Press releases
2023
28 September, 2023
Guard Therapeutics provides more information on the development strategy for RMC-035
Guard Therapeutics [GUARD], a biotechnology company specializing in kidney diseases, today announced further information regarding the development strategy for the investigational drug RMC-035. An advisory meeting with the U.S. Food and Drug Administration (FDA) will be requested to explore dose optimization and the framework for a future...
19 September, 2023
Guard Therapeutics reports robust efficacy of RMC-035 in Phase 2 (AKITA) and advances clinical development program
Guard Therapeutics [GUARD], a biotechnology company specializing in kidney diseases, today announced top-line results from its Phase 2 clinical study AKITA, evaluating RMC-035 for the prevention of kidney injury in open-heart surgery. In line with previous communication patient recruitment was prematurely stopped, and as expected the primary...
Guard Therapeutics [GUARD], a biotechnology company specializing in kidney diseases, announced today that the last patient's last visit (LPLV) in the clinical Phase 2 study AKITA has been completed. The study aims to evaluate the kidney protective effect of the investigational drug RMC-035 in relation to open heart surgery. This milestone...
14 June, 2023
Study results with Guard Therapeutics’ RMC-035 in kidney transplantation confirm previously positive data analysis
Guard Therapeutics [GUARD], a biotechnology company specialized in kidney diseases, today announced the full results from the company's Phase 1b clinical study of the investigational drug RMC-035 in patients undergoing kidney transplantation. The study results confirm the previously positive preliminary data analysis and demonstrate favorable...
Guard Therapeutics [GUARD] provides updated timelines and additional details on the plan for data analysis in the clinical phase 2 study AKITA, which aims to evaluate the kidney-protective effect of the investigational drug RMC-035 in connection with open heart surgery. The previously reported interim analysis focused on acute drug effects...
