{"id":51915,"date":"2024-07-08T19:29:34","date_gmt":"2024-07-08T18:29:34","guid":{"rendered":"https:\/\/www.innovationnewsnetwork.com\/?p=51915"},"modified":"2024-10-15T19:41:03","modified_gmt":"2024-10-15T18:41:03","slug":"defence-therapeutics-no-objection-health-canada-trial-accum-002-accutox","status":"publish","type":"post","link":"https:\/\/www.innovationnewsnetwork.com\/defence-therapeutics-no-objection-health-canada-trial-accum-002-accutox\/51915\/","title":{"rendered":"Defence Therapeutics receives no-objection letter from Health Canada for phase I trial of ACCUM-002 (AccuTOX)"},"content":{"rendered":"
Defence Therapeutics Inc, a Canadian biopharmaceutical company developing novel immune-oncology vaccines and drug delivery technologies, is pleased to announce that it received a No Objection Letter (\u201cNOL\u201d) from Health Canada for its Clinical Trial Study number ACCUM-002-01 entitled \u201cA Phase I trial of Intratumoral Administration of ACCUM-002TM as a Monotherapy and in Combination with Opdualag in Patients with Unresectables, Stage IIIB and IV, Melanoma\u201d.<\/p>\n
The primary objectives of this study are to determine the safety and tolerability of intratumoral administration of AccuTOX\u00ae, as a monotherapy and in combination with Opdualag which combines the LAG-3 checkpoint inhibitor relatlimab and PD-1 inhibitor nivolumab. The secondary objectives are to obtain preliminary efficacy data and to determine the Maximum Tolerated Dose (\u201cMTD\u201d) and recommended Phase 2 Dose (\u201cRP2D\u201d) of AccuTOX\u00ae exploits as an immune booster and anti-cancer molecule.<\/p>\n