[c09aa8]: / clusters / clusters9k / clust_73.txt

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Pregnant females are ineligibleXx_NEWLINE_xXNo patients that are known to be pregnant or nursingXx_NEWLINE_xXNot pregnant and not nursingXx_NEWLINE_xXSubject is pregnant, nursing or intends to become pregnant during the course of the study.Xx_NEWLINE_xXPregnant or nursing female patients.Xx_NEWLINE_xXFemale patients who are pregnant or nursingXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant and nursing females.Xx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant and nursing mothers are excluded from this study.Xx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnant or actively nursing an infant are not eligibleXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing mothers are excludedXx_NEWLINE_xXPregnant/nursingXx_NEWLINE_xXPregnant, or nursing female patient Previous treatmentXx_NEWLINE_xXTREATMENT: PregnantXx_NEWLINE_xXPregnant or nursing.Xx_NEWLINE_xXAre pregnant and/or nursingXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXFor female subjects of childbearing potential: Is pregnant or nursingXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXAny patient who is pregnant or who may have plans to become pregnantXx_NEWLINE_xXPregnant and nursing subjects are excludedXx_NEWLINE_xXPregnant/nursing femaleXx_NEWLINE_xXPregnant or planning to become pregnant during period of study participationXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXFemale subjects who are pregnant, intend to become pregnant or are nursingXx_NEWLINE_xXPatients who are pregnant.Xx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXPatients who are pregnant or nursing.Xx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXSubject is pregnant or trying to become pregnant.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients must not be pregnant or nursingXx_NEWLINE_xXNon-pregnant.Xx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXWomen who are pregnant or nursing or plan to become pregnant or nurse during the course of the studyXx_NEWLINE_xXFemale patients will not be eligible for this study if she is either pregnant or nursing at the time of enrollmentXx_NEWLINE_xXFemale patients who are pregnant or nursing.Xx_NEWLINE_xXSubjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.Xx_NEWLINE_xXIf you are pregnant, you will not be enrolled on this studyXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXSubjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infantsXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXMay not be pregnant or nursingXx_NEWLINE_xXBe female and pregnant or nursing.Xx_NEWLINE_xXWomen who are pregnant, nursing, or who plan to become pregnant while in the trialXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXPatient is known to be pregnantXx_NEWLINE_xXNon-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 studyXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatient is pregnantXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatient is pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant females are excludedXx_NEWLINE_xXSubjects who are pregnant or nursingXx_NEWLINE_xXPregnant patients will be excluded from this studyXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXFemale subjects who are pregnant, intend to become pregnant or are nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXPregnant or nursing patientsXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursing are excludedXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPHASE I: Patients must not be pregnant or nursing as the potential of this regimen to harm nursing infants has not been evaluatedXx_NEWLINE_xXPHASE II: Patients must not be pregnant or nursing as the potential of this regimen to harm nursing infants has not been evaluatedXx_NEWLINE_xXSubjects must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.Xx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXSubjects must not be pregnantXx_NEWLINE_xXSubjects who are pregnant or may become pregnantXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing patientsXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXPatient is not pregnantXx_NEWLINE_xXPregnant and nursing mothers are excluded from this studyXx_NEWLINE_xXFemale patients who are either pregnant or nursing.Xx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXFemales who are pregnantXx_NEWLINE_xXNot pregnant and not nursingXx_NEWLINE_xXPatients who are pregnant or nursing (Turnstile I)Xx_NEWLINE_xXSubjects who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXFemales who are pregnant, intend to become pregnant, or are nursing at the time of randomization.Xx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPatients who are pregnant or nursing (Turnstile I)Xx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXFemales who are pregnantXx_NEWLINE_xXAre pregnant and/or nursingXx_NEWLINE_xXPregnantXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPatient who is pregnantXx_NEWLINE_xXPregnant patients (Cohort D)Xx_NEWLINE_xXNot pregnant or nursingXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXFemale subjects who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing at the time of signing informed consentXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXNursing or pregnant females or females who plan pregnancy during the duration of the study.Xx_NEWLINE_xXAre not pregnant or nursing;Xx_NEWLINE_xXPatients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infantsXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXENROLLMENT: Pregnant females.Xx_NEWLINE_xXPatients must not be pregnant or nursingXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXMay not be pregnant or nursingXx_NEWLINE_xXPatients must not be pregnant or nursingXx_NEWLINE_xXSubjects known to be pregnant or nursing.