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Baton Rouge LA 膀胱癌临床试验
6项针对 膀胱癌的研究正在 Baton Rouge及周边约 30 英里内的站点招募参与者。打开研究详情可查看入选标准及联系研究团队的方式。
官方研究文本（英文）
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Testing the Addition of the Immunotherapy Drug, Pembrolizumab, to Radiation Therapy Compared to the Usual Chemotherapy Treatment During Radiation Therapy for Bladder Cancer, PARRC Trial
招募中2 期
- Louisiana Hematology Oncology Associates LLC, Baton Rouge
- Mary Bird Perkins Cancer Center, Baton Rouge
- Mary Bird Perkins Cancer Center - Gonzales, Gonzales · 距离 21 英里
Collecting Blood Samples From Patients With and Without Cancer to Evaluate Tests for Early Cancer Detection
招募中观察性研究欢迎健康志愿者
- LSU Health Baton Rouge-North Clinic, Baton Rouge
- Our Lady of the Lake Physician Group, Baton Rouge
- Our Lady of The Lake, Baton Rouge
- 以及另外 2 项
Testing the Effectiveness of Two Immunotherapy Drugs (Nivolumab and Ipilimumab) With One Anti-cancer Targeted Drug (Cabozantinib) for Rare Genitourinary Tumors
招募中2 期
- Louisiana Hematology Oncology Associates LLC, Baton Rouge
A Study of Vepugratinib (LY3866288) in Participants With Cancer in the Urinary Tract
招募中3 期
- Mary Bird Perkins Cancer Center, Baton Rouge
FORAGER-1: A Study of Vepugratinib (LY3866288; LOXO-435) in Participants With Cancer With a Change in a Gene Called FGFR3
招募中1 期
- Mary Bird Perkins Cancer Center, Baton Rouge
Testing Shorter Duration Radiation Therapy Versus the Usual Radiation Therapy in Patients Receiving the Usual Chemotherapy Treatment for Bladder Cancer, ARCHER Study
招募中3 期
- Louisiana Hematology Oncology Associates LLC, Baton Rouge
- Mary Bird Perkins Cancer Center, Baton Rouge
其他城市的 膀胱癌试验
- New York City, NY35 项研究
- Houston, TX31 项研究
- Nashville, TN31 项研究
- Dallas, TX27 项研究
- Washington, DC26 项研究
- Boston, MA26 项研究
- Baltimore, MD24 项研究
- Los Angeles, CA24 项研究
- St. Louis, MO22 项研究
- Seattle, WA21 项研究
- Edison, NJ21 项研究
- Philadelphia, PA21 项研究
Baton Rouge的其他研究
- 肥胖症15 项研究
- 超重10 项研究
- 非小细胞肺癌10 项研究
- 转移性癌症9 项研究
- 急性髓系白血病8 项研究
- 肺癌8 项研究
- 结直肠癌8 项研究
- 乳腺癌7 项研究
- 慢性淋巴细胞白血病5 项研究
- 前列腺癌5 项研究
- 慢性阻塞性肺病5 项研究
- 心力衰竭5 项研究
数据来自 ClinicalTrials.gov，检索日期：2026年10月6日。每项研究自行设定入选标准，由研究团队决定谁能参与。