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Orange、CAにおける卵巣がんの臨床試験

Orangeとその周辺地域(約30マイル以内)の拠点で、卵巣がんに関する16件の研究が参加者を募集しています。研究を開いて、参加資格と連絡方法を確認してください。

公式研究テキスト(英語)

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Testing the Addition of Paclitaxel Administered Into the Abdominal Cavity Combined With Chemotherapy for Patients With Gastric Cancer Spread to the Abdominal Cavity

被験者募集中第2/3相
  • UC Irvine Health/Chao Family Comprehensive Cancer Center, Orange
18歳以上 · 全性別 · 2026/10/05更新 · NCT07001748

Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial

被験者募集中第2相
  • Children's Hospital of Orange County, Orange
  • Saint Joseph Hospital - Orange, Orange
全年齢 · 全性別 · 2026/10/05更新 · NCT05564377

A Study to Find Out How Safe REGN5668 is and How Well it Works In Adult Women When Given With Either Cemiplimab, or Cemiplimab + Fianlimab, or Ubamatamab

被験者募集中第1/2相
  • Chao Family Comprehensive Cancer Center, Orange
18歳以上 · 女性 · 2026/09/24更新 · NCT04590326

Study of Elironrasib and Daraxonrasib as Monotherapies and Combination Therapy in Participants With Advanced KRAS G12C Mutant Solid Tumors

被験者募集中第1/2相
  • UC IRVINE Health, Orange
18歳以上 · 全性別 · 2026/09/22更新 · NCT06128551

Evaluate BL-B01D1 in Patients With Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors

被験者募集中第1相
  • University of California Irvine Medical Center, Orange
18歳以上 · 全性別 · 2026/09/21更新 · NCT05983432

Study to Evaluate INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression

被験者募集中第3相
  • Uci Health Chao Family Comprehensive Cancer Center, Orange
18歳以上 · 女性 · 2026/09/15更新 · NCT07214779

Efficacy & Safety of Olvi-Vec and Platinum-doublet + Bevacizumab Compared to Physician's Choice of Chemotherapy and Bevacizumab in Platinum-Resistant/Refractory Ovarian Cancer (PRROC) (OnPrime, GOG-3076)

被験者募集中第3相
  • UCI Health Chao Family Comprehensive Cancer Center, Orange
18歳以上 · 女性 · 2026/08/26更新 · NCT05281471

Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors

被験者募集中第1/2相
  • Children's Hospital of Orange County, Orange
12 Months – 30 Years · 全性別 · 2026/08/25更新 · NCT04851119

Patient Derived Vascularized MicroTumor Model of Gastrointestinal Peritoneal Carcinomatosis

被験者募集中
  • Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange
18歳以上 · 全性別 · 2026/08/14更新 · NCT05844865

Effect of NAC on Preventing Chemo-Related Cognitive Impairments in Ovarian Ca Pts Treated W/ PBT

被験者募集中第1/2相
  • Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange
18歳以上 · 女性 · 2026/07/17更新 · NCT04520139

Trial of Single Protein Encapsulated Doxorubicin, SPEDOX-6 in Advanced Malignancies

被験者募集中第1/2相
  • Chao Family Comprehensive Cancer Center University of California, Irvine, Orange
18歳以上 · 全性別 · 2026/07/17更新 · NCT07064018

Repurposing Riluzole for Cancer-Related Cognitive Impairment: A Pilot Trial

被験者募集中第2相
  • Chao Family Comprehensive Cancer Center, University of California Irvine, Orange
18歳以上 · 全性別 · 2026/07/14更新 · NCT06580002

A Study of Emiltatug Ledadotin (Emi-Le) in Participants With Solid Tumors

被験者募集中第1/2相
  • UC Irvine Health-Chao Family Comprehensive Cancer Center, Orange
18歳以上 · 全性別 · 2026/06/29更新 · NCT05377996

Riluzole For Preventing Cognitive Dysfunction in Ca Pts Receiving Chemo (REFOCUS): Pilot Trial

被験者募集中第2相
  • Chao Family Comprehensive Cancer Center, University of California Irvine, Orange
18歳以上 · 全性別 · 2026/03/03更新 · NCT07447050

PhI Pilot Study Pafolacianine Inject for Intraoperative Imaging on Outcomes of GI Cancer Peritoneal Carcinomatosis

被験者募集中早期第1相
  • Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange
18歳以上 · 全性別 · 2026/02/27更新 · NCT06511037

SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry

被験者募集中観察研究
  • Massive Bio SYNERGY-AI site, Orange
全年齢 · 全性別 · 2025/10/28更新 · NCT03452774

他の都市における卵巣がんの試験

Orangeにおける他の研究

ClinicalTrials.govより、2026/10/06時点のデータを取得。各研究には独自の参加資格があり、参加可否は研究チームが決定します。