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.
Women who are pregnant or breast-feeding
Pregnant or breast feeding women are excluded from this study
Women must not be pregnant or breast-feeding
Women must not be pregnant or breast-feeding
Pregnant or breast feeding women
ELIGIBILITY CRITERIA - PHASE I (ARMS A, B, C): Women must not be pregnant or breast-feeding
ELIGIBILITY CRITERIA - PHASE II (ARM D): Women must not be pregnant or breast-feeding
Pregnant or breast-feeding women
Pregnant or breast-feeding women
Pregnant or breast-feeding women, or intending to become pregnant during the study
Pregnant or breast-feeding women.
Women who are pregnant or breast feeding
Women who are pregnant or are breast feeding.
Women who are pregnant or breast-feeding
Women must not be breast-feeding
Pregnant women or women who are breast-feeding
Women who are pregnant or breast feeding.
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women.
Women who are breast feeding.
Pregnant or breast-feeding women
Women who are pregnant or breast-feeding.
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women
Women who are pregnant or breast feeding.
Women must not be pregnant or breast feeding; pregnant women are excluded from this study
Women who are pregnant or currently breast feeding
Pregnant or breast-feeding women
Pregnant or breast-feeding women
Women may not be pregnant or breast-feeding
Women who are pregnant or breast-feeding.
Pregnant or breast-feeding women
Women who are nursing must discontinue breast-feeding prior to the enrollment in the trial
Women must not be pregnant or breast-feeding
Women who are pregnant or breast-feeding at enrollment
Patients must not be women who are pregnant or breast feeding.
Pregnant or breast-feeding women will not be entered on this study due to risks of fetal and teratogenic adverse events as seen in animal/human studies. Women of childbearing age must obtain a pregnancy test and pregnant or breast feeding females are excluded
Pregnant or breast-feeding women
Women who are pregnant or breast feeding
Women who are pregnant or breast feeding
Women who are pregnant or breast-feeding
Pregnant or breast feeding women; women desiring to become pregnant within the time frame of the study are also excluded
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding.
Women who are breast feeding are not eligible
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women
Women who are breast feeding
Pregnant women and women who are breast-feeding
Pregnant or breast-feeding women
Pregnant or breast-feeding women are excluded
Women who are pregnant or breast-feeding
Women who are breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women.
Women who are pregnant or breast feeding.
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding.
Pregnant women or women who are breast-feeding
Women that are currently breast feeding
Pregnant women or women who are breast-feeding
Breast feeding women
Pregnant or breast feeding women due potential damage to the fetus
Breast feeding women
Pregnant, lactating or breast feeding women
Pregnant or breast-feeding women will not be entered on this study
Breast feeding and/or pregnant women
Pregnant or breast-feeding women will not be entered on this study
Pregnant and breast feeding women
Pregnant or breast-feeding women
Are pregnant or breast-feeding women.
Women who are pregnant or are breast-feeding
Pregnant or breast-feeding women
Pregnancy or breast feeding. Due to the potential teratogenic effects of retinoids, pregnant women are NOT eligible. Breast milk feeding by study patient is NOT allowed
Pregnant or breast-feeding women
Women of childbearing potential without effective contraception as well as pregnant or breast feeding women.
Pregnant women or women who are breast-feeding
Pregnant or breast-feeding women
Pregnant women or women who are breast-feeding
Pregnant or breast-feeding women are excluded
Pregnant or breast-feeding women due to the known birth defects association with the treatments used in this study
Women who are breast feeding.
Women who are pregnant or breast feeding
Women who are pregnant or breast feeding
Women who are pregnant or breast-feeding;
Women who are pregnant or breast-feeding
Breast feeding women.
Pregnant or breast-feeding women
Women who are pregnant or breast-feeding
Women who are pregnant or breast feeding.
Pregnant or breast feeding women are excluded from this study
Women who are actively breast feeding
Women who are nursing must discontinue breast-feeding prior to the enrollment in the trial
Women who are breast feeding
Breast feeding women are not eligible
-  Pregnant or breast-feeding women
Women who are pregnant or breast-feeding
Breast feeding women
Women who are pregnant or breast feeding
Women who are pregnant or breast feeding
Women who are pregnant or breast-feeding
Pregnant or breast-feeding (lactating) women or women who plan to become pregnant or breast-feed during the study
Women who are pregnant or breast-feeding
Subject is pregnant or breast-feeding. Women must not breast-feed until at 5 months after completion of study participation..
Women must not be pregnant or breast-feeding
Pregnant or breast-feeding women.
