Primary HypercholesterolemiaPhase 3NCT01294683
A Study to Evaluate Efficacy and Safety of Extended-Release Niacin + Laropiprant + Simvastatin in Participants With Primary Hypercholesterolemia or Mixed Dyslipidemia (MK-0524B-118)
A Phase 3 study testing Simvastatin, Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM) and Extended Release (ER) niacin/laropiprant (N/LRPT) in people with Primary Hypercholesterolemia and Dyslipidemia, run by Merck Sharp & Dohme LLC.
Trial summary
This study is being done to find out if tablets containing extended release (ER) niacin, laropiprant, and simvastatin (ERN/LRPT/SIM) are as effective as tablets containing ER niacin and laropiprant taken with simvastatin tablets (ERN/LRPT + SIM) for lowering high cholesterol and high lipid levels in the blood. Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Primary Hypercholesterolemia, Dyslipidemia
- What is being tested?
- Simvastatin, Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM) and Extended Release (ER) niacin/laropiprant (N/LRPT)
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 977 participants
- Where
- No sites listed yet
- Study dates
- 4 Feb 2011to 17 Jan 2012
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Participant has a history of primary hypercholesterolemia or mixed dyslipidemia and meets LDL-C and triglyceride criteria.
- Visit 2:
- Participant is high risk coronary heart disease (CHD) or CHD risk-equivalent.
Who cannot join
- Participant is pregnant or breast-feeding, or expecting to conceive during the study.
- Participant has a history of malignancy.
- Participant consumes more than 3 alcoholic drinks per day (14 per week).
- Participant is high risk CHD patient on statin therapy or any patient on statin therapy equivalent to 80 mg simvastatin.
- Participant with Type 1 or Type 2 diabetes mellitus that is poorly controlled, or on statin therapy.
- Participant currently engages in vigorous exercise or is on an aggressive diet regimen.
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- Participant uncontrolled endocrine or metabolic disease, uncontrolled gout, kidney or hepatic disease, heart failure, recent peptic ulcer disease, hypersensitivity or allergic reaction to niacin or simvastatin, recent heart attack, stroke or heart surgery.
- Participant is human immunodeficiency virus (HIV) positive.
- Participant has taken niacin >50 mg/day, bile-acid sequestrants, hydroxymethyl glutaryl coenzyme A (HMG-CoA) reductase inhibitors, ezetimibe, Cholestin™ [red yeast rice] and other red yeast products within 6 weeks, or fibrates within 8 weeks of randomization visit (Visit 3).
- Note: Fish oils, phytosterol margarines and other non-prescribed therapies are allowed provided participant has been on a stable dose for 6 weeks prior to Visit 2 and agrees to remain on this dose for the duration of the study.
- Participant is currently receiving cyclical hormonal contraceptives or intermittent use of hormone replacement therapies (HRTs) (e.g., estradiol, medroxyprogesterone, progesterone).
- Note: Participants who have been on a stable dose of non-cyclical HRT or hormonal contraceptive for greater than 6 weeks prior to Visit 1 are eligible if they agree to remain on the same regimen for the duration of the study.
- Participant is taking prohibited medications such as systemic corticosteroids, itraconazole or ketoconazole, erythromycin, clarithromycin, or telithromycin, nefazodone, HIV protease inhibitors, verapamil, amiodarone, cyclosporine, danazol, diltiazem or fusidic acid.
- Participant consumes >1 quart of grapefruit juice/day.
About this study
Official title: A Phase III Multicenter, Double-Blind, Crossover Design Study to Evaluate Lipid-Altering Efficacy and Safety of Extended-Release Niacin/Laropiprant/Simvastatin Combination Tablet in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia
This study is being done to find out if tablets containing extended release (ER) niacin, laropiprant, and simvastatin (ERN/LRPT/SIM) are as effective as tablets containing ER niacin and laropiprant taken with simvastatin tablets (ERN/LRPT + SIM) for lowering high cholesterol and high lipid levels in the blood. The primary hypothesis is that ERN/LRPT/SIM 2 g/40 mg is equivalent to ERN/LRPT 2 g co-administered with simvastatin 40 mg in reducing low-density lipoprotein cholesterol (LDL-C).
