TrialSignal
Clinical trial intelligence report
Ph 1b Dose Escalation Study of OXi4503 as a Single Agent and in Combination With Cytarabine With Subsequent Phase 2 Cohorts for Subjects With Relapsed/Refractory Acute AML and MDS
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 19, 2026
NCT ID
NCT02576301
Status
UNKNOWN
Phase
Phase 1b/2
Sponsor
Mateon Therapeutics
Executive brief
Investment-Ready Snapshot
Mateon Therapeutics is advancing OXi4503 through a dual-phase clinical trial aimed at addressing significant unmet needs in relapsed/refractory AML and MDS populations. The combination therapy with cytarabine targets a market with limited effective options post-chemotherapy failure. The successful completion of this trial could position Mateon favorably against competitors in the hematologic oncology space, particularly in the context of increasing demand for innovative therapies in these indications. The trial's outcomes may also attract interest from potential partners or acquirers looking to enhance their oncology portfolios.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02576301
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
OXi4503 (combretastatin A1-diphosphate) is a vascular-targeted therapy that disrupts tumor vasculature, potentially enhancing the efficacy of cytarabine in treating relapsed/refractory acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).
Intervention
Phase 1 - OXi4503, Phase 1 - OXi4503 + cytarabine, Phase 2 - OXi4503 + cytarabine, Phase 2 - OXi4503 + cytarabine
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.