A Study of Alisertib and Paclitaxel in Patients With Small Cell Lung Cancer (SCLC)
← catalyst calendarNCT07465757 · readout in 590 d
Sponsored by Puma Biotechnology, Inc. (industry) · PBYI — their whole pipeline →.
Phase
Phase 2
Status
Not yet recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
50estimated
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
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-09-30 | estimated | When the study began enrolling |
| Primary completion | 2028-03-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-09-30 | estimated | The whole study's end, after follow-up |
| First posted | 2026-03-12 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-03-12 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Small Cell Lung Cancer ( SCLC )
Interventions
- Drug: Alisertib — also filed as PB-8237, MLN8237
- Drug: Alisertib — also filed as PB-8237, MLN8237
- Drug: Alisertib — also filed as PB-8237, MLN8237
- Drug: Alisertib — also filed as PB-8237, MLN8237
- Drug: Alisertib — also filed as PB-8237, MLN8237
- Drug: Paclitaxel
Primary outcome
what the primary-completion date above is the date OFPercentage of Participants with Treatment-Emergent Adverse Events (Adverse Events and Serious Adverse Events)
measured From date of first dose through last dose plus 28 days, assessed up to 24 months
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