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Study identifier: NCT07028749 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: RecruitingTYDAL-TIMI 78

Study of MAR001 in Adults With Elevated Triglycerides and Remnant Cholesterol

Condition: Hypertriglyceridemia  ·  Sponsor: Marea Therapeutics

PhasePhase 2
Planned participants316
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where54 locations · 4 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The primary objective of the study is to evaluate the effect of MAR001 compared to placebo on levels of TG in adults with elevated TG and RC.

This description comes directly from the study's public registry record.

Talk to the study team

Matty Hughes  ·  415-766-3610  ·  TYDAL_info@mareatx.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Elevated fasting TGs and RC * Elevated nonfasting TGs and RC * Part A only: Fasting LDL-C ≥ 50 mg/dL (≥ 1.29 mmol/L) and ≤ 130 mg/dL (≤ 3.36 mmol/L) * Willingness to provide informed consent and comply with the intervention and all study assessments * Stable diet for a minimum of 3 months prior to screening and with no plans to change during screening or trial participation * Stable drug regimen (if relevant) prior to screening visit and no planned changes after enrollment; Part B only: adjustment of lipid-lowering therapy during the diet/lifestyle run-in period is permitted Exclusion Criteria: * Acute or chronic liver disease * Part A only: TG concentration ≥880mg/dl; Part B only: TG concentration ≥2000 mg/dL * History of type 1 diabetes mellitus or history of diabetic ketoacidosis * Newly diagnosed T2DM * Participants with known active hepatitis A, B, or C * Uncontrolled hypothyroidism * Part B only: recent history of active pancreatitis * Part B only: genetically confirmed Familial Chylomicronemia Syndrome (FCS) diagnosis due to biallelic loss of function mutations in LPL or GPIHBP1 * Part B only: use of ANGPTL3 and ApoC-III inhibitors * Any condition that prevents the participant from complying with study procedures

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (54)

Marea Site 328Anniston, Alabama, United StatesRecruiting
Marea Site 329Mobile, Alabama, United StatesRecruiting
Marea Site 313Little Rock, Arkansas, United StatesRecruiting
Marea Site 306Hamden, Connecticut, United StatesRecruiting
Marea Site 302Boca Raton, Florida, United StatesRecruiting
Marea Site 307Port Saint Lucie, Florida, United StatesRecruiting
Marea Site 310Columbus, Georgia, United StatesRecruiting
Marea Site 319Peachtree Corners, Georgia, United StatesRecruiting
Marea Site 317Park Ridge, Illinois, United StatesRecruiting
Marea Site 325Springfield, Illinois, United StatesRecruiting
Marea Site 301Louisville, Kentucky, United StatesRecruiting
Marea Site 316Baltimore, Maryland, United StatesRecruiting

+ 42 more locations — full list on the registry record.

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