[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"ApexCPG LLC\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":66},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100633659","efficacy-of-cl25216-on-hormonal-balance-and-menstrual-health-in-women-with-primary-dysmenorrhea-100633659",false,"NCT07529561","Efficacy of CL25216 on Hormonal Balance and Menstrual Health in Women With Primary Dysmenorrhea.","The Effect of CL25216 on Hormonal Balance and Menstrual Health in Women With Primary Dysmenorrhea: A Randomized, Double-blind, Placebo Controlled Clinical Trial","PD","Inclusion Criteria:\n\n* Healthy females aged between 25-40 years with a Body Mass Index (BMI) of approximately 25 to 29 kg\u002Fm2.\n* Healthy women with primary dysmenorrhea Grade 2 (measured using Verbal Multi-dimensional scoring system (VMSS)) at least for 1 day in 50 % of menstrual cycles and maximum pain intensity score ≥4 on a 10 cm VAS for at least 3 menstrual cycles before participating in the study.\n* Subjects with regular menstrual cycles that typically occur between every 21-35 days (menstrual period 3-7 days) in last 6 months.\n* Subjects with normal pelvic TVS and breast mammogram.\n* Subjects without any chronic diseases having symptoms such as burning, itching, abnormal vaginal discharge.\n* Subjects willing to provide their age of menarche and regularity in menstrual cycle.\n* Subjects without any clinical history of Gynaecological disorders or ovarian pathology, pelvic pathology like pelvic inflammatory disease, tumour and fibroma or without any history of pelvic surgery (screened using pelvic transvaginal sonography (TVS))\n* Subjects with normal thyroid profile\n* Subjects willing not to use any analgesics 24 hrs. prior screening and throughout the study.\n* Females of childbearing potential who are sexually active must agree to use adequate non-hormonal contraception during the study.\n* Normal vital signs, including electrocardiogram (ECG) and laboratory evaluations (including clinical chemistry, haematology, and complete urinalysis) within the reference range for the testing laboratory or the results are deemed not clinically significant for inclusion into this study by the investigator.\n* Subject understands the study procedures and provides signed informed consent to participate in the study\n\nExclusion Criteria:\n\n* Subjects with irregular menstrual cycle (shorter than 21 and longer than 35 days) affecting the treatment and efficacy judgment.\n* Subjects with secondary dysmenorrhea (menstrual pain associated with conditions such as endometriosis, pelvic inflammatory disease, leiomyomas, Mullerian anomalies, and adenomyosis and interstitial cystitis).\n* Subjects who are on related medications such as NSAIDs or hormonal contraceptive pills or intrauterine contraceptive devices in the past 3 months.\n* History of cerebrovascular disease, thrombo-embolic disorders, heart attack, or angina at any time or thrombophlebitis within the last 5 years, on anti-coagulant or anti-platelet drugs daily for any conditions.\n* Subjects with a high blood pressure (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥ 90 mmHg) and Fasting blood glucose level \\>125 mg\u002Fdl at screening.\n* Subjects who had any hormonal therapy or any other herbal products in the past 3 months.\n* Hypothyroidism, hyperthyroidism, hyperprolactinemia, Cushing's syndrome and congenital adrenal hyperplasia, following a special diet for the past 3 months, taking drugs affecting insulin sensitivity or lipid and hormonal profiles, including glucocorticoids, ovulation-stimulating drugs, anti-obesity, anti-diabetes, anti-hypertensive, anti-estrogenic, anti-androgenic during the last 3 months.\n* Active gall bladder disease, gynaecological or breast surgery in the last 6 months.\n* Subjects underwent hysterectomy or bilateral oophorectomy.\n* History of breast, endometrial, other gynaecological cancer at any time or other cancer within the last 5 years.\n* Smokers or tobacco users.\n* Alcohol intake (\\>2 standard drinks per day), or recreational drugs (such as cocaine, methamphetamine, marijuana, etc.) or psychiatric drug users.\n* Pregnant and lactating mothers.\n* History of hypersensitivity reactions attributed to investigational product (IP) or its components or related products.\n* History of positive hepatitis screening including Hepatitis B surface antigen or Hepatitis C virus (HCV) antibodies or subjects with human immunodeficiency virus (HIV) and \u002For syphilis.\n* History of clinically significant illness or any other medical disorder that may interfere with subject treatment, assessment or compliance with the protocol.\n* Any condition that in opinion of the Investigator, does not justify the subjects' participation in the study.\n* Subjects with a systemic disease including tuberculosis, leucosis, collagenosis, multiple sclerosis or other autoimmune diseases.