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Clinical Trial ● Currently Recruiting Phase III NCT06641414

Lisaftoclax (APG-2575) Combined With Azacytidine (AZA) in the Treatment of Patients With Higher-risk Myelodysplastic Syndrome (GLORA-4).

Lisaftoclax (APG-2575) Combined With Azacytidine (AZA) in the Treatment of Patients With Higher-risk Myelodysplastic Syndrome (GLORA-4). — Recruiting • Phase III • NCT06641414.

📅 13 Oct 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT06641414
Start
2025-01-22
Completion
2029-06
ClinicaliQ Trial Snapshot
  • Lisaftoclax (APG-2575) Combined With Azacytidine (AZA) in the Treatment of Patients With Higher-risk Myelodysplastic Syndrome (GLORA-4). — Recruiting • Phase III • NCT06641414.
  • GLORA-4 Trial Summary.
  • Adding lisaftoclax to azacitidine improves survival in newly diagnosed high-risk myelodysplastic syndrome compared to azacitidine alone.

Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

A global multicenter, randomized, double-blind, placebo-controlled, pivotal phase III study. To evaluate overall survival (OS) of lisaftoclax (APG-2575) combined with azacitidine (AZA) vs. placebo combined with azacitidine in newly diagnosed patients with HR-MDS. Conditions: Higher-risk Myelodysplastic Syndrome Interventions: Lisaftoclax (APG-2575), Azacitidine Injection, Placebo Lead Sponsor: Ascentage Pharma Group Inc. Planned Enrollment: 490 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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