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Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN

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NCT03386513

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
179actual
Sites
28
Countries
France, Germany, Italy +3

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
Start2018-01-02actualWhen the study began enrolling
Primary completion2023-09-06actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-30estimatedThe whole study's end, after follow-up
First posted2017-12-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-12-16actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Blastic Plasmacytoid Dendritic Cell Neoplasm
  • Myeloproliferative Neoplasm

Intervention

  • Drug: IMGN632

Primary outcome

what the primary-completion date above is the date OF
To assess the rate of composite CR in BPDCN patients
measured 21-day cycle

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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