\n* Subject consumes significant amounts of soya products in the diet or any products containing red clover, black cohosh, omega 3 or omega 6 fatty acids or any other Ayush or homeopathic preparations that can interfere with the study",true,"FEMALE","25 Years","40 Years",{"count":22,"type":23},80,"ESTIMATED","INTERVENTIONAL",[26],"NA","This study is to evaluate the effects of CL25216 on hormonal balance and menstrual health in women with primary dysmenorrhea. Enrolled subjects will receive either CL25216 - 250 mg\u002Fday or placebo.",[29,30],"Primary Dysmenorrhea","Menstural Cramps","NOT_YET_RECRUITING","2026-04-08",{"date":34,"type":35},"2026-04-14","ACTUAL",{"date":37,"type":23},"2026-04-13",{"date":39,"type":23},"2026-09-10",{"name":41,"class":42},"ApexCPG LLC","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":17,"sex":18,"minAge":20,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":24,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":43},"100601604","efficacy-of-cl25216-on-vasomotor-symptoms-in-women-during-perimenopause-100601604","NCT07112651","Efficacy of CL25216 on Vasomotor Symptoms in Women During Perimenopause","The Effects of CL25216 on Vasomotor Symptoms in Women During Perimenopause: a Randomised, Double-blind, Placebo-controlled Study","Inclusion Criteria:\n\n* Healthy overweight women (BMI: 25-29 kg\u002Fm2) aged between 40 to 55 years with reports of changes in their menstrual cycle for at least 3 months.\n* Participants needed to have a total score of greater than 16 on the Greene Climacteric Scale (GCS), have an intact uterus and ovaries.\n* Early Perimenopausal Women according \"The Stages of Reproductive Aging Workshop (STRAW) Classification (-2)\" irregular periods without skipping menstrual cycles and more than seven days difference in length of consecutive cycles.\n* Subjects with serum FSH \\>20 U\u002FL on 3-5 days of menstrual cycle.\n* Subjects with normal pelvic TVS and breast mammogram.\n* Subjects with normal fasting blood glucose level (\\\u003C125 mg\u002Fdl).\n* Subject understands the study procedures and provides signed informed consent to participate in the study.\n* Subjects with normal blood thyroid profile.\n* Females of childbearing potential who are sexually active must agree to use adequate contraception and can neither be pregnant nor lactating from screening throughout the duration of the study.\n* Clinical screening including vital signs, electrocardiogram (ECG) and laboratory evaluations (including clinical chemistry, haematology, and complete urinalysis) within the reference range for the testing laboratory or the results are deemed not clinically significant for inclusion into this study by the investigator.\n\nExclusion Criteria:\n\n* History of cerebrovascular disease, thrombo-embolic disorders, heart attack, or angina at any time or thrombophlebitis within the last 5 years, on anti-coagulant or anti-platelet drugs daily for any conditions.\n* Subjects who had received hormonal treatment or any other herbal products in the previous 6 months.\n* Subjects underwent treatment for COVID 19 within last 3 months or tested positive during the study will be excluded.\n* Subjects diagnosed with ovarian cysts ≥ 4 cm or any underlying pathology in pelvic ultrasonography (USG) performed during screening.\n* Chronic or acute life stressors relating to a major life change, experiencing depression and\u002For receiving medication for such illness or disorders, receiving statins or other drugs known to impact on steroid hormone levels.\n* Subjects having active gall bladder disease, gynaecological or breast surgery in the last 6 months.\n* History of breast, endometrial, other gynaecological cancer at any time or other cancer within the last 5 years.\n* Subjects with abnormal ECG.\n* Pregnant and breast feeding female.\n* History of hypersensitivity reactions attributed to investigational product (IP) or its components or related products.\n* Donation\u002Floss of blood 1 unit or 350 mL within 90 days prior to receiving the first dose of study medication.\n* Use of any recreational drugs (cocaine, amphetamine, barbiturates, benzodiazepines, cannabinoids, and morphine).\n* History of clinically significant illness or any other medical disorder that may interfere with subject treatment, assessment, or compliance with the protocol.\n* Participated in a clinical study with an investigational drug or biologic within the last 30 days.\n* Any condition that in opinion of the investigator, does not justify the subjects\" participation in the study.\n* Subjects with a high blood pressure at screening (systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥ 100 mmHg).\n* Subjects with progressive systemic diseases (e.g. tuberculosis, leucosis, collagenosis, multiple sclerosis, AIDS, HIV infections, Hepatitis B surface antigen or Hepatitis C virus (HCV) antibodies or other auto-immune diseases).\n* Evidence or history of clinically significant (in the judgment of the Investigator) haematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, neurologic diseases, or malignancies, hypothyroidism.\n* High alcohol intake (\\>2 standard drinks per day), smokers (\\>5 cigarettes per day).","55 Years",{"count":22,"type":23},[26],"This study is to evaluate the effects of CL25216 on vasomotor symptoms in women during Perimenopause. Enrolled subjects will receive either CL25216 - 250 mg\u002Fday or placebo.",[56],"Vasomotor Symptoms","RECRUITING","2025-11-28",{"date":60,"type":35},"2025-12-05",{"date":62,"type":23},"2025-11-24",{"date":64,"type":23},"2026-06-12",{"name":41,"class":42},""]