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临床试验/PER-084-12
PER-084-12未知未知

A RANDOMIZED, DOUBLE-BLIND, 12-WEEK, PARALLEL GROUP, PLACEBO-CONTROLLED STUDY OF THE EFFICACY AND SAFETY OF RO4917523 IN PATIENTS WITH FRAGILE X SYNDROME.

F. HOFFMANN-LA ROCHE LTD.,0 个研究点目标入组 0 人开始时间: 2013年2月5日最近更新:

试验速览

阶段
未知

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
16 至 50(—)

入选标准

  • 1. ADULTS AND ADOLESCENTS (AGES 16 TO 50)
  • 2. PATIENTS MUST AGREE TO EITHER REMAIN COMPLETELY ABSTINENT OR TO USE TWO EFFECTIVE CONTRACEPTIVE METHODS FROM SCREENING UNTIL 21 DAYS (5 HALF-LIVES) AFTER THE LAST DOSE OF STUDY TREATMENT AS FOLLOWS:
  • A) ALL MALES, INCLUDING MALE PARTNERS OF FEMALE PATIENTS, MUST USE A BARRIER METHOD OF CONTRACEPTION (E.G. CONDOM)
  • B) ALL FEMALES OF CHILDBEARING POTENTIAL AND FEMALE PARTNERS OF MALE PATIENTS, MUST CHOOSE FROM THE FOLLOWING CONTRACEPTIVE OPTIONS:
  • I. AN INTRAUTERINE DEVICE (IUD) WHICH WAS IMPLANTED AT LEAST 2 MONTHS PRIOR TO SCREENING
  • II. ESTABLISHED HORMONAL CONTRACEPTION (ORAL, VAGINAL, IMPLANTED OR INJECTABLE)
  • III. IN ADDITION TO A SPERMICIDAL AGENT (FOAM, GEL, CREAM, OR SUPPOSITORY), USE OF A BARRIER METHOD, SUCH AS A CONDOM, DIAPHRAGM, CERVICAL/VAULT CAP, OR VAGINAL SPONGE
  • 3. CGI-S OF 3 (MILDLY ILL) OR MORE
  • 4. ABC TOTAL SCORE OF 20 OR MORE
  • 5. DIAGNOSIS OF FXS WITH A CONFIRMED FMR1 FULL MUTATION
  • 6. THE PRESENCE OF A RELIABLE CAREGIVER, ABLE AND WILLING TO PROVIDE INFORMATION REGARDING PATIENT´S BEHAVIOR AND SYMPTOMS AND ABLE TO ADMINISTER TREATMENT
  • 7. LANGUAGE, HEARING AND VISION COMPATIBLE WITH THE STUDY MEASUREMENTS
  • 8. FOR THE MEDICATIONS ALLOWED (SECTION 4.4.1): STABLE REGIMEN FOR 4 WEEKS

排除标准

  • 1. HAVE PREVIOUSLY RECEIVED TREATMENT WITH ANOTHER MGIU5 RECEPTOR ANTAGONIST WITHIN 18 MONTHS OR R04917523
  • 2. ENROLLMENT/PARTICIPATION IN ANY INTERVENTIONAL STUDY (CLINICAL TRIAL) INVOLVING AN INVESTIGATIONAL DRUG (UNAPPROVED) OR NON-DRUG TREATMENT WITHIN THE PRIOR 3 MONTHS OR 5 TIMES THE HALF-LIFE (WHICHEVER IS LONGER)
  • 3. HYPERSENSITIVITY TO THE EXCIPIENTS OF THE STUDY DRUG [1]
  • 4. ANY UNCONTROLLED, UNSTABLE CLINICALLY SIGNIFICANT PSYCHIATRIC CONDITION OTHER THAN FXS THAT MAY INTERFERE WITH THE INTERPRETATION OF SAFETY AND EFFICACY EVALUATIONS
  • 5. CURRENT SYMPTOMS OR PRESUMPTION OF PSYCHOSIS OR EUPHORIA, HISTORY OF CATATONIA, HALLUCINATIONS OR DELUSIONAL THOUGHTS
  • 6. HISTORY OF SUICIDAL BEHAVIOR OR OTHERWISE CONSIDERED A HIGH SUICIDAL RISK BY THE INVESTIGATOR
  • 7. SEVERE SELF-INJURIOUS BEHAVIORS THAT ARE CURRENT OR IN THE PAST 5 YEARS, WITH THE EXCEPTION OF HAND BITING
  • 8. BEHAVIORAL DYSFUNCTION THAT WOULD PREVENT ADMINISTRATION OF THE STUDY PROCEDURES
  • 9. ALCOHOL AND SUBSTANCE ABUSE OR DEPENDENCE IN THE PAST 6 MONTHS

研究者

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