STEP I: The following patients will be excluded:\r\n* Pregnant women\r\n* Nursing women
STEP II: The following patients will be excluded:\r\n* Pregnant women\r\n* Nursing women
No patients that are known to be pregnant or nursing
Not pregnant and not nursing
Pregnancy and/or nursing females
Nursing mothers are excluded
Women who are pregnant or nursing
Subject is pregnant, nursing or intends to become pregnant during the course of the study.
Pregnant or nursing female patients.
Female patients who are pregnant or nursing
Pregnant and nursing women are excluded from this study
Pregnant and nursing females.
Pregnant or nursing women
Pregnant or nursing women
Female patients who are pregnant or nursing are not eligible
Pregnant and nursing mothers are excluded from this study.
Pregnant or nursing women
Pregnant or nursing (lactating) women.
Any of the following:\r\n* Pregnant women\r\n* Nursing women
Females who are pregnant or nursing
Patients who are pregnant or actively nursing an infant are not eligible
Nursing women
Pregnant or nursing (lactating) women
Pregnant or nursing
Pregnant or nursing mothers are excluded
Pregnant/nursing
Pregnant, or nursing female patient Previous treatment
Pregnant or nursing.
Pregnant or nursing women.
Are pregnant and/or nursing
Pregnant or nursing women will be excluded from the study
Women who are pregnant or nursing a child may not take part in this study
Pregnant or nursing females
Women who are pregnant or nursing
Pregnant or nursing women will be excluded from the study
Pregnant women are excluded from this study; nursing mothers should stop breastfeeding to be eligible
For female subjects of childbearing potential: Is pregnant or nursing
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing
Pregnant or nursing
Pregnant and nursing subjects are excluded
Nursing women
Pregnant/nursing female
Pregnant or nursing
Pregnant or nursing women are excluded
Patients who are pregnant or nursing
Pregnant or nursing females.
Pregnant or nursing female patients
Pregnant or nursing women
Pregnant or nursing women
Nursing women
Pregnant or nursing female subjects
Pregnant or nursing women
Female subjects who are pregnant, intend to become pregnant or are nursing
Pregnant or nursing women
Pregnant or nursing female participants
Patients who are pregnant or nursing.
Pregnant and nursing women
Pregnant or nursing women
Pregnant or nursing women
Women who are pregnant or nursing are not eligible as treatment involves unforeseeable risks to the fetus or child
Nursing or pregnant women
Patient is pregnant or nursing
Nursing or pregnant women
Pregnant or nursing female subjects
Pregnant or nursing female participants
Women who are pregnant or nursing.
Pregnant or nursing
Patients must not be pregnant or nursing
Pregnant or nursing female participants
Females who are pregnant or nursing
Pregnant or nursing women
Female patients who are pregnant or nursing are not eligible
Women who are pregnant or nursing or plan to become pregnant or nurse during the course of the study
Female patients will not be eligible for this study if she is either pregnant or nursing at the time of enrollment
Female patients who are pregnant or nursing.
Subjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.
Pregnant and nursing women are excluded because of the potential teratogenic effects and potential unknown effects on nursing newborns (please see above paragraph under inclusion criteria regarding WOCBP)
Pregnant or nursing women
Pregnant and nursing women are excluded from this study
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing women
Subjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants
Women who are pregnant or nursing.
Nursing or pregnant women
Any of the following:\r\n* Pregnant women\r\n* Nursing women
May not be pregnant or nursing
Be female and pregnant or nursing.
