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a b/clusters/3009knumclusters/clust_122.txt
1
Adequate bone marrow, cardiac, kidney and liver function
2
Adequate liver function, including:
3
Patients must have adequate renal function with serum creatinine level =< IULN within 21 days prior to registration
4
Adequate liver function must be demonstrated, defined as:
5
Subjects must have adequate renal function defined as a serum creatinine based on age/gender
6
Adequate bone marrow, kidney, and liver function
7
Adequate liver function must be demonstrated, defined as:
8
Liver function test must be obtained within 14 days prior to registration
9
Adequate hematological and biological function, confirmed by the following laboratory values within 96 hours prior to enrollment: Bone Marrow Function
10
Adequate bone marrow, renal, and liver function
11
Adequate bone marrow, kidney and liver function
12
Adequate bone marrow, kidney and liver function
13
Acceptable liver function:
14
Adequate bone marrow, liver and kidney function
15
Adequate renal function as evidenced by a serum/plasma creatinine < 1.5 x ULN
16
Acceptable liver function:
17
Adequate bone-marrow, renal and liver function.
18
Adequate renal function
19
Adequate blood coagulation function
20
Adequate liver function
21
Participants have adequate bone marrow, kidney and liver function.
22
Adequate performance status and hematological, liver, and kidney function
23
Adequate renal function
24
Adequate coagulation function
25
Acceptable hematological function:
26
Acceptable liver function:
27
Adequate bone marrow, kidney and liver function
28
Adequate renal function:
29
Adequate cardiovascular, hematological, liver and renal function
30
Good kidney and liver function
31
Adequate liver function:
32
Adequate Bone Marrow, Renal, and Liver Function.
33
Acceptable liver and renal function
34
Must have adequate bone marrow, liver, and renal function as described in protocol
35
Adequate renal function
36
Adequate liver function
37
Adequate bone marrow, cardiac, kidney and liver function
38
Adequate renal function
39
Acceptable liver function, as specified below:
40
Adequate liver function defined by:
41
Adequate liver and renal function
42
Inadequate liver function as evidenced by any of the following:
43
Adequate Bone Marrow, Liver, Renal, Pancreatic Function
44
Adequate Renal & Liver Function.
45
Adequate renal function within 28 days prior to study registration defined by either of the following criteria:
46
Combination Arm: adequate heart function
47
Adequate pulmonary and cardiac function
48
Adequate renal function.
49
Severe impairment of your kidney or liver function
50
Hematological function:
51
Acceptable liver function at Screening,
52
Have acceptable liver function defined as:
53
Patients must have adequate bone marrow, kidney, and liver function, (within 14 days prior to registration), defined as:
54
Acceptable liver function:
55
Acceptable liver function, serum creatinine and hematological status
56
Adequate organ function defined as absolute neutrophil count ?1,500×10^6/L, absolute lymphocyte count ?500/mm^3, and platelet count ?100,000×10^6/mm^3. Adequate liver function defined as aspartate aminotransferase and alanine aminotransferase ?2.5× the upper limit of institutional normal, bilirubin ?1.5 mg/dL or 25 µmol/L. Adequate renal function defined as blood urea nitrogen and serum creatinine of ?1.5 mg/dL or 130 µmol/L.
57
Subjects must have adequate liver function as defined by:
58
Subjects must have adequate renal function
59
Adequate bone marrow, liver, renal, and cardiac function at study entry, assessed as follows:
60
Adequate cardiac, hematological, liver and renal function
61
Adequate bone marrow, renal and liver function
62
Adequate liver function as demonstrated by:
63
Adequate bone marrow reserve, liver and renal function
64
Inadequate renal function as defined by serum creatinine > 3x normal for age
65
Acceptable liver function:
66
Adequate hematological function, defined as:
67
Adequate liver function, defined as:
68
Adequate renal function, defined as:
69
Adequate coagulation function
70
Adequate renal function
71
Adequate bone marrows, liver and renal function as assessed by the following laboratory requirements. Hemoglobin ?8.0 g/dL (may not be transfused or treated with erythropoietin in preceding week to maintain or exceed this level)
72
Must have adequate coagulation, hematology, kidney, and liver function, per protocol.
