A Study To Assess Adverse Events and Change in Disease Activity With Oral Cariprazine When Added to Antidepressant Therapies (ADTs) Compared to Placebo in Adult Participants With Generalized Anxiety Disorder (GAD) Who Have Had an Inadequate Response to ADTs Alone
- Conditions
- Generalized Anxiety Disorder
- Interventions
- Registration Number
- NCT04965272
- Lead Sponsor
- AbbVie
- Brief Summary
Generalized anxiety disorder (GAD) is usually treated with antidepressant therapy (ADT); however, sometimes ADTs alone are not enough to adequately treat GAD. The purpose of this study is to assess adverse events and the change in disease activity with cariprazine when added to ADTs compared with placebo in adult participants with GAD who have had an inadequate response to 1 or more prior ADTs alone.
Cariprazine is an approved drug being developed for the treatment of GAD. The participants are placed into 1 of 4 groups, called treatment arms. Each group receives a different treatment. There is a 1 in 4 chance that participants will be assigned to placebo. Around 1072 participants age 18-65 with GAD and an inadequate response to ADT alone will be enrolled in the study in the United States.
After a 2-week screening period, participants will receive daily oral capsules of cariprazine of varying doses or placebo for 6 weeks, followed by a 4-week safety follow-up period for a total study duration of 10 weeks.
There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
- Participants with generalized anxiety disorder (GAD).
- Taking one of the FDA-approved antidepressant therapies (ADTs) for the treatment of GAD (i.e., escitalopram, paroxetine, duloxetine, and venlafaxine XR).
- Continuing to exhibit anxiety symptoms (Hamilton Anxiety Scale [HAM-A] total score >= 22) at Visit 1 (Screening) and Visit 2 (Baseline, Week 0) despite being on an adequate dose and duration (at least 6 weeks of continuous use, with a minimum of 3 of 6 weeks above the minimum labeled dose for GAD).
- Documentation of inadequate response to at least 1 ADT must be confirmed on the GAD-Antidepressant Treatment Response Questionnaire (GAD-ATRQ).
- Must have a minimum score of 22 on the rater-administrated HAM-A and a minimum score of 4 on the rater-administered Clinical Global Impression of Severity Scale (CGI-S), at both Visit 1 (Screening) and Visit 2 (Baseline, Week 0).
- A score of less than 12 on the rater-administered Hamilton Depression Rating Scale-17-item (HAMD-17) at Visit 1 (Screening) and Visit 2 (Baseline, Week 0).
- Laboratory values must meet the criteria specified in the protocol within the screening period prior to the first dose of study drug.
- Psychiatric comorbidities, risk of suicide, self-injury, and/or harm to others; any current Diagnostic and Statistical Manual of Mental Disorders - 5th edition (DSM-5) psychiatric diagnosis other than generalized anxiety disorder (GAD) (other than specific phobias) or history of alcohol or any other substance-related disorders within the 6 months before Visit 1 (Screening).
- Pregnancy, current breastfeeding status, plans to become pregnant or to donate eggs during the study or for approximately 30 days after the last dose of investigational product (female participants).
- History of an allergic reaction, hypersensitivity, or intolerance to constituents of cariprazine (and its excipients) and/or other products of the same class or to any of the protocol-approved rescue medications.
- Any clinically relevant or significant electrocardiogram (ECG) abnormalities, including ECG with QT interval corrected for heart rate (QTc) using Fridericia's formula (QTcF) >450 msec (males) or >470 msec (females).
- History of seizure disorder, with the exception of febrile seizure, stroke, significant head injury, tumor of the central nervous system, or any other condition that predisposes to seizure.
