A DOUBLE-BLND, RANDOMIZED, PLACEBO-CONTROLLED, MULTICENTER, PARALLEL-GROUP, ADAPTIVE-DESIGN, DOSE-RANGING STUDY OF MK-1029 IN ADULT SUBJECTS WITH PERSISTENT ASTHMA.

MERCK SHARP & DOHME PERU S.R.L.,0 个研究点目标入组 60 人开始时间: 2013年3月4日最近更新: 2023年9月4日

试验速览

暂无简介。

•1.SUBJECT IS A FEMALE OR MALE SUBJECT BETWEEN 18 AND 75 YEARS OF AGE.
•2.SUBJECT IS NOT PREGNANT (AS EVIDENCED BY NEGATIVE SERUM PREGNANCY TEST FOR SUBJECTS OF CHILDBEARING POTENTIAL) OR BREASTFEEDING AND DOES NOT PLAN TO BECOME PREGNANT FOR THE DURATION OF THE STUDY AND POST STUDY FOLLOW-UP PERIOD.
•3.A SUBJECT WHO IS OF REPRODUCTIVE POTENTIAL AGREES TO REMAIN ABSTINENT OR USE (OR HAVE THEIR PARTNER USE) 2 ACCEPTABLE METHODS OF BIRTH CONTROL WITHIN THE PROJECTED DURATION OF THE STUDY. ACCEPTED METHODS OF BIRTH CONTROL ARE: INTRAUTERINE DEVICE (IUD), DIAPHRAGM WITH SPERMICIDE, CONTRACEPTIVE SPONGE, CONDOM, VASECTOMY, HORMONAL CONTRACEPTIVES.
•A FEMALE SUBJECT WHO IS NOT OF REPRODUCTIVE POTENTIAL IS ELIGIBLE WITHOUT REQUIRING THE USE OF CONTRACEPTION. A FEMALE SUBJECT WHO IS NOT OF REPRODUCTIVE POTENTIAL IS DEFINED AS: ONE WHO HAS EITHER 1) REACHED NATURAL MENOPAUSE (DEFINED AS 6 MONTHS OF SPONTANEOUS AMENORRHEA WITH SERUM FOLLICLE STIMULATING HORMONE (FSH) LEVELS IN THE POSTMENOPAUSAL RANGE AS DETERMINED BY THE LABORATORY, OR 12 MONTHS OF SPONTANEOUS AMENORRHEA), 2) 6 WEEKS POST SURGICAL BILATERAL OOPHORECTOMY WITH OR WITHOUT HYSTERECTOMY, OR 3) BILATERAL TUBAL LIGATION.

•1.SUBJECT IS, IN THE OPINION OF THE INVESTIGATOR, MENTALLY OR LEGALLY INCAPACITATED PREVENTING INFORMED CONSENT FROM BEING OBTAINED, UNABLE TO READ OR COMPREHEND WRITTEN MATERIAL, OR UNABLE TO COMPLY WITH THE STUDY PROCEDURES OR PROTOCOL.
•2.SUBJECT HAS A RECENT HISTORY (≤ 3 MONTHS) OF MYOCARDIAL INFARCTION, CONGESTIVE HEART FAILURE, OR UNCONTROLLED CARDIAC ARRHYTHMIA PRIOR TO VISIT 1.
•3.SUBJECT IS HOSPITALIZED OR HAS BEEN HOSPITALIZED IN THE 4 WEEKS PRIOR TO VISIT 1.
•4.SUBJECT INTENDS TO MOVE OR ANTICIPATES MISSING ANY CLINIC VISIT DAYS.
•5.SUBJECT HAS UNDERGONE ANY MAJOR SURGICAL PROCEDURE WITHIN THE 4 WEEKS PRIOR TO VISIT 1.
•6.SUBJECT HAS PARTICIPATED IN A CLINICAL STUDY INVOLVING AN INVESTIGATIONAL DRUG WITHIN THE 4 WEEKS PRIOR TO VISIT 1.
•7.SUBJECT IS CURRENTLY A REGULAR USER OR A RECENT PAST ABUSER (WITHIN THE PAST 5 YEARS) OF ALCOHOL (>14 DRINKS/WEEK) OR ILLICIT DRUGS.
•8.SUBJECT HAS DONATED A UNIT OF BLOOD WITHIN THE 2 WEEKS PRIOR TO VISIT 1 OR INTENDS TO DONATE A UNIT OF BLOOD AT ANY TIME DURING THE COURSE OF THIS STUDY.
•9.SUBJECT HAS EVIDENCE OF ANOTHER CLINICALLY SIGNIFICANT, ACTIVE PULMONARY DISORDER SUCH AS BRONCHIECTASIS OR CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD) DOCUMENTED BY HISTORY, PHYSICAL EXAMINATION, OR CHEST X-RAY.

发起方

MERCK SHARP & DOHME PERU S.R.L.,