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A drug, venetoclax, to treat non-Hodgkin's lymphoma (NHL) that has come back (relapsed) or has not gotten better with treatment (refractory) in people taking an oral contraceptive (ethinyl estradiol/levonogestrel)

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18 and older

Phase 1

3 Locations

NCT03557619

Clinical Trial Goal


To find out:
  • The highest dose of ethinyl estradiol/levonorgestrel that’s safe to give with venetoclax 
  • If venetoclax changes the effectiveness of an oral contraceptive (ethinyl estradiol/levonogestrel)

You may be able to join this trial if you:


  • Are 18 years or older 
  • Were assigned female at birth
  • Have NHL that has relapsed or is refractory. Some examples include:
    • Diffuse large B-cell lymphoma (DLBCL)
    • Follicular lymphoma
    • Lymphoplasmacytic lymphoma (LPL)
    • Mantle cell lymphoma (MCL)
    • Marginal zone lymphoma (MZL)
    • T-cell prolymphocytic lymphoma
    • Waldenstrom's macroglobulinemia 
  • Have not had an autologous (your own cells) or allogeneic (cells from a donor) blood or marrow transplant (BMT) in the last 3 months
  • Agree to have other standard tests done to see if you can be in the clinical trial 

Trial Details


Ethinyl estradiol/levonorgestrel is an oral contraceptive containing progestin and estrogen used to prevent pregnancy. 
Venetoclax is a small molecule inhibitor that blocks BCL2 in certain cells.

You’ll get:
  • Ethinyl estradiol/levonorgestrel – A pill that you take by mouth 2 times
  • Venetoclax –  A pill that you take by mouth 1 time each day

You'll have scans to see how well the treatment is working. The clinical trial doctors will check your health for up to 2 months.

The Food and Drug Administration (FDA) has approved all of the drugs used in this trial.

Contacts


ABBVIE CALL CENTER, 844-663-3742, abbvieclinicaltrials@abbvie.com

Locations


Duplicate_Henry Ford Health System /ID# 209090COMPLETED

Detroit, Michigan

Dartmouth-Hitchcock Medical Center /ID# 169097COMPLETED

Lebanon, New Hampshire

Gabrail Cancer Center Research /ID# 207039COMPLETED

Canton, Ohio

ClinicalTrials.gov record


NCT03557619. First posted on 6/15/18

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