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Chong Kun Dang Pharmaceutical clinical trials
Also known as CKD.
The registry lists 299 studies whose lead sponsor is Chong Kun Dang Pharmaceutical. 15 are recruiting or about to start. Per ClinicalTrials.gov, last updated Sep 30, 2026.
Keep track of what changes. Save the Chong Kun Dang Pharmaceutical studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesRegistry sponsor names on this page
Each name exactly as ClinicalTrials.gov lists it, and how it relates to Chong Kun Dang Pharmaceutical.
- Chong Kun Dang Pharmaceutical299 studiesSame company
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Focus areas
Conditions Chong Kun Dang Pharmaceutical leads ten or more studies in, by study count. A broader condition is left out when almost all its studies are already in a narrower one listed here.
Studies
Recruiting first, then most recently updated. Showing 50 of 299. Browse all 299 →
- Korean Study on Safety and Effectiveness of OAD Triple Therapy in Type 2 DiabetesRecruitingNCT06838286
- A Phase 3 Study to Evaluate the Safety and Efficacy of CKD-843 in Male Patients With Androgenetic AlopeciaRecruitingNCT06916793Phase 3
- Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-339 in Healthy VolunteersNot yet recruitingNCT07748702Phase 1
- A First-in-Human Study of CKD-703 in Advanced Solid Tumors and Non-Small Cell Lung CancerRecruitingNCT07439094Phase 1/2
- Study of CKD-215 and D215 in Adults With BRCA-mutated Advanced Ovarian, Fallopian Tube, or Primary Peritoneal CancerNot yet recruitingNCT07532148Phase 1
- Phase Ia/Ib Study of CKD-512 Alone and in Combination With Pembrolizumab in Subjects With Advanced or Metastatic Solid TumorsRecruitingNCT07215637Phase 1
- Evaluate the Efficacy and Safety of Empagliflozin or Glimepiride Combination Therapy in Type 2 Diabetes Mellitus PatientsNot yet recruitingNCT07365358Phase 4
- A Study to Compare the Pharmacokinetics, Pharmacodynamic, Immunogenicity, and Safety of CKD-706 With US-Dupixent®, and EU-Dupixent® in Healthy Adult Participants.RecruitingNCT07358156Phase 1
- Pharmacokinetic, Safety, Tolerability, and Immunogenicity Comparison of CKD-704 (Risankizumab Biosimilar), With EU-approved Skyrizi®, and US-licensed Skyrizi® in Healthy Adult ParticipantsRecruitingNCT07258745Phase 1
- Phase 3 Trial to Evaluate the Efficacy and Safety of CKD-202ARecruitingNCT06643819Phase 3
- Optimize Immunosuppressive Therapy Using Everolimus and Low-dose Calcineurin Inhibitors in Heart Transplant Patients in KoreaNot yet recruitingNCT06942156Phase 4
- To Evaluate the Food Effect on Pharmacokinetic Profiles and Safety in Healthy VolunteersNot yet recruitingNCT06492655Phase 1
- Efficacy and Safety of Telmisartan Compared With LosartanRecruitingNCT06431477Phase 4
- Efficacy and Safety of EsoDuo®RecruitingNCT06430047Phase 4
- A Clinical Trial to Evaluate the Blood Pressure Control of Telmisartan or Losartan in Essential Hypertensive Patients With Metabolic SyndromeNot yet recruitingNCT05843162Phase 4
- A Clinical Trial to Compare and Evaluate Evaluate the Pharmacokinetics and Safety of CKD-846CompletedNCT07404735Phase 1
- Efficacy and Safety of Everolimus Versus Mycophenolate Mofetil in Liver Transplant Recipients.CompletedNCT04471441Phase 4
- Study to Evaluate the Pharmacokinetics and Tolerability of Tacrolimus in Kidney Transplant Recipients.CompletedNCT04102943Phase 4
- MYREPTIC-N® or MY-REPT® in Stable Patients After Kidney Transplant RecipientsCompletedNCT06044493Phase 4
- Initial Pilot Study to Evaluate the Safety and Temporary Symptom Improvement Efficacy of CKD-981CompletedNCT06954766Phase 2
- A Study to Investigate the Safety, Tolerability, PK, and PD of CKD-508 in Healthy ParticipantsCompletedNCT06727396Phase 1
