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Trial to Compare Time to Response in the Symptoms of Anxiety to Concomitant Treatment With Niravam™ and an SSRI or SNRI to Treatment With an SSRI or SNRI Alone in Subjects With Generalized Anxiety Disorder or Panic Disorder
This study has been completed.
Study NCT00266409   Information provided by UCB, Inc.
First Received: December 15, 2005   Last Updated: November 5, 2009   History of Changes
Study Type: Interventional
Study Design: Randomized, Open Label, Parallel Assignment
Conditions: Generalized Anxiety Disorder
Panic Disorder
Interventions: Drug: Niravam
Drug: SSRI/SNRI

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
Participants Flow shows 418 subjects that have been enrolled and randomized. The safety population consists of 414 subjects that received at least one dose of SSRI/SNRI and/or Niravam.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
Baseline Characteristics are only available for the Intent-to-treat population (subjects who received one dose of SSRI/SNRI and/or Niravam and have an assessment beyond the Baseline assessment)

Reporting Groups
  Description
Panic: Niravam+SSRI/SNRI Panic Disorder: Niravam plus a newly prescribed SSRI or SNRI
Panic: SSRI/SNRI Alone Panic Disorder: Newly prescribed SSRI or SNRI alone
GAD : Niravam+SSRI/SNRI Generalized Anxiety Disorder: Niravam plus newly prescribed SSRI or SNRI
GAD: SSRI/SNRI Alone Generalized Anxiety Disorder: Newly prescribed SSRI or SNRI alone

Participant Flow:   Overall Study
  Panic: Niravam+SSRI/SNRI Panic: SSRI/SNRI Alone GAD : Niravam+SSRI/SNRI GAD: SSRI/SNRI Alone
STARTED   137     138     72     71  
COMPLETED   92     92     55     49  
NOT COMPLETED   45     46     17     22  
      Lack of Efficacy               2                 6                 1                 2  
      Adverse Event               7                 2                 1                 1  
      Lost to Follow-up               18                 21                 6                 8  
      Withdrawal by Subject               6                 10                 3                 9  
      Protocol Violation               5                 3                 4                 2  
      unspecified               7                 4                 2                 0  



  Baseline Characteristics
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Reporting Groups
  Description
Panic: Niravam+SSRI/SNRI Panic Disorder: Niravam plus a newly prescribed SSRI or SNRI
Panic: SSRI/SNRI Alone Panic Disorder: Newly prescribed SSRI or SNRI alone
GAD : Niravam+SSRI/SNRI Generalized Anxiety Disorder: Niravam plus newly prescribed SSRI or SNRI
GAD: SSRI/SNRI Alone Generalized Anxiety Disorder: Newly prescribed SSRI or SNRI alone

Baseline Measures
  Panic: Niravam+SSRI/SNRI Panic: SSRI/SNRI Alone GAD : Niravam+SSRI/SNRI GAD: SSRI/SNRI Alone Total
Number of Participants  
[units: participants]
125 120 67 62 374
Age  
[units: participants]
         
<=18 years 0 0 0 0 0
Between 18 and 65 years 120 119 66 61 366
>=65 years 5 1 1 1 8
Age  
[units: years]
Mean ± Standard Deviation
40.1 ± 12.24 38.1 ± 12.55 40.1 ± 12.64 43.6 ± 12.20 40 ± 12
Gender  
[units: participants]
         
Female 102 93 50 42 287
Male 23 27 17 20 87
Region of Enrollment  
[units: participants]
         
United States 125 120 67 62 374



  Outcome Measures
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1.  Primary:   Cumulative Percent of Participants Showing a Response in the Symptoms of Anxiety (Decrease in Total Hamilton Anxiety (HAM-A) -Score of >=50%) in the Intent-to-treat Population (Kaplan-Meier-estimates)   [ 10 weeks ]

2.  Primary:   Cumulative Percent of Participants Showing a Response in the Symptoms of Anxiety (Decrease in Total Hamilton Anxiety (HAM-A) -Score of >=50%) in the Per Protocol Population (Kaplan-Meier-estimates)   [ 10 weeks ]

3.  Secondary:   Change From Baseline in the Total HAM-A Score After 1 Week   [ Baseline and 1 week ]

4.  Secondary:   Change From Baseline in the Total HAM-A Score After 2 Weeks   [ Baseline and 2 Weeks ]

5.  Secondary:   Change From Baseline in the Total HAM-A Score After 3 Weeks   [ Baseline and 3 weeks ]

6.  Secondary:   Change From Baseline in the Total HAM-A Score After 4 Weeks   [ Baseline and 4 weeks ]

7.  Secondary:   Change From Baseline in the Total HAM-A Score After 5 Weeks   [ Baseline and 5 weeks ]

8.  Secondary:   Change From Baseline in the Total HAM-A Score After 6 Weeks   [ Baseline and 6 weeks ]

9.  Secondary:   Change From Baseline in the Total HAM-A Score After 7 Weeks   [ Baseline and 7 weeks ]

10.  Secondary:   Change From Baseline in the Total HAM-A Score After 8 Weeks   [ Baseline and 8 weeks ]

11.  Secondary:   Change From Baseline in the Total HAM-A Score at Endpoint During the 8 Week Treatment Period   [ Baseline and at endpoint during the 8 week treatment period ]