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant or nursing female patients are excluded from this studyXx_NEWLINE_xXDOSE ESCALATION COHORT: Pregnant or nursingXx_NEWLINE_xXDOSE EXPANSION COHORT: Pregnant or nursingXx_NEWLINE_xXNursing womanXx_NEWLINE_xXPregnant or nursing.Xx_NEWLINE_xXNursing and pregnant females. Patients of childbearing potential should practice effective methods of contraception. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing mothersXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPatients who are pregnant or nursing are excludedXx_NEWLINE_xXPatients who are pregnant or nursing are excludedXx_NEWLINE_xXPatients known or found to be pregnantXx_NEWLINE_xXNot pregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPregnant patients are ineligibleXx_NEWLINE_xXPatients 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 womenXx_NEWLINE_xXPregnant and nursing females.Xx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXKnown active or untreated central nervous system (CNS) metastases. - Pregnant, planning to become pregnant within 6 months of treatment, or nursing.Xx_NEWLINE_xXIs a female who is pregnant, nursing, or breastfeeding, or who intends to become pregnant during the participation in the studyXx_NEWLINE_xXPregnant, planning to become pregnant, or nursingXx_NEWLINE_xXPregnant or nursing women. NOTE: If a woman became pregnant or suspects she is pregnant while participating in this study, she must inform her treating physician immediately.Xx_NEWLINE_xXNot pregnant. Must agree not to become pregnant until at least 6 months after ceasing study treatmentXx_NEWLINE_xXNon-pregnant and non-nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXFemales who are pregnant, nursing or breastfeeding, or intend to become pregnant during the participation to the studyXx_NEWLINE_xXPregnant, planning to become pregnant, or nursingXx_NEWLINE_xXIs pregnant or nursingXx_NEWLINE_xXWomen who are pregnant, nursing, or who plan to become pregnant while in the trialXx_NEWLINE_xXIs a female who is pregnant, nursing, or breastfeeding, or who intends to become pregnant during the participation in the studyXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXCurrently pregnant, nursing, or wishing to become pregnant during the studyXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXnot be pregnantXx_NEWLINE_xXPatients must be non-pregnant and non-nursingXx_NEWLINE_xXFemales who are nursing must agree to discontinue nursing before the first dose of GS-5829Xx_NEWLINE_xXPregnant or nursing; orXx_NEWLINE_xXPatient is pregnant or nursing or physiologically capable of becoming pregnant and not using highly effective contraceptionXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXNursing and pregnant femalesXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXFemales who are nursing must agree to discontinue nursing before the first dose of study drugXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXFemale patients who are pregnant or nursing (lactating) are not eligibleXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXParticipants who are pregnant or nursingXx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing.Xx_NEWLINE_xXPregnant or nursing patients will be excluded from the studyXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXFemales who are nursing must agree to discontinue nursing before the first dose of MMBXx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXPatients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXAre not pregnant and do not plan to become pregnant during the clinical trialXx_NEWLINE_xXSubjects must not be pregnantXx_NEWLINE_xXPatient is pregnantXx_NEWLINE_xXPregnant or nursing within past 6 months, or plans to become pregnant in the next yearXx_NEWLINE_xXPatient is a pregnant womanXx_NEWLINE_xXPatient must not be pregnant or nursingXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXAre pregnant or nursing, or intending to become pregnant within the duration of the studyXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients pregnant or nursingXx_NEWLINE_xXPregnant or nursing within past 6 monthsXx_NEWLINE_xXNon-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 controlXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnant, nursing or of child-bearing potentialXx_NEWLINE_xXPregnant females are excludedXx_NEWLINE_xXFemales who are pregnantXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXnot pregnant or nursing; Female participants must not breastfeed during the study and for a period of 30 days following the last dose.