73
Liver function:
74
Adequate renal function.
75
Adequate renal function
76
Adequate liver function
77
Adequate hematological function
78
High screening liver function tests
79
Adequate renal function:
80
Adequate bone marrow, liver, and renal function.
81
Adequate renal function including creatinine < 2 unless related to the disease
82
Adequate bone marrow, liver, and renal function
83
Good kidney and liver function
84
Adequate bone marrow, renal, and liver function
85
Participant must have adequate liver function as demonstrated by:
86
Adequate bone marrow, liver and renal function
87
Adequate bone marrow, renal and liver function.
88
Subject has adequate liver function defined as:
89
Subject has adequate pulmonary function defined as:
90
Normal liver, kidney and bone marrow function
91
Participants must have adequate renal function, defined as:
92
Participants must have adequate liver function, defined as:
93
Adequate organ function, hematologic status, coagulation status, kidney function, and liver function as follows:
94
Adequate liver function:
95
Adequate bone marrow reserve, cardiac, liver, renal and metabolic function:
96
Acceptable liver function within 7 days of day 1 of therapy defined as:
97
Adequate marrow, liver, and renal function:
98
Participant must have adequate liver function as demonstrated by:
99
Patients must have adequate bone marrow, liver, coagulation and renal function within 7 days prior to study registration, as defined below:
100
Inadequate liver function at screening as demonstrated by the following:
101
Adequate renal function
102
Renal Function as follows:
103
Adequate renal function defined as follows:
104
Inadequate liver, renal function as defined below for both cohorts:
105
Adequate renal function, as indicated by creatinine =< 1.5 x ULN
106
Adequate liver function:
107
Adequate renal function:
108
Adequate renal function with creatinine (Cr) =< 2.5 mg/dL
109
Hematological function:
110
Renal function:
111
Adequate renal function assessed by: serum creatinine ? 1.5 × ULN
112
Adequate renal function: creatinine ?1.5 x ULN
113
Impaired renal function
114
Reproductive function:
115
Adequate blood cell counts, kidney function, liver function and Eastern Cooperative Oncology Group (ECOG) score of 0 or 1 (for the Recommended Phase 2 Cohort, a ECOG score of 2 may be allowed on a case-by-case basis)
116
Adequate bone marrow function, renal and liver functions
117
Renal Function:
118
Have adequate renal function as defined by the following criterion:
119
Adequate marrow function
120
Adequate bone marrow, liver and kidney function
121
Renal
122
Adequate organ function as defined below: • Liver function: a. Total bilirubin < 2.0 mg/dL (34 µmol/L) b. AST and/or ALT <3 x ULN
123
Adequate liver function as evidenced by:
124
Adequate renal function:
125
Adequate Renal Function:
126
Adequate Liver Function:
127
Evidence of inadequate renal function (creatinine > 2 g/dL)
128
Renal function: preservation of renal function, serum creatinine did NOT increase by more than 2 fold above the normal reference range
129
Renal function criteria: preservation of renal function, serum creatinine did NOT increase by more than 2 fold above the normal reference range
130
Subjects must have adequate liver function as defined by:
131
Subjects must have adequate renal function defined as: Serum creatinine based on age/gender.
132
Patients are required to have adequate renal function as indicated by a serum creatinine =< 2.5 mg/dL; this value must be obtained within four weeks before protocol entry
133
Adequate bone marrow, liver, renal and coagulation function
134
Impaired heart function
135
Acceptable liver function
136
Acceptable renal function
137
Patient must have adequate renal function as defined by serum creatinine < -2.5 mg/dl obtained within 28 days prior to registration
138
Liver function test must be obtained within 14 days prior to registration
139
Renal Function: Adequate renal function in the opinion of the Investigator with no clinically significant renal impairment or uncontrolled renal disease.