- Specific medical conditions precluding study drug use and/or study participation, such as history of neuroleptic malignant syndrome; cataracts or retinal detachment; allergic reactions/hypersensitivity to cariprazine and/or protocol-approved rescue medications; pregnancy per above; cardiovascular disease; seizure history; and any other disease that is clinically unstable or would make the participant an unsuitable candidate to participate in the study, based on the investigator's judgment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Cariprazine 1.5 mg/day + Antidepressant Therapy Cariprazine 1.5 mg/day Antidepressant (paroxetine, escitalopram, venlafaxine XR, or duloxetine) + cariprazine 1.5 mg/day oral, once daily for 6 weeks Cariprazine 0.75 mg/day + Antidepressant Therapy Cariprazine 0.75 mg/day Antidepressant (paroxetine, escitalopram, venlafaxine XR, or duloxetine) + cariprazine 0.75 mg/day oral, once daily for 6 weeks Cariprazine 3.0 mg/day + Antidepressant Therapy Cariprazine 3.0 mg/day Antidepressant (paroxetine, escitalopram, venlafaxine XR, or duloxetine) + cariprazine 1.5 mg/day oral for 2 weeks followed by cariprazine 3.0 mg/day oral, once daily for 4 weeks. Placebo + Antidepressant Therapy Placebo Antidepressant (paroxetine, escitalopram, venlafaxine XR, or duloxetine) + oral placebo, once daily for 6 weeks
- Primary Outcome Measures
Name Time Method Change from Baseline in the Hamilton Anxiety Scale (HAM-A) Total Score Week 6 The HAM-A is a 14-item, clinician-reported measure used to quantify and categorize the participant's anxiety over the past week. Items are rated on a 5-point Likert rating scale. The HAM-A total score ranges from 0 to 56, with higher scores indicating greater anxiety severity.
- Secondary Outcome Measures
Name Time Method Change from Baseline in Hamilton Depression Rating Scale-17 item, via Structured Interview Guide for the Hamilton Depression Scale (HAMD-17) Total Score Week 6 The HAMD-17 is a 17-item, clinician-reported measure used to quantify and categorize the participant's depression over the past week. The HAMD-17 total score ranges from 0 to 52 with higher scores indicating greater depression severity.
Change from Baseline in SDS: Anxiety Total Score Week 6 The SDS: Anxiety is a 5-item, patient-reported measure used to assess functional impairment in the domains of work/school, social life, and family life on a 10-point numeric rating scale with verbal anchors. The 3 items assessing work/school, social life, and home life or family responsibilities impairment are summed into a single dimensional measure of global functional impairment, with scores ranging from 0 (unimpaired) to 30 (highly impaired). Higher scores indicate greater impairment.
Change from Baseline in Clinical Global Impression of Severity Scale (CGI-S) Week 6 The CGI-S is a single, clinician-reported item that measures the clinician's impression of a subject's current anxiety severity considering their total clinical experience with the patient population. The measure uses a 5-point Likert rating scale, with higher scores indicating greater anxiety severity.
Percentage of Participants in Remission Week 6 Remission is defined as HAM-A total score \<=7, Clinical Global Impression of Improvement Scale (CGI-I) = 1, and Sheehan Disability Scale: Anxiety (SDS: Anxiety) total score \<= 5
Percentage of Participants with HAM-A Response Week 6 HAM-A response is defined as \>= 50% reduction from baseline in HAM-A total score
Percentage of Participants with CGI-I Responder Status of "Much Better" or "Very Much Better" Week 6 The CGI-I is a single, clinician reported item that measures the clinician's impression of how much a participant's anxiety has changed since starting the study medication compared to the participant's condition at baseline. The measure uses a 7-point Likert rating scale with responses ranging from "very much better" (1) to "very much worse" (7).
Percentage of Participants with Patient Global Impression of Change Scale (PGI-C) Responder Status of "Much Better" or "Very Much Better" Week 6 The PGI-C is a single, patient-reported item that assesses the participant's perceived overall change in their anxiety since they started taking the study medication. The measure uses a 7-point Likert rating scale with responses ranging from "very much better" (1) to "very much worse" (7).
