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a b/clusters/3009knumclusters/clust_210.txt
1
Ability to swallow entrectinib intact
2
Unable or unwilling to swallow napabucasin capsules daily.
3
Patients must be able to swallow tablets whole
4
Patients must be able to swallow capsules
5
Patients unable to swallow capsules whole are not eligible; nasogastric or gastric (G) tube administration is not allowed
6
Patients must be able to swallow tablets or capsules; a patient with any gastrointestinal disease that would impair ability to swallow, retain, or absorb drug is not eligible
7
Patients must be able to swallow whole capsules
8
Patients must be able to swallow tablets
9
Patients must be able to swallow tablets
10
Ability to swallow abiraterone acetate tablets as a whole
11
Patients must be able to swallow intact capsules
12
Patients who are unable to swallow whole tablets are not eligible
13
Patients who are unable to swallow intact tablets are not eligible
14
Patients must be able to swallow intact tablets
15
Patients must be able to swallow intact tablets
16
Patients must be able to swallow intact tablets
17
Patients must be able to swallow intact capsules
18
Patients must be able to swallow intact tablets
19
Able to swallow capsules
20
Inability to swallow capsules or known gastrointestinal malabsorption
21
Ability to swallow tablets
22
Able to swallow ribociclib capsules
23
Patients must be able to swallow tablets
24
Eligible patients have a body surface area >= 0.7 m^2 AND be able to swallow whole tablets at the time of study enrollment
25
Patients who are unable to swallow whole tablets are not eligible
26
Patient must be able to swallow capsules
27
Subjects who are unable to swallow pills
28
Ability to swallow the investigational product tablets.
29
Participants must be able to swallow ribociclib capsules or tablets
30
Inability to swallow intact tablets
31
Able to swallow capsules
32
Inability or unwillingness to swallow capsules; patients with any condition that may impair the ability to swallow or absorb oral medications/investigational product including:\r\n* Any lesion, whether induced by tumor, radiation or other conditions, which makes it difficult to swallow capsules or pills;\r\n* Prior surgical procedures affecting absorption including, but not limited to major resection of stomach or small bowel;\r\n* Active peptic ulcer disease;\r\n* Malabsorption syndrome
33
Able to swallow capsules
34
Inability to swallow intact tablets
35
The subject is unable to swallow capsules.
36
Ability to swallow pills or capsules
37
Participant is unable to swallow or absorb oral tablets.
38
Inability to swallow capsules
39
Subject is unable to swallow pills
40
Must be able to swallow ribociclib and everolimus capsules/tablets
41
Inability to swallow gelatin capsules, or any medical condition that interferes with normal gastrointestinal absorption
42
Must be able to swallow LEE011 and everolimus capsules/tablets
43
Patients must have the ability to swallow tablets
44
Patients who are unable to swallow tablets or liquid are not eligible.
45
Patients must be able to swallow capsules; nasogastric or gastrostomy feeding (G) tube administration is not allowed
46
The participant is unable to swallow tablets that are whole (do not crush or chew or administer via nasogastric [NG]-tube)
47
Gastrointestinal disorder affecting absorption or the ability to swallow tablets
48
Patients must be able to swallow tablets (or applesauce, if part of bioavailability \crushed\ six patient cohort)
49
Unable or unwilling to swallow napabucasin capsules daily.
50
Unable or unwilling to swallow tablets as per dosing schedule
51
Subjects that cannot swallow tablets.
52
Subject is unable to swallow or absorb oral tablets normally
53
Ability to swallow pills/capsules
54
Inability to swallow capsules, since capsules cannot be crushed or broken
55
Unable or unwilling to swallow tablets or capsules
56
Patients must be able to swallow capsules
57
Able to swallow tablets.
