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Expanded Access to Ziftomenib

Expanded Access to Ziftomenib

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05738538
Enrollment
Unknown
Registered
2023-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Lymphoblastic Leukemia, With Appropriate Mutations, Acute Myeloid Leukemia, With NPM1 Mutations

Brief summary

Requests for single patient expanded access to ziftomenib monotherapy may be considered for eligible adult patients with Acute Lymphoblastic Leukemia (ALL) with KMT2A rearrangements, or Acute Myeloid Leukemia (AML), with NPM1 mutations or KMT2A rearrangements. To request access, use Responsible Party contact information provided in this record. Expanded access for ziftomenib is only available in the United States.

Detailed description

• Subsection Condition: * NPM1 mutation in AML patients * KMT2A rearrangement in AML patients * KMT2A rearrangement in ALL patients

Interventions

Sponsors

Kura Oncology, Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

Inclusion/

Exclusion criteria

* Diagnosed with Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL). * Adult, ages 18+. * Has exhausted appropriate standard treatments without success and no comparable or satisfactory alternative treatment is available or exists to treat the disease or condition. For newly diagnosed AML patients with either NPM1-mutant, or KMT2A-rearranged AML, ziftomenib therapy will be considered for patients not eligible for ongoing clinical trials. In the case of patients with KMT2A-rearranged AML, Expanded Access to ziftomenib will only be provided for use in combination with FDA-approved therapies currently under clinical investigation at Kura Oncology (e.g., venetoclax + azacitidine, cytarabine + daunorubicin). * Is ineligible for participation in any ongoing clinical study of the investigational drug, which includes lack of access due to geographic limitations. * Meets any other pertinent medical criteria for access to the investigational drug, as established by Kura Oncology.

Contacts

Primary ContactClinical Operations
ExpandedAccess@kuraoncology.com617-588-3755

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026