NCT01185353 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Administered orally once daily (QD) for 12 weeks in Part A. Methotrexate (MTX) was administered orally as background therapy.
- id
- FG000
- title
- 1 Milligrams (mg) LY3009104 QD - Part A
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG001
- title
- 2 mg LY3009104 QD - Parts A and B
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG002
- title
- 4 mg LY3009104 QD - Parts A and B
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG003
- title
- 8 mg LY3009104 QD - Parts A and B
- description
- Placebo administered orally QD for 12 weeks in Part A. MTX was administered orally as background therapy.
- id
- FG004
- title
- Placebo QD - Part A
- description
- Participants who received Placebo or 1 mg LY3009104 in Part A were re-randomized at Week 12 to receive 2 mg LY3009104 twice daily (BID) in Part B. MTX was administered orally as background therapy.
- id
- FG005
- title
- 2 mg LY3009104 BID - Part B
- description
- Participants who received Placebo or 1 mg LY3009104 in Part A were re-randomized at Week 12 to receive 4 mg LY3009104 QD in Part B. MTX was administered orally as background therapy.
- id
- FG006
- title
- 4 mg LY3009104 QD - Part B
- description
- Participants who received 2 mg LY3009104 QD or BID in Part B were re-assigned at Week 24 to 4 mg LY3009104 QD in Part C. Participants who received 4 mg LY3009104 QD in Part B continued to receive 4 mg LY3009104 QD in Part C. Participants who completed Part C continued to receive 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG007
- title
- 4 mg LY3009104 QD - Parts C and D
- description
- Participants who received 2 mg LY3009104 QD or BID in Part B were re-assigned at Week 24 to 4 mg LY3009104 QD in Part C. Participants who received 4 mg LY3009104 QD in Part B continued to receive 4 mg LY3009104 QD in Part C. At Weeks 28 and 32, participants who met dose escalation criteria received 8 mg LY3009104 QD for the rest of the Part C. Dose escalation criteria: ≥ 6 tender and 6 swollen joints based on the 28-joint count assessments and the clinical judgment of the investigator. Participants who completed Part C received 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG008
- title
- 4 to 8 mg LY3009104 QD - Part C and 4 mg LY3009104 QD - Part D
- description
- Participants who received 8 mg LY3009104 QD in Part B remained on 8 mg LY3009104 QD in Part C. Participants who completed Part C received 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG009
- title
- 8 mg LY3009104 QD - Part C and 4 mg LY3009104 QD - Part D
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 5
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 4
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Entry Criteria Not Met
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 2
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 1
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 3
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 49
- group Id
- FG001
- num Subjects
- 52
- group Id
- FG002
- num Subjects
- 52
- group Id
- FG003
- num Subjects
- 50
- group Id
- FG004
- num Subjects
- 98
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 49
- group Id
- FG001
- num Subjects
- 52
- group Id
- FG002
- num Subjects
- 52
- group Id
- FG003
- num Subjects
- 50
- group Id
- FG004
- num Subjects
- 98
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Received at Least 1 Dose of Study Drug
- achievements
- group Id
- FG000
- num Subjects
- 44
- group Id
- FG001
- num Subjects
- 51
- group Id
- FG002
- num Subjects
- 50
- group Id
- FG003
- num Subjects
- 49
- group Id
- FG004
- num Subjects
- 82
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 5
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 16
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Part A (Weeks 0 Through 12)
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 1
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 1
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 1
- group Id
- FG003
- num Subjects
- 2
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 3
- group Id
- FG006
- num Subjects
- 4
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 1
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- Entry Criteria Not Met
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 51
- group Id
- FG002
- num Subjects
- 50
- group Id
- FG003
- num Subjects
- 49
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 63
- group Id
- FG006
- num Subjects
- 63
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 50
- group Id
- FG002
- num Subjects
- 48
- group Id
- FG003
- num Subjects
- 45
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 59
- group Id
- FG006
- num Subjects
- 57
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 2
- group Id
- FG003
- num Subjects
- 4
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 4
- group Id
- FG006
- num Subjects
- 6
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Part B (Weeks 12 Through 24)
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 8
