TrialSignal
Clinical trial intelligence report
A Phase I Study of Nivolumab in Combination With Ipilimumab for the Treatment of Patients With High Risk or Refractory/Relapsed Acute Myeloid Leukemia and Myelodysplastic Syndrome Following Allogeneic Stem Cell Transplantation
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03600155-Jul 28, 2026
NCT ID
NCT03600155
Status
COMPLETED
Phase
PHASE1
Sponsor
M.D. Anderson Cancer Center
Executive brief
Investment-Ready Snapshot
A Phase I Study of Nivolumab in Combination With Ipilimumab for the Treatment of Patients With High Risk or Refractory/Relapsed Acute Myeloid Leukemia and Myelodysplastic Syndrome Following Allogeneic Stem Cell Transplantation is a PHASE1 clinical asset sponsored by M.D. Anderson Cancer Center in Allogeneic Hematopoietic Stem Cell Transplantation Recipient, Myelodysplastic Syndrome, Recurrent Acute Myeloid Leukemia, Refractory Acute Myeloid Leukemia. SEO and diligence focus: Ipilimumab, Nivolumab, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03600155
Indication
Allogeneic Hematopoietic Stem Cell Transplantation Recipient
Modality
protein therapy
Target
Ipilimumab, Nivolumab
Intervention
Ipilimumab, Nivolumab
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.