Methyldopa for Reduction of DQ8 Antigen Presentation in At-Risk Subjects for Type 1 Diabetes

NCT03396484 | Withdrawn Phase 2 DMC FDA Drug

• 3 other identifiers: MethyldopaUC4DK106993UC4DK117009
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

A study is to see if methyldopa can change the immune system's attack on insulin producing cells in people at early stages of type 1 diabetes.

Conditions

Type1 Diabetes Mellitus

Keywords

TrialNet

Outcome Measures

Primary Outcomes (1)

• DQ8 Antigen Presentation

  insulin peptide-specific DQ8 antigen presentation

  6 months after initiation of treatment

Study Arms (2)

Methyldopa

EXPERIMENTAL

Adults: methyldopa 500mg twice daily for one week and then increased to 500mg three times a day Children: methyldopa dose based on weight twice daily for one week then increased to three times a day

Drug: Methyldopa

Placebo

PLACEBO COMPARATOR

Inactive agent to match active drug in appearance and dose frequency.

Drug: Placebo

Interventions

Methyldopa DRUG

Tablet for oral dosing

Also known as: Aldomet

Methyldopa

Placebo DRUG

Tablet for oral dosing

Placebo

Eligibility Criteria

• Age: 8 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Participant in TrialNet Pathway to Prevention Study (TN01)
• Willing to provide Informed Consent or, if the subject is \<18 years of age, have a parent or legal guardian provide Informed Consent
• Confirmed positive for one or more autoantibodies, one of which is insulin autoantibody (mIAA)
• Positive for at least one gene encoding HLA-DQ8 (DQB\*0302)
• If a female participant with reproductive potential, willing to avoid pregnancy and undergo pregnancy testing prior to randomization and during the study
• Have normal or abnormal glucose tolerance on OGTT performed within 7 weeks of randomization

You may not qualify if:

• Inability or unwillingness of a participant to give written informed consent or comply with study protocol
• History of clinically significant anemia or Hemoglobin \<10 g/dl
• Evidence of liver dysfunction
• History of renal insufficiency
• History of symptomatic hypotension including positional hypotension
• Systolic BP \< 100 mmHg for adults or blood pressure \< 5th percentile for age/height/gender in children and adolescents
• Use of a treatment that is known to cause a significant, ongoing change in the course of diabetes or immunologic status, within 4 weeks prior to participation. This includes high-dose inhaled, extensive topical or systemic glucocorticoids
• Females who are pregnant at the time of screening, breastfeeding or unwilling to defer pregnancy during the 16-month study period. (Female participant must be at least 100 days postpartum before enrollment into study)
• Unable to avoid concurrent antihypertensive medications, monoamine oxidase (MAO) inhibitors, lithium, or medications containing ferrous sulfate or ferrous gluconate
• Unable to avoid medications that affect stomach pH, such as proton pump inhibitors or histamine H2 receptor blockers
• Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study

Sponsors & Collaborators

• National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): lead

Related Links

• TrialNet Public Website

MeSH Terms

Interventions

Methyldopa

Intervention Hierarchy (Ancestors)

Dihydroxyphenylalanine; Catecholamines; Amines; Organic Chemicals; Catechols; Phenols; Benzene Derivatives; Hydrocarbons, Aromatic; Hydrocarbons, Cyclic; Hydrocarbons; Phenylalanine; Amino Acids, Aromatic; Amino Acids, Cyclic; Amino Acids; Amino Acids, Peptides, and Proteins; Tyrosine

Study Officials

• Carla Greenbaum, MD

  Type 1 Diabetes TrialNet

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: PREVENTION
• Intervention Model: CROSSOVER
• Sponsor Type: NIH
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 4, 2018
• First Posted: January 11, 2018
• Study Start: September 1, 2020
• Primary Completion: March 1, 2022
• Study Completion: March 1, 2022
• Last Updated: June 30, 2020

Record last verified: 2020-06