Pregnant or nursing women
Pregnant or nursing (lactating) women; breastfeeding should be discontinued
Pregnant or nursing women
Women who are pregnant, nursing, or who plan to become pregnant while in the trial
Pregnant or nursing female participants
Pregnant or nursing female participants
Non-pregnant and non-nursing; pregnant and nursing patients may not be enrolled; women and men of reproductive potential must agree to use acceptable forms of contraception during the study
Pregnant or nursing
Female patients who are pregnant or nursing are not eligible
Patients who are pregnant or nursing
Pregnant or nursing women
Nursing women
Pregnant and nursing women are excluded from this study
Pregnant or nursing
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing women
Pregnant or nursing women
Subjects who are pregnant or nursing
Pregnant or nursing women are excluded from this study
Patients who are pregnant or nursing
Female subjects who are pregnant, intend to become pregnant or are nursing
Pregnant or nursing
Subjects must not be pregnant or nursing
Pregnant or nursing patients
Pregnant and nursing women are excluded
Pregnant or nursing
Patients who are pregnant or nursing are excluded
Pregnant or nursing (lactating) women
Pregnant or nursing
PHASE I: Patients must not be pregnant or nursing as the potential of this regimen to harm nursing infants has not been evaluated
PHASE II: Patients must not be pregnant or nursing as the potential of this regimen to harm nursing infants has not been evaluated
Subjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing women
Pregnant or nursing (lactating) women
Nursing women
Patients who are pregnant or nursing
Pregnant or nursing women
Patients who are pregnant or nursing
Pregnant or nursing women.
Pregnant or nursing women
Pregnant or nursing patients
Pregnant women or nursing mothers
Pregnant and nursing mothers are excluded from this study
Female patients who are either pregnant or nursing.
Pregnant or nursing women
Pregnant or nursing women
Pregnant or nursing women
Nursing women may participate only if nursing is discontinued
Women who are pregnant or nursing
Subjects must not be pregnant or nursing
Pregnant or nursing women
Pregnant or nursing
Study drug must not be administered to pregnant women or nursing mothers
Patients who are pregnant or nursing
Subjects must not be pregnant or nursing
Pregnant or nursing (lactating) women
Pregnant women or nursing mothers
Not pregnant and not nursing
Pregnant or nursing (lactating) women
Women who are pregnant or nursing
Patients who are pregnant or nursing (Turnstile I)
Women who are pregnant or nursing.
Subjects who are pregnant or nursing
Pregnant or nursing female subjects
Pregnant women or nursing mothers
Women who are pregnant or nursing
Subjects must not be pregnant or nursing
Females who are pregnant, intend to become pregnant, or are nursing at the time of randomization.
Pregnant or nursing female patients
Patients who are pregnant or nursing (Turnstile I)
Pregnant women or nursing mothers
Patients who are pregnant or nursing
Are pregnant and/or nursing
Pregnant or nursing women are excluded from this study
EXCLUSION CRITERIA FOR REGISTRATION: pregnant or nursing women are excluded from this study
Patient must not be pregnant because of the risk of harm to the fetus; nursing women may participate only if nursing is discontinued, due to the possibility of harm to nursing infants from the treatment regimen; women/men of reproductive potential must agree to use an effective contraception method
Pregnant or nursing (lactating) women
Pregnant or nursing women
Pregnancy or nursing patients will be excluded from the study
Pregnant or nursing women
Pregnancy or nursing
Not pregnant or nursing
Pregnant and nursing women.
Pregnant or nursing female participants
Pregnancy or nursing
Women who are pregnant or nursing
Female subjects who are pregnant or nursing
Women who are pregnant or nursing
Pregnant or nursing at the time of signing informed consent
Lactating females must agree to discontinue nursing
Pregnant or nursing women
Pregnant or nursing females.
Nursing or pregnant females or females who plan pregnancy during the duration of the study.
Pregnant or nursing women.
Nursing women
Are not pregnant or nursing;
Patients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants
Pregnant or nursing
Pregnant or nursing
Female patients who are pregnant or nursing are not eligible
Patients must not be nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants
Patients must not be pregnant or nursing
May not be pregnant or nursing
Patients must not be pregnant or nursing
Subjects known to be pregnant or nursing.
Pregnant or nursing
Pregnant or nursing females
Nursing women who are unwilling to discontinue nursing
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing female patients are excluded from this study
ARM A: Pregnant or nursing women
ARM B: Pregnant or nursing women
DOSE ESCALATION COHORT: Pregnant or nursing
DOSE EXPANSION COHORT: Pregnant or nursing
Any of the following:\r\n* Pregnant women\r\n* Nursing women
Pregnant or nursing women
Pregnant or nursing women
Pregnant women are excluded from this study; nursing women are excluded from this study
Nursing woman
Pregnant women are excluded from this study; nursing women are excluded from this study
Any of the following:\r\n* Pregnant women\r\n* Nursing women
Pregnant or nursing.