140
Immunological Function: Adequate immune system function in the opinion of the Investigator with no known immunodeficiency disease.
141
Adequate bone marrow, renal and liver function.
142
Adequate renal function, defined as:
143
Adequate liver function, defined as:
144
Adequate liver function at Cycle 1 Day 1 pre-dosing defined as:
145
Acceptable renal function
146
Acceptable liver function
147
Adequate hematological, liver and kidney function.
148
Adequate hematological, liver, and kidney function
149
Adequate liver and renal function
150
Acceptable liver function
151
Adequate renal, liver and bone marrow function:
152
Have adequate values, bone marrow, renal and liver functions at screening as defined below:
153
Adequate liver and renal function and hematology laboratory values
154
Adequate liver function
155
Adequate renal function
156
Adequate bone marrow, renal and liver function.
157
Adequate bone marrow, liver, and renal function, as documented by the following laboratory assessments conducted within 28 days prior to dosing:
158
Adequate bone marrow, liver and renal function.
159
The patient has adequate pulmonary function
160
Adequate renal functions
161
Patients must have adequate renal function defined as age-adjusted serum creatinine =< 1.5 x normal for age
162
Have adequate renal function
163
Patient has adequate bone marrow, coagulation, liver and renal function
164
Acceptable renal function
165
Acceptable liver function
166
Adequate performance status and hematological, liver and kidney functions
167
Adequate liver and renal function
168
Adequate bone marrow function (absolute neutrophil count > 1,500/mm3 and platelet count of > 100,000/mm3), adequate liver function [ALT and AST <3 x upper limit normal (ULN), alkaline phosphatase <2 x ULN, and total bilirubin <1.5 mg/dL], & adequate renal function (BUN and creatinine <1.5 x ULN)
169
Adequate bone marrow, liver, kidney function
170
Liver function < 3 x normal
171
Renal function: CrCl < 15 ml/min.
172
Adequate renal function: serum creatinine =< 1.5 x ULN
173
Inadequate lung function
174
Inadequate renal function
175
Subject has adequate renal function, which is defined as:
176
Subjects must have adequate hematopoietic function as evidenced by:
177
Subjects must have adequate liver function, including all of the following:
178
Adequate bone marrow, kidney and liver function
179
Patients must have adequate heart, kidney, liver and bone marrow function.
180
Adequate Bone Marrow, Pancreatic Function, Renal Function and Liver Function.
181
Adequate hematological, renal, and liver function
182
Subject must have adequate kidney and liver function as described in the protocol
183
Renal function defined as:
184
Liver function defined as:
185
Have adequate coagulation function.
186
Have adequate renal function as defined by creatinine clearance >30 milliliters/minute.
187
Adequate hematological, liver, and renal function
188
Adequate renal function, defined as serum creatinine ?1.5x ULN or GFR >50 mL/min
189
Acceptable liver and renal function:
190
Adequate liver function:
191
Adequate blood clotting function
192
Bone marrow impairment, renal impairment, liver function abnormality and impaired cardiac function as defined in the protocol
193
Adequate liver function
194
Abnormal liver function test results
195
Adequate major organ function (normal or minimal alteration in liver, kidney, hematological, metabolic and cardiac function)
196
Adequate hematological, liver and kidney function.
197
Adequate cardiovascular function
198
Adequate renal, liver, and bone marrow function according to the following criteria:
199
Inclusion Criteria:\n\n        Patients with histologically or cytologically confirmed advanced solid malignancy or\n        Lymphoma\n\n        Relapsed or refractory disease after at least 1 prior systemic treatment for the primary\n        malignancy and not a candidate for other curative treatment.\n\n        Adequate hematologic status\n\n        Adequate coagulation function\n\n        Adequate hepatic function\n\n        Adequate renal function\n\n        Exclusion Criteria:\n\n        Known primary tumors of central nervous system disease\n\n        Known active brain metastases\n\n        Known cardiopulmonary disease
200
Adequate liver, bone marrow and renal function
201
Adequate liver function:
202
Participants with Hepatitis B or C are eligible on the condition that they have adequate liver function as defined by Inclusion Criterion 9.
