PTX secures EU Orphan Drug Designation for PTX-100 in CTCL
Filed with ASX · · 3 pages · English
• PTX-100 is a first-in-class therapy designed to disrupt cancer growth pathways, now in Phase 2a trials for relapsed/refractory CTCL. • Complements existing U.S. FDA Orphan Drug and Fast Track status • Join CEO, James McDonnell, for an online investor briefing on Tuesday, 25th November at 3pm (AEDT). Register here: https://prescienttherapeutics.investorportal.com.au/investor- briefing/ MELBOURNE,
Prescient Therapeutics Limited on 6ix
Earlier from Prescient Therapeutics
- September Quarterly Updated and Appendix 4C
- Appendix 4E and 2025 Annual Report
- Prescient successfully completes $3 million Placement
- June 2025 Quarterly Update and Appendix 4C
- Prescient announces results of SPP & Launches Placement
Later from Prescient Therapeutics
- PTX secures EU Authorisation to commence PTX-100 Trial
- December 2025 Quarterly Update and Appendix 4C
- Appendix 4D and Half Year Financial Report
- March 2026 Quarterly Update and Appendix 4C
- June 2026 Quarterly Update and Appendix 4C
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