Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
AbbVie (prior sponsor, Abbott)
This is an open-label extension study of navitoclax in subjects with chronic lymphocytic leukemia (CLL).
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
The subject has been dosing in Arm C of the ABT4710n study, has not discontinued for any reason prior to study closure and the investigator believes that continued treatment with navitoclax is in the best interest of the subject
The subject must meet defined hematology and coagulation lab criteria as specified in the protocol
The subject must meet defined chemistry criteria as specified in the protocol
Women of childbearing potential and men must agree to use adequate contraception (as per protocol) prior to study entry, for the duration of study participation and up to 90 days following completion of therapy
The subject is capable of understanding and complying with parameters as outlined in the protocol and able to sign the Informed Consent Form
You may not be if
The subject discontinued navitoclax administration in Arm C of the ABT4710n study for reasons of disease progression, Adverse Event toxicity, withdrawal of consent or Investigator decision prior to study completion.
The subject has any medical condition which in the opinion of the investigator places the subject at an unacceptably high risk for toxicities.
