Ignite Creation Date:
2025-12-24 @ 7:41 PM
Ignite Modification Date:
2026-01-04 @ 10:33 AM
Study NCT ID:
NCT06701903
Status:
RECRUITING
Last Update Posted:
2025-02-20
First Post:
2024-11-20
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Study of ITI-1284 as Monotherapy Treatment in Patients With Generalized Anxiety Disorder
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D000098647', 'term': 'Generalized Anxiety Disorder'}], 'ancestors': [{'id': 'D001008', 'term': 'Anxiety Disorders'}, {'id': 'D001523', 'term': 'Mental Disorders'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 570}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2024-11-21', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-02', 'completionDateStruct': {'date': '2027-06', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-02-19', 'studyFirstSubmitDate': '2024-11-20', 'studyFirstSubmitQcDate': '2024-11-20', 'lastUpdatePostDateStruct': {'date': '2025-02-20', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2024-11-22', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2027-06', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Hamilton Anxiety Rating Scale (HAM-A)', 'timeFrame': 'Week 6', 'description': 'The HAM-A Scale is a clinician-rated scale measuring both psychic anxiety (mental agitation and psychological distress) and somatic anxiety (physical complaints related to anxiety). It is comprised of 14 items that are rated on a 5-point scale ranging from 0'}], 'secondaryOutcomes': [{'measure': 'Clinical Global Impression Scale-Severity (CGI-S)', 'timeFrame': 'Week 6', 'description': "The CGI-S is a clinician-rated scale to assess a patient's overall mental health. The scale ranges from 1 (normal, not at all ill) to 7 (among the most extremely ill patients)"}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Generalized Anxiety Disorder']}, 'descriptionModule': {'briefSummary': 'This is a multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy, safety, and tolerability of ITI-1284 as monotherapy treatment in patients meeting Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria for GAD in patients who have had inadequate response to generalized anxiety disorder treatment.', 'detailedDescription': 'The study will be conducted in 3 periods:\n\n* Screening Period (up to 2 weeks) during which patient eligibility will be assessed and the washout of prohibited medications will occur;\n* Double-blind Treatment Period (6 weeks) during which a total of approximately 570 patients are planned to be randomized in a 1:1:1 ratio to receive one of the 3 treatments (ITI-1284 10 mg, ITI-1284 20 mg, or placebo);\n* Safety Follow-up Period (1 week) during which all patients will return for a safety follow-up visit approximately 1 week after the last dose of study drug.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Provide written informed consent before the initiation of any study specific procedures;\n* At Screening, meet Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) diagnostic criteria for moderate or severe GAD as confirmed by the Investigator or Sponsor-approved rater using the Structured Clinical Interview for DSM-5 Clinical Trials Version (SCID-5-CT), and meets all of the following at Screening and Baseline:\n\n * HAM-A Total score of ≥ 22;\n * HAM-A Items 1 (anxious mood) and 2 (tension) scores ≥ 2;\n * CGI-S score of ≥ 4;\n* History of inadequate response (\\< 50% improvement in anxiety symptoms as measured by the modified Antidepressant Treatment Response Questionnaire \\[ATRQ\\] for GAD) to at least 2 of the following GAD-approved treatments: paroxetine, venlafaxine XR, duloxetine, escitalopram, or buspirone taken at an adequate dose (at least the minimum GAD-approved dose per package insert) and duration (ie, for at least 6 weeks prior to Screening) for the treatment of ongoing GAD symptoms.\n\nExclusion Criteria:\n\n* Within the patient\'s lifetime, has one of the following confirmed DSM-5-TR psychiatric diagnoses:\n\n * Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorder or other psychotic disorder;\n * Bipolar Disorder;\n* MADRS total score \\> 18 at Screening or Baseline;\n* In the opinion of the Investigator, the patient has a significant risk for suicidal behavior during his/her participation in the study or\n\n * At Screening, the patient scores "yes" on Suicidal Ideation Items 4 or 5 of the C-SSRS within 6 months prior to Screening or, at Baseline, the patient scores "yes" on Suicidal Ideation Items 4 or 5 since the Screening Visit;\n * At Screening, the patient has had 1 or more suicidal attempts within the 2 years prior to Screening;\n * At Screening or Baseline MADRS Item 10 score ≥ 5; or\n * The patient is considered to be an imminent danger to him/herself or others based on the assessment of the Investigator;\n* Lifetime history of failure to respond to \\> 3 of the approved treatments for GAD (ie, paroxetine, venlafaxine XR, duloxetine, escitalopram, or buspirone) at an adequate dose (ie, at least the minimum dose approved for GAD per package insert) and for an adequate duration (ie, at least 6 weeks).'