203
Adequate bone marrow, renal, liver and pancreatic function
204
Adequate liver and renal function
205
Have adequate organ function including hematology, renal, and liver.
206
Adequate bone marrow, liver, and renal function as assessed by the following laboratory requirements:
207
Abnormal hematological, renal, or liver function
208
Adequate liver function
209
Adequate renal function
210
Renal function: • Creatinine less than or equal to 1.5 x ULN
211
Inadequate renal or liver function
212
Acceptable renal function
213
Acceptable liver function
214
Adequate bone marrow, kidney and liver function
215
Adequate liver function, defined as:
216
Adequate cardiac function as assessed clinically
217
Adequate cardiac function as measured by echocardiogram
218
Inadequate hematological, liver, renal, cardiac function
219
Adequate coagulation function
220
Adequate renal function
221
Eligible study subjects must exhibit acceptable liver, renal, and coagulation function as assessed by laboratory tests.
222
Has a history or presence of inadequate liver, renal, hematopoietic and/or cardiac function parameters outside protocol-defined range
223
Inadequate hematologic function, renal function, and liver function
224
Adequate bone marrow, liver and renal function
225
Adequate renal function (defined as serum creatinine =< 1.5 X ULN)
226
Adequate bone marrow function, renal and liver functions
227
Adequate hematological and biological function
228
Adequate liver, kidney, and bone marrow function
229
Adequate bone marrow, liver and renal function
230
Adequate bone marrow, liver, and renal functions.
231
Adequate renal function within 28 days prior to registration for protocol therapy defined by either of the following criteria:
232
Inadequate liver, renal or bone marrow function within 2 weeks of first dose
233
Patient has adequate renal function defined as: Serum creatinine ?1.5 the institutional ULN
234
Inadequate renal function
235
Subject must have adequate liver function as demonstrated by:
236
Adequate liver function
237
Inadequate renal function
238
Renal
239
Inadequate bone marrow, renal, or liver function
240
Adequate hematological function defined as:
241
Adequate liver function defined as:
242
Acceptable liver function defined as:
243
Adequate bone marrow, kidney and liver function.
244
Performance Status of 0 or 1 - Adequate bone marrow, kidney and liver function
245
Adequate liver function, defined as both of the following:
246
Adequate bone marrow, renal, and liver function.
247
Adequate renal function
248
Adequate liver function
249
Adequate cardiac function
250
Adequate neurologic function
251
Adequate pancreatic function
252
Adequate liver function, defined as:
253
Adequate bone marrow, liver and renal function renal function
254
Adequate cardiac function
255
Adequate bone marrow, liver and renal function as assessed by the following laboratory tests conducted within 7 days before randomization.
256
Abnormal heart function
257
Adequate bone marrow, liver and renal function as assessed within 7 days before starting study treatment
258
Adequate renal function, defined as serum creatinine ?1.5x ULN
259
Adequate renal function
260
Adequate organ function (bone marrow, kidney and liver)
261
Adequate kidney function
262
Adequate liver function
263
Normal pancreatic function
264
Patients must have adequate renal function (creatinine < 1.5 mg/dL) before starting therapy and the test must be performed within 14 days prior to registration
265
Renal
266
Inadequate liver function at screening and Day 1 (before drug administration) as demonstrated by:
267
Adequate haematological, renal (creatinine < 2xULN), cardiac and liver functions
268
Abnormal/inadequate blood values, liver and kidney function
269
Adequate cardiac and renal function
270
abnormal/inadequate blood values, liver, and kidney function
271
Adequate liver function (bilirubin less than or equal to 3.0 mg/dl, unless considered due to tumor), and renal function (creatinine less than or equal to 3.0 mg/dl, unless considered due to tumor)
272
Adequate cardiac function as assessed clinically.