Women who are pregnant or breast feeding.
Pregnant or breast feeding women
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women
Women who are either breast feeding or pregnant.
Women who are pregnant or breast-feeding.
Breast-feeding women
Women who are pregnant or breast feeding are not to be included.
Pregnant or breast-feeding women
Pregnant or lactating/breast-feeding women.
Women who are pregnant or breast feeding
Pregnant or breast-feeding women will not be entered on this study; women of child-bearing age must obtain a pregnancy test, and pregnant or breast feeding females are excluded
Women who are pregnant or breast-feeding
Women must not be pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast feeding
Women who are breast feeding
Women who are pregnant or breast-feeding
Pregnant, lactating, or breast feeding women
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are pregnant or breast feeding
Pregnant or breast-feeding women.
Lactating women who are breast-feeding
Women who are pregnant or breast feeding
Breast feeding women.
Women who are pregnant or breast-feeding and women or men not practicing effective birth control
Pregnant patients or women who are breast-feeding (patients must be postmenopausal)
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding.
Pregnant or breast-feeding women
Pregnant women or women who are breast-feeding
Women of childbearing potential who are pregnant or breast feeding.
For women only - currently pregnant or breast feeding.
Pregnant or breast-feeding women
Pregnant women or women who are breast-feeding
Pregnant or breast feeding women
Women who are pregnant or breast-feeding
Pregnant or breast feeding women
Women who are pregnant or breast-feeding
Breast feeding women;
Pregnant women; breast feeding should be discontinued during treatment
Women who are pregnant or breast-feeding and women or men not practicing effective birth control
Pregnant or breast feeding women
Pregnant or breast-feeding women are excluded
Pregnant or breast-feeding women are ineligible
Women who are pregnant or breast feeding.
Pregnant women or women who are breast-feeding
Women who are pregnant or breast-feeding.
Women who are breast-feeding or pregnant.
Women who are pregnant or breast-feeding.
Women who are pregnant or breast-feeding
Pregnant, lactating or breast feeding women
Women currently pregnant or breast feeding.
Pregnant or breast-feeding women are excluded.
Pregnant or breast-feeding women
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Women who are breast feeding or pregnant as evidenced by pregnancy test.
Pregnant women and women who are breast-feeding
Breast-feeding women
Women who are pregnant or breast feeding.
Pregnant or breast-feeding women
Pregnant or breast feeding women
Women who are pregnant or breast feeding.
Women who are pregnant or breast-feeding
Women who are pregnant or breast feeding are not to be included.
Pregnant women or women presently breast-feeding
Women who are pregnant or breast feeding
Pregnant or breast-feeding women will not be entered on this study
Women who are pregnant or breast-feeding.
Women of childbearing potential who are pregnant or breast feeding.
Pregnant or breast-feeding women and women of childbearing age who are unwilling to use adequate contraception
Breast feeding women
Pregnant and/or breast-feeding women.
Pregnant or breast-feeding women
Pregnant or breast-feeding women will not be entered on this study due to risks of fetal and teratogenic adverse events.
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Pregnant or breast-feeding women.
Pregnant or breast-feeding women
Women who are currently pregnant or breast-feeding
Women who are pregnant or breast feeding or women of childbearing potential (WOCBP) not using 2 reliable forms of birth control
Women who are pregnant or breast feeding.
Pregnant or breast-feeding (lactating) women or women who plan to become pregnant or breast-feed during the study
Women who are pregnant or breast feeding
Women who are pregnant, become pregnant, or are breast-feeding
Women who are currently breast-feeding are not eligible for this study
Breast feeding women.
Women who are pregnant or breast feeding will not be included in the study
Pregnant and breast-feeding women are ineligible
Women who are pregnant or breast feeding
Pregnant women or women who are breast feeding are not eligible for the study
Women who are currently pregnant or breast feeding
Pregnant or breast-feeding women
At the beginning of the study, pregnant women and women who are breast-feeding will not be enrolled
CONTROL (HEALTHY) GROUP: At the beginning of the study, pregnant women and women who are breast-feeding will not be enrolled
Women currently pregnant or breast-feeding at time of study consent
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Breast feeding women
Women who are currently pregnant or breast-feeding
Women must not be pregnant or breast-feeding
Pregnant women or those who are breast feeding
Children, minors, pregnant women, women who are breast feeding, institutionalized patients
Women that are pregnant or breast-feeding
Pregnant, lactating, or breast feeding women
Women who are pregnant or breast-feeding
Women who are pregnant or breast-feeding
Pregnant women or women who are breast-feeding
Pregnant women or women who are breast feeding
Women who are pregnant of breast-feeding
Women who are pregnant or breast feeding
Women who are pregnant or breast-feeding
Women who are either pregnant or breast feeding
Pregnant or breast-feeding women
Women must not be pregnant or breast-feeding
Pregnant or breast feeding women
Women who are pregnant or breast feeding
Pregnant women or women who are breast feeding
Pregnant or breast feeding women
Pregnant or breast-feeding women will not be entered on this study; women of child-bearing age must obtain a pregnancy test and pregnant or breast feeding females are excluded
Woman who are pregnant or breastfeeding
Pregnant or breastfeeding.