- Conditions
- Primary Hypercholesterolemia, Dyslipidemia
- Being tested
- Simvastatin, Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM), Extended Release (ER) niacin/laropiprant (N/LRPT), Placebo
- Keywords
- Low-density lipoprotein, LDL, High-density lipoprotein, HDL, Niacin, Lipid modifying therapy, Cholesterol, High cholesterol, Triglycerides, Mixed Dyslipidemia
- Medical subject headings
- Dyslipidemias, Hypercholesterolemia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
SimvastatinDrug
Also called Zocor
Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM)Drug
Also called MK-0524B
Extended Release (ER) niacin/laropiprant (N/LRPT)Drug
Also called MK-0524A
PlaceboDrug
| Study group | Role | What they receive |
|---|---|---|
| Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg | Experimental | After a 2-week placebo run-in, participants received extended release (ER) niacin/laropiprant (N/LRPT) 1 g/20 mg combination tablet (MK-0524B) once daily for 4 weeks, then ERN/LRPT/Simvastatin (SIM) 2 g/40 mg combination tablet once daily for 8 weeks. Participants then received ERN/LRPT 2 g (MK-0524A) co-administered with SIM 40 mg once daily for 8 weeks. Receives: Drug: Simvastatin; Drug: Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM); Drug: Extended Release (ER) niacin/laropiprant (N/LRPT); Drug: Placebo |
| Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g | Experimental | After a 2-week placebo run-in, participants received ERN/LRPT 1 g (MK-0524A) co-administered with SIM 20 mg once daily for 4 weeks then received ERN/LRPT 2 g (MK-0524A) co-administered with SIM 40 mg once daily for 8 weeks. Participants then received ERN/LRPT/SIM 2 g/40 mg combination tablets (MK-0524B) once daily for 8 weeks. Receives: Drug: Simvastatin; Drug: Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM); Drug: Extended Release (ER) niacin/laropiprant (N/LRPT); Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline in Low-density Lipoprotein Cholesterol (LDL-C)
Blood samples were taken at baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III) to determine the LDL-C levels. The change from baseline after 8 weeks of treatment was recorded.
Results from recent studies indicated that the combination tablet formulations used in the study did not meet the pre-specified pharmacokinetic bounds used to establish the equivalence of the combination tablet (MK-0524B; ERN/LRPT/SIM) to the coadministration of MK-0524A (ERN/LRPT) and SIM. Therefore, efficacy data were not analyzed, as the study was stopped early. Only safety data were evaluated.
Measured: Baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III)
Secondary outcomes (11)
Change From Baseline in High-density Lipoprotein Cholesterol (HDL-C)
Blood samples were taken at baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III) to determine the HDL-C levels. The change from baseline after 8 weeks of treatment was recorded.
Results from recent studies indicated that the combination tablet formulations used in the study did not meet the pre-specified pharmacokinetic bounds used to establish the equivalence of the combination tablet (MK-0524B; ERN/LRPT/SIM) to the coadministration of MK-0524A (ERN/LRPT) and SIM. Therefore, efficacy data were not analyzed, as the study was stopped early. Only safety data were evaluated.
Measured: Baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment during each period (Week 12 for Period II and Week 20 for Period III)
Percentage of Participants With Consecutive Elevations in Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) of >=3 x Upper Limit of Normal (ULN)
Participants had AST and ALT levels assessed during Period I (4 weeks ) and throughout each 8 week treatment period (20 weeks total). Participants who had an assessment of either AST or ALT that was 3 x ULN or greater were recorded. The AST UNLs for males and females were 43 U/L and 36 U/L, respectively. The ALT UNLs for males and females were 40 U/L and 33 U/L, respectively.
Measured: Up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Elevations in ALT and/or AST of >=5 x ULN
Participants had AST and ALT levels assessed during Period I (4 weeks ) throughout each 8 week treatment period (20 weeks total). Participants who had an assessment of either AST or ALT that was 5 x ULN or greater were recorded. The AST UNLs for males and females were 43 U/L and 36 U/L, respectively. The ALT UNLs for males and females were 40 U/L and 33 U/L, respectively.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Elevations in ALT and/or AST of >=10 x ULN
Participants had AST and ALT levels assessed during Period I (4 weeks ) throughout each 8 week treatment period (20 weeks total). Participants who had an assessment of either AST or ALT that was 10 x ULN or greater were recorded. The AST UNLs for males and females were 43 U/L and 36 U/L, respectively. The ALT UNLs for males and females were 40 U/L and 33 U/L, respectively.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Creatine Kinase (CK) >=10 x ULN
Participants had CK levels assessed throughout the treatment periods. Participants who had any CK level that was >=10 x ULN were recorded. The UNLs for males and females were 207 U/L and 169 U/L, respectively.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With CK >=10 x ULN With Muscle Symptoms - Drug Related
Participants had CK levels assessed throughout the treatment periods. 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 UNLs for males and females were 207 U/L and 169 U/L, respectively.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants Who Experienced at Least 1 Hepatitis-related Adverse Event (AE)