12.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 1 Week   [ 1 week ]

13.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 2 Weeks   [ 2 weeks ]

14.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 3 Weeks   [ 3 weeks ]

15.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 4 Weeks   [ 4 weeks ]

16.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 5 Weeks   [ 5 weeks ]

17.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 6 Weeks   [ 6 weeks ]

18.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 7 Weeks   [ 7 weeks ]

19.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) After 8 Weeks   [ 8 weeks ]

20.  Secondary:   Clinical Response (Decrease From Baseline in Total HAM-A-score >=50%) at Endpoint During the 8 Week Treatment Period   [ at endpoint during the 8 week treatment period ]

21.  Secondary:   Change in Severity of Illness From Baseline Using the Clinical Global Impression Improvement (CGI-I) Score After 2 Weeks   [ Baseline and 2 weeks ]

22.  Secondary:   Change in Severity of Illness From Baseline Using the Clinical Global Impression - Improvement (CGI-I) Score After 4 Weeks   [ Baseline and 4 weeks ]

23.  Secondary:   Change in Severity of Illness From Baseline Using the Clinical Global Impression - Improvement (CGI-I) Score After 8 Weeks   [ Baseline and 8 weeks ]

24.  Secondary:   Change in Severity of Illness From Baseline Using the Clinical Global Impression - Improvement (CGI-I) Score at Endpoint During the 8 Week Treatment Period   [ Baseline and at endpoint during the 8 week treatment period ]

25.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 1 Week   [ 1 week ]

26.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 2 Weeks   [ 2 weeks ]

27.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 3 Weeks   [ 3 weeks ]

28.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 4 Weeks   [ 4 weeks ]

29.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 5 Weeks   [ 5 weeks ]

30.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 6 Weeks   [ 6 weeks ]

31.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 7 Weeks   [ 7 weeks ]

32.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score After 8 Weeks   [ 8 weeks ]

33.  Secondary:   Subject's Assessment of Treatment Effect as Measured by the Patient Global Impression (PGI) Score at Endpoint During the 8 Week Treatment Period   [ at endpoint during the 8 week treatment period ]

34.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 1 Week   [ Baseline and 1 week ]

35.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 2 Weeks   [ Baseline and 2 weeks ]

36.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 3 Weeks   [ Baseline and 3 weeks ]

37.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 4 Weeks   [ Baseline and 4 weeks ]

38.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 5 Weeks   [ Baseline and 5 weeks ]

39.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 6 Weeks   [ Baseline and 6 weeks ]

40.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 7 Weeks   [ Baseline and 7 weeks ]

41.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore After 8 Weeks   [ Baseline and 8 weeks ]

42.  Secondary:   Change From Baseline in HAM-A-insomnia Subscore at Endpoint During the 8 Week Treatment Period   [ Baseline and at endpoint during the 8 week treatment period ]

43.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 1 Week   [ Baseline and 1 week ]

44.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 2 Weeks   [ Baseline and 2 weeks ]

45.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 3 Weeks   [ Baseline and 3 weeks ]

46.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 4 Weeks   [ Baseline and 4 weeks ]

47.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 5 Weeks   [ Baseline and 5 weeks ]

48.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 6 Weeks   [ Baseline and 6 weeks ]

49.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 7 Weeks   [ Baseline and 7 weeks ]

50.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore After 8 Weeks   [ Baseline and 8 weeks ]

51.  Secondary:   Change From Baseline in HAM-A-psychic Factors Subscore at Endpoint During the 8 Week Treatment Period   [ Baseline and at endpoint during the 8 week treatment period ]

52.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 1 Week   [ Baseline and 1 week ]

53.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 2 Weeks   [ Baseline and 2 weeks ]

54.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 3 Weeks   [ Baseline and 3 weeks ]

55.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 4 Weeks   [ Baseline and 4 weeks ]

56.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 5 Weeks   [ Baseline and 5 weeks ]

57.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 6 Weeks   [ Baseline and 6 weeks ]

58.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 7 Weeks   [ Baseline and 7 weeks ]

59.  Secondary:   Change From Baseline in HAM-A-somatic Subscore After 8 Weeks   [ Baseline and 8 weeks ]

60.  Secondary:   Change From Baseline in HAM-A-somatic Subscore at Endpoint During the 8 Week Treatment Period   [ Baseline and at endpoint during the 8 week treatment period ]

61.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 1 Week   [ 1 week ]

62.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 2 Weeks   [ 2 weeks ]

63.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 3 Weeks   [ 3 weeks ]

64.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 4 Weeks   [ 4 weeks ]

65.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 5 Weeks   [ 5 weeks ]

66.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 6 Weeks   [ 6 weeks ]

67.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 7 Weeks   [ 7 weeks ]

68.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) After 8 Weeks   [ 8 weeks ]

69.  Secondary:   Presence of Any Panic Attack(s) (for Subjects With Panic Disorder Only) at Endpoint During the 8 Week Treatment Period   [ at endpoint during the 8 week treatment period ]


  Serious Adverse Events
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  Other Adverse Events
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