Currently breast feeding.
The subject is pregnant or breast feeding
Pregnant or breast-feeding
Patients who are pregnant or breast-feeding
Patients found to be pregnant/breast feeding
Patients who are breast feeding
Pregnant or breast feeding or plans to become pregnant within 6 months of AVB-620 administration.
Not breast feeding at any time during the study.
Not currently pregnant or breast feeding
Not breast feeding at any time during the study.
Not breast feeding at any time during the study.
Breast feeding or pregnant
Patients who are pregnant or breast-feeding will NOT be eligible for participation
Patients who are pregnant or breast-feeding
Pregnant or breast feeding.
The participant is pregnant or breast-feeding
The subject is pregnant or breast-feeding
Pregnant or breast feeding
The participant is pregnant or breast-feeding
Participant is breast feeding or pregnant.
Not pregnant or breast feeding
Not breast feeding at any time during the study.
Breast feeding
The patient is pregnant or breast feeding.
Subject is pregnant or breast-feeding.
Pregnant or breast feeding
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding.
Pregnant and breast-feeding patients are not eligible for the study
Pregnant or breast-feeding
Pregnant or breast feeding.
Breast feeding or pregnant.
Pregnant or breast feeding
Pregnant or breast feeding
Pregnant or breast-feeding woman will not be entered on this study
The patient is pregnant or breast-feeding
Pregnant or breast feeding
Pregnant or breast-feeding
Subject is pregnant, breast-feeding or lactating.
Patient is pregnant or breast-feeding
Patients who are pregnant or breast feeding
Breast feeding after pregnant
Patient is pregnant or breast feeding.
Pregnant or currently breast-feeding
Pregnant or breast feeding
Pregnant or breast feeding
Pregnant or breast feeding
Currently pregnant or breast-feeding
Pregnant and breast-feeding subjects
Pregnant or breast-feeding
Patients must not be pregnant/breast feeding and must agree to practice adequate contraception.
Patient is pregnant or breast-feeding
Breast feeding or pregnant
Pregnant or breast feeding
DONOR: Pregnant or breast-feeding
Patient is pregnant or breast-feeding
Not breast feeding
DONOR: Not breast feeding
Pregnant or breast feeding
Patient is pregnant or breast-feeding
Breast feeding or pregnant
Pregnant or currently breast-feeding
Pregnant or breast-feeding
Pregnant, lactating or breast feeding woman
Patient is pregnant or breast-feeding
Pregnant or breast feeding
Subjects who are pregnant or breast-feeding
Patient is breast feeding.
The patient is pregnant or breast-feeding
Breast feeding
Breast-feeding, pregnant, or likely to become pregnant during the study
Pregnant or breast-feeding
Patient is pregnant or breast-feeding
Pregnant or breast-feeding
TREATMENT: Pregnant or breast feeding
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding patients
The subject is pregnant or breast-feeding
Not breast feeding
DONOR: Not breast feeding
DONOR: Pregnant or breast-feeding
Patients who are pregnant or breast-feeding.
Patients who are pregnant or breast-feeding.
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding patients
Pregnant or breast-feeding patients are excluded from this study
Not pregnant or breast-feeding
Pregnant or breast feeding
Patient is pregnant or breast-feeding.
Pregnant or breast-feeding
Pregnant or breast-feeding
Pregnant or breast-feeding
Pregnant or breast-feeding.
Pregnant or breast feeding
Individuals who are pregnant or breast feeding or who become pregnant while enrolled on this trial will be excluded from participation
Pregnant or breast feeding
Pregnant or breast feeding
Participants cannot be breast feeding
Pregnant or breast-feeding
Pregnant or breast-feeding patients
Patients known or found to be pregnant or who is unwilling to stop breast-feeding
Patients who are pregnant or breast-feeding
Currently breast feeding.
They are pregnant or breast feeding.
Patients that are pregnant, breast feeding, or unwilling to use effective contraception during the study
Patients who are pregnant or breast-feeding
Patients who are pregnant or breast feeding
Is pregnant or breast-feeding
Currently pregnant or breast-feeding
The patient is pregnant or breast feeding.
Pregnant or breast-feeding
Patients who are breast-feeding
Subject is pregnant or breast feeding
Pregnant or breast feeding
Pregnant or breast-feeding
Subject is pregnant or breast feeding
Patients who are pregnant or breast-feeding.
Pregnant or breast feeding patients
Subjects are pregnant or breast-feeding at entry.
The patient is pregnant or breast feeding.
Not pregnant or breast-feeding
Is pregnant or breast-feeding
Pregnant or breast feeding at time of consent
Patient is pregnant or breast-feeding.
Participant is pregnant or breast feeding.