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 6
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 2
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 2
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 1
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 0
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- type
- Entry Criteria Not Met
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 0
- group Id
- FG009
- num Subjects
- 1
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 0
- group Id
- FG008
- num Subjects
- 1
- group Id
- FG009
- num Subjects
- 0
- type
- Reason missing
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 108
- group Id
- FG008
- num Subjects
- 61
- group Id
- FG009
- num Subjects
- 32
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 92
- group Id
- FG008
- num Subjects
- 53
- group Id
- FG009
- num Subjects
- 24
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 16
- group Id
- FG008
- num Subjects
- 8
- group Id
- FG009
- num Subjects
- 8
- type
- NOT COMPLETED
- title
- Part C (Weeks 24 Through 76)
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 3
- group Id
- FG009
- num Subjects
- 0
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 1
- group Id
- FG008
- num Subjects
- 2
- group Id
- FG009
- num Subjects
- 0
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 79
- group Id
- FG008
- num Subjects
- 47
- group Id
- FG009
- num Subjects
- 18
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
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- 0
- group Id
- FG002
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- FG003
- num Subjects
- 0
- group Id
- FG004
- num Subjects
- 0
- group Id
- FG005
- num Subjects
- 0
- group Id
- FG006
- num Subjects
- 0
- group Id
- FG007
- num Subjects
- 76
- group Id
- FG008
- num Subjects
- 40
- group Id
- FG009
- num Subjects
- 17
- type
- COMPLETED
- achievements
- group Id
- FG000
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- 0
- group Id
- FG001
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- FG002
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- FG003
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- 7
- group Id
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- NOT COMPLETED
- title
- Part D (Weeks 76 Through 128)
- pre Assignment Details
- This study consisted of 4 parts and a follow-up up to 28 days post the last dose of study drug.
Complete source fields
- groups
- description
- Administered orally once daily (QD) for 12 weeks in Part A. Methotrexate (MTX) was administered orally as background therapy.
- id
- FG000
- title
- 1 Milligrams (mg) LY3009104 QD - Part A
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG001
- title
- 2 mg LY3009104 QD - Parts A and B
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG002
- title
- 4 mg LY3009104 QD - Parts A and B
- description
- Administered orally QD for 24 weeks in Parts A and B. MTX was administered orally as background therapy.
- id
- FG003
- title
- 8 mg LY3009104 QD - Parts A and B
- description
- Placebo administered orally QD for 12 weeks in Part A. MTX was administered orally as background therapy.
- id
- FG004
- title
- Placebo QD - Part A
- description
- Participants who received Placebo or 1 mg LY3009104 in Part A were re-randomized at Week 12 to receive 2 mg LY3009104 twice daily (BID) in Part B. MTX was administered orally as background therapy.
- id
- FG005
- title
- 2 mg LY3009104 BID - Part B
- description
- Participants who received Placebo or 1 mg LY3009104 in Part A were re-randomized at Week 12 to receive 4 mg LY3009104 QD in Part B. MTX was administered orally as background therapy.
- id
- FG006
- title
- 4 mg LY3009104 QD - Part B
- description
- Participants who received 2 mg LY3009104 QD or BID in Part B were re-assigned at Week 24 to 4 mg LY3009104 QD in Part C. Participants who received 4 mg LY3009104 QD in Part B continued to receive 4 mg LY3009104 QD in Part C. Participants who completed Part C continued to receive 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG007
- title
- 4 mg LY3009104 QD - Parts C and D
- description
- Participants who received 2 mg LY3009104 QD or BID in Part B were re-assigned at Week 24 to 4 mg LY3009104 QD in Part C. Participants who received 4 mg LY3009104 QD in Part B continued to receive 4 mg LY3009104 QD in Part C. At Weeks 28 and 32, participants who met dose escalation criteria received 8 mg LY3009104 QD for the rest of the Part C. Dose escalation criteria: ≥ 6 tender and 6 swollen joints based on the 28-joint count assessments and the clinical judgment of the investigator. Participants who completed Part C received 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG008
- title
- 4 to 8 mg LY3009104 QD - Part C and 4 mg LY3009104 QD - Part D
- description
- Participants who received 8 mg LY3009104 QD in Part B remained on 8 mg LY3009104 QD in Part C. Participants who completed Part C received 4 mg LY3009104 QD in Part D. MTX was administered orally as background therapy.
