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A Phase Ib, Open-Label Study Evaluating the Safety and Pharmacokinetics of Atezolizumab (Anti-PD-L1 Antibody) Administered in Combination With Hu5F9-G4 to Patients With Relapsed and/or Refractory Acute Myeloid Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03922477-Jul 28, 2026
NCT ID
NCT03922477
Status
TERMINATED
Phase
Phase 1
Sponsor
Hoffmann-La Roche
Executive brief
Investment-Ready Snapshot
The Phase Ib study evaluating the combination of Atezolizumab and Hu5F9-G4 in relapsed or refractory acute myeloid leukemia (AML) was terminated by Hoffmann-La Roche due to the decision to discontinue development for this indication. This outcome suggests potential challenges in the therapeutic efficacy or safety profile of the combination therapy in this patient population. The AML market remains competitive with several emerging therapies, including other immunotherapies and targeted agents. The termination of this trial may impact Roche's positioning in the AML space, necessitating a reassessment of their pipeline and strategic focus on alternative indications or combinations.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03922477
Indication
Acute Myeloid Leukemia
Modality
small molecule
Target
PD-L1 (Programmed Death-Ligand 1) and Hu5F9-G4 (anti-CD47 antibody)
Intervention
Atezolizumab, Hu5F9-G4
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.