Pregnant or breast feeding
Patient is pregnant or breast-feeding
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding patients
Pregnant or breast-feeding
The subject is pregnant or breast-feeding
Breast feeding or pregnant
Breast feeding or pregnant.
Breast feeding or pregnant
Subjects who are pregnant or breast feeding.
Pregnant or breast-feeding
Pregnant patients or currently breast-feeding
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding patients
Patients who are pregnant or breast-feeding
Patients who are pregnant or breast-feeding
Patients who are pregnant or breast feeding are NOT eligible for participation
Pregnant or breast-feeding
Pregnant or breast-feeding
Patients who are breast-feeding
Patients who are pregnant or breast-feeding will NOT be eligible for participation
Pregnant, inadequate contraception, breast feeding
Pregnant or breast feeding
Pregnant or breast feeding
Breast feeding must be discontinued
Pregnant or breast feeding
A woman who is pregnant or breast feeding
Pregnant or intending to become pregnant or breast-feeding patents
Breast feeding
Subject who is pregnant or breast feeding
Pregnant or breast-feeding patients.
Pregnant or breast feeding
Patients who are pregnant or breast-feeding
Pregnant or breast-feeding
Is pregnant or breast-feeding
Pregnant or breast feeding
Pregnant or breast-feeding
Subjects who are pregnant or are breast-feeding
Pregnant or breast-feeding
Patients may not be pregnant or breast feeding
are pregnant or breast-feeding.
Are pregnant and or breast feeding.
Patients who are pregnant or breast-feeding.
Pregnant or breast feeding
Subjects who are pregnant or breast feeding.
Pregnant or breast feeding within the projected duration of trial participation through 4 months after the last dose of study treatment.
Is pregnant or breast feeding
Currently pregnant or breast-feeding.
Pregnant or breast feeding
Pregnant or breast feeding
Breast feeding
Not breast feeding
DONOR: Not breast feeding
Patient is breast feeding
Not breast feeding
Pregnant or breast-feeding
Is pregnant or breast-feeding
Pregnant or breast feeding
Pregnant or breast feeding
Pregnant or breast feeding
Pregnant or breast feeding
The patient is pregnant or breast feeding.
Subjects who are pregnant or are breast-feeding.
Not breast feeding
DONOR: Not breast feeding
Patients who are pregnant or breast-feeding
Pregnant or breast feeding.
Pregnant or breast feeding
Pregnant or breast-feeding
Not pregnant or breast-feeding
pregnant or breast feeding
Patients must not be pregnant or breast feeding and must practice adequate contraception
Patient is pregnant or nursing/breast-feeding.
Pregnant or breast feeding
Pregnant or breast-feeding.
If you are pregnant or breast feeding
Patient is pregnant or breast-feeding
Currently pregnant or breast-feeding
Pregnant or breast feeding
Must not be pregnant or breast feeding
May not be pregnant, lactating or breast feeding
Not pregnant or breast?feeding
Pregnant or breast feeding
Pregnant or breast-feeding
Pregnant or breast feeding
Patients who are pregnant or breast feeding
Females who are pregnant, breast-feeding or intending to become pregnant; this exclusion criterion will be assessed by questioning the patient about the pregnancy status, breast-feeding status, the intent to become pregnant, the menopausal status, and the date of the last menstrual period
Pregnant or breast feeding
Pregnant or breast-feeding.
Subject is not pregnant or breast feeding, and cannot become pregnant within 30 days after the end of treatment
Pregnant patients or actively breast-feeding
Pregnant or breast feeding
Breast feeding
Pregnant or breast feeding
Pregnant and/or breast-feeding
Patient is pregnant or breast-feeding
Not be currently pregnant or breast feeding
Pregnant or breast-feeding
Pregnant or breast feeding
Pregnant or breast feeding
Breast feeding
Is pregnant or breast feeding
Patient must NOT be pregnant or breast-feeding
Not pregnant or breast feeding
Pregnant or currently breast-feeding
Breast-feeding
Breast-feeding
Subjects who are pregnant or breast feeding
No breast-feeding
Not pregnant or breast-feeding
Not pregnant or breast feeding
Breast feeding
Pregnant or breast-feeding
OVARIAN CANCER PARTICIPANTS: Patient is pregnant or breast-feeding
BREAST CANCER PARTICIPANTS: Patient is pregnant or breast-feeding
Not breast-feeding, if applicable
Pregnant or breast feeding.
Patients who are pregnant or are breast feeding
Is breast-feeding or pregnant
Subjects who are pregnant or breast feeding
The patient is pregnant or breast feeding
Pregnant or breast-feeding
Participant is pregnant or breast-feeding
Patients who are breast feeding
Pregnant or breast feeding
Patient is pregnant or breast-feeding.