TrialSignal
Clinical trial intelligence report
Open-label, Phase I, Multi-center Study to Determine in Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome Patients the Recommended Dose of CYAD-02 After a Non-myeloablative Preconditioning Chemotherapy Followed by a Potential Consolidation Cycle
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT04167696-Jul 28, 2026
NCT ID
NCT04167696
Status
RECRUITING
Phase
PHASE1
Sponsor
Celyad Oncology SA
Executive brief
Investment-Ready Snapshot
Open-label, Phase I, Multi-center Study to Determine in Relapsed/Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome Patients the Recommended Dose of CYAD-02 After a Non-myeloablative Preconditioning Chemotherapy Followed by a Potential Consolidation Cycle is a PHASE1 clinical asset sponsored by Celyad Oncology SA in Acute Myeloid Leukemia, Myelodysplastic Syndrome. SEO and diligence focus: CYAD-02, ENDOXAN, Fludara, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04167696
Indication
Acute Myeloid Leukemia
Modality
cell therapy
Target
CYAD-02, ENDOXAN, Fludara
Intervention
CYAD-02, ENDOXAN, Fludara
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.