Study to Investigate Luveltamab Tazevibulin in Adults With Advanced or Metastatic Non-small Cell Lung Cancer
← catalyst calendarSponsored by Sutro Biopharma, Inc. (industry) · STRO — their whole pipeline →.
Phase
Phase 2
Status
Withdrawn
Study type
Interventional
Design
Na · None · Treatment
Enrollment
0actual
Sites
7
Country
United States
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 | 2024-08-21 | actual | When the study began enrolling |
| Primary completion | 2025-05-01 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-05-01 | actual | The whole study's end, after follow-up |
| First posted | 2024-08-15 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-08-22 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Lung Cancer
- Lung Cancer Metastatic
- Lung Cancer, Nonsmall Cell
- Lung Cancer Non-Small Cell Stage IIIB
- Lung Cancer Non-small Cell Stage IV
- Lung Cancer, Non-small Cell
Intervention
- Drug: Luveltamab tazevibulin — also filed as STRO-002, luvelta
Primary outcome
what the primary-completion date above is the date OFObjective Response Rate (ORR)
measured up to 24 months
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