Currently pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding, or intending to become pregnant during the study
Pregnant or breastfeeding.
Patients may not be pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Are pregnant or breastfeeding.
Is not pregnant or breastfeeding
Patients must not be pregnant or breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Currently pregnant or breastfeeding
Breastfeeding or pregnant.
Pregnant or breastfeeding, or intending to become pregnant during the study
Subjects that are pregnant or breastfeeding an infant.
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Currently pregnant or breastfeeding
Patients that are pregnant or breastfeeding
Pregnant or breastfeeding, or intending to become pregnant during the study or within 140 days after the last dose of BTRC4017A
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding, or intending to become pregnant during the study
Pregnant or breastfeeding
The participant is pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
WOCBP who are pregnant or breastfeeding.
Pregnant, breastfeeding, or plan to become pregnant during the study duration
Pregnant and/or breastfeeding
DONOR: WOCBP: Pregnant or =< 6 months breastfeeding
Pregnant or breastfeeding
Pregnant and/or breastfeeding
DONOR: Pregnant and/or breastfeeding
Subjects who are pregnant or breastfeeding.
Patients who are pregnant or breastfeeding
Breastfeeding or pregnant
Is pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Subjects who are pregnant or breastfeeding are excluded
Pregnant and/or breastfeeding
DONOR: Pregnant and/or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Is pregnant or breastfeeding
Pregnant or breastfeeding
DONOR: Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding participants
Pregnant or breastfeeding
Pregnant or breastfeeding
ADDITIONAL CRITERIA FOR STUDY CONTINUATION: Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding
PART 1: Pregnant or breastfeeding
PART 2: Pregnant or breastfeeding
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Are pregnant or breastfeeding.
Pregnant or breastfeeding woman.
Pregnant or breastfeeding
Patients who are currently pregnant or breastfeeding.
Are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant and/or breastfeeding
WOCBP: Pregnant or breastfeeding
Pregnant or is breastfeeding
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding.
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Participants who are pregnant or breastfeeding
Pregnant or breastfeeding patients are not eligible
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Subjects who are pregnant or breastfeeding.
Currently pregnant or breastfeeding
Patients who are pregnant or breastfeeding.
Pregnant or breastfeeding
Breastfeeding or pregnant.
Pregnant or breastfeeding
Participants who are breastfeeding, or intending to become pregnant during the study
Is pregnant or breastfeeding.
Pregnant or breastfeeding patients;
Pregnant or breastfeeding
Pregnant or breastfeeding.
are pregnant or breastfeeding
Breastfeeding or pregnant
Pregnant or breastfeeding
Pregnant or breastfeeding
Are pregnant or breastfeeding.
Pregnant and/or breastfeeding
Patients who are pregnant or breastfeeding
Breastfeeding and pregnant.
Breastfeeding or pregnant
WOCBP who are pregnant or breastfeeding
Pregnant and/or breastfeeding
Breastfeeding or pregnant
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Be pregnant or breastfeeding.
Pregnant or breastfeeding.
Are pregnant or breastfeeding
A participant who is pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or patients who are breastfeeding
Is pregnant or breastfeeding
Participant is pregnant or breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Be a woman who is pregnant or breastfeeding
Must not be pregnant or breastfeeding.
Patients who are pregnant or breastfeeding
The participant is pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding patients
Pregnant (positive ?-HCG) or breastfeeding.
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding patients
Currently pregnant or breastfeeding.
Breastfeeding or pregnant.
Breastfeeding or pregnant
Are pregnant or breastfeeding
Are pregnant or breastfeeding.
Participants who are pregnant or breastfeeding
Patients may not be pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding, or intending to become pregnant during the study
Pregnant or breastfeeding
Be pregnant or breastfeeding
Recipient must not be pregnant and/or breastfeeding.
