Luveltamab Tazevibulin (STRO-002) in Infants and Children < 12 Years of Age With Relapsed/Refractory CBFA2T3::GLIS2 AML
← catalyst calendarSponsored by Sutro Biopharma, Inc. (industry) · STRO — their whole pipeline →. With Children's Oncology Group, Innovative Therapies For Children with Cancer Consortium.
Phase
Phase 1/2
Status
Terminated
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
24actual
Sites
36
Countries
Austria, Canada, Denmark +6
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Why the sponsor stopped it
Terminated Early
As filed on the registry record, in the sponsor's own words.
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-12-04 | actual | When the study began enrolling |
| Primary completion | 2025-06-01 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-06-01 | actual | The whole study's end, after follow-up |
| First posted | 2024-11-07 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-08-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Acute Myeloid Leukemia (AML)
Intervention
- Drug: Luveltamab tazevibulin — also filed as STRO-002, Luvelta
Primary outcome
what the primary-completion date above is the date OFEvaluate efficacy of luveltamab tazevibulin monotherapy
measured Up to 12 weeks
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