Phase 2
Completed N=112
Randomized Study of Obicetrapib in Combination With Ezetimibe
Dyslipidemias · High Cholesterol · Hypercholesterolemia
Source: ClinicalTrials.gov NCT04770389 ↗
Enrolled (actual)
112
Serious AEs
1.8%
Results posted
Apr 2024
Primary outcomePrimary: Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [Friedewald] — -45.63; -0.17 percent change from baseline — p=<0.0001
Summary
This study will be a placebo-controlled, double-blind, randomized, phase 2 study in participants with mild dyslipidemia to evaluate the efficacy, safety, and tolerability of obicetrapib and ezetimibe combination therapy.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [Friedewald] |
-45.63; -0.17 | <0.0001 sig |
| PRIMARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [Friedewald] |
-51.95; -1.40 | <0.0001 sig |
| PRIMARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [Friedewald] |
-43.55; 1.37 | <0.0001 sig |
| PRIMARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [PUC] |
-44.38; -1.53 | <0.0001 sig |
| PRIMARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [PUC] |
-51.40; -2.00 | <0.0001 sig |
| PRIMARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo [PUC] |
-44.10; -0.78 | <0.0001 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [Friedewald] |
-31.88; -0.17 | <0.0001 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [Friedewald] |
-34.40; -1.40 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [Friedewald] |
-31.99; 1.37 | <0.0001 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [PUC] |
-27.94; -1.53 | <0.0001 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [PUC] |
-30.10; -2.00 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo [PUC] |
-28.98; -0.78 | <0.0001 sig |
| SECONDARY Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo |
-31.62; -1.17 | <0.0001 sig |
| SECONDARY Median Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo |
-34.75; -0.90 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Placebo |
-29.73; -0.11 | <0.0001 sig |
| SECONDARY Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo |
-22.15; -1.17 | <0.0001 sig |
| SECONDARY Median Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo |
-23.50; -0.90 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Placebo |
-22.46; -0.11 | <0.0001 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy [Friedewald] |
-45.63; -12.69 | <0.0001 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy [Friedewald] |
-51.95; -14.80 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy [Friedewald] |
-43.55; -13.42 | <0.0001 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Ezetimibe Monotherapy [Friedewald] |
-31.88; -12.69 | 0.0005 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Ezetimibe Monotherapy [Friedewald] |
-34.40; -14.80 | 0.0005 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Obicetrapib Monotherapy Compared to Ezetimibe Monotherapy [Friedewald] |
-31.99; -13.42 | 0.0005 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [Friedewald] |
-12.69; -0.17 | 0.0051 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [Friedewald] |
-14.80; -1.40 | 0.0051 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [Friedewald] |
-13.42; 1.37 | 0.0051 sig |
| SECONDARY Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [PUC] |
-13.68; -1.53 | 0.0245 sig |
| SECONDARY Median Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [PUC] |
-14.90; -2.00 | 0.0245 sig |
| SECONDARY LS Mean Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 57: Ezetimibe Monotherapy Compared to Placebo [PUC] |
-13.55; -0.78 | 0.0245 sig |
| SECONDARY Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy |
-31.62; -8.78 | <0.0001 sig |
| SECONDARY Median Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy |
-34.75; -8.90 | <0.0001 sig |
| SECONDARY LS Mean Percent Change in Apolipoprotein-B (ApoB) From Baseline to Day 57: Obicetrapib in Combination With Ezetimibe Compared to Ezetimibe Monotherapy |
-29.73; -8.92 | <0.0001 sig |
Eligibility Criteria
Inclusion Criteria
- Understanding of the study procedures, willingness to adhere to the study schedules and diet, and agreement to participate in the study by giving written informed consent prior to Screening procedures
- Men or women 18 to 70 years of age, inclusive
- Women may be enrolled if all 3 of the following criteria are met:
- They are not pregnant;
- They are not breastfeeding; and
- They do not plan on becoming pregnant during the study
- Women of childbearing potential must have a negative urine pregnancy test at the Screening Visit.
- Women of childbearing potential must agree to use an effective method of avoiding pregnancy from the Screening Visit to 90 days after the last visit. Men whose partners are of childbearing potential must agree to use an effective method of avoiding pregnancy from the Screening Visit to 90 days after the last visit.
- Fasting LDL-C levels >2.5 mmol/L (>100 mg/dL) and = 40 kg/m2
- Participation in another clinical study involving an investigational or marketed drug within 30 days prior to the Screening Visit
- Currently taking any lipid-altering therapy
- Any clinical manifestation of atherosclerotic CVD or any evidence of ischemic coronary disease present on the 12-lead ECG at the Screening Visit
- Diagnosis of type 1 or type 2 diabetes mellitus; or HbA1c >= 6.5% at the Screening visit if no prior diagnosis of diabetes mellitus
- Uncontrolled hypertension ie, sitting systolic blood pressure >160 mmHg and/or sitting diastolic blood pressure >90 mmHg taken as the average of triplicate measurements.
One retest will be allowed, at which point if the retest result is no longer exclusionary, the participant may be randomized
- Active muscle disease or persistent creatine kinase concentration >3 x the upper limit of normal (ULN). One retest will be allowed after 1 week to verify the result, at which point if the retest result is no longer exclusionary, the participant may be randomized
- History of torsades de pointes
- Estimated glomerular filtration rate 2 x ULN, or total bilirubin >1.5 x ULN
- Anemia, defined as hemoglobin concentration <11 g/dL for males and hemoglobin concentration <9 g/dL for females
- History of malignancy within the past 5 years, with the exception of non-melanoma skin cancers
- Evidence of any other clinically significant non-cardiac disease or condition that, in the opinion of the Investigator, would preclude participation in the study
- Known ezetimibe or CETP inhibitor allergy or intolerance
Data sourced from ClinicalTrials.gov (NCT04770389). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.