Pregnant (positive total HCG) or breastfeeding
Pregnant and/or breastfeeding
Pregnant, breastfeeding or considering becoming pregnant within 6 months following the last dose of investigational product;
Pregnant or breastfeeding
Pregnant and/or breastfeeding
As per self-report participants who are pregnant or who are breastfeeding
Pregnant or breastfeeding
Not pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Is pregnant or breastfeeding
Patients who are pregnant or breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant, contemplating getting pregnant, or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding
Is pregnant, intends to become pregnant during study, or is breastfeeding
Pregnant and/or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant, contemplating getting pregnant, or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding.
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding
Not pregnant and/or breastfeeding
Pregnant or breastfeeding.
Not pregnant and/or breastfeeding
Pregnant and breastfeeding patients
Pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant and breastfeeding patients
Pregnant or breastfeeding
Pregnant and/or breastfeeding
Is pregnant or breastfeeding
Pregnant or breastfeeding
Not pregnant, not breastfeeding
You are pregnant or breastfeeding
Pregnant or breastfeeding
Pregnant or breastfeeding at time of consent
Patients who are pregnant or breastfeeding
Participants who are breastfeeding, pregnant or trying to become pregnant
Breastfeeding, pregnant, or likely to become pregnant during the study
Pregnant or breastfeeding
Patients may not be pregnant or breastfeeding
Patients who are pregnant or breastfeeding or likely to become pregnant
pregnant or breastfeeding
Participants must not be known to be pregnant or breastfeeding
Pregnant
TREATMENT: Pregnant
Any patient who is pregnant or who may have plans to become pregnant
Not pregnant
Pregnant
Subject is pregnant or trying to become pregnant.
Non-pregnant.
Currently pregnant
Patient is known to be pregnant
Patient is pregnant
Patient is pregnant
Subjects must not be pregnant
Subjects who are pregnant or may become pregnant
Are pregnant
Patient is not pregnant
Pregnant
Patient who is pregnant
Not pregnant
Not pregnant
Women who are pregnant, plan to become pregnant, and/or breastfeed during the study.
Not pregnant. Must agree not to become pregnant until at least 6 months after ceasing study treatment
not be pregnant
Pregnant
Are not pregnant and do not plan to become pregnant during the clinical trial
Subjects must not be pregnant
Patient is pregnant
Patient is a pregnant woman
Are pregnant
The donor is pregnant or lactating, or was pregnant in the previous 6 months, or intends to get pregnant during the study or within 30 days after the last dose of study drug
Pregnant
Pregnant
Subjects who are pregnant or may become pregnant during metformin administration
Subjects who are pregnant.
Females: neither pregnant nor intending to become pregnant during the course of the study, defined as:
Not pregnant
PHASE II: Pregnant (per patient report); if participant becomes pregnant during the course of the study, she will be removed from further participation
Patient is pregnant
Pregnant
Are pregnant
Pregnant
Pregnant
Pregnant
Pregnant
Currently pregnant
Pregnant or thinking about becoming pregnant during the study period
Pregnant
Currently pregnant
pregnant
Pregnant females are ineligible; all subjects of childbearing potential will be asked if they are pregnant or could be pregnant; the patient must respond “no” to continue with radiation and to participate in this clinical study
Pregnant
Pregnant
Participants who are pregnant
Are pregnant or intend to become pregnant during the study period
Non-pregnant
Plan to become pregnant in the next two years, as mammography is not typically performed for screening pregnant women
PRELIMINARY TEST: Not currently pregnant or was not pregnant in the last 3 months
Not currently pregnant or was not pregnant in the last 3 months
Pregnant or possibly pregnant
Currently pregnant
They do not plan to become pregnant during the study; and
Being pregnant
Currently pregnant. However, participants enrolled who become pregnant after randomization can remain on the study.
If female, must not be pregnant, plan to become pregnant, or nurse a child during the study and through 30 days after completion of the study
Pregnant
Are pregnant
Currently pregnant
Women who are pregnant or plan to become pregnant in the study period
Participants who are pregnant
Pregnant
Participants who are pregnant
Patient is pregnant
Are pregnant
Not pregnant
Patient is not pregnant
Patients who are pregnant or are trying to become pregnant are excluded from this study
Pregnant
Currently pregnant
Participants who are pregnant
Pregnant
Is pregnant;
Pregnant
Pregnant
Women who are pregnant or trying to get pregnant
Not pregnant
Are pregnant
Pregnant
Pregnant
Be pregnant
Patient who is pregnant
Are pregnant
Participants who are currently pregnant
Not pregnant
Women who are pregnant or intending to become pregnant during the study
Currently pregnant