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A Phase 1/2 Study of KK2430 in Participants With Hematologic Neoplasms

← catalyst calendar

NCT07629726 · readout ≤ 254 d

Sponsored by Kyowa Kirin Co., Ltd. (industry) · 4151.T — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
72estimated
Sites
1
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

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartAug 2026estimatedWhen the study began enrolling
Primary completionApr 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2027estimatedThe whole study's end, after follow-up
First posted2026-06-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hematologic Neoplasms

Intervention

  • Drug: KK2430

Primary outcomes

what the primary-completion date above is the date OF
Dose Level Toxicity (DLT)
measured Endpoint 28 days after first dose
Adverse Events (AEs)
measured Signing of ICF through study completion for an average of 1.5 years
Pregnancy Test
measured Screening through study completion, an average of 1.5 years
ECG QT Interval
measured Treatment period, an average of 3months
ECG QRS Interval
measured Treatment period, an average of 3months
Vital Sign Measurements
measured Treatment period, an average of 3 months
Vital Sign Measurements
measured Treatment period, an average of 3 months
Vital Sign Measurements
measured Treatment period, an average of 3 months
Vital Sign Measurements
measured Treatment period, an average of 3 months

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