A Study of the Efficacy and Safety of MK-0653H in Japanese Participants With Hypercholesterolemia (MK-0653H-832)

Hypercholesterolemia Clinical Trial

Official title:

A Phase III, Randomized, Active Comparator-controlled, Clinical Trial to Study the Efficacy and Safety of MK-0653H in Japanese Patients With Hypercholesterolemia.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02741245
• Other study ID #: 0653H-832
• Secondary ID: 163336
• Status: Completed
• Phase: Phase 3
• Start date: June 9, 2016
• Est. completion date: January 18, 2017

Study information

• Verified date: February 2022
• Source: Organon and Co
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the efficacy and safety and tolerability of 2 dose levels of MK-0653H in Japanese participants. The primary hypotheses are that the administration of MK-0653H is safe and tolerable and that MK-0653H is superior to single entity of Ezetimibe and Rosuvastatin in percent reduction from baseline in low-density lipoprotein-cholesterol (LDL-C) after 12 weeks of treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 321
• Est. completion date: January 18, 2017
• Est. primary completion date: January 18, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 80 Years

Eligibility

Inclusion Criteria:

• Japanese

• Outpatient with hypercholesterolemia

• Female participant who is of reproductive potential has to agree to remain abstinent or use (or partner use) two acceptable methods of birth control from date of signed informed consent to the 14 days after the last dose of study drug

• Will maintain a stable diet that is consistent with the Japan Atherosclerosis Society Guideline 2012 (JAS 2012) for prevention of atherosclerotic cardiovascular diseases for the duration of the study

Exclusion Criteria:

• Uncontrolled hypertension (treated or untreated)

• Uncontrolled type 1 or type 2 diabetes mellitus

• History of coronary artery disease (CAD), CAD-equivalent disease

• Familial hypercholesterolemia or has undergone LDL apheresis

• Uncontrolled endocrine or metabolic disease known to influence serum lipids or lipoproteins

• Has had a gastrointestinal tract bypass, or other significant intestinal malabsorption

• History of cancer within the past 5 years (except for successfully treated dermatological basal cell or squamous cell carcinoma or in situ cervical cancer)

• Human Immunodeficiency Virus (HIV) positive

• History of drug/ alcohol abuse within the past 5 years or psychiatric illness not adequately controlled and stable on pharmacotherapy

• Consumes more than 25 g of alcohol per day

• Currently following an excessive weight reduction diet

• Currently engages in a vigorous exercise regimen (e.g.; marathon training, body building training etc.) or intends to start training during the study

• Hypersensitivity or intolerance to Ezetimibe or Rosuvastatin

• Myopathy or rhabdomyolysis with Ezetimibe or any statin

• Pregnant or lactating

• Taking any other investigational drugs and/or has taken any investigational drugs within 30 days

Related Conditions & MeSH terms

• Hypercholesterolemia

Intervention

Drug:
• Ezetimibe 10 mg

• Rosuvastatin 2.5 mg

• Placebo for Ezetimibe

• Placebo for Rosuvastatin

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Organon and Co

References & Publications (1)

Teramoto T, Yokote K, Nishida C, Oshima N, Takase T. A phase III clinical trial to study the efficacy and safety of ezetimibe plus rosuvastatin combination therapy in Japanese patients with hypercholesterolemia - A randomized, double-blind comparative stu