58
Patient must be able to swallow capsules
59
Patients who are unable to swallow erlotinib tablets are not eligible
60
Patients must be able to swallow whole tablets or capsules; nasogastric or gastrostomy tube (G-tube) administration is not allowed
61
Patients must be able to swallow whole tablets or capsules; nasogastric or gastrostomy tube (G-tube) administration is not allowed; any gastrointestinal disease which would impair ability to swallow, retain, or absorb drug is not allowed
62
Are able to swallow capsules
63
Participant must be able to swallow tablets or capsules. A participant with any gastrointestinal disease that would impair ability to swallow, retain, or absorb drug is not eligible.
64
Patients who are unable to swallow tablets or have a gastrointestinal disease that could hinder the absorption of enzalutamide.
65
Ability to swallow oral tablets without difficulty
66
Unable to swallow capsules or disease significantly affecting gastrointestinal function
67
Patients must be able to swallow intact tablets
68
Patients who are not able to swallow intact tablets are not eligible
69
Patients must be able to swallow intact capsules
70
Patients must be able to swallow capsules
71
Unable to swallow tablets.
72
Are able to swallow capsules.
73
Inability to swallow intact tablets
74
Unable to swallow or take anything orally
75
Unable or unwilling to swallow tablets or capsules
76
Inability to swallow intact tablets
77
Inability to swallow intact tablets
78
Men unable to swallow pills
79
Has an inability to swallow tablets or capsules
80
Patients who are unable to swallow pills
81
Able to swallow intact capsules
82
Inability to swallow capsules, since capsules cannot be crushed or broken
83
The subject is unable to swallow capsules
84
Unable or unwilling to swallow tablets
85
Able to swallow bicalutamide and ribociclib capsules/tablets.
86
Patient must be capable of swallowing the ruxolitinib capsules (tablets)
87
Be able to swallow tablets.
88
Must be able to swallow pills or capsules
89
The subject is unable to swallow tablets
90
Ability to swallow capsules unless enrolled in Part E
91
Part E: Any patient unable to swallow capsules who otherwise meet all other eligibility criteria for Part A (expansion) B, C or D
92
Patients must be able to swallow whole capsules; nasogastric or gastrointestinal (G)-tube administration is not allowed
93
Is unable to swallow capsules or malabsorption syndrome, disease or condition significantly affecting gastrointestinal function
94
Able to swallow capsules
95
Is unable to swallow capsules or malabsorption syndrome, disease or condition significantly affecting gastrointestinal function
96
Are able to swallow capsules and tablets.
97
Patients must be able to swallow AZD1775 capsules
98
Ability to swallow and retain capsules.
99
Patients must be able to swallow intact tablets; patients who cannot swallow intact tablets are not eligible
100
Ability to swallow capsules
101
Inability to swallow capsules, since capsules cannot be crushed or broken
102
PART 2 GROUP 1 INCLUSION CRITERIA: Subjects taking capsule formulations must be able to swallow capsules
103
PART 2 GROUP 2A INCLUSION CRITERIA: Subjects taking capsule formulations must be able to swallow capsules
104
PART 2 GROUP 3 INCLUSION CRITERIA: Subjects taking capsule formulations must be able to swallow capsules
105
Able to swallow the study drugs whole as tablets
106
Patients must be able to swallow whole tablets
107
Unable or unwilling to swallow tablets
108
Patients unable to swallow pills.
109
CAPMATINIB EXCLUSION CRITERIA: Inability to swallow intact tablets or capsules
110
CERITINIB EXCLUSION CRITERIA: Inability to swallow intact tablets or capsules
111
REGORAFENIB EXCLUSION CRITERIA: Inability to swallow intact tablets or capsules
112
ENTRECTINIB EXCLUSION CRITERIA: Inability to swallow intact tablets or capsules
113
Patient has a condition that would prevent him or her from being able to swallow Toca FC tablets or absorb flucytosine.
