--- a
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+All females must have a negative serum or urine pregnancy test (minimum sensitivity  IU/L or equivalent units of beta-human chorionic gonadotropin [?-hCG]) at the Screening Visit and the Baseline Visit. A pregnancy test needs to be performed within  hours of the first dose of study drug. Females of childbearing potential must agree to use a highly effective method of contraception for the entire study period and for  days after study discontinuation, ie
+Females who are breastfeeding or pregnant at screening or baseline (as documented by a positive beta-human chorionic gonadotropin [beta-hCG] (or human chorionic gonadotropin [hCG]) test with a minimum sensitivity of  IU/L or equivalent units of beta-hCG [or hCG]); a separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic gonadotropin [-hCG] (or human chorionic gonadotropin [hCG]) test with a minimum sensitivity of  International units per liter [IU/L] or equivalent units of -hCG [or hCG]). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic gonadotropin [?-hCG] (or human chorionic gonadotropin [hCG]) test with a minimum sensitivity of  International Units per Liter [IU/L] or equivalent units of ?-hCG [or hCG]). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females who are breastfeeding or pregnant at Screening or Baseline. A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  h before the first dose of study drug.
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [?-hCG] test with a minimum sensitivity of  International Units per Liter [IU/L] or equivalent units of -hCG). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug. Females of childbearing potential (all females will be considered to be of childbearing potential unless they are postmenopausal [amenorrheic for at least  consecutive months, in the appropriate age group, and without other known or suspected cause] or have been sterilized surgically [ie, bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy, all with surgery at least  month before dosing]) who:
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic gonadotropin [-hCG] (or human chorionic gonadotropin [hCG]) test with a minimum sensitivity of  IU/L or equivalent units of -hCG [or hCG]). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug. Cohort B (Combination Expansion): Osteosarcoma participants who progressed in Cohorts  or B and opt to receive combination therapy.
+Pregnancy, breastfeeding, contraception: Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic [?-hCG] or human chorionic gonadotropin [hCG] test with a minimum sensitivity of  International Units per Liter [IU/L] or equivalent units of ?-hCG [or hCG]). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic gonadotropin [-hCG] or human chorionic gonadotropin [hCG] test with a minimum sensitivity of  international units/liter (IU/L) or equivalent units of -hCG [or hCG]). A separate Baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females must not be lactating or pregnant at screening or baseline (as documented by a negative beta-human chorionic gonadotropin [B-hCG] test with a minimum sensitivity of  IU/L or equivalent units of B-hCG). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Pregnant and/or lactating females are excluded; a negative beta-human chorionic gonadotropin [B-hCG]) is required during Screening, and a separate local assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of Test Article
+Females must not be lactating or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [B-hCG] test with a minimum sensitivity of  IU/L or equivalent units of B-hCG). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females must not be breast-feeding or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [B-hCG] test with a minimum sensitivity of  IU/L or equivalent units of B-hCG). A separate baseline assessment is required if a negative Screening pregnancy test was obtained more than  hours before the first dose of study drug.
+All females must have a negative serum or urine pregnancy test (minimum sensitivity  IU/L or equivalent units of beta-human chorionic gonadotropin [?-hCG]) at the screening visit and the baseline visit; a pregnancy test needs to be performed within  hours of the first dose of study drug
+Females must not be lactating or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [B-hCG] (or human chorionic gonadotropin [hCG]) test with a minimum sensitivity of  International units per litre (IU/L) or equivalent units of B-hCG [or hCG]). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive beta-human chorionic gonadotropin [?-hCG] or human chorionic gonadotropin [hCG] test with a minimum sensitivity of  International Units [IU]/L or equivalent units of ?-hCG or hCG). A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.
+Females must not be lactating or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [-hCG] test with a minimum sensitivity of  IU/L or equivalent units of -hCG).
+Females must not be lactating or pregnant at Screening or Baseline (as documented by a negative beta-human chorionic gonadotropin [B-hCG] test with a minimum sensitivity of  IU/L or equivalent units of B-hCG. A separate baseline assessment is required if a negative screening pregnancy test was obtained more than  hours before the first dose of study drug.