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage Change From Baseline in Low-density Lipoprotein-cholesterol (LDL-C)	Participants had LDL-C levels assessed at baseline and after 12 weeks of study drug administration. The change from baseline was calculated. Results were reported as a M-estimate.	Baseline and Week 12
Primary	Percentage of Participants Who Experience at Least 1 Adverse Event (AE)	An AE was defined as any untoward medical occurrence in a subject which does not necessarily have a causal relationship with the treatment. An AE was any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with use of a medicinal product, whether or not considered related to the medicinal product. The percentage of participants that reported at least 1 AE was summarized	up to 14 weeks
Primary	Percentage of Participants Who Had Study Drug Discontinued Due to Adverse Event	An AE was defined as any untoward medical occurrence in a subject which does not necessarily have a causal relationship with the treatment. An AE was any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with use of a medicinal product, whether or not considered related to the medicinal product. The percentage of participants that had study drug discontinued due to an AE was summarized.	up to 12 weeks
Primary	Percentage of Participants Who Experience 1 or More Gastrointestinal-related AEs	Gastrointestinal-related AEs included all preferred terms within system organ class of Gastrointestinal Disorders except Chapped Lips and Toothache.	up to 14 weeks
Primary	Percentage of Participants Who Experience 1 or More Gallbladder-related AEs	Gallbladder-related AEs included Bile Duct Obstruction, Bile Duct Stone, Bile Duct Stenosis, Biliary Colic, Cholangitis, Cholecystectomy, Cholecystitis, Cholelithiasis, Gallbladder Disorder, Gallbladder Perforation, Hepatic Pain, and Hydrocholecystis.	up to 14 weeks
Primary	Percentage of Participants Who Experience 1 or More Allergic Reaction or Rash AEs	Allergic Reaction or Rash AEs included Allergy to Arthropod Sting, Anaphylactoid Reaction, Anaphylactic Reaction, Anaphylatic Shock, Anaphylactoid Shock, Angioedema, Conjunctivitis Allergic, Contrast Media Reaction, Dermatitis, Dermatitis Allergic, Dermatitis Atopic, Dermatitis Bullous, Dermatitis Contact, Dermatitis Psoriasiform, Drug Hypersensitivity, Eczema, Eosinophila, Erythema, Eye Allergy, Face Oedema, Hypersensitivity, Mechanical Urticaria, Palmar Erythema, Periorbital Oedema, Photodermatosis, Photosensitivity Allergic reaction, Photosensitivity Reaction, Pigmentation Disorder, Pruritus, Pruritus Generalised, Rash, Rash Erythematous, Rash Follicular, Rash Generalised, Rash Maculo-Papular, Rash Papulosquamous, Rash Pruritic, Rash Pustular, Rash Vesicular, Rhinitis, Rhinitis Allergic, Rosacea, Skin Exfoliation, Skin Disorder, Skin Hyperpigmentation, Skin Lesion, Skin Mass, Skin Ulcer, Subcutaneous Nodule, Swelling Face, Systemic Lupus Erythematosus Rash, Urticaria.	up to 14 weeks
Primary	Percentage of Participants Who Experience 1 or More Hepatitis-related AEs	Hepatitis-related AEs included Cholestasis, Cytolytic Hepatitis, Hepatic Cyst, Hepatic Failure, Hepatic Lesion, Hepatic Necrosis, Hepatitis, Hepatitis Cholestatic, Hepatitis Fulminant, Hepatitis Infectious, Hepatocellular Injury, Hepatomegaly, Jaundice, Jaundice Cholestatic.	up to 14 weeks
Primary	Percentage of Participants Who Experience Consecutive Elevations in Alanine Aminotransferase (ALT) =3 Times Upper Normal Limit (ULN)	Participants had ALT levels assessed throughout the 12 week treatment period. Participants who had 2 consecutive assessments of ALT that were 3 x ULN or greater were recorded. The ALT ULN was 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Consecutive Elevations in Aspartate Aminotransferase (AST) =3 Times Upper Normal Limit (ULN)	Participants had AST levels assessed throughout the 12 week treatment period. Participants who had 2 consecutive assessments of AST that were 3 x ULN or greater were recorded. The AST ULN was 40 U/L..	up to 12 weeks
Primary	Percentage of Participants Who Experience Consecutive Elevations in Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) =3 Times Upper Normal Limit (ULN)	Participants had ALT and AST levels assessed throughout the 12 week treatment period. Participants who had 2 consecutive assessments of ALT and/or AST that were 3 x ULN or greater were recorded. The ALT and AST ULNs were 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevation in Alanine Aminotransferase (ALT) =5 Times Upper Normal Limit (ULN)	Participants had ALT levels assessed throughout the 12 week treatment period. Participants who had an assessments of ALT that was 5x ULN or greater were recorded. The ALT ULN was 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevation in Aspartate Aminotransferase (AST) =5 Times Upper Normal Limit (ULN)	Participants had AST levels assessed throughout the 12 week treatment period. Participants who had an assessments of AST that was 5x ULN or greater were recorded. The AST ULN was 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevation in Alanine Aminotransferase (ALT) =10 Times Upper Normal Limit (ULN)	Participants had ALT levels assessed throughout the 12 week treatment period. Participants who had an assessments of ALT that was 10x ULN or greater were recorded. The ALT ULN was 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevation in Aspartate Aminotransferase (AST) =10 Times Upper Normal Limit (ULN)	Participants had AST levels assessed throughout the 12 week treatment period. Participants who had an assessments of AST that was 10x ULN or greater were recorded. The AST ULN was 40 U/L.	up to 12 weeks
Primary	Percentage of Participants Who Experience Consecutive Elevations in Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) =10 Times Upper Normal Limit (ULN)	Participants had ALT and AST levels assessed throughout the 12 week treatment period. Participants who had 2 consecutive assessments of ALT and/or AST that were 10x ULN or greater were recorded. The ALT and AST ULNs were 40 U/L.	up to 12 weeks
Primary	Percentage of Participants With Potential Hy's Law Condition	Percentage of Participants with Potential Hy's Law Condition (defined as serum ALT or serum AST elevations >3xULN, with serum alkalinephosphatase <2xULN and total bilirubin (TBL) =2xULN) was summarized. The ALT and AST ULNs were 40 U/L. The ULN for alkaline phosphatase was 359 IU/L and the ULN for total bilirubin was 1.2 mg/dL.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevations in Creatine Kinase (CK) =10 Times ULN	Participants had creatine phosphokinase (CK) levels assessed throughout the 12 week treatment period. Participants who had any CK level that was =10 x ULN were recorded. The CK ULNs for males and females were 287 IU/L and 163 IU/L, respectively.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevations in Creatine Kinase (CK) =10 Times ULN With Muscle Symptoms	Participants had CK levels assessed throughout the 52 week treatment period. Participants who had any CK level that was =10 x ULN and had associated muscle symptoms present within +/- 7 days were recorded. The CK ULNs for males and females were 287 IU/L and 163 IU/L, respectively.	up to 12 weeks
Primary	Percentage of Participants Who Experience Elevations in Creatine Kinase (CK) =10 Times ULN and Drug-Related Muscle Symptoms	Participants had CK levels assessed throughout the 52 week treatment period. Participants who had any CK level that was =10 x ULN and had associated muscle symptoms present within +/- 7 days that were reported as at least possibly-related to study drug were recorded. The CK ULNs for males and females were 287 IU/L and 163 IU/L, respectively.	up to 12 weeks