- id
- FG009
- title
- 8 mg LY3009104 QD - Part C and 4 mg LY3009104 QD - Part D
- periods
- drop Withdraws
- reasons
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- 1
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- 0
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- Physician Decision
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- group Id
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- reasons
- group Id
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- 2
- group Id
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- group Id
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- 52
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- FG003
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- 50
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- FG004
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- 98
- group Id
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- type
- Received at Least 1 Dose of Study Drug
- achievements
- group Id
- FG000
- num Subjects
- 44
- group Id
- FG001
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- 51
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- FG002
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- 50
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- FG003
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- 49
- group Id
- FG004
- num Subjects
- 82
- group Id
- FG005
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- FG006
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- FG007
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- COMPLETED
- achievements
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- 1
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- 16
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- 0
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- 0
- group Id
- FG008
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- 0
- group Id
- FG009
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- 0
- type
- NOT COMPLETED
- title
- Part A (Weeks 0 Through 12)
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
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- 1
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- FG003
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- 0
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- FG004
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- 0
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- 0
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- FG008
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- Adverse Event
- reasons
- group Id
- FG000
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- FG002
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- Lack of Efficacy
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- 0
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- 0
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- Entry Criteria Not Met
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- achievements
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- FG000
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- 51
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- 50
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- FG003
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- 49
- group Id
- FG004
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- 0
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- 63
- group Id
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- 63
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- type
- STARTED
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- NOT COMPLETED
- title
- Part B (Weeks 12 Through 24)
- drop Withdraws
- reasons
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- FG000
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- group Id
- FG004
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- Reason missing
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- group Id
- FG002
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- group Id
- FG003
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- 0
- group Id
- FG004
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- 0
- group Id
- FG005
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- 0
- group Id
- FG006
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- 0
- group Id
- FG007
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- 108
- group Id
- FG008
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- 61
- group Id
- FG009
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- 32
- type
- STARTED
- achievements
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- FG003
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- group Id
- FG004
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- group Id
- FG005
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- group Id
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- group Id
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- 92
- group Id
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- group Id
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- 24
- type
- COMPLETED
- achievements
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- 16
- group Id
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- group Id
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- type
- NOT COMPLETED
- title
- Part C (Weeks 24 Through 76)
- drop Withdraws
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- group Id
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- 2
- group Id
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- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
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- 0
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- FG006
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- 0
- group Id
- FG007
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- 1
- group Id
- FG008
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- FG009
- num Subjects
- 0
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
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- 0
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- FG001
- num Subjects
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- FG002
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- FG003
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- FG004
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- FG005
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- FG006
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- group Id
- FG007
- num Subjects
- 79
- group Id
- FG008
- num Subjects
- 47
- group Id
- FG009
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- 18
- type
- STARTED
- achievements
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- FG003
- num Subjects
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- FG004
- num Subjects
- 0
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- FG005
- num Subjects
- 0
- group Id
- FG006
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- 0
- group Id
- FG007
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- 76
- group Id
- FG008
- num Subjects
- 40
- group Id
- FG009
- num Subjects
- 17
- type
- COMPLETED
- achievements
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- FG000
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- FG001
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- FG002
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- FG003
- num Subjects
- 0
- group Id
- FG004
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- FG005
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- FG006
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- FG007
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- group Id
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- 1
- type
- NOT COMPLETED
- title
- Part D (Weeks 76 Through 128)
- pre Assignment Details
- This study consisted of 4 parts and a follow-up up to 28 days post the last dose of study drug.
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Preserved source evidence · Not medical advice
Triangle