| Primary | Change From Baseline in the Pain Anxiety Symptoms Scale (PASS) Total Score at Approximately Week 5 | The change from baseline to approximately week 5 in the PASS total score. PASS asks participants to indicate how often they engage in each of the 40 thoughts or activities that represent anxiety symptoms on a scale of 0=never to 5=always. The total score has a range of 0-200. | | Posted | | Mean | Standard Deviation | units on a scale | | Day 0 (baseline), approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| | Group IDs | Group Description | Statistical Method | Statistical Comment | P-Value | P-Value Comment | Parameter Type | Parameter Value | Dispersion Type | Dispersion Value | Confidence Interval Sides | Confidence Interval % | CI Lower Limit | CI Upper Limit | CI Lower Limit Comment | CI Upper Limit Comment | Estimate Comment | Tested Non-Inferiority | Non-Inferiority Type | Non-Inferiority Comment | Other Analysis Description |
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| | t-test, 2 sided | | 0.3223 | | Mean Difference (Net) | -1.6 | | | 2-Sided | 95 | -4.64 | 1.54 | | | | No | Superiority or Other | | |
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| Secondary | Change From Baseline in the Pain Anxiety Symptoms Scale (PASS) Subscale Scores at Approximately Week 5 | The change from baseline to approximately week 5 in the PASS subscale scores. PASS asks participants to indicate how often they engage in each of the 40 thoughts or activities that represent anxiety symptoms on a scale of 0=never to 5=always. Those 40 questions are organized into four subscales: fear, cognitive anxiety, somatic anxiety, and escape/avoidance. Each subscale score is obtained by summing the answers to the ten items in the subscore resulting in a range of 0-50. | | Posted | | Mean | Standard Deviation | units on a scale | | Day 0 (baseline), approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Change From Baseline in the Beck Depression Inventory at Approximately Week 5 | Change from baseline to endpoint (week 4 of Treatment period or last post baseline visit) in the Beck Depression Inventory (BDI). The BDI is a self-reporting instrument that asks 21 questions regarding how the participant felt in the past few days. Answers are in sentence form, and offer a scale where the first answer (worth 0 points) indicates no depression and the fourth answer (worth 3 points) indicates significant depression. Totals (0-63) are grouped so that totals of 1-10 are interpreted as 'These ups and downs are considered normal' and scores >40 indicate extreme depression. | Full analysis set of participants who answered the questions. | Posted | | Mean | Standard Deviation | units on a scale | | Day 0 (baseline), approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Change From Baseline in the West Haven-Yale Multidimensional Pain Inventory Subscales at Approximately Week 5 | Change from baseline to endpoint (week 4 of Treatment period or last post baseline visit) in the Multidimensional Pain Inventory Subscales. Answers to questions in the MPI are captured on a 7-point scale, with 0=most positive answer and 6= least positive answer. Twenty questions focus on pain, fourteen on a significant other's response when participant is in pain, and eighteen questions about daily activities. There are a total of 13 subscales with variable ranges. Subscales and corresponding ranges are listed in the results table. The General Activity category combines the Household Chores, Outdoor Work, Activities Away from Home, and Social Activities categories. | | Posted | | Mean | Standard Deviation | units on a scale | | Day 0 (baseline), approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Medication Preference From the Pain Flare Treatment Satisfaction Questionnaire at Approximately Week 5 | The summary question from the Pain Flare Treatment Satisfaction Questionnaire asked participants which medication they preferred to use for their break-through pain. Options were 1) Prior medication 2) Study medication 3) no preference | Full analysis set of participants who answered the questions. | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Go to Work at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to go to work. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Perform at Work at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to perform at work and includes both work outside the home and housework. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Walk at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to walk. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Exercise at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to exercise. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Participate in Social Events at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to participate in social events. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Have Sex at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to have sex. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Patient Assessment of Ability to Enjoy Life at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) participants completed the Patient Assessment of Function Scale which asks 7 questions about the effect of study treatment on the patient's ability to function. This question asks about the ability to enjoy life. | Full analysis set of participants who answered the question | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Clinical Assessment of Patient Function - General Activities - at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) investigators completed the Clinical Assessment of Patient Function Scale which asks 5 questions about the effect of study treatment on the patient's ability to function. This question asks about the patient's general activities. | | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Clinical Assessment of Patient Function - Patient's Walking Ability - at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) investigators completed the Clinical Assessment of Patient Function Scale which asks 5 questions about the effect of study treatment on the patient's ability to function. This question asks about the patient's walking ability. | Full analysis set. One participant was not assessed by the investigator. | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Clinical Assessment of Patient Function - Patient's Ability to Work/Perform Activities of Daily Living - at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) investigators completed the Clinical Assessment of Patient Function Scale which asks 5 questions about the effect of study treatment on the patient's ability to function. This question asks about the patient's ability to work and perform activities of daily living. | | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Clinical Assessment of Patient Function - Patient's Relationship With Others - at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) investigators completed the Clinical Assessment of Patient Function Scale which asks 5 questions about the effect of study treatment on the patient's ability to function. This question asks about the patient's relationship with others. | | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Clinical Assessment of Patient Function - Patient's Enjoyment of Life - at Approximately Week 5 | At the endpoint of the study (week 4 of Treatment period or last post baseline visit) investigators completed the Clinical Assessment of Patient Function Scale which asks 5 questions about the effect of study treatment on the patient's ability to function. This question asks about the patient's enjoyment of life. | | Posted | | Number | | participants | | approximately week 5 | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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| Secondary | Summary of Participants' Successful Dosing Levels of Fentanyl Buccal Tablets to Control Episodes of Breakthrough Pain (BTP) | During the dose titration period, participants self-administered FBT, starting at 100, 200 or 400 mcg (depending on analgesic used pre-study) and titrated to 600 and 800 mcg if needed. For each breakthrough pain (BTP) episode, participants took a dose, and did not take further study drug if adequate pain relief was achieved. If pain was not controlled within 30 minutes, the same dose level was repeated. If pain relief was inadequate 30 minutes after the second dose, usual rescue medication was taken for that BTP episode. Doses were adjusted until pain relief was adequate and side effects were tolerated. This outcome summarizes the successful dose levels identified during the titration period. | | Posted | | Number | | participants | | up to 10 days | | | | ID | Title | Description |
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| OG000 | Fentanyl Buccal Tablets | Successful dose strength for each participant was determined during a titration period of no more than 10 days. Participants used the successful dose of 100, 200, 400, 600, or 800 mcg during the four week open-label treatment period. |
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