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NCT ID: NCT00239252 Completed - Hepatitis C Clinical Trials

Comparison in Efficacy and Safety Between Interferon Alfacon-1 Alone and Concomitant Dosing With Ribavirin for the Treatment of Hepatitis C

Start date: n/a
Phase: Phase 3
Study type: Interventional

Efficacy and safety is compared between interferon alfacon-1 alone and concomitant dosing of interferon alfacon-1 and ribavirin in hepatitis C patients.

NCT ID: NCT00239213 Completed - Influenza Infection Clinical Trials

Catechin Gargling for Influenza Infection

Start date: November 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to clarify the preventive effects of catechin gargling on the influenza infection.

NCT ID: NCT00238875 Completed - Clinical trials for T1N0M0 Non-small Cell Lung Cancer

A Phase II Study of Stereotactic Body Radiation Therapy in Patients With T1N0M0 Non-small Cell Lung Cancer (JCOG0403)

Start date: July 2004
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of SBRT for T1N0M0 non-small cell lung cancer

NCT ID: NCT00238160 Withdrawn - Clinical trials for Localized Resectable Adult Primary Liver Cancer

Surgery With or Without Hepatic Arterial Chemotherapy in Treating Patients With Liver Cancer

Start date: n/a
Phase: Phase 3
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as fluorouracil and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving drugs directly into the arteries around the tumor may kill more tumor cells. Giving chemotherapy after surgery may kill any remaining tumor cells. It is not yet known whether surgery and hepatic arterial chemotherapy are more effective than surgery alone in treating patients with liver cancer that has spread to the portal vein. PURPOSE: This randomized phase III trial is studying surgery and hepatic arterial chemotherapy to see how well they work compared to surgery alone in treating patients with liver cancer that has spread to the portal vein.

NCT ID: NCT00237211 Completed - Clinical trials for Postmenopausal Women With Advanced Breast Cancer

Study of High-dose Letrozole Therapy in Postmenopausal Patients With Breast Cancer

Start date: June 2001
Phase: Phase 2
Study type: Interventional

To investigate the safety and efficacy of letrozole monotherapy at a dose of 2.5 mg/day in postmenopausal patients with breast cancer, and to determine the blood concentrations of letrozole and hormones.

NCT ID: NCT00237198 Completed - Clinical trials for Postmenopausal Women With Advanced Breast Cancer

Study of Safety and Efficacy of Letrozole Monotherapy as Second-line Endocrine Therapy in Postmenopausal Patients With Advanced Breast Cancer Who Received Previous Anti-estrogen Treatment

Start date: March 2004
Phase: Phase 2
Study type: Interventional

- Safety and efficacy of letrozole 2.5 mg/day monotherapy as second-line endocrine therapy in postmenopausal patients with advanced breast cancer who received previous anti-estrogen treatment - To investigate changes in blood drug concentrations and blood hormone kinetics. - To investigate gene polymorphisms of CYP2A6, an enzyme involved in the metabolism of letrozole

NCT ID: NCT00235872 Completed - Clinical trials for Rheumatoid Arthritis

Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis

Start date: August 2004
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the long-term safety and tolerability of repeated administration of adalimumab in Japanese subjects with rheumatoid arthritis.

NCT ID: NCT00235833 Completed - Clinical trials for Rheumatoid Arthritis

Adalimumab in Adult Japanese Subjects With Rheumatoid Arthritis

Start date: June 2003
Phase: Phase 2
Study type: Interventional

The purpose of the study is to assess the long-term safety, tolerability, and efficacy of repeated administration of adalimumab in adult Japanese subjects with rheumatoid arthritis.

NCT ID: NCT00234104 Completed - Clinical trials for Heart Failure, Congestive

A Dose-finding Study of OPC-41061 in Treatment of Cardiac Edema (Congestive Heart Failure)

Start date: August 2004
Phase: Phase 2
Study type: Interventional

This drug is being developed to treat cardiac edema. The primary purpose of this study is to investigate the dose response for body weight in seven-day repeated oral administration of OPC-41061 at 15, 30, and 45 mg or placebo in patients with extracellular volume expansion secondary to CHF despite taking furosemide at 40 mg/d or more. This study is being conducted in Japan.

NCT ID: NCT00234078 Completed - Dry Eye Syndromes Clinical Trials

Dose-response Study of OPC-12759 Ophthalmic Suspension

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the dose-response of OPC-12759 ophthalmic suspension in dry eye patients.