Women who are pregnant or nursing
Pregnant or nursing women
Pregnant or nursing
Pregnant or nursing mothers
Pregnant or nursing women
Women who are pregnant or are nursing
Pregnant or nursing female patients
Women who are pregnant or nursing
Patients who are pregnant or nursing are excluded
Pregnancy or nursing Mother
Patients who are pregnant or nursing are excluded
Pregnant/nursing women are excluded from this study because oxaliplatin is an agent with the potential for teratogenic or abortifacient effects
Pregnant and nursing women are excluded from this study
Not pregnant or nursing
Pregnant women or nursing mothers
Pregnant or nursing
Pregnant or nursing
Patients who are pregnant or nursing
Patients of childbearing potential, not practicing adequate contraception, patients who are pregnant or patients who are nursing are not eligible for this trial; bevacizumab should not be administered to nursing women
Pregnant and nursing females.
Patients who are pregnant or nursing
Is a female who is pregnant, nursing, or breastfeeding, or who intends to become pregnant during the participation in the study
Pregnant or nursing (lactating) women
Pregnant, planning to become pregnant, or nursing
Pregnant or nursing (lactating) women
Pregnant or nursing women
Non-pregnant and non-nursing
Pregnant or nursing
Females who are pregnant, nursing or breastfeeding, or intend to become pregnant during the participation to the study
Pregnant or nursing women.
Pregnant, planning to become pregnant, or nursing
Pregnant or nursing women
Is pregnant or nursing
Women who are pregnant, nursing, or who plan to become pregnant while in the trial
Is a female who is pregnant, nursing, or breastfeeding, or who intends to become pregnant during the participation in the study
Pregnant or nursing
Pregnant or nursing female participants
Women who are pregnant or nursing.
No women who are pregnant or nursing
Currently pregnant, nursing, or wishing to become pregnant during the study
Pregnant or nursing female participants
Pregnant women or nursing women
Women who are pregnant or nursing (lactating).
Patients must be non-pregnant and non-nursing
Pregnant women and/or nursing patients will be excluded from the study
Females who are nursing must agree to discontinue nursing before the first dose of GS-5829
Pregnant or nursing; or
Women who are pregnant or nursing
Patient is pregnant or nursing or physiologically capable of becoming pregnant and not using highly effective contraception
Patients who are pregnant or nursing
Nursing and pregnant females
Pregnant or nursing (lactating) women.
Pregnancy or nursing
Pregnant or nursing
Females who are nursing must agree to discontinue nursing before the first dose of study drug
Women who are pregnant or nursing/breastfeeding
Pregnant or nursing women
Pregnant or nursing females.
Women who are pregnant or nursing (lactating) women
Female patients who are pregnant or nursing (lactating) are not eligible
Pregnant or nursing women will be excluded from the study
Female patients who are pregnant or nursing are not eligible
Female patients who are pregnant or nursing are not eligible
Participants who are pregnant or nursing
Subjects must not be pregnant or nursing
Pregnant or nursing
Women that are pregnant or nursing
Pregnant or nursing.
Pregnant and nursing women
Pregnant or nursing patients will be excluded from the study
Any of the following\r\n* Pregnant women\r\n* Nursing women
Pregnant or nursing women will be excluded from the study
Patients who are pregnant or nursing
Pregnant women and nursing mothers
Pregnant or nursing (lactating) women
Pregnant or nursing women
Pregnant or nursing females
Pregnant and nursing women are excluded from this study
Pregnant or nursing (lactating) women
Patients who are pregnant or nursing
Females who are nursing must agree to discontinue nursing before the first dose of MMB
Pregnant or nursing female subjects
Patients who are pregnant or nursing are not eligible
Pregnant or nursing
Nursing women
Pregnant and nursing women are excluded from this study
Women who are pregnant or nursing/breastfeeding.