273
Adequate Bone Marrow, Renal and liver Functions.
274
Adequate liver, kidney, and bone marrow function
275
Participants must have adequate liver, kidney, and bone morrow function
276
Adequate bone marrow, renal and liver function.
277
Adequate hematological, liver and kidney function.
278
Adequate renal function.
279
Adequate glucose control, bone marrow, kidney, liver, and heart function.
280
Inadequate heart function
281
Inadequate lung function
282
Adequate hematological function, defined as:
283
Adequate liver function, defined as:
284
Adequate bone marrow, liver and renal function
285
Adequate hematological function, defined as:
286
Adequate liver function, defined as:
287
Adequate hematological, liver, and renal function
288
Adequate bone marrow, liver and renal function
289
Adequate renal and liver function
290
Must have adequate hematological function
291
Must have adequate renal function
292
Patients must be suitable candidates for treatment with standard regimens; this includes having adequate hematologic parameters, liver function and renal function based on labs that are deemed acceptable for treatment by the investigators
293
Adequate bone marrow, kidney and liver function
294
Severe impairment of your kidney or liver function
295
Adequate white blood cell counts (with low blast counts), liver function, and renal function
296
Acceptable hematological status, liver and renal function as defined in the protocol
297
Adequate bone marrow function [absolute neutrophil count (ANC) > 1,500/mm3 & platelet count of > 100,000/mm3], adequate liver function [alanine aminotransferase (ALT) & aspartate aminotransferase (AST) <3 x upper limit normal (ULN), alkaline phosphatase <2 x ULN, & total bilirubin <1.5 mg/dL], & adequate renal function (BUN & creatinine <1.5 x ULN)
298
Adequate bone marrow, renal, liver, cardiac and pulmonary function.
299
Inadequate renal function (Blood creatinine > 1.5 times the institutional ULN)
300
Adequate renal function
301
Have adequate bone marrow function, liver function, and renal function, as measured by the following laboratory assessments conducted within 7 days prior to the initiation of study treatment:
302
Adequate bone marrow, kidney, liver, and heart function.
303
Acceptable liver function
304
Acceptable renal function
305
Adequate renal function
306
Acceptable liver function:
307
Adequate bone marrow, liver and renal function
308
Adequate renal function, defined by serum creatinine ? 1.5 x ULN.
309
Adequate hematological, renal and liver function
310
Patients must have adequate liver function
311
Patients must have adequate renal function as defined by a serum creatinine =< 1.5 times ULN within one week prior to treatment
312
Adequate bone marrow, liver and renal function
313
Adequate coagulation function as defined by the following criteria:
314
Adequate blood, liver, and kidney function as defined by laboratory tests.
315
Subjects must have adequate liver function
316
Subjects must have adequate kidney function
317
Adequate bone marrow, liver, and renal function
318
Adequate liver function, defined as:
319
Patients must have adequate bone marrow function (ANC >/= 1,500/mm3 and platelet count of >/= 100,000/mm3), adequate liver function (SGPT and serum glutamate oxaloacetate transaminase (SGOT) </= 2.5 times normal, bilirubin </= 2 mg/dl), and adequate renal function (BUN and creatinine </=1.5 times institutional normal) prior to starting therapy.
320
Adequate bone marrow, liver, and renal functions
321
Adequate bone marrow, liver, and renal functions, defined as:
322
Inadequate hematopoietic, liver, endocrine or renal function
323
Inadequate lung function
324
Inadequate heart function
325
Adequate bone morrow and kidney function
326
Adequate bone marrow, liver, cardiac, and renal function
327
Adequate haematological, liver and renal function
328
Adequate renal function
329
Adequate liver, renal and cardiac function
330
Adequate bone marrow, kidney and liver function
331
Patient must have adequate renal function documented by a serum creatinine of ? 1.5 times the ULN for the reference lab.