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursing.Xx_NEWLINE_xXNot pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPatients who are pregnant;Xx_NEWLINE_xXCurrently pregnant or nursing, or planning pregnancy (in the period up to 6 months) following the index procedure(s),Xx_NEWLINE_xXFemales who are pregnantXx_NEWLINE_xXSubject is nursing or intends to begin nursing during the course of the studyXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXNursing or pregnant.Xx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXPregnant and nursing patients will be excluded from the studyXx_NEWLINE_xXPregnant or nursing patients will be excluded from the studyXx_NEWLINE_xXPregnant, nursing or planning to become pregnantXx_NEWLINE_xXPatients who are pregnant, nursing, or who wish to become pregnant during the studyXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXFemales who are pregnant or nursing.Xx_NEWLINE_xXPregnant or nursing female patients.Xx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXIs nursing or pregnantXx_NEWLINE_xXFemales who are pregnant or currently nursing.Xx_NEWLINE_xXSubjects who are pregnant or may become pregnant during metformin administrationXx_NEWLINE_xXFemales who are pregnant, nursing, or not inclined to use adequate contraceptive methods if necessary to prevent pregnancy during the studyXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXSubjects who are pregnant.Xx_NEWLINE_xXFemales: neither pregnant nor intending to become pregnant during the course of the study, defined as:Xx_NEWLINE_xXPregnant or planning to become pregnantXx_NEWLINE_xXCurrently pregnant or nursing.Xx_NEWLINE_xXIs nursing or pregnantXx_NEWLINE_xXPregnant or nursing females;Xx_NEWLINE_xXpatient was pregnant or nursing at the time of entryXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXFemales who are nursing.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients must not be pregnant or nursingXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPatients must not be pregnant or nursingXx_NEWLINE_xXParticipant is nursing or intends to begin nursing during the course of the studyXx_NEWLINE_xXFemales who are pregnant or nursing a child at Baseline (within 24 hours prior to surgical procedure).Xx_NEWLINE_xXSubject is pregnant or nursing an infantXx_NEWLINE_xXAre pregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXPregnant femalesXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPatients who are pregnant may not be treated on this studyXx_NEWLINE_xXPregnant or nursing mothersXx_NEWLINE_xXPregnant or nursing women. Pregnant and nursing patients are excluded because the effects of CWP232291 on a fetus or nursing child are unknown.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXParticipants who are pregnant or nursingXx_NEWLINE_xXFemale subjects cannot be pregnant or nursing.Xx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXNursing or pregnant females; should a woman become pregnant or suspect she is pregnant while participating in the study, she should inform her treating physician immediatelyXx_NEWLINE_xXNot pregnant or nursingXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligibleXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursing are ineligibleXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXFemales who are nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXFemales who are pregnantXx_NEWLINE_xXSubject is pregnant at time of enrollmentXx_NEWLINE_xXSubject is pregnant, nursing, or planning to get pregnant during study duration.Xx_NEWLINE_xXFemale patients who are pregnant or nursing are not eligible.Xx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXPregnant or nursing female subjects; may be determined in the preoperative evaluationXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXThose who are currently pregnant, have been pregnant within the last 6 months, or are planning to become pregnant in the next 6 months.Xx_NEWLINE_xXNot currently pregnant or planning to become pregnant throughout the duration of cancer treatmentXx_NEWLINE_xXPatient is pregnantXx_NEWLINE_xXPregnant patients will be excludedXx_NEWLINE_xXNon-pregnant femalesXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXParticipant is pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXWomen who are pregnant, lactating/nursing or plan to become pregnantXx_NEWLINE_xXCurrently pregnant, nursing or planning to become pregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnant or thinking about becoming pregnant during the study periodXx_NEWLINE_xXCurrently pregnant or planning to become pregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXSubject is pregnant or nursingXx_NEWLINE_xXNo exclusion criteria for pregnant or nursing patients from participating in this study (of note, pregnant patients will not be treated with vaginal brachytherapy, a requirement for enrolling on this