NEXUS Study: A Study to Test Single and Multiple Doses of MER511 Given to Adults With Graves' Disease

Trial details

Who runs it

Merida Biosciences

Trial code

NCT07305818EU 2025-523823-23-00

Record updated

29 October 2026

Original description

The purpose of this study is to evaluate how well MER511 is tolerated and what side effects may occur in adults who have Graves' disease. The study drug will be administered either intravenously (into a vein in the arm) or subcutaneously (under the skin).Read full original descriptionShow less

A Phase 1, First-in-Human, Placebo-Controlled, Single and Multiple Ascending Dose Study to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of Intravenous and Subcutaneous Administration of MER511 in Adults With Graves' Disease

The purpose of this study is to evaluate how well MER511 is tolerated and what side effects may occur in adults who have Graves' disease. The study drug will be administered either intravenously (into a vein in the arm) or subcutaneously (under the skin).

Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body.

Inclusion: Adults 18 to 65 years of age, inclusive, at the time of signing the ICF; Documented GD diagnosis,; Receiving stable dose of ATD (Antithyroid drug); Body weight at least 50 kg (110 lb) and body mass index (BMI) 18.0-35.0 kg/m2, inclusive; Women of childbearing potential must agree to use highly effective contraceptive methods; Men with partners of childbearing potential or who are pregnant must agree to use a condom or strict abstinence; Signed informed consent to participate in the study; Willingness and ability, in the opinion of the investigator, to comply with protocol requirements and restrictions (eg, dosing, schedule of assessments).

Exclusion: History of:; total thyroidectomy; History of hyperthyroidism not caused by GD (eg, toxic adenoma, toxic multinodular goiter); History of thyroid storm; History of agranulocytosis, anemia, leukopenia, thrombocytopenia, vasculitis, or liver toxicity due to prior ATD therapy Treatment with RAI therapy within 12 months prior to Screening; Likely to require definitive treatment for GD (RAI therapy or thyroidectomy) during the study, based on GD history and anticipated prognosis; Use of levothyroxine, desiccated thyroid extract, or T3 at any dose within 6 weeks prior to Screening; History of TED-directed medical treatment (including IV/oral steroids, immunosuppressants, or teprotumumab), surgical treatment, and/or orbital radiation within 3 months prior to Screening, or per required prohibited concomitant therapy washout criteria in the protocol (whichever is longer); Major surgery or use of iodinated contrast within 3 months prior to planned IMP dosing; Treatment with prohibited medications prior to planned IMP dosing or likely to require prohibited concomitant therapy during the study; Live vaccine(s) or mRNA vaccine(s) within 1 month prior to IMP dosing, or plans to receive such vaccines during the study; Treatment with any investigational drug within within 3 months or 5 half-lives (whichever is longer) prior to enrollment; Positive drug screen or positive test for alcohol; Donated more than 500 mL of blood in the 2 months prior to signing the ICF; Current enrollment or past participation within 3 months or 5 half-lives (whichever is longer) prior to signing the ICF in any other clinical trial involving an IMP; Active systemic autoimmune disease requiring treatment that causes undue risk in the opinion of the investigator; History of cardiovascular, respiratory, renal, gastrointestinal, endocrinological (other than GD), hematological, immunodeficiency, or neurological disorders that may constitute a risk when taking the IMP or interfere with data interpretation; History of liver disease; Positive result for HIV antibody, HBsAg, or hepatitis C antibody with detectable viral RNA levels at Screening; Heart rate <45 bpm or >100 bpm; Any other conditions that, in the opinion of the investigator or the sponsor, could interfere with participation in or completion of the study; Total IgG level <700 mg/dL at Screening; Any of the following at Screening (confirmed by single repeat measurement, if deemed necessary):; ALT or AST >1.5 × ULN; Total bilirubin >1.5 × ULN; Estimated glomerular filtration rate (eGFR) <75 mL/min/1.73 m2 using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine equation; Current active or chronic moderate-to-severe TED per EUropean Group On Graves' Orbitopathy (EUGOGO) criteria as judged by the investigator at Screening; Pregnant, breastfeeding, or planning to become pregnant during the study; 12-lead ECG demonstrating any of the following at Screening:; QTcF interval >450 ms; QRS interval >120 ms; PR interval >220 ms; Blood pressure measurements demonstrating any of the following at Screening:; Systolic blood pressure ≥140 mmHg; Diastolic blood pressure ≥90 mmHg; Refusal to adhere to lifestyle considerations as defined in the protocol; Employee of the investigator, clinic, or sponsor with direct involvement in the proposed study or other studies under the direction of the investigator or clinic, as well as family members of the employee or investigator.

ClinicalTrials.gov NCT07305818 · EU CTIS 2025-523823-23-00