Study of ITI-1284 as an Adjunctive Treatment in Patients With Generalized Anxiety Disorder

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorIntra-Cellular Therapies, Inc.

About this trial

This is a multicenter, randomized, double-blind, placebo-controlled study evaluating the efficacy, safety, and tolerability of ITI-1284 compared with placebo as adjunctive therapy to GAD treatment in patients meeting Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria for GAD who have an inadequate response to ongoing GAD treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Provide written informed consent before the initiation of any study specific procedures;

Male or female patients ≥ 18 years of age;

HAM-A Total score of ≥ 22;

HAM-A Items 1 (anxious mood) and 2 (tension) scores ≥ 2;

Disqualifiers

Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorder or other psychotic disorder;

Bipolar Disorder;

MADRS total score > 18 at Screening or Baseline;

In the opinion of the Investigator, the patient has a significant risk for suicidal behavior during his/her participation in the study or

Trial design

Design model

Parallel

Treatments tested in this trial

  • ITI-1284 10 mg

    Drug

    ITI-1284 10 mg tablet, taken once daily, sublingual administration.

  • ITI-1284 20 mg

    Drug

    ITI-1284 20 mg tablet, taken once daily, sublingual administration.

  • Placebo

    Drug

    Matching placebo tablet, taken once daily, sublingual administration

Treatment groups

705 Participants
are divided into 3 treatment groups
Group A: ITI-1284 10 mgExperimental treatment 1 intervention
Group B: ITI-1284 20 mgExperimental treatment 1 intervention
Group C: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Hamilton Anxiety Rating Scale (HAM-A)

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 comprises of 14 items that are rated on a 5-point scale ranging from 0 = not present to 4 = very severe, disabling symptoms. The HAM-A total score ranges from 0 to 56 with a higher score indicating increased severity of anxiety symptoms.

Time frame
Week 6

Secondary outcomes

1

Clinical Global Impression Scale-Severity (CGI-S)

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)

Time frame
Week 6

Other outcomes

Sponsors and contacts

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