Luye Pharma Group
Luye Pharma Group sponsors 22 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 21 completed. 1 of these trials are in Phase 3-4 (later-stage) and 21 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Schizophrenia, with 3 trials.
Trial Pipeline
22 total, page 1 of 1
Comparative Efficacy, Safety, PK, and Immunogenicity Study
NCT05853354
A Study of LY03015 in Healthy Chinese and Caucasian Adult Subjects
NCT07671833
Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder
NCT05321602
Relative Bioavailability of LY03010 Compared to Listed Drug
NCT04922593
A Randomized, Open-Label, Crossover Study to Evaluate the Pharmacokinetic Profiles of Rotigotine After a Single Dose of LY03003 (28 mg) Versus After a Week of Daily NEUPRO® Transdermal Patch (4 mg Every 24 Hours) in Healthy Volunteers
NCT04384666
Evaluate the PK of LY03010 Process 1 and Process 2 Drug Product vs INVEGA SUSTENNA After Intramuscular Injection in Schizophrenia Patients
NCT04572685
A Relative Bioavailability Food Effect Study of LY03005
NCT03822065
A Study to Determine Pharmacokinetic Characteristics of LY03010 Versus INVEGA SUSTENNA® in Schizophrenia Patients
NCT03751488
A Study to Assess Pharmacokinetic Profiles of LY03003 and Neupro
NCT03733561
A Study of LY03005 vs Pristiq
NCT03733574
Pharmacokinetic Study of LY03003 in Patients With Parkinson's Disease
NCT03589066
A Study to Assess LY01005 Versus Goserelin Comparator (ZOLADEX®) in Patients With Prostate Cancer
NCT03450109
Relative Bioavailability (RBA) Study of LY03005 vs Pristiq®
NCT03357796
Pilot BA Study of New LY03005 vs Pristiq
NCT02988024
Pharmacokinetic Profile of Neupro Patch Administrated at 2 mg, 4 mg, 6 mg and 8 mg/Day Weekly in Patients With Early-stage Parkinson's Disease
NCT02728947
Compare Pharmacokinetic(PK) Profiles of XZK vs Lovastatin in Healthy Male Volunteers
NCT02603770
Multiple Ascending Dose Study in Healthy Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY03005
NCT02271412
Bioavailability of LY03004 and Risperdal® Consta®
NCT02091388
An Randomized Open-Label PK Study of LY03004 Compared to Risperdal® Consta® in Stable Patients With Schizophrenia or Schizoaffective Disorder
NCT02186769
Safety, Tolerability and Pharmacokinetics Study of LY03005
NCT02055300
Pharmacokinetics and Safety Study of LY03003 in Patients With Early-stage Parkinson's Disease
NCT02055274
Pharmacokinetic and Safety Study of LY03004 in Stable Patients With Schizophrenia or Schizoaffective Disorder
NCT02055287
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 21 |
| Phase 3 | 1 |
What the Pipeline for Luye Pharma Group Shows
According to the ClinicalTrials.gov registry, Luye Pharma Group is linked to 22 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 21 are already marked complete, representing roughly 95% of the total.
The phase mix for Luye Pharma Group reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 21 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Luye Pharma Group is Schizophrenia with 3 linked trials, and 9 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.