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Recruiting Phase 3

An Open-Label, Single-Arm Study to Investigate the Efficacy and Safety of North Star Desiccated Porcine Thyroid Extract Tablets.

NCT07747103 · tracked via the Priya Life Science USA tracker
Sponsor
Neuvosyn Laboratories, LLC
Phase
Phase 3
Started
2026-06-30
Last updated
2026-08-05

Condition(s) studied

Hypothyroidism

Investigational drug(s) / intervention(s)

Desiccated Porcine Thyroid Extract Tablets

Desiccated Porcine Thyroid Extract Tablets: North Star

Study summary

The North Star study is a multi-center, Phase 3, open-label, single-arm clinical study to evaluate the Efficacy and Safety of North Star therapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with primary hypothyroidism, including Hashimoto's Thyroiditis, and on therapy with a stable dose of LT4 (minimum 50 mcg per day, administered 7 days per week) for at least 12 weeks prior to Screening * Have had euthyroid status for at least 6 weeks and up to 12 months prior to Screening (Visit 1), with at least one documented minimum stable dose of 50 mcg LT4. * Agree to practice a method of contraception * Female patients not pregnant or lactating at Screening * Agree to practice a method of contraception of greater than 90% reliability * Willing to give written informed consent for the Study * Provide written authorization for use and disclosure of protected health information Exclusion Criteria: * Any clinical condition or previous surgery that might affect the absorption, distribution, biotransformation or excretion of North Star * Hospitalization for a major illness within 5 weeks prior to Screening * Concomitant use of prohibited medications or supplements * Have uncontrolled diabetes * Taking or having taken prescription or over-the-counter weight loss medications within 6 weeks prior to Screening * Participated in another investigational new drug study within 30 days or 5 half-lives of the IMP, whichever is longer, prior to the first study drug administration. * For female subjects, be pregnant, nursing or planning to become pregnant during the study

Primary outcome measure(s)

  • Thyroid-stimulating hormone (TSH) levels within the normal reference range at 24 weeks and at a prior post-baseline visit with no intervening out of range values — 24 weeks

Trial sites (25)

FacilityCityRegionStatus
Paradigm Clinical Research Centers, LLC Modesto California Not Yet Recruiting
Paradigm Clinical Research Centers, LLC Redding California Not Yet Recruiting
Paradigm Clinical Research Centers, LLC San Diego California Not Yet Recruiting
Sunwise Clinical Research Walnut Creek California Not Yet Recruiting
Paradigm Clinical Research Centers, LLC Aurora Colorado Not Yet Recruiting
Accel Research Lakeland Florida Not Yet Recruiting
Accel Research Largo Florida Not Yet Recruiting
AppleMed Research Group, LLC Miami Florida Recruiting
Advanced Medical Research Institute, LLC Miami Florida Recruiting
3Sync LLC Miami Lakes Florida Not Yet Recruiting
3Sync Research Palm Springs Florida Not Yet Recruiting
Precision Clinical Research Sunrise Florida Not Yet Recruiting
Paradigm Clinical Research Centers, LLC Boise Idaho Not Yet Recruiting
Boston Clinical Trials Boston Massachusetts Not Yet Recruiting
ActivMed Practices and Research Methuen Massachusetts Not Yet Recruiting
M3 Wake Research - Las Vegas Wellness Way Las Vegas Nevada Not Yet Recruiting
M3 Wake Research Raleigh North Carolina Not Yet Recruiting
Progressive Medicine of the Triad, LLC Winston-Salem North Carolina Not Yet Recruiting
M3 Wake Research Charleston South Carolina Not Yet Recruiting
Coastal Carolina Research Center, LLC North Charleston South Carolina Not Yet Recruiting
M3 Wake Research Chattanooga Tennessee Not Yet Recruiting
M3 Wake Research Dallas Texas Not Yet Recruiting
Advanced Medical Trials, LLC Georgetown Texas Not Yet Recruiting
Olympus Clinical Research Sugar Land Texas Not Yet Recruiting
Charlotteville Medical Research Center, LLC Charlottesville Virginia Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07747103 on ClinicalTrials.gov ↗ ← All trials in the USA