Primary Hypercholesterolemia or Mixed Hyperlipidemia

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Review clinical trials related to Primary Hypercholesterolemia or Mixed Hyperlipidemia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

QLC7401 in the Treatment of Primary Hypercholesterolemia or Mixed Hyperlipidemia With Elevated Low Density Lipoprotein Cholesterol (LDL-C)

To evaluate the efficacy, safety and immunogenicity of QCL7401 subcutaneous administration in patients with primary hypercholesterolemia or mixed hyperlipidemia with poorly controlled LDL-C elevated on optimized lipid-lowering therapy.

Participants needed: 780
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Qilu Pharmaceutical Co., Ltd.Updated: Mar 4, 2026
Eligibility criteria

Male or female participants aged ≥18 years of age. [+4]

Having the following diseases or treatment history: (1) cardiac function as defi... [+3]

Status: Not yet recruiting

QLC7401 Monotherapy in Non-familial Hypercholesterolemia or Mixed Dyslipidemia

This Phase III clinical trial aims to assess the efficacy and safety of QLC7401 monotherapy in adults with non-familial primary hypercholesterolemia or mixed dyslipidemia who are not receiving lipid-lowering therapy. Participants will be randomly assigned to receive subcutaneous injections of either QLC7401 or a placebo according to the study schedule.

Participants needed: 510
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Qilu Pharmaceutical Co., Ltd.Updated: Mar 2, 2026
Eligibility criteria

Aged ≥18 years. [+5]

History of AAtherosclerotic cardiovascular disease (ASCVD)(e.g., myocardial infa... [+7]

Status: Not yet recruiting

Study of QLC7401 in the Treatment of Primary Hypercholesterolemia or Mixed Hyperlipidemia With Elevated LDL Cholesterol

To evaluate the efficacy, safety, pharmacodynamics and immunogenicity of QLC7401 subcutaneous administration in patients with primary hypercholesterolemia or mixed hyperlipidemia with poorly controlled LDL-C elevated on optimized lipid-lowering therapy.

Participants needed: 156
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Qilu Pharmaceutical Co., Ltd.Updated: Dec 27, 2024
Eligibility criteria

Male or female participants aged ≥18 years of age. [+4]

Having the following diseases or treatment history: (1) cardiac function as defi... [+3]