An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. Hepatitis-related AEs were identified by a collective review using the following pre-specified set of preferred terms: cholestasis, hepatic necrosis, hepatocellular damage, cytolytic hepatitis, hepatitis, hepatomegaly, jaundice, hepatic failure, hepatitis cholestatic, jaundice cholestatic, hepatitis fulminant, hyperbilirubinaemia, jaundice hepatocellular, ocular icterus, yellow skin, hepatic function abnormal, acute hepatic failure, subacute hepatic failure, hepatitis acute, hepatitis toxic, hepatotoxicity, and mixed hepatocellular-cholestatic injury.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With New Onset of Diabetes
Participants who with newly diagnosed of diabetes were recorded. A participant was classified as having new onset diabetes if they experienced an AE related to a diagnosis of diabetes (based on a pre-defined set of Medical Dictionary for Regulatory Activities [MedDRA] terms), or if they started taking an anti-diabetic medication during the course of the study. The MedDRA terms were as follows: diabetes mellitus, diabetes mellitus insulin-dependent, diabetes mellitus non-insulin dependent, insulin-requiring type II diabetes mellitus, insulin resistant diabetes, diabetes with hyperosmolarity, latent autoimmune diabetes in adults.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With a Confirmed Adjudicated Cardiovascular Event
Select serious adverse cardiovascular events and all-cause mortality that occurred during the treatment phase of the study were adjudicated by an expert committee external to the sponsor. Those events confirmed by the committee a cardiovascular events were recorded.
Measured: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants Who Experienced at Least 1 AE
An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE.
Measured: up 22 weeks (12 weeks in Periods I/II and 10 weeks in Period III)
Percentage of Participants Who Were Discontinued From the Study Due to an AE
An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. Participants who were discontinued from the study due to an AE were recorded.
Measured: up 22 weeks (12 weeks in Periods I/II and 10 weeks in Period III)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Feb 2011 (estimated)
- Study start4 Feb 2011
- Primary completion17 Jan 2012
- Study completion17 Jan 2012
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Primary HypercholesterolemiaStudies of the same condition, open and under way.
- More trials run by Merck Sharp & Dohme LLCThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 977 participants (actual)
Sponsor and investigators
- Lead sponsor
- Merck Sharp & Dohme LLC
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Medical Director, Study director, Merck Sharp & Dohme LLC
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01294683
- Sponsor's protocol ID
- 0524B-118
- Other IDs
- 2010-023939-42
- Status last verified
- Jul 2018
- First submitted
- 10 Feb 2011
- Last updated
- 16 Aug 2018
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- Individual data sharing
- Yes: https://www.merck.com/clinical-trials/pdf/ProcedureAccessClinicalTrialData.pdf
Study at a glance
From the registry record, last updated by the sponsor on 16 Aug 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase III Multicenter, Double-Blind, Crossover Design Study to Evaluate Lipid-Altering Efficacy and Safety of Extended-Release Niacin/Laropiprant/Simvastatin Combination Tablet in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia
- ClinicalTrials.gov ID
- NCT01294683
- Acronym / sponsor ID
- 0524B-118
- Conditions
- Primary Hypercholesterolemia, Dyslipidemia
- Keywords
- Low-density lipoprotein, LDL, High-density lipoprotein, HDL, Niacin, Lipid modifying therapy, Cholesterol, High cholesterol
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Terminated
- Enrolment
- 977 participants (actual)
- Lead sponsor
- Merck Sharp & Dohme LLCIndustry (pharma, biotech, devices)
- Study start
- 4 Feb 2011 (actual)
- Primary completion
- 17 Jan 2012 (actual)
- Study completion
- 17 Jan 2012 (actual)
- First posted
- 11 Feb 2011 (estimated)
- Results
- Posted 13 Dec 2016
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is being done to find out if tablets containing extended release (ER) niacin, laropiprant, and simvastatin (ERN/LRPT/SIM) are as effective as tablets containing ER niacin and laropiprant taken with simvastatin tablets (ERN/LRPT + SIM) for lowering high cholesterol and high lipid levels in the blood. The primary hypothesis is that ERN/LRPT/SIM 2 g/40 mg is equivalent to ERN/LRPT 2 g co-administered with simvastatin 40 mg in reducing low-density lipoprotein cholesterol (LDL-C).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg | Experimental | Drug: Simvastatin, Drug: Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM), Drug: Extended Release (ER) niacin/laropiprant (N/LRPT), Drug: PlaceboAfter a 2-week placebo run-in, participants received extended release (ER) niacin/laropiprant (N/LRPT) 1 g/20 mg combination tablet (MK-0524B) once daily for 4 weeks, then ERN/LRPT/Simvastatin (SIM) 2 g/40 mg combination tablet once daily for 8 weeks. Participants then received ERN/LRPT 2 g (MK-0524A) co-administered with SIM 40 mg once daily for 8 weeks. |
| Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g | Experimental | Drug: Simvastatin, Drug: Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM), Drug: Extended Release (ER) niacin/laropiprant (N/LRPT), Drug: PlaceboAfter a 2-week placebo run-in, participants received ERN/LRPT 1 g (MK-0524A) co-administered with SIM 20 mg once daily for 4 weeks then received ERN/LRPT 2 g (MK-0524A) co-administered with SIM 40 mg once daily for 8 weeks. Participants then received ERN/LRPT/SIM 2 g/40 mg combination tablets (MK-0524B) once daily for 8 weeks. |
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Participant has a history of primary hypercholesterolemia or mixed dyslipidemia and meets LDL-C and triglyceride criteria.