Change from Baseline in Patient Global Impression of Severity Scale (PGI-S) Week 6 The PGI-S is a single, patient-reported item that assesses the participant's perceived level of anxiety over the past 7 days. The measure uses a 5-point Likert rating scale with responses ranging from "none" (1) to "very severe" (5), with higher scores indicating greater anxiety severity.
Trial Locations
- Locations (36)
ATP Clinical Research, Inc /ID# 230445
🇺🇸Costa Mesa, California, United States
FutureSearch Trials of Dallas, LP /ID# 230535
🇺🇸Dallas, Texas, United States
Anderson Clinical Research /ID# 230440
🇺🇸Redlands, California, United States
Baber Research Group /ID# 230447
🇺🇸Naperville, Illinois, United States
Galiz Research - Palmetto Medical Plaza /ID# 230446
🇺🇸Hialeah, Florida, United States
Viking Clinical Research /ID# 230379
🇺🇸Temecula, California, United States
Great Lakes Clinical Trials /ID# 231296
🇺🇸Chicago, Illinois, United States
California Neuroscience Research Medical Group, Inc. /ID# 230453
🇺🇸Sherman Oaks, California, United States
Fieve Clinical Research, Inc. /ID# 230452
🇺🇸New York, New York, United States
Clinilabs, Inc. /ID# 230958
🇺🇸New York, New York, United States
Manhattan Behavioral Medicine PLLC /ID# 229713
🇺🇸New York, New York, United States
Carolina Institute for Clinical Research - Fayetteville /ID# 230961
🇺🇸Fayetteville, North Carolina, United States
Ohio State Harding Hospital /ID# 231302
🇺🇸Columbus, Ohio, United States
CincyScience /ID# 229719
🇺🇸West Chester, Ohio, United States
Integrative Clinical Trials /ID# 230955
🇺🇸Brooklyn, New York, United States
SPRI Clinical Trails /ID# 230957
🇺🇸Brooklyn, New York, United States
WR-PRI, LLC - Encino /ID# 230434
🇺🇸Encino, California, United States
Pharmacology Research Inst /ID# 230869
🇺🇸Newport Beach, California, United States
ProScience Research Group /ID# 231520
🇺🇸Culver City, California, United States
Synergy San Diego /ID# 231006
🇺🇸Lemon Grove, California, United States
Axiom Research /ID# 230728
🇺🇸Colton, California, United States
Pharmacology Research Institute - Wake LLC /ID# 230722
🇺🇸Los Alamitos, California, United States
Pacific Clinical Research Management Group /ID# 229725
🇺🇸Upland, California, United States
Research Strategies of Memphis /ID# 230443
🇺🇸Memphis, Tennessee, United States
Earle Research /ID# 230969
🇺🇸Houston, Texas, United States
Grayline Research Center /ID# 230455
🇺🇸Wichita Falls, Texas, United States
Alivation Research /ID# 230449
🇺🇸Lincoln, Nebraska, United States
ActivMed Practices and Research, LLC. /ID# 230441
🇺🇸Methuen, Massachusetts, United States
Center for Emotional Fitness /ID# 230450
🇺🇸Cherry Hill, New Jersey, United States
Hassman Research Institute Marlton /ID# 233252
🇺🇸Marlton, New Jersey, United States
Woodstock Research Center /ID# 231005
🇺🇸Woodstock, Vermont, United States
Clinical Neuroscience Solutions - Memphis /ID# 230734
🇺🇸Memphis, Tennessee, United States
Boston Clinical Trials /ID# 231003
🇺🇸Boston, Massachusetts, United States
Preferred Research Partners /ID# 232286
🇺🇸Little Rock, Arkansas, United States
Sooner Clinical Research /ID# 229731
🇺🇸Oklahoma City, Oklahoma, United States
Austin Clinical Trial Partners /ID# 229727
🇺🇸Austin, Texas, United States