114
Impaired gastrointestinal (GI) function or GI disease that may alter absorption of ceritinib or inability to swallow up to five ceritinib capsules daily; although, patients unable to swallow capsules will be allowed to participate in this study, by following the specific instructions on making a slurry of the medication
115
The subject is unable to swallow tablets
116
Patients who are unable to swallow pills/capsules are ineligible
117
Patients must be able to swallow intact capsules whole
118
Inability to swallow tablets or capsules
119
Patient must be able to swallow capsules
120
Ability to swallow pills or capsules
121
Subject is unable to swallow or absorb oral tablets normally
122
Inability or unwillingness to swallow capsules
123
Unable to swallow capsules
124
Patients with malabsorption syndrome or other condition that would interfere with intestinal absorption; patients must be able to swallow capsules
125
Unable to swallow tablets
126
Patients who cannot swallow whole tablets (i.e. medication tablets)
127
Unwilling or unable to swallow tablets BID
128
The subject is unable to swallow tablets
129
The subject is unable to swallow tablets
130
COHORTS 1 AND 2: HEALTHY VOLUNTEERS: Ability to swallow capsules or tablets
131
Patient must be able to swallow capsules
132
Capacity to swallow
133
Part E: Are able to swallow capsules or tablets
134
Patients who are unable to swallow pills
135
Patients who are unable to swallow oral gel capsules are not eligible
136
Ability to swallow medication capsules by mouth (which may include taking nilotinib mixed in apple sauce)
137
Participants must be able to swallow capsules
138
The subject must be able to swallow tablets, or receive tablets crushed and/or dispensed in water via nasogastric or orogastric tube.
139
Patients must be able to swallow tablets and have no significant impairment in gastrointestinal absorption
140
Able to swallow capsules whole (pomalidomide capsules cannot be crushed, dissolved or broken)
141
The subject is unable to swallow tablets
142
Patients must be able to swallow whole capsules
143
Patients must be able to swallow capsules
144
Patient must be able to swallow capsules
145
TUMOR BIOPSY SEQUENCING: Patients with gastrointestinal conditions that might predispose for drug intolerability or poor drug absorption (e.g., inability to take oral medication or a requirement for IV alimentation, prior surgical procedures affecting absorption, malabsorption syndrome, and active peptic ulcer disease) are excluded; subjects with Crohn’s disease or a partial or complete small bowel obstruction are also excluded, as are any patients who cannot swallow tablets or capsules whole; tablets or capsules must not be crushed or chewed; nasogastric or gastrostomy tube (G-tube) administration is not allowed
146
TREATMENT: Patients with gastrointestinal conditions that might predispose for drug intolerability or poor drug absorption (e.g., inability to take oral medication or a requirement for IV alimentation, prior surgical procedures affecting absorption, malabsorption syndrome, and active peptic ulcer disease) are excluded; subjects with Crohn's disease or a partial or complete small bowel obstruction are also excluded, as are any patients who cannot swallow tablets or capsules whole; tablets or capsules must not be crushed or chewed; nasogastric or G-tube administration is not allowed
147
Patients who are not able to swallow capsules or tablets
148
The subject is unable to swallow capsules or tablets
149
Inability to swallow lenalidomide capsules whole; capsules of 13-isotretinoin may be opened
150
Patients must be able to swallow capsules
151
Must be able to swallow ribociclib and tamoxifen capsules/tablets
152
Patients unable to swallow tablets or patients with malabsorption syndrome, or any other disease significantly affecting gastrointestinal function
153
Must be able to swallow ribociclib capsules
154
Subject is able to swallow capsules and is able to take or tolerate oral medications on a continuous basis
155
Patients must be able to swallow capsules whole
156
PHASE II: Patients must be able to swallow capsules whole
157
Known inability to swallow capsules
158
Patients must be able to swallow tablets whole
159
Patients must be able to swallow whole capsules
160
Patients must be able to swallow capsules whole
161
Patients who are unable to swallow pills
162
Unable or unwilling to swallow tablets BID
163
Patients must be able to swallow whole tablets or capsules; nasogastric or gastrostomy (G)-tube administration is not allowed; any gastrointestinal disease which would impair ability to swallow, retain, or absorb drug is not allowed
164
Patients must be able to swallow capsules/tablets
165
Patients who are unable to swallow pills are excluded
166
Part C: Patients must be able to swallow intact capsules
167
Patients must be able to swallow whole tablets; nasogastric or gastrostomy (G) tube administration is not allowed; tablets must not be crushed or chewed
168
Patients must be able to swallow whole capsules and tolerate oral medications
169
Patients unable to swallow whole capsules
170
Able to swallow whole capsules
171
Patients taking the capsule formulation must be able to swallow capsules; feeding tube administration is allowed for patients receiving the oral solution (OS)
172
Patients must be able to take oral medications; patients must be able to swallow capsules whole without crushing or altering them in any way
173
are able to swallow capsules
174
Unable to swallow pills
175
Patients must have the ability to swallow tablets
176
Unable or unwilling to swallow tablets
177
Unable to swallow tablets
178
The subject is unable to swallow tablets
179
Patients must be able to swallow whole capsules
180
Inability to swallow capsules.