- Visit 2:
- Participant is high risk coronary heart disease (CHD) or CHD risk-equivalent.
Key exclusion criteria (14 listed)
- Participant is pregnant or breast-feeding, or expecting to conceive during the study.
- Participant has a history of malignancy.
- Participant consumes more than 3 alcoholic drinks per day (14 per week).
- Participant is high risk CHD patient on statin therapy or any patient on statin therapy equivalent to 80 mg simvastatin.
- Participant with Type 1 or Type 2 diabetes mellitus that is poorly controlled, or on statin therapy.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| SimvastatinAlso: Zocor | Drug | Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg, Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g |
| Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM)Also: MK-0524B | Drug | Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg, Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g |
| Extended Release (ER) niacin/laropiprant (N/LRPT)Also: MK-0524A | Drug | Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg, Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g |
| Placebo | Drug | Sequence 1: MK-0524B 2g/40g→MK-0524A 2g + Simvastatin 40 mg, Sequence 2: MK-0524A 2g + Simvastatin 40 mg→ MK-0524B 2g/40g |
Primary outcome
Change From Baseline in Low-density Lipoprotein Cholesterol (LDL-C)
Time frame: Baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III)
Blood samples were taken at baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III) to determine the LDL-C levels. The change from baseline after 8 weeks of treatment was recorded. Results from recent studies indicated that the combination tablet formulations used in the study did not meet the pre-specified pharmacokinetic bounds used to establish the equivalence of the combination tablet (MK-0524B; ERN/LRPT/SIM) to the coadministration of MK-0524A (ERN/LRPT) and SIM. Therefore, efficacy data were not analyzed, as the study was stopped early. Only safety data were evaluated.
11 secondary outcomes
Change From Baseline in High-density Lipoprotein Cholesterol (HDL-C)
Time frame: Baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment during each period (Week 12 for Period II and Week 20 for Period III)
Percentage of Participants With Consecutive Elevations in Alanine Aminotransferase (ALT) and/or Aspartate Aminotransferase (AST) of >=3 x Upper Limit of Normal (ULN)
Time frame: Up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Elevations in ALT and/or AST of >=5 x ULN
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Elevations in ALT and/or AST of >=10 x ULN
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With Creatine Kinase (CK) >=10 x ULN
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With CK >=10 x ULN With Muscle Symptoms - Drug Related
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants Who Experienced at Least 1 Hepatitis-related Adverse Event (AE)
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With New Onset of Diabetes
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants With a Confirmed Adjudicated Cardiovascular Event
Time frame: up 20 weeks (12 weeks in Periods I/II and 8 weeks in Period III)
Percentage of Participants Who Experienced at Least 1 AE
Time frame: up 22 weeks (12 weeks in Periods I/II and 10 weeks in Period III)
Percentage of Participants Who Were Discontinued From the Study Due to an AE
Time frame: up 22 weeks (12 weeks in Periods I/II and 10 weeks in Period III)
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Aug 2018.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: Yes. https://www.merck.com/clinical-trials/pdf/ProcedureAccessClinicalTrialData.pdf
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Medical Director study director
Merck Sharp & Dohme LLC
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Simvastatin, Extended Release (ER) niacin/laropiprant/simvastatin (N/LRPT/SIM) and Extended Release (ER) niacin/laropiprant (N/LRPT) in people with Primary Hypercholesterolemia and Dyslipidemia, run by Merck Sharp & Dohme LLC.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 16 Aug 2018. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 13 Dec 2016). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change From Baseline in Low-density Lipoprotein Cholesterol (LDL-C) (time frame: Baseline (Week 4 for Period II; Week 12 for Period III) and after 8 weeks of treatment (Week 12 for Period II and Week 20 for Period III)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Aug 2018.