Oryzon Genomics (ORY) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
16 Mar, 2026Epigenetic drug development and clinical pipeline
Focus on potent, selective LSD1 inhibitors for oncology, hematology, and CNS diseases, with well-defined registrational pathways and multiple ongoing Phase I-III trials.
ladademstat shows strong efficacy in unfit 1L AML (100% ORR, 90% CRs) and is being tested in various combinations for AML, MDS, SCD, ET, and SCLC, leveraging collaborations with NCI and top-tier US institutions.
Vafidemstat is Phase III-ready for aggression in BPD, with ongoing trials in schizophrenia and ASD, and demonstrated significant reduction in agitation/aggression in PoC studies.
ORY-4001, a selective HDAC6 inhibitor, is advancing for ALS and CMT, with preclinical efficacy and first-in-man readiness expected in 2H2026.
Robust financial position with over $60 million raised in 2025, providing cash runway through 1H 2027.
Clinical data and regulatory strategies
ladademstat achieved 100% ORR and 90% CR in 1L AML, with final ALICE-2 data expected Q4 2026 and a seamless Phase II-III ALICE-3 trial planned for accelerated and full approval.
RESTORE Phase Ib in SCD is recruiting, with PoC data expected in 2026 and a registrational RESTORE-2 trial planned for 2027.
IDEAL Phase II trial in ET approved by EMA, planned to start 1Q2026, aiming to follow positive results from competitor LSD1i.
Vafidemstat's PORTICO Phase III protocol for BPD submitted to FDA, incorporating STAXI-2 Trait Anger and OAS-M as endpoints, with protocol resubmission targeted before year-end.
EVOLUTION Phase IIb trial in schizophrenia is ongoing, with EU expansion in 2026 and readout expected in 2H2027.
Market opportunities and competitive positioning
Significant unmet needs in AML, SCD, ET, BPD, schizophrenia, and ASD, with large addressable patient populations and high commercial potential (e.g., BPD market >$3Bn, schizophrenia drug market >$10Bn).
ladademstat and vafidemstat are positioned as first- or best-in-class assets, with broad applicability across multiple indications and strong safety profiles.
Strategic collaborations with leading pharma and biotech companies, and engagement with world-renowned clinical and regulatory experts.
Ongoing expansion of aggression program in ASD and rare neurodevelopmental disorders, supported by EU grants.
ORY-4001 available for partnering, with grant support from the ALS Association.
Latest events from Oryzon Genomics
- ALICE-2 responses underpin a planned 2027 two-cohort Phase III AML trial.ORY
Global Markets Forum Conference - FDA feedback advances vafidemstat toward Phase III amid lower FY24 R&D spending.ORY
Q4 2024 - Iadademstat AML progress and new financing support continued pipeline development.ORY
Q2 2026 - Iadademstat delivers 100% AML response rates, targeting $1B+ US peak sales and broad expansion.ORY
Jefferies Global Healthcare Conference 2026 - Positive AML trial results and robust cash position drive continued clinical expansion.ORY
Q1 2026 - Year-end cash reached €28.354m ($33.3m) as clinical programs advanced across oncology and CNS.ORY
Q4 2025 - Improved net result, strong cash position, and positive clinical progress in CNS and oncology.ORY
Q3 2025 - Vafidemstat advanced toward Phase III as €31.1m cash and a €13.264m grant supported funding.ORY
Q2 2025 - AML programs advanced as PORTICO missed primary endpoints amid ongoing funding needs.ORY
Q2 2024