}, 'identificationModule': {'nctId': 'NCT06701903', 'briefTitle': 'Study of ITI-1284 as Monotherapy Treatment in Patients With Generalized Anxiety Disorder', 'organization': {'class': 'INDUSTRY', 'fullName': 'Intra-Cellular Therapies, Inc.'}, 'officialTitle': 'A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of ITI-1284 as an Adjunctive Treatment in Patients With Generalized Anxiety Disorder Who Have an Inadequate Response to Generalized Anxiety Disorder Treatment', 'orgStudyIdInfo': {'id': 'ITI-1284-302'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'ITI-1284 10mg', 'description': 'ITI-1284 10 mg tablet, taken once daily, sublingual administration.', 'interventionNames': ['Drug: ITI-1284 10 mg']}, {'type': 'EXPERIMENTAL', 'label': 'ITI-1284 20mg', 'description': 'ITI-1284 20 mg tablet, taken once daily, sublingual administration.', 'interventionNames': ['Drug: ITI-1284 20 mg']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'description': 'Matching placebo tablet, taken once daily, sublingual administration', 'interventionNames': ['Drug: Placebo']}], 'interventions': [{'name': 'ITI-1284 10 mg', 'type': 'DRUG', 'description': 'ITI-1284 10 mg tablet, taken once daily, sublingual administration.', 'armGroupLabels': ['ITI-1284 10mg']}, {'name': 'ITI-1284 20 mg', 'type': 'DRUG', 'description': 'ITI-1284 20 mg tablet, taken once daily, sublingual administration.', 'armGroupLabels': ['ITI-1284 20mg']}, {'name': 'Placebo', 'type': 'DRUG', 'description': 'Matching placebo tablet, taken once daily, sublingual administration', 'armGroupLabels': ['Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '72211', 'city': 'Little Rock', 'state': 'Arkansas', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 34.74648, 'lon': -92.28959}}, {'zip': '90230', 'city': 'Culver City', 'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 34.02112, 'lon': -118.39647}}, {'zip': '91316', 'city': 'Encino', 'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 34.15917, 'lon': -118.50119}}, {'zip': '90024', 'city': 'Los Angeles', 'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '92056', 'city': 'Oceanside', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 33.19587, 'lon': -117.37948}}, {'zip': '32607', 'city': 'Gainesville', 'state': 'Florida', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 29.65163, 'lon': -82.32483}}, {'zip': '33176', 'city': 'Miami', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 25.77427, 'lon': -80.19366}}, {'zip': '32803', 'city': 'Orlando', 'state': 'Florida', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Cinical Site', 'geoPoint': {'lat': 28.53834, 'lon': -81.37924}}, {'zip': '30030', 'city': 'Decatur', 'state': 'Georgia', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 33.77483, 'lon': -84.29631}}, {'zip': '02131', 'city': 'Boston', 'state': 'Massachusetts', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '73116', 'city': 'Oklahoma City', 'state': 'Oklahoma', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 35.46756, 'lon': -97.51643}}, {'zip': '19063', 'city': 'Media', 'state': 'Pennsylvania', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 39.91678, 'lon': -75.38769}}, {'zip': '75231', 'city': 'Dallas', 'state': 'Texas', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 32.78306, 'lon': -96.80667}}, {'zip': '75243', 'city': 'Dallas', 'state': 'Texas', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 32.78306, 'lon': -96.80667}}, {'zip': '98007', 'city': 'Bellevue', 'state': 'Washington', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Clinical Site', 'geoPoint': {'lat': 47.61038, 'lon': -122.20068}}], 'centralContacts': [{'name': 'ITI Clinical Trials', 'role': 'CONTACT', 'email': 'ITCIClinicalTrials@itci-inc.com', 'phone': '6464409333'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Intra-Cellular Therapies, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}