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A Study to Assess the Effect of Venetoclax on Ethinyl Estradiol and Levonorgestrel in Female Participants With Different Hematological Malignancies

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NCT03557619

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Na · None · Basic science
Enrollment
12estimated
Sites
4
Countries
Australia, 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
Start2019-07-30actualWhen the study began enrolling
Primary completion2026-03-21estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-03-21estimatedThe whole study's end, after follow-up
First posted2018-06-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-08-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hematologic Malignancies

Interventions

  • Drug: Venetoclax — also filed as ABT-199, GDC-0199, Venclexta
  • Drug: ethinyl estradiol/levonorgestrel — also filed as Levora

Primary outcomes

what the primary-completion date above is the date OF
Tmax of Venetoclax
measured Up to approximately 59 days after initial study drug dose
Tmax of (ethinyl estradiol) EE/Levonorgestrel
measured Up to approximately 59 days after initial study drug dose
Cmax of Venetoclax
measured Up to approximately 59 days after initial study drug dose
Cmax of EE/Levonorgestrel
measured Up to approximately 59 days after initial study drug dose
t1/2 of Venetoclax
measured Up to approximately 59 days after initial study drug dose
t1/2 of EE/Levonorgestrel
measured Up to approximately 59 days after initial study drug dose
AUCt of Venetoclax
measured Up to approximately 59 days after initial study drug dose
AUCt of EE/Levonorgestrel
measured Up to approximately 59 days after initial study drug dose
AUCinf of EE/Levonorgestrel
measured Up to approximately 59 days after initial study drug dose

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