Promontory Therapeutics Inc. today presented Phase 2a clinical safety and efficacy data on lead therapeutic candidate PT-112 in combination with PD-L1 inhibition, in patients with advanced non-small cell lung cancer (NSCLC) at the European Society for Medical Oncology Immuno-Oncology (ESMO I-O) Congress 2022.
| Data suggest that PT-112 and PD-L1 combination is well-tolerated and has meaningful clinical benefits in pretreated patients without known predictive markers for immunotherapy response NEW YORK, Dec. 8, 2022 /PRNewswire/ -- Promontory Therapeutics Inc., a clinical stage pharmaceutical company advancing small molecule immunotherapies in oncology, today presented Phase 2a clinical safety and efficacy data on lead therapeutic candidate PT-112 in combination with PD-L1 inhibition, in patients with advanced non-small cell lung cancer (NSCLC) at the European Society for Medical Oncology Immuno-Oncology (ESMO I-O) Congress 2022.
The poster titled, “A phase 2a study of the novel immunogenic cell death (ICD) inducer PT-112 plus avelumab in advanced non-small cell lung cancer patients,” demonstrated that the PT-112 and avelumab combination is well-tolerated with manageable safety profile, and showed meaningful clinical benefits in patients without known predictive markers for immunotherapy response. Based on the clinical activity observed, the study’s results support further evaluation of PT-112 combinations with immuno-oncology agents and assessment of PT-112’s immunological effects in patients. “These data give us proof of principle for the use of immunogenic cell death inducer PT-112 in combination with immune checkpoint inhibition in NSCLC patients, and are supportive of future opportunities to bring our intended immunotherapy combinations to cancer patients,” said Matthew Price, Promontory Therapeutics co-founder and Chief Operating Officer. “Along with immune correlative findings, the results are encouraging. As the field of immunogenic small molecules continues to evolve, we are pleased to continue to demonstrate the ICD effects of PT-112 in human patients. Our published clinical and non-clinical studies to date have shown the potential of this approach.” The 18 patients enrolled in the study were treated with 360 mg/m2 of PT-112 on days one, eight, and 15, and 800 mg of avelumab on days one and 15, of a 28-day cycle. Eligible patients received no more than 4 prior lines of therapy and were required to have progressive disease and to have received prior anti-PD-1/PD-L1 and platinum treatment. Findings from the study include:
Based on preclinical models, PT-112 is an immunogenic small molecule that induces ICD, recruits immune effector cells in the tumor microenvironment, and synergizes with immune checkpoint inhibitors. For more information about PT-112 and Promontory Therapeutics’ clinical pipeline visit www.PromontoryTx.com. About PT-112 PT-112 is the first small-molecule conjugate of pyrophosphate in oncology, and possesses a unique pleiotropic mechanism of action that promotes immunogenic cell death (ICD), through the release of damage associated molecular patterns (DAMPs) that bind to dendritic cells and lead to downstream immune effector cell recruitment in the tumor microenvironment. PT-112 represents a highly potent inducer of this immunological form of cancer cell death. Further, PT-112 harbors a property known as osteotropism, or the propensity of the drug to reach its highest concentrations in certain areas of the bone, making it a candidate for treatment of patients with cancers that originate in, or metastasize to, the bone. The first in-human study of PT-112 demonstrated an attractive safety profile and evidence of long-lasting responses among heavily pre-treated patients and won “Best Poster” within the Developmental Therapeutics category at the ESMO 2018 Annual Congress. The combination Phase 1b dose escalation study of PT-112 with PD-L1 checkpoint inhibitor avelumab in solid tumors was reported in an oral presentation at the ESMO 2020 Virtual Congress and the Phase 2a dose confirmation cohort in non-small cell lung cancer (NSCLC) patients reported at ESMO IO 2022. The Phase 1 study in patients with relapsed or refractory multiple myeloma presented at ASH is the third completed Phase 1 study of PT-112. Monotherapy Phase 2 development is ongoing in mCRPC, and now includes the Phase 2 proof of concept study in thymic epithelial tumors under the company’s formal collaboration with the NCI. About Promontory Therapeutics Promontory Therapeutics Inc. is a privately held, clinical stage pharmaceutical company focused on small molecule immunotherapy. The company’s lead candidate, PT-112, is the first small molecule conjugate of pyrophosphate in oncology, and possesses a unique pleiotropic mechanism of action that promotes immunogenic cell death, through the release of damage associated molecular patterns (DAMPs) that bind to pattern recognition receptors on dendritic cells and promote the adaptive immune response in the tumor microenvironment. Clinical data generated across three Phase 1 studies have demonstrated single-agent anti-cancer activity and an attractive tolerability profile, and three Phase 2 studies of PT-112 are underway. The company’s research and development work has been conducted in the United States, Europe and Asia, along with a sub-license agreement for the development, commercialization and use of PT-112 in Greater China. The company also sponsors the ongoing clinical study of PT-112 in combination with the PD-L1 inhibitor avelumab under a collaboration agreement with Pfizer and Merck KGaA, Darmstadt, Germany (operating as EMD Serono in the US and Canada), and has an active Phase 2 trial underway with the NCI utilizing PT-112 in thymic epithelial tumors where PT-112 has received Orphan Drug designation. To learn more about Promontory Therapeutics, visit the company’s website here. CONTACTS: Promontory Therapeutics ICR Westwicke Investors: Media:
SOURCE Promontory Therapeutics Inc. |
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