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.
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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