer Research UK Centre for Drug Development has been pioneering the development of new cancer treatments for 25 years, taking over 140 potential new anti-cancer agents into clinical trials in patients. It currently has a portfolio of 21 new anti-cancer agents in preclinical development, Phase I or early Phase IIa clinical trials. Six of these new agents have made it to market including temozolomide for brain cancer, abiraterone for prostate cancer and rucaparib for ovarian cancer. Two other drugs are in late development Phase III trials. About Cancer Research UK Cancer Research UK is the world’s leading cancer charity dedicated to saving lives through research. Cancer Research UK’s pioneering work into the prevention, diagnosis and treatment of cancer has helped save millions of lives. Cancer Research UK receives no funding from the UK government for its life-saving research. Every step it makes towards beating cancer relies on vital donations from the public. Cancer Research UK has been at the heart of the progress that has already seen survival in the UK double in the last 40 years. Today, 2 in 4 people survive their cancer for at least 10 years. Cancer Research UK’s ambition is to accelerate progress so that by 2034, 3 in 4 people will survive their cancer for at least 10 years. Cancer Research UK supports research into all aspects of cancer through the work of over 4,000 scientists, doctors and nurses. Together with its partners and supporters, Cancer Research UK's vision is to bring forward the day when all cancers are cured. For further information about Cancer Research UK's work or to find out how to support the charity, please call 0300 123 1022 or visit Follow us on Twitter and Facebook. About Sosei Heptares Sosei Heptares is a fully integrated biopharmaceutical company focused on bringing life-changing medicines based on world-class science to patients globally. Our vision is to become one of Japan’s global biopharmaceutical champions. Our global business combines our world-leading GPCR-targeted StaR® technology, structure-based drug design and early development capabilities in the UK with a highly experienced clinical development capability and a commercial operation in Japan. We are leveraging these capabilities to generate and advance a broad and deep pipeline of novel medicines across multiple therapeutic areas, including neurology, immunology, gastroenterology and inflammatory diseases. We intend to develop these opportunities for patients in Japan and globally both internally and through our partnerships with global biopharmaceutical companies and emerging technology companies. Sosei Heptares operates from key locations in Tokyo and Osaka (Japan), London and Cambridge (UK) and Seoul (South Korea). “Sosei Heptares” is the corporate brand and trademark of Sosei Group Corporation, which is listed on the Tokyo Stock Exchange (ticker: 4565). Sosei, Heptares, the logo and StaR® are trademarks of Sosei Group companies. For more information, please visit LinkedIn: @soseiheptaresco | Twitter: @soseiheptaresco | YouTube: @soseiheptaresco Enquiries: Sosei Heptares – Media and Investor Relations Hironoshin Nomura, Chief Financial Officer Shinichiro Nishishita, VP Investor Relations, Head of Regulatory Disclosures Maya Bennison, Communications Manager +81 (0)3 5210 3399 | +44 (0)1223 949390 | IR@SoseiHeptares.com MEDiSTRAVA Consulting (for International Media) Mark Swallow, Frazer Hall +44 (0)203 928 6900 | SoseiHeptares@medistrava.com Forward-looking statements This press release contains forward-looking statements, including statements about the discovery, development, and commercialization of products. Various risks may cause Sosei Group Corporation’s actual results to differ materially from those expressed or implied by the forward-looking statements, including: adverse results in clinical development programs; failure to obtain patent protection for inventions; commercial limitations imposed by patents owned or controlled by third parties; dependence upon strategic alliance partners to develop and commercialize products and services; difficulties or delays in obtaining regulatory approvals to market products and services resulting from development efforts; the requirement for substantial funding to conduct research and development and to expand commercialization activities; and product initiatives by competitors. As a result of these factors, prospective investors are cautioned not to rely on any forward-looking statements. We disclaim any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

It’s been six years since Otsuka got its Lundbeck-partnered antipsychotic Rexulti approved to treat schizophrenia in the US. Now, the company has its sights set on a new approach for the difficult-to-treat disease — and it’s putting down close to $1 billion to snag that candidate and three others from fellow Japanese drugmaker Sumitomo Dainippon Pharma. Otsuka is shelling out $270 million upfront and another $620 million in biobucks for joint development and commercialization rights to four neuropsychiatric compounds from Sumitomo Dainippon’s subsidiary Sunovion, the companies said on Thursday. Ulotaront (SEP-363856), a schizophrenia treatment that entered Phase III back in 2019, is the furthest along. The company’s bipolar depression candidate SEP-4199 isn’t far behind, having entered a Phase III trial earlier this month. Meanwhile, SEP-378614 and SEP-380135, discovered in collaboration with PsychoGenics, are still in Phase I. Last April, Sunovion uncorked some positive Phase II results for ulotaront, showing an average 17.2-point improvement on the Positive and Negative Syndrome Scale used to assess schizophrenia, compared to a 9.7-point improvement for the placebo group. Schizophrenia is assessed according to both “positive” symptoms, such as movement issues and abnormal thoughts or perceptions, and “negative” ones, such as the loss of motivation or pleasure. While researchers still have much to learn about the disease, they traced part of those effects to excess dopamine. Current drugs that block the dopamine receptor D2 help mitigate the positive symptoms but have had less success treating the negative ones. Rexulti, on the other hand, is a D2 receptor partial agonist. Ulotaront is designed to act on two dopamine-affecting receptors, called TAAR1 and 5-HT1A, while leaving D2 alone. While Phase II study’s secondary endpoints weren’t powered to be statistically significant, researchers reported seeing promising results on the negative symptoms. Next in line is SEP-4199, which produced some mixed results in bipolar I depression last summer. A Phase II trial enrolled 344 patients who were experiencing major depressive episodes associated with bipolar I disorder. But at the topline readout, the study failed to meet its primary endpoint: a significant improvement on the Montgomery-Åsberg Depression Rating Scale after six weeks of treatment. CSO Kenneth Koblan blamed the results on a high placebo response, adding: “Despite the high placebo response in this study, which is known to diminish the effect size and the ability to detect a signal, the topline results suggest that SEP-4199 has the potential to be an effective advance in treatment for people with bipolar depression.” SEP-378614 and SEP-380135 are in Phase I trials for treatment-resistant depression and agitation in Alzheimer’s disease, respectively. According to the terms of their new deal, Sunovion and Otsuka will share profits from the four compounds, as well as all expenses for clinical studies, regulatory filings, and commercialization. “Otsuka has been committed to providing new antipsychotics that contribute to patients worldwide in the field of neuropsychiatry by leveraging internal capabilities and external collaborations, starting with the launch of antipsychotics in the U.S. in 2002,” Makoto Inoue, president and representative director of Otsuka, said in a statement. “Through this agreement, we are confident the companies will be able to deliver even more value to patients through the experience and networks that we have cultivated over many years worldwide,” he added.