332
Adequate hematological, renal and liver function For solid tumors only:
333
Impaired bone marrow, liver or renal function (as defined by protocol)
334
Reproductive Function
335
Adequate renal function
336
Adequate liver function
337
Adequate cardiac function
338
normal immune function
339
Acceptable bone marrow, liver and kidney function.
340
Adequate renal function
341
Adequate liver function within 72 hours of enrollment, defined as:
342
Adequate renal function, defined as serum creatinine ? 1.5x ULN
343
Adequate hematological and biological function; LVEF ?50%
344
Acceptable renal function
345
Acceptable liver function
346
Adequate cardiac function:
347
Inadequate bone marrow, liver, and renal function, as assessed by the following laboratory parameters:
348
Impaired heart function
349
Adequate bone marrow, renal and liver functioning
350
Chemistry, liver function tests, renal function, total CPK and hematology lab results must be ? Grade 1 at the time of screening;
351
Adequate bone marrow and renal function
352
Adequate bone marrow, renal and liver function
353
Adequate bone marrow, kidney, and liver function
354
Adequate hematology, liver and renal function laboratory values within 14 days prior to first dose of study treatment.
355
Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements conducted within 7 days of starting the study treatment:
356
Adequate liver function as demonstrated by
357
Have adequate complete blood counts and liver function tests
358
Have adequate cardiac function
359
Has adequate organ function (bone marrow, kidney and liver)
360
Inadequate lung function
361
Adequate bone marrow, and liver function as assessed by the following laboratory requirements conducted within 7 days of starting the study treatment
362
For subjects with SEVERELY IMPAIRED renal function:
363
Protocol-defined renal , liver and bone marrow function
364
Adequate hematological function (as defined in the study protocol)
365
Adequate renal function (as defined in the study protocol)
366
Adequate liver function (as defined in the study protocol)
367
Have adequate cardiac, bone marrow, liver and kidney function
368
Abnormal heart function
369
Renal:
370
Adequate bone marrow, liver, and renal function within the 14 days prior to Day 1 of Cycle 1 of study drug up until pre-dose of Cycle 1
371
Renal function, as follows:
372
Liver function:
373
Renal function:
374
Adequate hematological function unless inadequate function is due to underlying disease
375
Adequate bone marrow, liver, and renal function
376
Adequate hematological and biological function
377
Abnormal renal function tests (creatinine > 1.5)
378
Inclusion Criteria:\n\n          -  Life expectancy of at least 3 months\n\n          -  Histological or cytological documentation of advanced solid tumors\n\n          -  ECOG Performance Status of ? 1 (ECOG: Eastern Cooperative Oncology Group)\n\n          -  Adequate bone marrow, liver and renal function\n\n          -  Women of childbearing potential and men must agree to use adequate contraception
379
Adequate liver and renal functions
380
Hematological function, as follows:
381
Adequate hematological, renal and liver function
382
Adequate hematological function
383
Adequate renal function:
384
Normal renal function: estimated CrCl ?90 ml/min
385
Participants with adequate hematological, liver, and renal function
386
Adequate liver function, defined as:
387
Adequate bone marrow, renal and liver function as defined in the protocol.
388
Renal Function Creatinine >1.5 mg%
389
Adequate bone marrow, liver and renal function
390
Adequate liver function, as indicated by bilirubin =< 1.5 x ULN
391
Adequate Renal function
392
Inadequate kidney, liver, blood clotting function
393
Adequate renal function.
394
Adequate cardiac function.
395
Adequate renal function.
396
Adequate pulmonary function
397
Patients must have acceptable neutrophil and platelet counts as well as adequate kidney and liver function.