study)Xx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXFemale participants who are pregnant or lactating/nursingXx_NEWLINE_xXNot pregnant or nursingXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXpregnantXx_NEWLINE_xXPregnant or nursing patients will not be included in the studyXx_NEWLINE_xXSelf-report that they are not pregnant or planning to become pregnant in the next four monthsXx_NEWLINE_xXPregnant 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 studyXx_NEWLINE_xXPregnantXx_NEWLINE_xXFemales of childbearing potential who are pregnant or nursingXx_NEWLINE_xXPregnant or planning to become pregnant during the course of the studyXx_NEWLINE_xXPregnantXx_NEWLINE_xXCurrently pregnant, nursing, or wishing to become pregnant during the studyXx_NEWLINE_xXWomen who are pregnant, nursing, or who may become pregnant in the next 3 monthsXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPregnant patients-excluded by historyXx_NEWLINE_xXAre pregnant or intend to become pregnant during the study periodXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXNon-pregnantXx_NEWLINE_xXPatients who are currently pregnantXx_NEWLINE_xXPRELIMINARY TEST: Not currently pregnant or was not pregnant in the last 3 monthsXx_NEWLINE_xXNot currently pregnant or was not pregnant in the last 3 monthsXx_NEWLINE_xXPregnant or possibly pregnantXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXThey do not plan to become pregnant during the study; andXx_NEWLINE_xXBeing pregnantXx_NEWLINE_xXNot pregnant or planning on becoming pregnantXx_NEWLINE_xXPregnant or nursing female participantsXx_NEWLINE_xXNon-pregnant and non-nursingXx_NEWLINE_xXPregnant or planning to become pregnant within the next yearXx_NEWLINE_xXCurrently pregnant. However, participants enrolled who become pregnant after randomization can remain on the study.Xx_NEWLINE_xXBeing pregnant or planning on becoming pregnant within the next yearXx_NEWLINE_xXPregnantXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXNursing or pregnant femalesXx_NEWLINE_xXSubject is pregnant or nursingXx_NEWLINE_xXNursing or pregnant femalesXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXIf a woman is or becomes pregnant or is nursing at any time before or during the treatment period, she will be excluded from the studyXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXPregnantXx_NEWLINE_xXPatient is pregnantXx_NEWLINE_xXPregnant patients will be includedXx_NEWLINE_xXPregnant or nursing participantsXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXPatient is not pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXThe subject is pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXThe patient must not be pregnant or nursingXx_NEWLINE_xXPatients who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnant or are trying to become pregnant are excluded from this studyXx_NEWLINE_xXPregnantXx_NEWLINE_xXHEALTHY VOLUNTEER: Females who are pregnant or nursing or are actively lactatingXx_NEWLINE_xXPATIENT: Females who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXFemale patients who are pregnant or nursingXx_NEWLINE_xXFemale participants/volunteers who are pregnant or nursingXx_NEWLINE_xXFemale patients who are pregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xXPregnant or nursing females.Xx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXPregnant or nursing femalesXx_NEWLINE_xXPregnantXx_NEWLINE_xXIs pregnant;Xx_NEWLINE_xXPatient is pregnant or nursing;Xx_NEWLINE_xXFemales who are pregnant or nursing.Xx_NEWLINE_xXPatients must not be pregnantXx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXPregnant or nursing patients will be excluded from the studyXx_NEWLINE_xXPatient is pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnant or nursing female subjectsXx_NEWLINE_xXPregnantXx_NEWLINE_xXSubjects must not be pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXPregnant or nursing femaleXx_NEWLINE_xXFemales must not be pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXAre pregnant or nursingXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXPatients who are pregnant are excludedXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXKnown pregnant or nursing patientsXx_NEWLINE_xXPregnant patients are to be excludedXx_NEWLINE_xXSubjects who are pregnant or nursingXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPatients who are known to be pregnant.Xx_NEWLINE_xXPregnant or nursing patients will be excluded from the studyXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXPregnant patientsXx_NEWLINE_xXFemales who are pregnant or nursingXx_NEWLINE_xXPregnantXx_NEWLINE_xXPregnantXx_NEWLINE_xXPatients who are pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXBe pregnantXx_NEWLINE_xXPatient who is pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXAre pregnantXx_NEWLINE_xXPregnant or nursingXx_NEWLINE_xXPatients pregnant at the time of enrollmentXx_NEWLINE_xXPregnant or nursing female patientsXx_NEWLINE_xXPregnant patients are excludedXx_NEWLINE_xXPregnant or nursing patients will be excluded from the studyXx_NEWLINE_xXNot pregnantXx_NEWLINE_xXCurrently pregnantXx_NEWLINE_xX