Clinical trials

21

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study to Evaluate the Pharmacokinetics and the Safety After Administration of BR1015-A and Co-administration of BR1015-3 and BR1015-2 Under Fed Conditions

The purpose of this clinical trial is to evaluate the pharmacokinetics and the safety after administration of BR1015-A and co-administration of BR1015-3 and BR1015-2 in healthy volunteers under fed conditions

Participants needed: 48
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Feb 19, 2026
Eligibility criteria

Subjects with a body mass index (BMI) of more than 18.0 kg/m² and less than 30.0... [+2]

Subjects who have taken drugs that induce or inhibit metabolizing enzymes, such... [+5]

Status: Not yet recruiting

A Study to Evaluate the Pharmacokinetics and the Safety After Administration of BR1015-A and Co-administration of BR1015-3 and BR1015-2 Under Fasting Conditions

The purpose of this clinical trial is to evaluate the pharmacokinetics and the safety after administration of BR1015-A and co-administration of BR1015-3 and BR1015-2 in healthy volunteers under fasting conditions

Participants needed: 58
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Feb 19, 2026
Eligibility criteria

Subjects with a body mass index (BMI) of more than 18.0 kg/m² and less than 30.0... [+2]

Subjects who have taken drugs that induce or inhibit metabolizing enzymes, such... [+5]

Status: Not yet recruiting

A Study to Evaluate the Pharmacokinetics and the Safety After Administration of BR1015-A and Co-administration of BR1015-1 and BR1015-2 Under Fasting Conditions

The purpose of this clinical trial is to evaluate the pharmacokinetics and the safety after administration of BR1015-A and co-administration of BR1015-1 and BR1015-2 in healthy volunteers under fasting conditions

Participants needed: 58
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Feb 19, 2026
Eligibility criteria

Subjects with a body mass index (BMI) of more than 18.0 kg/m² and less than 30.0... [+2]

Subjects who have taken drugs that induce or inhibit metabolizing enzymes, such... [+5]

Status: Not yet recruiting

A Study to Evaluate the Pharmacokinetics and the Safety After Administration of BR1015-A and Co-administration of BR1015-1 and BR1015-2 Under Fed Conditions

The purpose of this clinical trial is to evaluate the pharmacokinetics and the safety after administration of BR1015-A and co-administration of BR1015-1 and BR1015-2 in healthy volunteers under fed conditions

Participants needed: 48
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Feb 19, 2026
Eligibility criteria

Subjects with a body mass index (BMI) of more than 18.0 kg/m² and less than 30.0... [+2]

Subjects who have taken drugs that induce or inhibit metabolizing enzymes, such... [+5]

Status: Not yet recruiting

A Study of Bosmolisib (BR101801) in Participants With R/R PTCL.

The objective of this phase II study is to evaluate the efficacy and safety of BR101801 in patients with peripheral T-cell lymphoma(PTCL).

Participants needed: 44
Trial details
Phase: Phase 2Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Jan 28, 2026
Eligibility criteria

The ECOG performance status ≤ 2. [+8]

The presence of overt leptomeningeal or active central nervous system (CNS) meta... [+6]

Status: Not yet recruiting

A Study of BR1400-1, BR1400-2, BR1400-3, BR1400-4, and BR1400-5 in Patients With Essential Hypertension

The objective of this clinical trial is to evaluate the antihypertensive efficacy and safety of BR1400-1, BR1400-2, BR1400-3, BR1400-4, and BR1400-5 with essential hypertension.

Participants needed: 330
Trial details
Phase: Phase 2Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Jan 28, 2026Locations: 1
Eligibility criteria

For patients not currently receiving antihypertensive therapy: 140 mmHg ≤ MSSBP... [+3]

Patients with blood pressure results showing MSSBP ≥ 180 mmHg or MSDBP ≥ 110 mmH... [+3]

Status: Recruiting

A Study of Second- and Later-line Palliative Chemotherapy in Patients With Metastatic Colorectal Cancer.

This study aims to comprehensively identify the various treatment patterns of second- or subsequent-line palliative chemotherapy used in patients with metastatic colorectal cancer who have experienced failure of first-line palliative chemotherapy and to evaluate the prognosis of each treatment.

Participants needed: 1,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Dec 4, 2025Locations: 1
Eligibility criteria

Patients who have signed the informed consent after receiving information about... [+3]

Female patients who are pregnant, have childbearing potential, or are breastfeed... [+2]

Status: Recruiting

A Study of Olanzapine in Participants With Bipolar Disorder.

