ARG-007 Efficacious Dose Validated in New Preclinical Study
Filed with ASX · · 5 pages · English
• Argenica engaged clinical research organisation MD Biosciences to independently validate the efficacy of ARG-007 in a rat model of ischemic stroke that mimics human large vessel occlusion strokes to provide further conviction on the efficacy and dosing of ARG-007. • Consistent with previous studies conducted by Argenica’s Chief Scientific Officer at the Perron Institute, a dose of 325 nmol/kg AR
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Story so far
Earlier from Argenica Therapeutics
- Phase 2 Trial Promising Improvements in Functional Outcomes
- Topline Phase 2 Trial Results of ARG-007 in AIS Patients
- Trading Halt
- Appendix 4E & Annual Report to 30 June 2025
- Argenica Receives IND Feedback From FDA
Later from Argenica Therapeutics
- Positive TNK Study Results Fulfil Key FDA Requirement
- AI Analysis Reveals Efficacy In Severe Stroke Patients
- Quarterly Activities/Appendix 4C Cash Flow Report
- Successful Applicaton for EMA Paediatric Waiver
- Half Yearly Report and Accounts
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