181
Unable to swallow capsules or disease significantly affecting gastrointestinal function
182
Patients must be able to swallow whole capsules
183
Are able to swallow capsules and tablets.
184
Subject is able to swallow capsules
185
Unable to swallow capsules or disease significantly affecting gastrointestinal function
186
Unable or unwilling to swallow BBI608 and/or BBI503 capsules daily
187
Any condition causing an inability to swallow tablets.
188
Unable or unwilling to swallow BBI608 capsules daily.
189
Must be able to swallow lenalidomide capsules
190
Unable or unwilling to swallow BBI608 capsules daily
191
Are able to swallow capsules
192
The subject is unable to swallow tablets
193
Unable to swallow capsules
194
Must be able to swallow ribociclib / placebo capsules/tablets
195
Patients must be able to swallow capsules
196
Inability to swallow capsules
197
Patients unable to swallow tablets or patients with malabsorption syndrome, or any other disease significantly affecting gastrointestinal function
198
Inability to swallow tablets
199
The subject is unable to swallow tablets
200
Unable to swallow tablets, or diagnosed malabsorption syndrome, or any other disease significantly affecting gastrointestinal function
201
Patients must be able to swallow whole capsules
202
Inability to swallow tablets or capsules
203
Inability to swallow capsules.
204
Able to swallow tablets
205
Inability to swallow tablets
206
Patients must be willing and able to swallow oral tablets
207
Patients must have the ability to swallow tablets
208
Inability to swallow tablets or use of a feeding tube
209
Patients who are unable or unwilling to swallow tablets
210
Unable or unwilling to swallow BBI608 capsules daily.
211
Able to swallow capsules
212
Participant is unable or unwilling to swallow tablets
213
Willing to take abiraterone acetate on an empty stomach; no food should be consumed at least two hours before and for at least one hour after the dose of abiraterone acetate is taken, and should be able to swallow tablets whole, without crushing/chewing tablets
214
Unable or unwilling to swallow BBI503 capsules daily
215
Unable or unwilling to swallow BBI608 capsules daily.
216
The subject is unable to swallow tablets
217
Are able to swallow tablets
218
Patients must be able to swallow tablets
219
Patients with an inability to swallow tablets or capsules
220
The subject is unable to swallow capsules tablets
221
Patients who are unable to swallow pills
222
The participant is unable to swallow capsules or tablets
223
Patients who cannot swallow capsules
224
Patients who are unable to swallow pills are not eligible
225
Patients must be able to swallow intact capsules
226
Inability to swallow capsules or known gastrointestinal malabsorption
227
Unable to swallow pills
228
Ability to swallow oral capsules
229
Are able to swallow capsules
230
Are able to swallow capsules or tablets
231
Unable or unwilling to swallow the complete daily dose of ARQ 087 capsules
232
Patients must be able to swallow the vorinostat capsules or have a feeding tube to allow for drug suspension
233
Patients who are unable to swallow tablets
234
Inability to swallow the HKI-272 capsules
235
Able to swallow capsules
236
Able to swallow capsules
237
Inability to swallow capsules
238
Ability to swallow tablets without difficulty;
239
Patients must be able to swallow tablets
240
Able to swallow tablets
241
The subject is unable to swallow tablets
242
Patients must be able to swallow whole capsules; capsules must not be crushed or chewed; capsules must not be opened
243
RECURRENT/ PROGRESSIVE DIPG (STRATUM 1): Patient must be able to swallow capsules whole
244
NON-PROGRESSED DIPG (STRATUM 2): Patient must be able to swallow capsules whole
245
Known inability to swallow up to five ceritinib (LDK378) capsules daily
246
Ability to swallow intact palbociclib capsules and bicalutamide tablets
247
The subject is unable to swallow tablets
248
Inability to swallow oral capsules
249
Unable to swallow tablets, or patients with malabsorption syndrome, or any other disease significantly affecting gastrointestinal function.