Pregnant or nursing (lactating) women
Pregnant or nursing (lactating) women
Pregnant or nursing within past 6 months, or plans to become pregnant in the next year
Pregnant or nursing (lactating) women
Pregnant or nursing women
Pregnant women and nursing women are excluded from this study
Patient must not be pregnant or nursing
Are pregnant or nursing, or intending to become pregnant within the duration of the study
Pregnant or nursing
Pregnant or nursing
Patients pregnant or nursing
Pregnant or nursing (lactating) women.
Pregnant or nursing women
Pregnant or nursing within past 6 months
Non-pregnant and non-nursing; pregnant or nursing patients may not be enrolled; women and men of reproductive potential should agree to use an effective means of birth control
Pregnant or nursing women
Patients who are pregnant or nursing
Pregnant or nursing (lactating) women.
Nursing female.
Pregnant or nursing women
Pregnant or nursing females
Nursing women
Pregnant women and nursing patients will be excluded
Patient is pregnant or nursing
not pregnant or nursing; Female participants must not breastfeed during the study and for a period of 30 days following the last dose.
Pregnant or nursing
Patients who are pregnant or nursing.
Nursing women
Not pregnant or nursing
Nursing women.
Pregnant or nursing women
Pregnancy and/or nursing mothers
Pregnant or nursing (lactating) women
Subject is nursing or intends to begin nursing during the course of the study
Pregnant or nursing
Pregnant or nursing (lactating) women
Pregnancy or nursing
Pregnant or nursing female patients
Nursing or pregnant.
Pregnant or nursing women may not participate in this trial
Pregnant or nursing female subjects
Pregnant and nursing patients will be excluded from the study
Pregnant or nursing patients will be excluded from the study
Pregnant, nursing or planning to become pregnant
Pregnant or nursing women.
Patients who are pregnant, nursing, or who wish to become pregnant during the study
Nursing women
Patients who are pregnant or nursing
Is, within 2 weeks prior to Day 1, nursing.
Pregnant and nursing women are excluded from this study
Females who are pregnant or nursing.
Pregnant or nursing female patients.
Pregnant or nursing women
Pregnant or nursing female patients
Pregnant or nursing women
Pregnant or nursing
Is nursing or pregnant
Females who are pregnant or currently nursing.
Pregnant or nursing women.
Pregnant or nursing women
Pregnant or nursing (lactating) women
Pregnant or nursing females
Women who are pregnant and/or nursing
Pregnant women or nursing women
Currently pregnant or nursing.
Is nursing or pregnant
Pregnant or nursing females;
patient was pregnant or nursing at the time of entry
Pregnant or nursing women; breastfeeding must be discontinued prior to treatment
Pregnant or nursing females.
Females who are nursing.
Pregnant or nursing
Patients must not be pregnant or nursing
Pregnant or nursing female patients
Patients must not be pregnant or nursing
Participant is nursing or intends to begin nursing during the course of the study
Subject is pregnant or nursing an infant
Are pregnant or nursing
Pregnant or nursing women
Pregnant or nursing
Pregnant or nursing females.
Women who are pregnant or nursing.
Pregnant or nursing women
Pregnant or nursing mothers
Pregnant or nursing women. Pregnant and nursing patients are excluded because the effects of CWP232291 on a fetus or nursing child are unknown.
Pregnant or nursing
Participants who are pregnant or nursing
Pregnant or nursing women Part 3 Exclusion Criteria:
Pregnant or nursing women Part 4 Exclusion Criteria:
Pregnant or nursing women
Pregnant or nursing women
Female subjects cannot be pregnant or nursing.
Pregnant or nursing
Pregnant or nursing women will be excluded from study.
Not pregnant or nursing
Pregnant or nursing women are excluded
Women who are pregnant or nursing (pregnancy test to be performed within 24 hours prior to HIFU treatment)
Pregnant and nursing women
Female patients who are pregnant or nursing are not eligible
Pregnant or nursing female patients
Patients who are pregnant or nursing
Women who are pregnant or nursing (pregnancy test to be performed within 24 hours prior to HIFU treatment)
Patients who are pregnant or nursing are ineligible
Pregnant or nursing female patients
Pregnant or nursing female patients
Females who are nursing
Pregnant or nursing
Pregnant or nursing
Patient is pregnant or nursing
Subject is pregnant, nursing, or planning to get pregnant during study duration.
