University of Mary Hardin-Baylor
University of Mary Hardin-Baylor sponsors 10 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 8 completed. The most-studied condition in this pipeline is Evaluation of Bioavailability of Supplemental Forms of Iron, with 1 trials.
Trial Pipeline
10 total, page 1 of 1
Glycoprotein Matrix-Bound Iron Improves Iron Absorption
NCT06738199
The Effect of Blood Flow Restriction With and Without Arginine on Physical Performance and Growth Hormone
NCT04079010
Pain and Neck Dysfunction Following Dry Needling With and Without Intramuscular Electrical Stimulus.
NCT04057781
Effect of Spinal Manipulation on Vulvar Pain
NCT04016467
Leg Muscle Activity Measured Via Electromyography in Back Squat Variations
NCT03902730
Effects of A-GPC on Reaction Time and Cognitive Function
NCT03903250
Effects of a Thermogenic Dietary Supplement on Metabolic, Hemodynamic, and Mood Responses
NCT03678116
Efficacy and Safety of Fenugreek Extract on Markers of Muscle Damage and Inflammation in Untrained Males
NCT03318731
Iron Aid IPS on Performance, Fatigue and Iron Levels During 12 Weeks of Supplementation and Aerobic Training
NCT03523455
The Effect of a Caffeine Blend on Reaction Time, Mental Performance and Focus in Athletic Males
NCT03019523
Therapeutic Areas
What the Pipeline for University of Mary Hardin-Baylor Shows
According to the ClinicalTrials.gov registry, University of Mary Hardin-Baylor is linked to 10 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 8 are already marked complete, representing roughly 80% of the total.
The phase mix for University of Mary Hardin-Baylor reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for University of Mary Hardin-Baylor is Evaluation of Bioavailability of Supplemental Forms of Iron with 1 linked trial, and 8 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.