Luye Pharma Group

22 total trials 21 completed

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

ACTIVE NOT RECRUITING Phase 3

Comparative Efficacy, Safety, PK, and Immunogenicity Study

NCT05853354

COMPLETED Phase 1

A Study of LY03015 in Healthy Chinese and Caucasian Adult Subjects

NCT07671833

COMPLETED Phase 1

Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder

NCT05321602

COMPLETED Phase 1

Relative Bioavailability of LY03010 Compared to Listed Drug

NCT04922593

COMPLETED Phase 1

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

COMPLETED Phase 1

Evaluate the PK of LY03010 Process 1 and Process 2 Drug Product vs INVEGA SUSTENNA After Intramuscular Injection in Schizophrenia Patients

NCT04572685

COMPLETED Phase 1

A Relative Bioavailability Food Effect Study of LY03005

NCT03822065

COMPLETED Phase 1

A Study to Determine Pharmacokinetic Characteristics of LY03010 Versus INVEGA SUSTENNA® in Schizophrenia Patients

NCT03751488

COMPLETED Phase 1

A Study to Assess Pharmacokinetic Profiles of LY03003 and Neupro

NCT03733561

COMPLETED Phase 1

A Study of LY03005 vs Pristiq

NCT03733574

COMPLETED Phase 1

Pharmacokinetic Study of LY03003 in Patients With Parkinson's Disease

NCT03589066

COMPLETED Phase 1

A Study to Assess LY01005 Versus Goserelin Comparator (ZOLADEX®) in Patients With Prostate Cancer

NCT03450109

COMPLETED Phase 1

Relative Bioavailability (RBA) Study of LY03005 vs Pristiq®

NCT03357796

COMPLETED Phase 1

Pilot BA Study of New LY03005 vs Pristiq

NCT02988024

COMPLETED Phase 1

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

COMPLETED Phase 1

Compare Pharmacokinetic(PK) Profiles of XZK vs Lovastatin in Healthy Male Volunteers

NCT02603770

COMPLETED Phase 1

Multiple Ascending Dose Study in Healthy Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY03005

NCT02271412

COMPLETED Phase 1

Bioavailability of LY03004 and Risperdal® Consta®

NCT02091388

COMPLETED Phase 1

An Randomized Open-Label PK Study of LY03004 Compared to Risperdal® Consta® in Stable Patients With Schizophrenia or Schizoaffective Disorder

NCT02186769

COMPLETED Phase 1

Safety, Tolerability and Pharmacokinetics Study of LY03005

NCT02055300

COMPLETED Phase 1

Pharmacokinetics and Safety Study of LY03003 in Patients With Early-stage Parkinson's Disease

NCT02055274

COMPLETED Phase 1

Pharmacokinetic and Safety Study of LY03004 in Stable Patients With Schizophrenia or Schizoaffective Disorder

NCT02055287

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.