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The U.S. National Library of Medicine provides a database of clinical trials worldwide. Use the fields below to search the database. Expand your results and select terms or phrases and right-click to search using Google, MalaCards, MedlinePlus, PubMed, or Wikipedia.

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Clinical Trials Search Results

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NCT IDTitle
NCT06467409Phase II Clinical Trial to Evaluate the Efficacy and Safety of LPM3480392 Injection for Moderate to Severe Pain After Orthopedic Surgery
NCT05856630Pharmacokinetics Pharmacodynamics and Safety of LY01022 in Patients With Prostate Cancer Compared With Zoladex® 10.8mg
NCT03427853A Study to Evaluate the Denosumab in Healthy Adults
NCT06240546First-in-Human Study of LPM6690176 in Patients With Advanced Solid Tumors.
NCT07230652A Phase 1 MAD Study to Evaluate the Safety and Tolerability of LY03020
NCT04627155A Study to Evaluate the Human Tolerance and Pharmacokinetics of LY03003
NCT06496048Lurbinectedin or in Combination with Irinotecan Versus Topotecan in Patients with Relapsed SCLC
NCT02055287Pharmacokinetic and Safety Study of LY03004 in Stable Patients With Schizophrenia or Schizoaffective Disorder
NCT04044547A Study of LY03003 in Patients With Early-stage Parkinson's Disease
NCT04853407A Study to Evaluate the Efficacy and Safety of Ansofaxine Hydrochloride Extended-release Tablets in the Treatment of Major Depressive Disorder (MDD)
NCT02988024Pilot BA Study of New LY03005 vs Pristiq
NCT04922593Relative Bioavailability of LY03010 Compared to Listed Drug
NCT03450109A Study to Assess LY01005 Versus Goserelin Comparator (ZOLADEX®) in Patients With Prostate Cancer
NCT06216054Safety, Tolerability and Pharmacokinetic of Multiple-ascending Doses of LPM3770164 in Healthy Subjects
NCT06980207A Phase 1, MAD Study to Evaluate the Safety, Tolerability and Pharmacokinetics of LY03017
NCT02055300Safety, Tolerability and Pharmacokinetics Study of LY03005
NCT03357796Relative Bioavailability (RBA) Study of LY03005 vs Pristiq®
NCT07292233A Food Effect Study of LY03020 in Healthy Subjects
NCT05853341Rivastigmine Bioequivalence Trial With Multiple Application of Transdermal Patches (13.3mg/24h)
NCT05110170Efficacy and Safety of LY01005 in Patients With Breast Cancer Compared to ZOLADEX®
NCT03733574A Study of LY03005 vs Pristiq
NCT07236476Identify Effective Doses of LY01021 in Controlled Ovarian Hyperstimulation (COH) for Female Subjects Undergoing Assisted Reproductive Technology (ART)
NCT05865925Safety, Tolerability, Pharmacokinetics (PK), and Primary Clinical Efficacy of LY01616 in Patients With Advanced Solid Tumors
NCT04638491Safety Tolerability Pharmacokinetic and Preliminary Efficacy in Chinese Advanced Solid Tumors Patients
NCT05238701A Dose-escalation Study to Evaluate the Safety, Tolerability and Pharmacokinetic of LPM3770164 in Healthy Subjects
NCT03822065A Relative Bioavailability Food Effect Study of LY03005
NCT04973735A Phase I Study of LY-CovMab Injection in Chinese Healthy Subjects
NCT06426485To Evaluate the Long-term Efficacy and Safety of Toludevenlafaxine Hydrochloride Sustained-release Tablets
NCT03844438A Study Evaluating the Safety, Tolerability of LPM3480226 Tablets in Patients With Advanced Solid Tumors
NCT04198636A Study to Evaluate LY01011 and Xgeva® in Healthy Adults
NCT03533127A Study of LY01008 and Bevacizumab Combined With Paclitaxel and Carboplatin for Treatment of Naïve Subjects With Metastatic or Recurrent Nonsquamous Non-small Cell Lung Cancer
NCT06098599Comparing the Pharmacokinetic Profile of LY01612 and CAELYX® in Chinese Subjects With Advanced Breast Cancer
NCT02091388Bioavailability of LY03004 and Risperdal® Consta®
NCT06095427A Pharmacokinetic Similarity Study in Healthy Male Subjects to Evaluate Pharmacokinetics, Pharmacodynamics, Safety and Immunogenicity of LY06006 Versus US-Prolia and EU-Prolia by Single-dose Subcutaneous Injection
NCT04381910Irinotecan Hydrochloride Liposome Injection (LY01610) For Small Cell Lung Cancer
NCT03785652Dose-Finding Clinical Trial to Evaluate the Efficacy and Safety of LY03005 Extended-release Tablets in the Treatment of Major Depressive Disorder (MDD)
NCT02728947Pharmacokinetic 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
NCT04571164A Study to Evaluate the Effectiveness and Safety of LY03003 in Patients With Early Primary PD
NCT05853354Comparative Efficacy, Safety, PK, and Immunogenicity Study
NCT04593511to Evaluate the Safety, Tolerability and Pharmacokinetics of Four Formulations of LY03009 in Healthy Volunteers
NCT03733561A Study to Assess Pharmacokinetic Profiles of LY03003 and Neupro
NCT04572698A Study to Compare LY09004 and Eylea in the Treatment of Wet Age-related Macular Degeneration(wAMD)
NCT04973722A Study to Evaluate LY06006 and Prolia in Healthy Adults
NCT05140512Pharmacokinetics, Pharmacodynamics and Safety of LY01005 in Patients With Prostate Cancer Compared to ZOLADEX®
NCT04629404A Clinical Trial to Evaluate the Pharmacodynamics/Pharmacokinetics and Safety of LY03003 in Early PD Patients
NCT04572685Evaluate the PK of LY03010 Process 1 and Process 2 Drug Product vs INVEGA SUSTENNA After Intramuscular Injection in Schizophrenia Patients
NCT05970510A Study to Evaluate Efficacy and Safety of Toludesvenlafaxine Hydrochloride Sustained-release Tablets in Generalized Anxiety Disorder.
NCT02055274Pharmacokinetics and Safety Study of LY03003 in Patients With Early-stage Parkinson's Disease
NCT05060406A Study to Evaluate the Efficacy and Safety of LY06006 in Postmenopausal Women With Osteoporosis at High Risk for Fracture
NCT04384666A 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