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A Study of Inclisiran in Participants With Homozygous Familial Hypercholesterolemia (HoFH) (ORION-5)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03851705
Recruitment Status : Completed
First Posted : February 22, 2019
Results First Posted : November 10, 2022
Last Update Posted : January 30, 2023
Sponsor:
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )

Brief Summary:
This study was a Phase III,A two-part (double-blind placebo-controlled/open-label) multicenter study to evaluate safety, tolerability, and efficacy of inclisiran in subjects with homozygous familial hypercholesterolemia (HoFH).

Condition or disease Intervention/treatment Phase
Homozygous Familial Hypercholesterolemia Drug: Inclisiran Sodium for injection Drug: Placebo Drug: Placebos Phase 3

Detailed Description:

This study had two sequential parts:

  • Part 1: 6-month double-blind period in which subjects were randomized to receive either inclisiran or placebo
  • Part 2: 18-month open-label follow-up period; placebo-treated subjects from Part 1 were transitioned to inclisiran at Day 180 and all subjects who participated in an open-label follow-up period of inclisiran only

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 56 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Masking Description: Double-blind
Primary Purpose: Treatment
Official Title: A Two-Part (Double-Blind Placebo Controlled/Open-Label) Multicenter Study to Evaluate Safety, Tolerability, and Efficacy of Inclisiran in Subjects With Homozygous Familial Hypercholesterolemia (Hofh) (ORION-5)
Actual Study Start Date : February 6, 2019
Actual Primary Completion Date : March 2, 2020
Actual Study Completion Date : September 9, 2021


Arm Intervention/treatment
Experimental: Part 1 - Inclisiran
Participants who received a dose of 300 milligram (mg) inclisiran sodium for injection administered by SC injection on Day 1 and Day 90.
Drug: Inclisiran Sodium for injection
Inclisiran is a synthetic, chemically modified small interfering ribonucleic acid (siRNA) targeting proprotein convertase subtilisin kexin type 9 (PCSK9) messenger ribonucleic acid (mRNA) with a covalently attached triantennary N-acetylgalactosamine (GalNAc) ligand.
Other Names:
  • ALN-PCSSC; KJX839
  • ALN-PCSSC

Placebo Comparator: Part 1 - Placebo
Participants who received a dose of placebos administered by SC injection on Day 1 and Day 90.
Drug: Placebo
Sterile normal saline (0.9% sodium chloride in water for injection)

Drug: Placebos
Sterile normal saline (0.9% sodium chloride in water for injection)

Experimental: Part 2 - Inclisiran
Participants who received a dose of 300 mg inclisiran sodium for injection administered by SC injection on Day 270, Day 450 and Day 630. In addition, participants who were assigned to the placebo arm in Part 1 will receive a dose of 300 mg inclisiran sodium administered by SC injection on Day 180 after completion of Part 1.
Drug: Inclisiran Sodium for injection
Inclisiran is a synthetic, chemically modified small interfering ribonucleic acid (siRNA) targeting proprotein convertase subtilisin kexin type 9 (PCSK9) messenger ribonucleic acid (mRNA) with a covalently attached triantennary N-acetylgalactosamine (GalNAc) ligand.
Other Names:
  • ALN-PCSSC; KJX839
  • ALN-PCSSC




Primary Outcome Measures :
  1. Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 150 [ Time Frame: Baseline, Day 150 ]
    Percentage Change in LDL-C levels from Baseline to Day 150


Secondary Outcome Measures :
  1. Absolute Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 150 [ Time Frame: Baseline, Day 150 ]
    Absolute Change in LDL-C levels (mg/dL) from baseline to Day 150

  2. Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in LDL-C levels from baseline to subsequent visits on Days 90, 150, and 180

  3. Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Percentage Change in LDL-C levels from baseline to subsequent visits up to Day 720

  4. Absolute Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute change in LDL-C levels (mg/dL) from baseline to subsequent visits on Days 90, 150 and 180 based on the

  5. Absolute Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Absolute change in LDL-C levels from Baseline to Subsequent Visits up to Day 720