- A Drug-drug Interaction Study to Investigate the Pharmacokinetic Interactions Between CKD-508, Midazolam, and Rosuvastatin in Healthy Adult Male ParticipantsCompletedNCT06979973Phase 1
- Study to Compare the Efficacy and Safety After Conversion to RaparoBell® or My-Rept® in Kidney Transplant PatientsActive, not recruitingNCT05193565Phase 4
- A Clinical Trial to Compare and Evaluate Evaluate the Pharmacokinetics and Safety of CKD-846CompletedNCT06110923Phase 1
- Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-383 0.5/10/1000mg in Healthy VolunteersCompletedNCT07304700Phase 1
- Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-383 0.5/25/1000mg in Healthy VolunteersCompletedNCT07304687Phase 1
- Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-383 0.25/12.5/1000mg in Healthy VolunteersCompletedNCT07304726Phase 1
- Clinical Study to Evaluate the Food Effect of CKD-383 0.5/10/1000mg in Healthy VolunteersCompletedNCT06695572Phase 1
- Clinical Study to Evaluate the Food Effect of CKD-378 in Healthy VolunteersCompletedNCT06709807Phase 1
- Clinical Study to Evaluate the Food Effect of CKD-383 0.5/25/1000mg in Healthy VolunteersCompletedNCT06695598Phase 1
- Clinical Study to Evaluate Drug-drug Interaction and Safety After Co-administration of D352 and D794 in Healthy Adult VolunteersCompletedNCT06758661Phase 1
- Retrospective Observational Study on GERD Management in General Hospitals in KoreaCompletedNCT06974903
- A Clinical Trial to Evaluate the Food Effect of CKD-379CompletedNCT06652971Phase 1
- The Efficacy and Safety of D745 Added to D150 Plus D759 Therapy in Patients with Type 2 DiabetesCompletedNCT05566028Phase 3
- A Clinical Trial to Evaluate the Food Effect of CKD-378CompletedNCT06386328Phase 1
- Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetic of CKD-501, D745, and D150 for Healthy Subjects in Fed State.CompletedNCT06483243Phase 1
- A Phase 2 Study to Evaluate the Safety and Efficacy of CKD-498 in Female Patients With Androgenetic AlopeciaCompletedNCT05677438Phase 2
- Clinical Trial to Evaluate the Efficacy and Safety of D064 and D702 Combination TherapyCompletedNCT05931224Phase 3
- Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetic After Oral Administration of CKD-341 and D956 in Healthy AdultsCompletedNCT06281132Phase 1
- Impact of Lymphocyte Anti-metabolite Immunosuppressions on Donor-Specific Anti-HLA Antibody and Kidney Graft OutcomeCompletedNCT03794492Phase 4
- Clinical Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-387 in Healthy Volunteers Under Fasting ConditionsCompletedNCT06399055Phase 1
- Clinical Study to Evaluate Pharmacokinetic Profiles and Safety of CKD-387 Under Fasting ConditionCompletedNCT05673369Phase 1
- Clinical Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-387 in Healthy Volunteers Under Fed ConditionsCompletedNCT06399068Phase 1
- Clinical Trial to Evaluate the Efficacy and Safety of D064 and D702 Combination Therapy Versus D064 or D702 MonotherapyCompletedNCT06121518Phase 3
- A Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetics of CKD-391(2)CompletedNCT06088017Phase 1
- A Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of CKD-348(6)CompletedNCT06112678Phase 1
- A Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetics of D745, D759, and D150CompletedNCT05928637Phase 1
- A Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetics of CKD-378CompletedNCT05741437Phase 1
- Evaluation of the Safety and Tolerability of CKD-508 in Healthy SubjectsCompletedNCT04488900Phase 1
- Clinical Trial to Compare and Evaluate the Safety and Pharmacokinetic After Oral Administration of CKD-341 and D958 in Healthy AdultsCompletedNCT05921435Phase 1