250
Subject is unable to swallow capsules or tablets
251
Inability or unwillingness to swallow capsules
252
Patients must be able to swallow whole tablets (for MK-2206); nasogastric or gastrostomy (G) tube administration is not allowed; tablets must not be crushed or chewed
253
Able to swallow capsules and maintain adequate hydration
254
Patients will be excluded if they are unable to swallow capsules whole.
255
Unable to swallow a whole tablet or capsule.
256
Patients who are not able to swallow capsules or tablets
257
Must be able to swallow whole capsules
258
Ability to swallow tablets.
259
Unable or unwilling to swallow BBI608/placebo capsules daily.
260
Patients must be able to swallow capsules
261
Inability or unwillingness to swallow capsules
262
Patients must be able to swallow whole tablets; nasogastric or gastrostomy (G) tube administration is not allowed; tablets must not be crushed or chewed
263
Unable or unwilling to swallow BBI608, BBI503, or sorafenib capsules or tablets
264
Patients must be able to swallow tablets whole, without crushing
265
Patients must be able to swallow whole capsules
266
Patients must be able to swallow whole tablets; tablets must not be crushed or chewed
267
The subject is unable to swallow tablets
268
The subject is unable to swallow tablets
269
Patients must be able to swallow whole tablets and capsules
270
PHASE I: >= 3 years and =< 18 years of age at the time of study enrollment, if able to swallow whole capsules
271
PHASE II: >= 2 and =< 18 years; body surface area (BSA) >= 0.55 m^2, and able to swallow whole capsules
272
Inability to swallow capsules, since capsules cannot be crushed or broken
273
Inability to swallow tablets for everolimus arm
274
Patient must be able to swallow whole tablets
275
Patients must be able to swallow oral medications (capsules and tablets) without chewing, breaking, crushing, opening or otherwise altering the product formulation
276
Patients must be able to swallow capsules whole; nasogastric or gastrostomy (G) tube administration is not allowed
277
Able to swallow whole capsules
278
Patients must be able to swallow tablets
279
Patients must be able to swallow capsules
280
Patients must be able to swallow tablets
281
Subject is able to swallow enzalutamide capsules and comply with study requirements.
282
Patients must be able to swallow either intact capsules or mini-tabs without chewing
283
Must be able to swallow tablets and capsules
284
Patient must have the ability to swallow multiple capsules
285
Participants who are unable to swallow pills
286
Able to swallow capsules
287
Inability to swallow tablets
288
Inability to swallow tablets
289
Able to swallow oral capsules without difficulty.
290
Able to swallow capsules
291
Ability to swallow oral tablets
292
Ability to swallow and tolerate oral tablets
293
GENERAL INCLUSION CRITERIA FOR SUBPROTOCOLS: Patients must be able to swallow intact capsules/tablets, unless otherwise specified in the subprotocol to which they are assigned
294
Patient must be able to swallow capsules (phase III only)
295
Subjects must be able to swallow capsules/tablets
296
Inability or unwillingness to swallow capsules
297
Patients must be able to swallow whole capsules
298
Unable or unwilling to swallow BBI608 capsules daily
299
Subjects that are unable to swallow a tablet/pill
300
Patients must be able to swallow whole tablets or capsules; nasogastric or g-tube administration is not allowed; any gastrointestinal disease which would impair ability to swallow, retain, or absorb drug is not allowed
301
Unable to swallow capsules or disease significantly affecting gastrointestinal function