  6. Percent Change in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in PCSK9 from baseline to subsequent visits up to Day 180

  7. Percent Change in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Percentage Change in PCSK9 from baseline to subsequent visits up to Day 720

  8. Absolute Change in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in PCSK9 from baseline to subsequent visits up to Day 180

  9. Absolute Change in Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Absolute Change in PCSK9 from baseline to subsequent visits up to Day 720

  10. Percent Change in Total Cholesterol From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150 and 180 ]
    Percentage change in total cholesterol from baseline to subsequent visits up to Day 180

  11. Absolute Change in Total Cholesterol From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in total cholesterol from baseline to subsequent visits up to Day 180

  12. Percent Change in Total Cholesterol From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Percentage change in total cholesterol from baseline to subsequent visits up to Day 720

  13. Absolute Change in Total Cholesterol From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Absolute Change in total cholesterol from baseline to subsequent visits up to Day 720

  14. Percent Change in Apolipoprotein B (apoB) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage change in Apolipoprotein B (apoB) from baseline to subsequent visits up to Day 180 demonstrated by Mixed Model Repeated Measures statisitical method.

  15. Percent Change in Apolipoprotein B (apoB) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Percentage Change in Apolipoprotein B (apoB) from baseline to subsequent visits up to Day 720

  16. Absolute Change in Apolipoprotein B (apoB) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute change in Apolipoprotein B (apoB) from baseline to subsequent visits up to Day 180

  17. Absolute Change in Apolipoprotein B (Apo B) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Absolute Change in Apolipoprotein B (Apo B) from baseline to subsequent visits up to Day 720

  18. Percent Change in Non-HDL Cholesterol (Non-HDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage change in non-HDL-C levels from baseline to subsequent visits up to Day 180

  19. Percent Change in Non-HDL Cholesterol (Non-HDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Percentage Change in non-HDL-C from Baseline to subsequent visits up to Day 720

  20. Absolute Change in Non-HDL Cholesterol (Non-HDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute change in non-HDL-C levels from Baseline to subsequent visits up to Day 180

  21. Absolute Change in Non-HDL Cholesterol (Non-HDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 270, 330, 450, 510, 630, 690, and 720 ]
    Absolute Change in non-HDL Cholesterol (non-HDL-C) from Baseline to Subsequent Visits up to Day 720

  22. Individual Responsiveness of Subjects: Part 1 [ Time Frame: Days 150, 180 ]
    Individual Responsiveness of Subjects defined as the number of subjects reaching on treatment LDL-C levels of <25 mg/dL, <50 mg/dL, <70 mg/dL, and <100 mg/dL up to Day 180

  23. Individual Responsiveness of Subjects: Part 2 [ Time Frame: Days 330, 510, 690 and 720 ]
    Individual Responsiveness of Subjects defined as the number of subjects reaching on treatment LDL-C levels of <25 mg/dL, <50 mg/dL, <70 mg/dL, and <100 mg/dL up to Day 720

  24. Proportional Responsiveness: Part 1 [ Time Frame: Days 150, 180 ]
    Number of participants in each group who attain global lipid targets for their indication

  25. Proportional Responsiveness of Subjects: Part 2 [ Time Frame: Days 330, 510, 690 and 720 ]
    Number of participants in each group who attain global lipid targets for their indication

  26. LDL-C Reduction ≥20% or ≥30% From Baseline: Part 1 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Proportion of subjects in each group with ≥20% or ≥30% LDL-C reduction from Baseline in Part 1 (Days 90, 150, 180)

  27. LDL-C Reduction ≥20% or ≥30% From Baseline: Part 2 [ Time Frame: Baseline, Days 330, 510, 690, and 720 ]
    Proportion of subjects in each group with ≥20% or ≥30% LDL-C reduction from Baseline in Part 2 (Days 330, 510, 690, and 720)

  28. Percent Change in High-Density Lipoprotein Cholesterol Levels (HDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in HDL-C levels (mg/dL) from baseline to subsequent visits on Day 90, 150, and 180

