Positive TNK Study Results Fulfil Key FDA Requirement
Filed with ASX · · 3 pages · English
• ARG-007 confirmed not to interfere with tenecteplase (TNK), meeting a critical FDA requirement and significantly de-risking ARG-007’s development for use alongside standard-of-care clot dissolving agents. • This drug-drug-interaction study compliments the previously completed study assessing ARG-007’s drug-drug interaction with alteplase, a standard of care clot dissolving drug similar to TNK, i
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Earlier from Argenica Therapeutics
- ARG-007 Efficacious Dose Validated in New Preclinical Study
- 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
Later from Argenica Therapeutics
- 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
- Argenica Receives $3.97m R&D Tax Incentive Cash Rebate
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