A Study to Evaluate the Pharmacodynamics of a Combination of QCZ484 and Inclisiran in Participants With Hypertension and Concomitant Hypercholesterolemia
Novartis Pharmaceuticals · NCT07610278
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–75 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 120
- US sites recruiting
- 29
- Study start
- May 29, 2026
- Record last updated
- July 30, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is a multicenter, randomized, double-blind, factorial design Phase 2 study to evaluate the pharmacodynamics, safety and tolerability of a combination of QCZ484 and inclisiran compared to QCZ484, inclisiran, and placebo in participants with hypertension and concomitant hypercholesterolemia.
Being studied: QCZ484; Inclisiran; QCZ484 placebo; Inclisiran placebo
Conditions: Hypercholesterolaemia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Males or females aged 18 to 75 years.
- Diagnosis of primary hypertension.
- Treatment with either no, or up to 2 antihypertensive medications at a stable dose for at least 4 weeks preceding screening.
- Systolic blood pressure ≥140 and \<165 mmHg based on the mean of 3 sitting measurements based on office blood pressure monitoring.
- Diagnosis of hypercholesterolemia including heterozygous familial hypercholesterolemia unable to reach LDL-C goals with a stable dose of statin treatment for at least 4 weeks prior to screening as per Investigator judgement, guidelines and local practice (if tolerated and not contraindicated) with or without bempedoic acid and with or without ezetimibe prescribed according to local guidance, at a stable dose for at least 4 weeks preceding Screening Visit 1.
The following parameters must be confirmed at Screening Visit 2:
- Fasting serum LDL-C ≥70 mg/dL and \<190 mg/dL using Friedewald equation.
- Fasting triglyceride \<400 mg/dL.
Exclusion Criteria
- Symptomatic orthostatic hypotension.
- Treatment with certain medications and/or unable to comply with prohibited medications requirements.
Other protocol inclusion/exclusion criteria may apply
Recruiting US locations
G and L Research LLC
Foley, AL 36535
Site contact: Christine S Fuller · glresearch5@gmail.com
The Center for Clinical Trials
Saraland, AL 36571
Site contact: JoAnn Ladner · joann@thecenterforclinicaltrials.com
Clinical Trials Research
Lincoln, CA 95648
Site contact: Stacy Woodward · +1 916 434 8230 · stacy@ctrsites.com
Downtown L A Research Center Inc
Los Angeles, CA 90017
Site contact: Claudia Cisneros · +1 213 261 3680 · ccisneros@dtlaresearch.com
Valley Clinical Trials
Northridge, CA 91325
Site contact: Haydee Gutierrez · hgutierrez@flourishresearch.com
Flourish Medical Clinical Trials
Boca Raton, FL 33434
Site contact: Cassandra Duff · cduff@flourishresearch.com
Clinical Research of Brandon LLC
Brandon, FL 33511
Site contact: Erika Santos · esantos@crofb.com
ALL Medical Research LLC
Cooper City, FL 33024
Site contact: Alejandro Marin · +1 754 263 2001 · amarin@allmedicalresearch.com
AMR Miami
Coral Gables, FL 33134
Site contact: Odalys Fundora · odalys.fundora@amr-clinical.com
Universal Axon Clinical Research
Doral, FL 33166
Site contact: Glenda Padron · glenda.padron@roviaclinical.com
East Coast Institute for Research
Jacksonville, FL 32216
Site contact: Carol Tunsil · +1 386 868 5625 · carol.tunsil@roviaclinical.com
Entrust Clinical Research
Miami, FL 33176
Site contact: Daimelys Garcia · Dgarcia@entrustclinicalresearch.com
Inpatient Research Clinical LLC
Miami Lakes, FL 33014
Site contact: Ilianys Marino · +1 786 502 4303 · imarino@inpatientresearch.com
Inpatient Research Clinical LLC
Miami Lakes, FL 33014
Site contact: Enrique Pacheco · epacheco@inpatientresearch.com
American Research Centers of FL
Pembroke Pines, FL 33027
Site contact: Liliana Portal · lportal@americanresearchcenters.com
East Coast Inst for Research LLC
Saint Augustine, FL 32086
Site contact: Rebecca Fink · +1 904 824 1776#116 · becca.fink@roviaclinical.com
East Coast Research
Canton, GA 30114
Site contact: Marvelyn Brentum · marvelyn.brentum@roviaclinical.com
Great Lakes Clinical Trials
Chicago, IL 60640
Site contact: Megi Stafa · +1 773 275 3500 · mstafa@flourishresearch.com
AMR Chicago
Niles, IL 60714
Site contact: Unnathi Nagelli · +1 630 491 1901 · unnathi.nagelli@amr-clinical.com
Alliance for Multispecialty Research
Wichita, KS 67207
Site contact: Shaunacie Mc Callum · shaunacie.mccallum@amr-clinical.com
Monroe Research Llc
West Monroe, LA 71291
Site contact: Nina Parrott · ninaparrottlpncrc@monroeresearch.net
Anderson Medical Research
Ft. Washington, MD 20744
Site contact: Ann-Marie Cobb · andersonmedicalresearch@gmail.com
Capitol Cardiology Associates
Lanham, MD 20706
Site contact: Iluyomade Adeusi · +1 301 312 0575 · iluyomade@capitolcardiology.com
Monroe Biomedical Research
Monroe, NC 28112
Site contact: Avrie Torres · +1 704 283 7359 · atorres@onsiteclinical.com
Walker Family Care
Little River, SC 29566
Site contact: Madelyn Poore · mpoore@littlerivercr.com
Synergy Group Medical LLC
Houston, TX 77061
Site contact: Graciela Lopez · +1 281 206 0068 · glopez@synergygroupus.com
Synergy Group Medical LLC
Houston, TX 77061
Site contact: Reina Romero · +1 832 532 4210 · rromero@synergygroupus.com
Manassas Clinical Research Center
Manassas, VA 20110
Site contact: Arleth Lopez · +1 703 330 1112 · arleth@manassasclinic.com
Dominion Medical Associates
Richmond, VA 23219
Site contact: Tara Snead · +1 804 836 6540 · tara@dominionmedicalinc.com
Study contacts (from the official record)
- Novartis Pharmaceuticals · 1-888-669-6682 · novartis.email@novartis.com
- Novartis Pharmaceuticals
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