398
Inadequate liver function as evidenced by any of the following:
399
Hepatic and renal function meeting the strata as outlined below; nota bene (NB): patients must fulfill both total bilirubin and serum glutamic-oxaloacetic transaminase (SGOT)/aspartate aminotransferase (AST) criteria and creatinine function to be included in a group; however, if a patient’s total bilirubin and SGOT/AST and creatinine levels indicate different groups, the patient may be enrolled in the indicated group with the greatest degree of liver dysfunction; all liver and renal function tests must be completed within 24 hours prior to the start of treatment; Note: patients on dialysis will not be eligible\r\n* Group A: hepatic function: normal function (bilirubin =< upper limit of normal [ULN]; AST =< ULN); renal function: normal function (creatinine clearance [CrCl] >= 60 mL/min) \r\n* Group B: hepatic function: normal function (bilirubin =< ULN; AST =< ULN); renal function: moderate dysfunction (CrCl >= 30 and < 60 ml/min)\r\n* Group C: hepatic function: normal function (bilirubin =< ULN; AST =< ULN); renal function: severe dysfunction (CrCl >= 15 and < 30 ml/min)\r\n* Group D: hepatic function: mild dysfunction D1: bilirubin =< ULN; AST > ULN, D2: bilirubin > ULN and =< 1.5 x ULN; any AST; renal function: normal function (creatinine clearance [CrCl] >= 60 mL/min)\r\n* Group E: hepatic function: mooderate dysfunction (bilirubin 1.5 x > ULN and =< 3 x ULN; any AST); renal function: normal function (creatinine clearance [CrCl] >= 60 mL/min)\r\n* Group F: hepatic function: severe dysfunction (bilirubin > 3 x ULN and up to investigator’s discretion; any AST); renal function: normal function (creatinine clearance [CrCl] >= 60 mL/min)
400
Patients with solitary kidneys, bilateral renal tumors, compromised renal function (baseline creatinine > 1.4)
401
Have adequate liver function defined as:
402
Have adequate heart function defined as:
403
Adequate hematologic and organ function, including blood counts, liver and kidney function Stage I Arm A (GDC-0077):
404
Renal function at screening and enrollment as defined by the Modification of Diet in Renal Disease (MDRD) equation.
405
Adequate liver function:
406
Impaired heart function
407
Normal kidney and liver function (lab results must be within 45 days prior enrollment)
408
Adequate renal and liver function as indicated by:
409
Adequate bone marrow, liver, and renal function, as assessed by the following requirements conducted within 21 days prior to dosing:
410
Adequate bone marrow, liver, and renal functions
411
Adequate bone marrow, liver, cardiac, and renal function
412
Patients must have normal renal function test and no prior renal disease; the screening cut off for serum creatinine is < 1.5 mg/dL
413
Patients with normal renal function according to MD Anderson testing standards and no prior renal disease
414
Adequate bone marrow, liver, and renal function
415
Adequate bone marrow, liver and kidney function
416
Participants with renal insufficiency or failure, as determined by a point of care renal function blood test.
417
Liver: Subjects must have adequate liver function
418
Renal: Adequate renal function
419
Cardiac and pulmonary function that is adequate for ASCT
420
Adequate renal function
421
Adequate hematological, liver and kidney function.
422
Adequate bone marrow reserves and liver and kidney function, as assessed by the following laboratory requirements:
423
Compromised renal function
424
Patients must have adequate liver function as defined by AST or ALT <10x normal
425
Have adequate bone marrow reserves and liver and kidney function, as assessed by the following laboratory requirements:
426
Inadequate renal function
427
Adequate renal function: serum creatinine ? 1.5x ULN;
428
Adequate bone marrow, liver and renal function
429
Participants with renal insufficiency or failure, as determined by a point of care renal function blood test
430
Adequate performance status and hematological, liver, and kidney function
431
Good kidney and liver function
432
Adequate renal function within 28 days prior to C1D1
433
Adequate hematopoietic function within 7 days prior to C1D1
434
Adequate bone marrow, liver, and kidney function within 2 weeks prior to first dose
435
Adequate liver function:
436
Adequate hematological, liver, and renal functions
437
Adequate renal function defined as:
438
Adequate liver function defined as:
439
Adequate function of kidney:
440
Adequate function of liver:
441
Adequate liver function:
442
Adequate bone marrow, kidney and liver function
443
Adequate bone marrow, liver, and renal function