  29. Percent Change in High-Density Lipoprotein Cholesterol Levels (HDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Percentage change in LDL-C levels from Baseline to Subsequent Visits up to Day 720

  30. Absolute Change in High-Density Lipoprotein Cholesterol Levels (HDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in HDL-C levels (mg/dL) from baseline to subsequent visits on Day 90, 150, and 180

  31. Absolute Change in High-Density Lipoprotein Cholesterol Levels (HDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Absolute change in LDL-C levels from Baseline to Subsequent Visits up to Day 720

  32. Absolute Change in Very-Low-Density Lipoprotein Cholesterol (VLDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in VLDL-C levels from baseline to subsequent visits on Days 90, 150, and 180

  33. Absolute Change in Very-Low-Density-Lipoprotein Cholesterol Levels (VLDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Absolute change in VLDL-C levels from Baseline to Subsequent Visits up to Day 720

  34. Percent Change in Very-Low-Density Lipoprotein Cholesterol (VLDL-C) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in VLDL-C levels (mg/dL) from baseline to subsequent visits on Days 90, 150, and 180

  35. Percent Change in Very-Low-Density-Lipoprotein Cholesterol Levels (VLDL-C) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Percentage change in VLDL-C levels from Baseline to Subsequent Visits up to Day 720

  36. Absolute Change in Apolipoprotein A-1 (Apo-A1) mg/dL From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in Apolipoprotein A-1 (Apo-A1) from baseline to subsequent visits on Days 90, 150, and 180

  37. Absolute Change Apolipoprotein A-1 (Apo-A1) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Absolute change in Apolipoprotein A-1 (Apo-A1) from Baseline to Subsequent Visits up to Day 720

  38. Percent Change in Apolipoprotein A-1 (Apo-A1) From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in Apolipoprotein A-1 (Apo-A1) from baseline to subsequent visits on Day 90, 150, and 180

  39. Percent Change Apolipoprotein A-1 (Apo-A1) From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Percentage change in Apolipoprotein A-1 (Apo-A1) from Baseline to Subsequent Visits up to Day 720

  40. Percent Change in Lipoprotein(a) [Lp(a)] From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percentage Change in Lp(a) from Baseline to Subsequent Visits up to Day 180

  41. Percent Change in Lipoprotein(a) [Lp(a)] From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Percentage change in Lp(a) from Baseline to Subsequent Visits up to Day 720

  42. Absolute Change in Lipoprotein(a) [Lp(a)] From Baseline to Subsequent Visits up to Day 180 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in Lp(a) from baseline to subsequent visits up to Day 180

  43. Absolute Change in Lipoprotein(a) [Lp(a)] From Baseline to Subsequent Visits up to Day 720 [ Time Frame: Baseline, Days 330, 450, 510, 630, 690, and 720 ]
    Absolute change in Lp(a) from Baseline to Subsequent Visits up to Day 720

  44. Percent Change in High-Sensitivity C-Reactive Protein (hsCRP) From Baseline to Subsequent Visits up to Day 180: Part 1 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Percent change in hsCRP from Baseline to subsequent visits up to Day 180

  45. Percent Change in High-Sensitivity C-Reactive Protein (hsCRP) From Baseline to Subsequent Visits up to Day 720: Part 2 [ Time Frame: Baseline, Days 330, 510 ,690, 720 ]
    Percentage change in hsCRP from baseline to subsequent visits up to Day 720

  46. Absolute Change in High-Sensitivity C-Reactive Protein (hsCRP) From Baseline to Subsequent Visits up to Day 180: Part 1 [ Time Frame: Baseline, Days 90, 150, 180 ]
    Absolute Change in High-Sensitivity C-Reactive Protein (hsCRP) from Baseline to subsequent visits up to Day 180

  47. Absolute Change in High-Sensitivity C-Reactive Protein (hsCRP) From Baseline to Subsequent Visits up to Day 720: Part 2 [ Time Frame: Baseline, Days 330, 510, 690, 720 ]
    Absolute Change in High-Sensitivity C-Reactive Protein (hsCRP) from baseline to subsequent visits up to Day 720

  48. Percent Change in Apo-B From Baseline to Day 150 [ Time Frame: Baseline, Day 150 ]
    Percentage change in Apo-B from baseline to Day 150 as demonstrated using the ANCOVA statisitical model.

