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 20, 2026
NCT ID
NCT02576301
Status
UNKNOWN
Phase
Phase 1b/2
Sponsor
Mateon Therapeutics
Executive brief
Investment-Ready Snapshot
Mateon Therapeutics is investigating OXi4503 in a Phase 1b/2 clinical trial for relapsed/refractory Acute Myeloid Leukemia (AML) and Myelodysplastic Syndromes (MDS). The market for AML and MDS therapies is significant, with a growing demand for effective treatments due to high relapse rates and limited options post-chemotherapy. The combination of OXi4503 with intermediate-dose cytarabine could provide a competitive edge if shown to improve response rates compared to existing therapies. Diligence should focus on the trial's recruitment progress and preliminary efficacy data, as well as potential partnerships for commercialization.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02576301
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
OXi4503 (combretastatin A1-diphosphate) targets the tumor vasculature by disrupting the microtubule network, leading to vascular shutdown and subsequent tumor cell death.
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.