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Kusajili – Clinical trials directory
Result
of your search per sponsor: Merck & Co., Inc
Woman and Man Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Phase IIa Randomized, Double-Blind, Parallel-Groups, Placebo-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0724 Intravenous Infusion on the Amelioration of Neurological Damage and Recovery from Middle Cerebral Artery Ischemic Stroke
To compare the efficacy MK-0724 8 mg/kg/hr x 1 hr daily for 7 days to placebo in patients with middle cerebral artery ischemic stroke using the Day 90 Action Research Arm Test (ARAT) scores.
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Multicenter, Randomized, Double-Blind Study to Evaluate the Safety of MK-0431 Monotherapy in Patients With Type 2 Diabetes Mellitus and Chronic Renal Insufficiency Who Have Inadequate Glycemic Control
In patients with type 2 diabetes mellitus and chronic renal insufficiency with inadequate glycemic control Primary: To assess the safety and tolerability of MK-0431 after 12 weeks.
Country
None
organs
None
Specialty
None
unknown
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Man Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Phase III Study to Assess the Safety, Tolerability, and Efficacy of MK-0822 (Odanacatib) in Prolonging Bone Metastasis-Free Survival in Men with Castration-Resistant Prostate Cancer
• To assess the effect of treatment with MK-0822 5 mg once daily on bone metastasis-free survival (defined as time to first bone metastasis or death from any cause) compared to placebo. • To assess th...
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Phase III Study to Assess the Tolerability and Efficacy of MK-0822 (Odanacatib) in Reducing the Risk of Bone Metastases and Prolonging Disease-Free Survival in Women with Breast Cancer
Objective: To assess the effect of treatment with MK-0822 5 mg once daily on the risk of developing a first bone metastasis (first disease recurrence) compared to placebo Objective: To assess the ...
Country
None
organs
None
Specialty
None
unknown
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Woman Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Phase II Study to Assess the Safety, Tolerability, and Efficacy of MK-0822 (Cathepsin-K Inhibitor) in the Treatment of Women with Breast Cancer and Established Bone Metastases (MBD)
E.2.1 Main objective: To assess the safety, tolerability, and biochemical efficacy (changes in urinary NTx) of MK-0822 in women with breast cancer and MBD
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc
Update Il y a 5 ans
The effect and long-term safety of MK-0887A in children with asthma
Primary Efficacy Objective: To demonstrate the efficacy of MF/F 100/10 mcg twice daily, compared with MF 100 mcg twice daily, by evaluating lung function during the first 12 weeks of double-blind tre...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., N.J., USA
Update Il y a 5 ans
A Randomized, Double-Blind, Active-Controlled, Multicenter Study of Patients with Cardiovascular Disease and Diabetes Mellitus Not Adequately Controlled with Simvastatin 20 mg or Atorvastatin 10 mg: A Comparison of Switching to a Combination Tablet Ezetimibe/Simvastatin (10mg/20mg) Versus Switching to Rosuvastatin 10mg or Doubling the Statin Dose
In patients with cardiovascular disease (CVD) and diabetes mellitus treated with simvastatin 20 mg or atorvastatin 10 mg with LDL-Cholesterol blood level (LDL-C) ≥70 mg/dl (1.81 mmol/L) and ≤160 mg/dl...
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc
Update Il y a 5 ans
Vaginal ring dose-finding study on ovarian function and vaginal bleeding in healthy women aged 18-35 years
1. Inhibition of ovulation, which is considered confirmed if in the subset of subjects for whom the test will be performed, ovulation is observed in less than 15% of the subjects at any time during th...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Merck & Co., Inc
Update Il y a 5 ans
A Phase III Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Prospectively Evaluate Efficacy of Montelukast in Patients Aged 6 Months to 5 Years With Chronic Asthma
E.2.1 Main objective: To demonstrate that montelukast, compared with placebo, improves asthma control (as measured by the percentage of days without asthma ) over a 24-week treatment period in patien...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc
Update Il y a 5 ans
Pembrolizumab (MK-3475) in High Risk Non-muscle Invasive Bladder Cancer (NMIBC) Patients Unresponsive to Bacillus Calmette-Guerin (BCG) Therapy
Objective 1: To evaluate anti-tumor activity of pembrolizumab (MK-3475), with regards to absence of high risk NMIBC or progressive disease, as determined by cystoscopy, cytology, biopsy (if applicable...
Country
None
organs
None
Specialty
None
unknown
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