Female patients who are pregnant or nursing are not eligible.
Known pregnancy or nursing
Patient is pregnant or nursing
Pregnant or nursing women
Pregnant or nursing female subjects; may be determined in the preoperative evaluation
Pregnant or nursing female participants
Pregnant or nursing women
Participant is pregnant or nursing
Pregnant or nursing women
Women who are pregnant, lactating/nursing or plan to become pregnant
Currently pregnant, nursing or planning to become pregnant
Pregnant women will be excluded; nursing patients will be included
Pregnant or nursing women
Pregnant and nursing women
Pregnant or nursing female patients
Women who are known to be pregnant or nursing
Nursing women
Pregnant or nursing female patients
Subject is pregnant or nursing
Nursing women
Pregnant or nursing (lactating) women
Women who are pregnant or nursing; pregnancy will be confirmed by urine test
Female participants who are pregnant or lactating/nursing
Women who are nursing
Women who are nursing
Not pregnant or nursing
Pregnant or nursing patients will not be included in the study
Females of childbearing potential who are pregnant or nursing
Currently pregnant, nursing, or wishing to become pregnant during the study
Women who are pregnant, nursing, or who may become pregnant in the next 3 months
Pregnant women or nursing women
Women who are pregnant or nursing
Pregnant or nursing female participants
Women who are pregnant or nursing, or intend to be/do so during the course of the study
Women who are pregnant or nursing
Non-pregnant and non-nursing
Pregnant or nursing women
Pregnancy or nursing women
Nursing women
Pregnant or nursing women
Pregnant or nursing (lactating) women
Nursing or pregnant females
Subject is pregnant or nursing
Nursing or pregnant females
Pregnant or nursing (lactating) women.
Pregnant or nursing
Pregnant or nursing
If a woman is or becomes pregnant or is nursing at any time before or during the treatment period, she will be excluded from the study
Women who are pregnant or nursing except when the indication is an abnormal cell-free DNA test
Females who are pregnant or nursing
Females who are pregnant or nursing
Women who are pregnant or nursing
Pregnant or nursing participants
Pregnant or nursing
Pregnant or nursing
Nursing female subjects
Females who are pregnant or nursing
Pregnant or nursing (lactating) women
Patient is pregnant or nursing
Pregnant or nursing
Pregnant or nursing
Pregnant or nursing females
The patient must not be pregnant or nursing
Pregnant and/or nursing women
Patients who are pregnant or nursing
HEALTHY VOLUNTEER: Females who are pregnant or nursing or are actively lactating
PATIENT: Females who are pregnant or nursing
Pregnant or nursing female
Female patients who are pregnant or nursing
Female participants/volunteers who are pregnant or nursing
Female patients who are pregnant or nursing
Pregnancy or nursing patients
Pregnant or nursing
Women who are pregnant or nursing
Pregnant or nursing females.
Pregnant or nursing (lactating)
Pregnant or nursing female
Pregnant or nursing female
Pregnant or nursing female
Pregnant or nursing female
Pregnant or nursing females
Pregnant or nursing female
Pregnant or nursing females
Pregnant or nursing women
Patient is pregnant or nursing;
Females who are pregnant or nursing.
Patient is pregnant or nursing
Females who are pregnant or nursing
Pregnancy or nursing mothers
Pregnant or nursing patients will be excluded from the study
Patient is pregnant or nursing
Pregnant or nursing female subjects
Women who are pregnant or nursing
Subjects must not be pregnant or nursing
Pregnant or nursing female
Pregnant or nursing
Are pregnant or nursing
Females who are pregnant or nursing
Pregnant or nursing
Known pregnant or nursing patients
Subjects who are pregnant or nursing
Pregnant or nursing patients will be excluded from the study
Females who are pregnant or nursing
Pregnant or nursing women
Pregnant or nursing
Pregnant and nursing women
Pregnant or nursing women
Pregnant or nursing
Pregnant or nursing
Pregnant or nursing
Pregnant or nursing female patients
Pregnant or nursing patients will be excluded from the study