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New York City、NYにおける直腸がんの臨床試験

New York Cityとその周辺地域(約30マイル以内)の拠点で、直腸がんに関する17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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A Clinical Study of Calderasib (MK-1084) With Targeted Therapy and Chemotherapy in People With Colorectal Cancer (MK-1084-012/KANDLELIT-012)

被験者募集中第3相
  • Memorial Sloan Kettering Cancer Center ( Site 0095), New York
18歳以上 · 全性別 · 2026/10/01更新 · NCT06997497

A Study of Botensilimab and Balstilimab for Colorectal Cancer With ctDNA+ After Surgery and Chemotherapy

被験者募集中第2相
  • Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York
18歳以上 · 全性別 · 2026/09/22更新 · NCT07227636

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
  • Columbia University, New York
  • NYU Langone Health, New York
  • Memorial Sloan Kettering Cancer Center, New York
18歳以上 · 全性別 · 2026/09/22更新 · NCT06128551

A First-in-Human Trial of BLU-924 (SAR449336) in Advanced Solid Tumors Harboring KRAS Mutations

被験者募集中第1/2相
  • NYU Langone Health Perlmutter Cancer Center, New York
18歳以上 · 全性別 · 2026/09/21更新 · NCT07629960

Study of Induction PD-1 Blockade in Subjects With Locally Advanced Mismatch Repair Deficient Solid Tumors

被験者募集中第2相
  • Memorial Sloan Kettering Cancer Center, New York
18歳以上 · 全性別 · 2026/09/15更新 · NCT04165772

Five or Ten Year Colonoscopy for 1-2 Non-Advanced Adenomatous Polyps

被験者募集中
  • Laura and Isaac Perlmutter Cancer Center at NYU Langone, New York
  • NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center, New York
45歳〜70歳 · 全性別 · 2026/09/02更新 · NCT05080673

A Phase I-II Study to Test the Safety and Efficacy of PD1 (AB122) and Adenosine Receptor (AB928) Antagonists With Chemotherapy After Short-Course Radiation for Rectal Cancer.

被験者募集中第2相
  • Weill Cornell Medical College, New York
  • Brooklyn Methodist Hospital - NewYork Presbyterian, New York
  • New York Presbyterian Hospital - Queens, New York
18歳〜90歳 · 全性別 · 2026/07/29更新 · NCT05024097

Neoadjuvant Chemotherapy, Excision And Observation vs Chemoradiotherapy For Rectal Cancer

被験者募集中第3相
  • Memorial Sloan Kettering Cancer Center, New York
18歳以上 · 全性別 · 2026/07/14更新 · NCT06205485

The Radiation Oncology-Biology Integration Network (ROBIN) Molecular Characterization Trial (MCT) of Standard Short Course Radiotherapy for Rectal Cancer

被験者募集中
  • Weill Cornell Medical College, New York
  • New York Presbyterian Hospital - Queens, New York
18歳〜90歳 · 全性別 · 2026/06/15更新 · NCT05943210

A Study to Evaluate the Safety and Efficacy of Mesothelin-Targeting Logic-gated CAR T, in Participants With Solid Tumors That Express MSLN and Have Lost HLA-A*02 Expression

被験者募集中第1/2相
  • NYU Langone Medical Center, New York
18歳以上 · 全性別 · 2026/06/12更新 · NCT06051695

A Study of Response to Standard Treatment Before Surgery in People With Rectal Cancer

被験者募集中
  • Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York
18歳以上 · 全性別 · 2026/06/02更新 · NCT06637462

Brodalumab in the Treatment of Immune-Related Adverse Events

被験者募集中第1相
  • Columbia University Irving Medical Center, New York
18歳以上 · 全性別 · 2026/05/13更新 · NCT06673329

A Study of Tucatinib and Trastuzumab in People With Rectal Cancer

被験者募集中第2相
  • Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York
18歳以上 · 全性別 · 2026/05/12更新 · NCT05672524

Biopsy After Radioembolization to Identify Changes in Tumor Cells From the Radiation

被験者募集中観察研究
  • Memorial Sloan Kettering Cancer Center, New York
18歳以上 · 全性別 · 2026/03/12更新 · NCT04668872

Gemcitabine, Cisplatin, Nab-paclitaxel (GAP) and Cemiplimab for Locally Advanced Biliary Tract Cancer (BTC)

被験者募集中第2相
  • Columbia University Irving Medical Center, New York
18歳以上 · 全性別 · 2026/02/25更新 · NCT07433673

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, New York
全年齢 · 全性別 · 2025/10/28更新 · NCT03452774

他の都市における直腸がんの試験

New York City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。