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asparaginase

Generic: asparaginase·Brand: Erwinaze, Rylaze

asparaginase: 11 clinical trials tracked.

asparaginase evidence translation

What we can confirm

11 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about asparaginase, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence5 indications · 5 study sponsors
Clinical Trials (11)showing 10 most recent

A Phase 1/1b Study Evaluating Asparaginase Erwinia Chrysanthemi- Recombinant-Rywn (Recombinant Erwinia Asparaginase) and Venetoclax in Combination With Blinatumomab in Adults With Relapsed or Refractory B-Cell Acute Lymphoblastic Leukemia

NCT07133997·Phase 1
Recruiting

Primary endpoint: Incidence of adverse events (AEs) (Phase I)

Interventionalopen26 targetStarted 2026-05Completion 2028-061 site · United StatesCity of Hope Medical Center

Dose-Adjusted Etoposide, Prednisone, Vincristine, Cyclophosphamide, and Doxorubicin (DA-EPOCH) ± Rituximab + Recombinant Erwinia Asparaginase (JZP458; Rylaze®) for the Treatment of Newly-Diagnosed Adults With Philadelphia Chromosome-Negative Acute Lymphoblastic Lymphoma/Leukemia

NCT06738368·Phase 2
Recruiting

Primary endpoint: Measurable residual disease (MRD) negativity

Interventionalopen30 targetStarted 2026-05Completion 2028-071 site · United StatesUniversity of Washington

A Phase 2 Study Evaluating the Safety and Efficacy of Asparaginase Erwinia Chrysanthemi- Recombinant-Rywn (Recombinant Erwinia Asparaginase) During Pediatric-Inspired Regimen in High-Risk Adults With Newly Diagnosed ALL or LBL

NCT06918431·Phase 2·ASRT
Recruiting

Primary endpoint: Incidence of adverse events (AEs) (Safety Lead-in)

Interventionalopen53 targetStarted 2025-10Completion 2029-038 sites · United StatesCity of Hope Medical Center

A Phase 2 Study of Blinatumomab in Combination With Chemotherapy for Infants With Newly Diagnosed Acute Lymphoblastic Leukemia With Randomization of KMT2A-Rearranged Patients to Addition of Venetoclax

NCT06317662·Phase 2·COSM
Recruiting

Primary endpoint: Incidence of dose-limiting toxicities (DLTs) (safety phase)

InterventionalRandomizedopen153 targetStarted 2025-06Completion 2028-1250 sites · United StatesNational Cancer Institute (NCI)

A Phase 3 Randomized Trial for Patients With De Novo AML Comparing Standard Therapy Including Gemtuzumab Ozogamicin (GO) to CPX-351 With GO, and the Addition of the FLT3 Inhibitor Gilteritinib for Patients With FLT3 Mutations

NCT04293562·Phase 3
Recruiting

Primary endpoint: Event-free survival (EFS)

InterventionalRandomizedopen1,186 targetStarted 2020-07Completion 2029-0650 sites · United StatesChildren's Oncology Group

A Phase 3 Trial Investigating Blinatumomab (NSC# 765986) in Combination With Chemotherapy in Patients With Newly Diagnosed Standard Risk or Down Syndrome B-Lymphoblastic Leukemia (B-ALL) and the Treatment of Patients With Localized B-Lymphoblastic Lymphoma (B-LLy)

NCT03914625·Phase 3·COSM
Active, not recruiting

Primary endpoint: Disease free survival (DFS) in randomization eligible patients with higher risk features (SR-High) or standard risk average (SR-Avg) B-ALL patients based on randomization with addition of blinatumomab

InterventionalRandomizedopen6,720 targetStarted 2019-07Completion 2027-0950 sites · United StatesNational Cancer Institute (NCI)

A Phase 2 Study of Inotuzumab Ozogamicin (NSC# 772518) in Children and Young Adults With Relapsed or Refractory CD22+ B-Acute Lymphoblastic Leukemia (B-ALL)

NCT02981628·Phase 2
Active, not recruiting

Primary endpoint: Morphologic response (complete response [CR]+ incomplete hematologic recovery [CRi]) following one cycle of treatment with inotuzumab ozogamicin (Cohort 1)

Interventionalopen80 targetStarted 2017-06Completion 2026-1250 sites · United StatesChildren's Oncology Group

A Phase 2 Study of the JAK1/JAK2 Inhibitor Ruxolitinib With Chemotherapy in Children With De Novo High-Risk CRLF2-Rearranged and/or JAK Pathway-Mutant Acute Lymphoblastic Leukemia

NCT02723994·Phase 2·INCY
Completed

Primary endpoint: Part 1: Safety/tolerability of ruxolitinib in combination with chemotherapy as measured by adverse events (AEs), vital signs, clinical laboratory tests, and echocardiograms

Interventionalopen171 enrolledStarted 2016-09Completion 2026-0350 sites · United StatesIncyte Corporation

Total Therapy for Infants With Acute Lymphoblastic Leukemia (ALL) I

NCT02553460·Phase 1/Phase 2·GHRS
Active, not recruiting

Primary endpoint: Percentage of Treatment-related Mortality (TRM)

Interventionalopen50 targetStarted 2016-01Completion 2031-1015 sites · Canada, United StatesSt. Jude Children's Research Hospital

Risk-Stratified Therapy for Acute Myeloid Leukemia in Down Syndrome

NCT02521493·Phase 3
Active, not recruiting

Primary endpoint: Event-free Survival (EFS)

Interventionalopen280 enrolledStarted 2015-12Completion 2027-0650 sites · United StatesChildren's Oncology Group