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临床试验/PER-123-12
PER-123-12未知未知

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PAHSE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ONCE A DAY, TAK-375 (RAMELTEON) TABLET FOR SUBLINGUAL ADMINISTRATION (TAK-375SL TABLET) 0.1, 04, AND 0.8 MG AS ADJUNCTIVE THERAPY IN THE TREATMENT O ACUTE DEPRESSIVE EPISODES ASSOCIATED WITH BIPOLAR 1 DISORDER IN ADULT SUBJECTS

TAKEDA GLOBAL RESEARCH & DEVELOPMENT CENTER, INC.,0 个研究点目标入组 0 人开始时间: 2013年8月2日最近更新:

试验速览

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 75(—)

入选标准

  • 1. IN THE OPINION OF THE INVESTIGATOR, THE SUBJECT IS CAPABLE OF UNDERSTANDING AND COMPLYING WITH PROTOCOL REQUIREMENTS.
  • 2. THE SUBJECT OR, WHEN APPLICABLE, THE SUBJECT´S LEGALLY ACCEPTABLE REPRESENTATIVE SIGNS AND DATES A WRITTEN, INFORMED CONSENT FORM AND ANY REQUIRED PRIVACY AUTHORIZATION PRIOR TO THE INITIATION OF ANY STUDY PROCEDURES.
  • 3. THE SUBJECT IS A MAN OR WOMAN AGED BETWEEN 18 AND 75 YEARS, INCLUSIVE.
  • 4. THE SUBJECT SUFFERS FROM BIPOLAR 1 DISORDER, MOST RECENT EPISODE DEPRESSED AS THE PRIMARY DIAGNOSIS ACCORDING TO DSM-IV-TR CRITERIA (CLASSIFICATION CODE 296.5X) AND CONFIRMED BY THE STRUCTURED CLINICAL INTERVIEW FOR DSM DISORDERS (SCID).
  • 5. THE REPORTED DURATION OF THE CURRENT MAJOR DEPRESSIVE EPISODE (MDE) IS AT LEAST FOUR WEEKS AND LESS THAN 6 MONTHS.
  • 6. THE SUBJECT HAS A YMRS SCORE OF ≤ 10 BOTH AT THE SCREENING AND BASELINE VISITS.
  • 7. THE SUBJECT HAS A MADRS TOTAL SCORE ≥ 24 AT THE SCREENING AND BASELINE VISITS.
  • 8. THE SUBJECT HAS A CGI-S SCORE OF ≥ 4 AT THE SCREENING AND BASELINE VISITS.
  • 9. HAM- A SCORE IS≤ 21 AT SCREENING AND BASELINE VISITS.

排除标准

  • 1. THE SUBJECT HAS RECEIVED ANY INVESTIGATIONAL COMPOUND <30 DAYS BEFORE SCREENING OR 5 HALF-LIVES WHICHEVER IS LONGER PRIOR TO SCREENING.
  • 2. THE SUBJECT HAS RECEIVED TAK-375 OR TAK-375SL IN A PREVIOUS CLINICAL STUDY OR HAS EVER USED RAMELTEON.
  • 3. THE SUBJECT IS AN IMMEDIATE FAMILY MEMBER, STUDY SITE EMPLOYEE, OR IS IN A DEPENDENT RELATIONSHIP WITH A STUDY SITE EMPLOYEE WHO IS INVOLVED IN CONDUCT OF THIS STUDY (EG, SPOUSE, PARENT, CHILD, SIBLING) OR MAY CONSENT UNDER DURESS.
  • 4. THE SUBJECT HAS ONE OR MORE OF THE FOLLOWING:
  • A. ANY CURRENT PSYCHIATRIC DISORDER WHICH IS THE PRIMARY FOCUS OF TREATMENT OTHER THAN BIPOLAR 1 DISORDER, MOST RECENT EPISODE DEPRESSED AS DEFINED IN THE DSM-IV-TR, AS ASSESSED BY THE SCID.
  • B. CURRENT OR HISTORY OF: SCHIZOPHRENIA, SCHIZOAFFECTIVE DISORDER, UNIPOLAR DEPRESSION WITH PSYCHOTIC FEATURES, BIPOLAR DEPRESSION WITH PSYCHOTIC FEATURES, ANY OTHER PSYCHOTIC DISORDER (WITH THE EXCEPTION OF PSYCHOSIS ASSOCIATED WITH A MANIC OR MIXED EPISODE), OCD, MENTAL RETARDATION, ORGANIC MENTAL DISORDERS, OR MENTAL DISORDERS DUE TO A GENERAL MEDICAL CONDITION AS DEFINED IN THE DSM-IV-TR.

研究者

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