  49. Percent Change in Non-HDL-C From Baseline to Day 150 [ Time Frame: Baseline, Day 150 ]
    Percentage Change in non-HDL-C from baseline to Day 150 as demonstrated using the ANCOVA statisitical model.

  50. Percent Change in Total Cholesterol From Baseline to Day 150 [ Time Frame: Baseline, Day 150 ]
    Percentage change in total cholesterol from baseline to Day 150 as demonstrated using the ANCOVA statisitical model.

  51. Proportion of Subjects With ≥30% LDL-C Reduction of From Baseline at Day 150 [ Time Frame: Baseline, Day 150 ]
    Number of participants in each group with ≥30% LDL-C reduction from baseline at Day 150 using the Regression Logistic Statistical Model



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Diagnosis of HoFH by genetic confirmation or a clinical diagnosis based on a history of an untreated LDL-C concentration >500 mg/dL (13 mmol/L) together with either xanthoma before 10 years of age or evidence of heterozygous familial hypercholesterolemia in both parents
  2. Stable on a low-fat diet.
  3. Subjects on statins should be receiving a maximally tolerated dose. Maximum tolerated dose is defined as the maximum dose of statin that can be taken on a regular basis without intolerable adverse events.
  4. Subjects not receiving statins must have documented evidence of intolerance to at least two different statins.
  5. Subjects on lipid-lower therapies (such as statin and/or ezetimibe) should be on a stable dose for ≥30 days before screening with no planned medication or dose change during study participation.
  6. Fasting central laboratory LDL-C concentration ≥130 mg/dL (3.4 mmol/L).
  7. Triglyceride concentration <400 mg/dL (4.5 mmol/L)
  8. No current or planned renal dialysis or renal transplantation
  9. Subjects on a documented regimen of LDL or plasma apheresis will be allowed to continue the apheresis during the study, if needed.
  10. Subjects must be willing and able to give written informed consent before initiation of any study-related procedures. The subject should be willing to comply with all required study procedures.
  11. Willing to follow all study procedures including adherence to dietary guidelines, study visits, fasting blood draws, and compliance with study treatment regimens.

Exclusion Criteria:

  1. Use of Mipomersen or Lomitapide therapy within 5 months of screening
  2. Treatment (within 90 days of screening) with monoclonal antibodies directed towards PCSK9
  3. New York Heart Association (NYHA) class IV heart failure or last known left ventricular ejection fraction <25%
  4. Major adverse cardiovascular event within 3 months prior to randomization
  5. Planned cardiac surgery or revascularization
  6. Uncontrolled severe hypertension: systolic blood pressure >180 mmHg or diastolic blood pressure >110 mmHg prior to randomization despite anti-hypertensive therapy
  7. Active liver disease defined as any known current infectious, neoplastic, or metabolic pathology of the liver or unexplained alanine aminotransferase (ALT), aspartate aminotransferase (AST), elevation >3x ULN, or total bilirubin >2x upper limit of normal (ULN) at screening confirmed by a repeat measurement at least 1 week apart
  8. Severe concomitant noncardiovascular disease that carries the risk of reducing life expectancy to less than the duration of the trial
  9. History of malignancy that required surgery (excluding local and wide-local excision), radiation therapy and/or commencement of systemic therapy as treatment during the 3 years prior to randomization
  10. Females who are pregnant or nursing, or who are of childbearing potential and unwilling to use at least one acceptable effective method of contraception (eg, oral contraceptives, barrier methods, approved contraceptive implant, long- term injectable contraception, intrauterine device) for the entire duration of the study. Exemptions from this criterion:

    1. Women >2 years postmenopausal (defined as 1 year or longer since their last menstrual period) AND more than 55 years of age
    2. Postmenopausal women (as defined above) and less than 55 years of age with a negative pregnancy test within 24 hours of enrolment
    3. Women who are surgically sterilized at least 3 months prior to enrolment
  11. Known history of alcohol and/or drug abuse within 5 years
  12. Any condition that according to the investigator could interfere with the conduct of the study, such as but not limited to:

    1. Subjects who are unable to communicate or to cooperate with the investigator.
    2. Unable to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study (including subjects whose cooperation is doubtful due to drug abuse or alcohol dependency)
    3. Unlikely to comply with the protocol requirements, instructions, and study-related restrictions (eg, uncooperative attitude, inability to return for follow-up visits, and improbability of completing the study)
    4. Have any medical or surgical condition, which in the opinion of the investigator would put the subject at increased risk from participating in the study
    5. Persons directly involved in the conduct of the study
  13. Any uncontrolled or serious disease, or any medical or surgical condition, that may either interfere with participation in the clinical study, and/or put the subject at significant risk (according to investigator's [or delegate] judgment) if he/she participates in the clinical study
  14. Any underlying known disease, or surgical, physical, or medical condition that, in the opinion of the Investigator, might interfere with the interpretation of clinical study results
  15. Treatment with other investigational medicinal products or devices within 30 days or 5 half-lives of the screening visit, whichever is longer
  16. Previous participation in the study
  17. Hypersensitivity to any of the ingredients of Inclisiran

The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03851705


Locations
Layout table for location information
Hong Kong
(50852-001) Queen Mary Hospital
Hong Kong, Hong Kong
Israel
(50972-001) Hadassah Hospital Lipid Research Ein Kerem
Jerusalem, Israel, 91120
Russian Federation
(50007-001) Research Institute of Complex Issues of Cardiovascular Diseases
Kemerovo, Russian Federation, 650002
(50007-003) National Medical Research Centre of Cardiology
Moscow, Russian Federation, 121552
(50007-002) Hospital for War Veterans
Saint Petersburg, Russian Federation, 193079
Serbia
(50381-001) Clinical Center of Serbia
Belgrad, Serbia, 11000
South Africa
(50027-001) Johannesburg Hospital
Johannesburg, South Africa, 2193
Taiwan
(50886-001) Taipei Veterans General Hospital
Taipei, Taiwan, 11217
Turkey
(50090-002) University of Health Sciences
Etlik, Turkey, 06010
(50090-003) Istanbul University
Istanbul, Turkey, 34093
(50090-001) Ege Universitesi
İzmir, Turkey, 35040
Ukraine
(50380-002) IMunicipal Non-commercial Enterprise "Ivano-Frankivsk Regional Clinical Cardiology Center Ivano-Frankivsk Regional Council"
Ivano-Frankivs'k, Ukraine, 76018
(50380-001) National Scientific Center
Kyiv, Ukraine, 03680
Sponsors and Collaborators
Novartis Pharmaceuticals
  Study Documents (Full-Text)

Documents provided by Novartis ( Novartis Pharmaceuticals ):
Study Protocol  [PDF] October 8, 2020
Statistical Analysis Plan  [PDF] March 23, 2021

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Layout table for additonal information
Responsible Party: Novartis Pharmaceuticals
ClinicalTrials.gov Identifier: NCT03851705    
Other Study ID Numbers: MDCO-PCS-17-02
CKJX839A12302 ( Other Identifier: Novartis Pharmaceuticals )
2018-000893-31 ( EudraCT Number )
First Posted: February 22, 2019    Key Record Dates
Results First Posted: November 10, 2022
Last Update Posted: January 30, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description:

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com.


Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Novartis ( Novartis Pharmaceuticals ):
HoFH
Additional relevant MeSH terms:
Layout table for MeSH terms
Hyperlipoproteinemia Type II
Hypercholesterolemia
Hyperlipidemias
Dyslipidemias
Lipid Metabolism Disorders
Metabolic Diseases
Lipid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Genetic Diseases, Inborn
Hyperlipoproteinemias