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PDS Phase 2 Clinical Trial Update

PDS Phase 2 Clinical Trial Update.

articleEmv Capital PlcDecember 6, 20214/company/emv-capital-plc/news/pds-phase-2-clinical-trial-update
PDS Phase 2 Clinical Trial Update

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[{"type":"text","content":"\n \n \n \n RNS Number : 7206U\n NetScientific PLC\n 06 December 2021\n  \n \n \n \n NetScientific plc\n \n \n  \n \n \n (\"NetScientific\", the \"Group\" or the \"Company\")\n \n \n  \n \n \n PDS Phase 2 Clinical Trial Update\n \n \n  \n \n \n PDS Biotech Provides Recruitment update for National Cancer Institute-Led Phase 2 Clinical Trial of PDS0101-Based Combination\n \n \n  \n \n \n London, UK - 06 December 2021 - NetScientific plc (AIM: NSCI), the international life sciences and sustainability technology investment and commercialisation Group,  announces that its portfolio company, PDS Biotechnology Corporation (Nasdaq: PDSB), has announced the reopening of recruitment in the National Cancer Institute (NCI)-led Phase 2 clinical trial (NCT04287868) evaluating PDS0101 (Versamune®-HPV16) in combination with two investigational immune-modulating agents in advanced HPV cancers.\n \n  \n \n \n The suspension of recruitment was administrative in nature and was unrelated to any specific safety or efficacy concerns associated with the triple combination being studied. As a result, during the recruitment suspension, patients already enrolled in the study continued to receive scheduled treatment. The timing of clinical results from this trial is not expected to be affected by the pause in recruitment of new patients.\n \n \n  \n \n \n The trial is evaluating the novel triple combination in two groups of patients. Firstly, in second line treatment of recurrent or metastatic HPV-positive cancers including anal, cervical, head and neck, penile, vaginal, and vulvar cancers in patients who are naïve to checkpoint inhibitors and have not responded to at least one standard of care therapy. Secondly in third line treatment of the above recurrent or metastatic HPV-positive cancers in patients who have not responded to at least two standard of care therapies including checkpoint inhibitor treatment.\n \n \n  \n \n \n \n Dr. Lauren V. Wood, PDS Biotech's Chief Medical Officer commented:\n \n \n \"We are pleased that the NCI, part of the National Institutes of Health, quickly obtained IRB approval to resume recruitment in this important trial. We believe the interim data demonstrated that this combination has the potential to significantly improve clinical outcomes for patients with advanced, ...

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