This study aimed to identify treatment patterns in patients with bipolar disorder receiving olanzapine according to demographic and clinical characteristics and to evaluate the effectiveness of education on weight gain, a side effect of olanzapine, in preventing weight gain.

Participants needed: 3,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Dec 4, 2025Locations: 1
Eligibility criteria

Patients who have signed the informed consent after receiving information about... [+2]

Female patients who are pregnant, have childbearing potential, or are breastfeed... [+2]

Status: Recruiting

Observational Study to Evaluate the Safety and Efficacy of Zepzelca™ Injection

The purpose of this study is to evaluate the safety and efficacy of Zepzelca™ inj. in real-world practice and to investigate important identified risks and gaps in information related to risk management plans.

Participants needed: 300
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 16, 2025Locations: 1
Eligibility criteria

Patients who voluntarily provide written consent for personal information collec... [+2]

Patients with no prior history of platinum-based anticancer chemotherapy for can... [+4]

Status: Recruiting

A Phase IV Clinical Trial to Compare the Efficacy and Safety of Metformin+Sodium-Glucose Cotransporter 2 Inhibitor(SGLT2-i)+Thiazolidinedione (TZD) in Patients With Type 2 Diabetes

This is a randomized, open-label, active-controlled, parallel, multicenter, phase IV clinical study evaluating the efficacy and safety of switching Metformin+SGLT2-i+DPP4-i to Metformin+SGLT2-i+TZD in patients with type 2 diabetes.

Participants needed: 204
Trial details
Phase: Phase 4Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Has voluntarily agreed to participate in this clinical trial. [+2]

Has severe renal and liver disorders [+3]

Status: Recruiting

A Clinical Trial to Evaluate the Safety and Efficacy of Olanzapine Titration Schedule in Patients With Schizophrenia

The objective of this clinical trial is to evaluate the safety and efficacy of olanzapine titration schedule in patients with schizophrenia

Participants needed: 120
Trial details
Phase: Phase 2Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 15, 2025Locations: 2
Eligibility criteria

Of patients with schizophrenia in accordance with DSM(Diagnostic and Statistical... [+1]

Patients diagnosed schizophrenia spectrum and other psychotic disorder(e.g. schi... [+1]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of Dapagliflozin in Patient With Type 2 Diabetes Mellitus and Hypertension

The purpose of this clinical trial is to evaluate the efficacy and safety of dapagliflozin in patient with type 2 diabetes mellitus and hypertension

Participants needed: 9,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Those diagnosed with type 2 diabetes mellitus accompanied by hypertension who ar... [+2]

Patients with secondary hypertension: Secondary hypertension is not limited to t... [+3]

Status: Recruiting

A Study to Evaluate Ethanol-induced Symptoms and Safety in Breast Cancer Patients

The purpose of this study is to evaluate ethanol-induced symptoms and safety in breast cancer patients with neoadjuvant/adjuvant chemotherapy including Non-ethanol formulation docetaxel before and after surgery

Participants needed: 1,052
Trial details
Age: 19+Biological sex: FemaleType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 12, 2025Locations: 2
Eligibility criteria

Those who voluntarily signed a written personal information collection and usage... [+5]

Those are diagnosed with other primary cancer that can influence the treatment o... [+2]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of Fixed-Dose Combination of Pitavastatin/Ezetimib

The purpose of this study is to evaluate the efficacy and safety of fixed-Dose combination of Pitavastatin/Ezetimibe under the real-world condition

Participants needed: 8,606
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Those who taking statins or statins and ezetimibe in addition to dietary and exe... [+1]

Those who are taking a fixed-dose combination of pitavastatin/ezetimibe at study... [+2]

Status: Recruiting

An OS to Evaluate Effectiveness and Safety of Fixed-dose Combinations of FMS/AML or FMS/AML/HCTZ

The main purpose of this observation study is to collect data on the effects and side effects for 12 weeks of the medication administration of the single-pill combinations, which are fimasartan/amlodipine or fimasartan/amlodipine/hydrochlorothiazide, based on fimasartan. (Stage 1). Also, this study will evaluate major cardiovascular events, long-term blood pressure control, and the safety by follow-up of those who consent to the extended study for about 2 years (96 weeks).(Stage 2)

Participants needed: 20,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Patients who voluntarily consent on the informed consent form and understand the... [+6]

The patients who are suspected of having secondary hypertension or confirmed to... [+3]

Status: Recruiting

A Study to Evaluate the Pharmacokinetics and Safety Between "BR3006" and Co-administration of "BR3006A", "BR3006B", and "BR3006C" in Healthy Adult Volunteers (Fasting)

This was an open-label, randomized, fasting, single-dose, 2-sequence, 2-period crossover study to evaluate the pharmacokinetics and safety between single oral administration of "BR3006" and co-administration of "BR3006A", "BR3006B," and "BR3006C" in healthy adult volunteers.

