Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 75/100

Failure Rate

17.6%

15 terminated/withdrawn out of 85 trials

Success Rate

76.9%

-9.6% vs industry average

Late-Stage Pipeline

12%

10 trials in Phase 3/4

Results Transparency

44%

22 of 50 completed trials have results

Key Signals

8 recruiting22 with results10 terminated5 withdrawn

Enrollment Performance

Analytics

Phase 1
39(45.9%)
Phase 2
33(38.8%)
Phase 3
9(10.6%)
Early Phase 1
2(2.4%)
Phase 4
1(1.2%)
N/A
1(1.2%)
85Total
Phase 1(39)
Phase 2(33)
Phase 3(9)
Early Phase 1(2)
+2 more

Activity Timeline

Global Presence

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Clinical Trials (85)

Showing 20 of 85 trials
NCT06191978Phase 1Recruiting

A Phase Ia/Ib Open-label, Multiple Dose, Study to Determine the Recommended Dose, Evaluate PKs, PDs, Safety, and Activity of Venetoclax in Combination With Oral Decitabine/Cedazuridine (ASTX727) in Pediatric Patients With Relapsed/Refractory Acute Myeloid Leukemia (AML)

Role: collaborator

NCT06802146Early Phase 1Recruiting

Early Intervention in High Risk CCUS

Role: collaborator

NCT04061421Phase 1Recruiting

Active Myeloid Target Compound Combinations in MDS/MPN Overlap Syndromes Overlap Syndromes (ABNL-MARRO)

Role: collaborator

NCT03922555Phase 1Recruiting

ASTX727 in Recurrent/Progressive Non-enhancing IDH Mutant Gliomas

Role: collaborator

NCT05360160Phase 1Recruiting

A Phase I-II Study Investigating the All-Oral Combination of the Menin Inhibitor SNDX-5613 With Decitabine/Cedazuridine (ASTX727) and Venetoclax in Acute Myeloid Leukemia (SAVE)

Role: collaborator

NCT06297629Phase 2Withdrawn

A Phase I/II Trial to Assess the Efficacy and Toxicity of ASTX727 (Oral Decitabine/Cedazuridine) for the Treatment of Hematological Neoplasms After Allogeneic Stem Cell Transplantation

Role: collaborator

NCT04655755Phase 1Active Not Recruiting

Venetoclax in Combination With ASTX727 for the Treatment of Treatment-Naive High-Risk Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

Role: collaborator

NCT05007873Phase 2Recruiting

ASTX727 and Dasatinib for the Treatment of Newly Diagnosed Philadelphia Chromosome or BCR-ABL Positive Chronic Myeloid Leukemia in Chronic Phase

Role: collaborator

NCT05082259Phase 1Recruiting

ASTEROID: A Trial of ASTX660 in Combination With Pembrolizumab

Role: collaborator

NCT03875287Phase 1Active Not Recruiting

Dose-Escalation Study of E7727, an Oral Cytidine Deaminase Inhibitor With Oral Decitabine in Subjects With Solid Tumors

Role: collaborator

NCT05245682Early Phase 1Active Not Recruiting

Tolinapant and Radiation for Cisplatin-Ineligible, Previously Untreated, Locally Advanced Head and Neck Cancer

Role: collaborator

NCT03019003Phase 1Completed

Oral Decitabine (ASTX727) and Durvalumab in Recurrent and/or Metastatic Head and Neck Cancer Patients

Role: collaborator

NCT02998567Phase 1Recruiting

Combination Study of Guadecitabine/ASTX727 and Pembrolizumab

Role: collaborator

NCT03220477Phase 1Active Not Recruiting

Pembrolizumab (Immunotherapy Drug) in Combination With Guadecitabine and Mocetinostat (Epigenetic Drugs) for Patients With Advanced Lung Cancer.

Role: collaborator

NCT04857645Phase 2Completed

ASTX727 and Donor Lymphocyte Infusions After Allogenic Stem Cell Transplantation in Very High Risk MDS or AML Patients

Role: collaborator

NCT01261312Phase 1Completed

SGI-110 in Participants With Myelodysplastic Syndromes (MDS) or Acute Myelogenous Leukemia (AML)

Role: lead

NCT05835011Phase 2Terminated

A Study of Oral Decitabine/Cedazuridine in Combination With Magrolimab in Participants With Intermediate- to Very High-Risk Myelodysplastic Syndromes (MDS)

Role: lead

NCT02920008Phase 3Completed

Phase 3 Randomized, Open-Label Study of Guadecitabine vs Treatment Choice in Previously Treated Acute Myeloid Leukemia

Role: lead

NCT02103478Phase 1Completed

Pharmacokinetic Guided Dose Escalation and Dose Confirmation With Oral Decitabine and Oral Cytidine Deaminase Inhibitor (CDAi) in Patients With Myelodysplastic Syndromes (MDS)

Role: lead

NCT03603964Phase 2Terminated

Guadecitabine Extension Study

Role: lead