A Study to Evaluate the Safety, Tolerability of INCB160058 in Participants With Myeloproliferative Neoplasms
← catalyst calendarNCT06313593 · readout in 782 d
Sponsored by Incyte Corporation (industry) · INCY — their whole pipeline →.
Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
37actual
Sites
30
Countries
Canada, France, Germany +5
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 | 2024-08-08 | actual | When the study began enrolling |
| Primary completion | 2028-10-09 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-10-09 | estimated | The whole study's end, after follow-up |
| First posted | 2024-03-15 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-12 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Myeloproliferative Neoplasms
Interventions
- Drug: INCB160058
- Drug: Standard disease-directed therapy
Primary outcomes
what the primary-completion date above is the date OFNumber of participants with Dose Limiting Toxicities (DLTs)
measured Up to 28 days
Number of participants with Treatment-emergent Adverse Events (TEAEs)
measured Up to 2 years and 30 days
Number of participants with TEAEs leading to dose modification or discontinuation
measured Up to 2 years and 30 days
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