Participants needed: 52
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Jul 24, 2025Locations: 1
Eligibility criteria

Adults aged over 19 at the time of consent [+2]

Those who have administered investigational products within 6 months from the fi... [+2]

Status: Recruiting

A Study to Evaluate the Pharmacokinetics and Safety Between "BR3006" and Co-administration of "BR3006A", "BR3006B", and "BR3006C" in Healthy Adult Volunteers (Fed)

This was an open-label, randomized, fed, single-dose, 2-sequence, 2- period crossover study to evaluate the pharmacokinetics and safety between single oral administration of "BR3006" and co-administration of "BR3006A", "BR3006B," and "BR3006C" in healthy adult volunteers.

Participants needed: 40
Trial details
Phase: Phase 1Age: 19+Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Jul 24, 2025Locations: 1
Eligibility criteria

Adults aged over 19 at the time of consent [+2]

Those who have administered investigational products within 6 months from the fi... [+2]

Status: Recruiting

A Bioequivalence Study to Evaluate Pharmacokinetics and Safety of BR2022 and BR2022-1 in Patients With Deleterious or Suspected Deleterious Germline BRCA-Mutated Advanced Ovarian Cancer

This was a multicenter, open-label, randomized, crossover bioequivalence study to evaluate the pharmacokinetics and safety of BR2022 and BR2022-1 in Patients with deleterious or suspected deleterious germline BRCA-mutated advanced ovarian cancer.

Participants needed: 24
Trial details
Phase: Phase 1Age: 19-74Biological sex: FemaleType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Jul 16, 2025Locations: 1
Eligibility criteria

Females aged 19 -74 at the time of consent [+2]

Those who have a history of severe hypersensitivity to drugs that include the in... [+2]

Status: Recruiting

A Study to Compare and Evaluate the Pharmacokinetic Characteristics and the Safety Between Administration of BR2021 and BR2021-1

The purpose of this clinical study is to compare and evaluate the pharmacokinetic characteristics and the safety between administration of BR2021 and BR2021-1 in patients with metastatic adenocarcinoma of the pancreas

Participants needed: 20
Trial details
Phase: Phase 1Age: 19-74Biological sex: AllType: InterventionalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Apr 10, 2025Locations: 2
Eligibility criteria

Those with histologically or cytologically proven metastatic adenocarcinoma of t... [+2]

In the case of a female subject, pregnant woman or those suspected pregnancy or... [+4]

Status: Recruiting

A Observational Study to Evaluate the Efficacy and Safety of Pacitol Inj.

The purpose of this study is to evaluate the efficacy and safety of pacitol Inj.(paricalcitol) for secondary hyperparathyroidism with stage 5D chronic kidney disease (CKD 5D) receiving hemodialysis

Participants needed: 1,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Dec 12, 2024Locations: 1
Eligibility criteria

Among hemodialysis patients with secondary hyperparathyroidism due to chronic ki... [+2]

Those with a history of hypersensitivity reactions to this drug or its component... [+6]

Status: Recruiting

A Study to Identify the Risk of Non-alcoholic Fatty Liver Disease (NAFLD) in Patients With Type 2 Diabetes in Clinical Practice and to Evaluate the Clinical Usefulness of Dapagliflozin/Pioglitazone Combination Therapy

The purpose of this study is to identify the risk of non-alcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes in clinical practice and to evaluate the clinical usefulness of Dapagliflozin/Pioglitazone combination therapy

Participants needed: 10,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Boryung Pharmaceutical Co., LtdUpdated: Oct 18, 2024Locations: 2
Eligibility criteria

Among patients with type 2 diabetes, those who are scheduled to administer a fix... [+1]

Those who have a history of taking a fixed-dose combination of dapagliflozin/pio... [+1]