Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Cancer Chemotherapy from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 25
- Active, not recruiting: 15
- Completed: 3
- Other: 7
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT01810913 — Testing Docetaxel-Cetuximab or the Addition of an Immunotherapy Drug, Atezolizumab, to the Usual Chemotherapy and Radiation Therapy in High-Risk Head and Neck Cancer
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 613 |
| Study Type | INTERVENTIONAL |
| Conditions | Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma; Stage III Hypopharyngeal Squamous Cell Carcinoma AJCC v7; Stage III Laryngeal Squamous Cell Carcinoma AJCC v6 and v7; Stage III Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7; Stage III Oropharyngeal Squamous Cell Carcinoma AJCC v7 |
| Interventions | ; ; |
This phase II/III trial studies how well radiation therapy works when given together with cisplatin, docetaxel, cetuximab, and/or atezolizumab after surgery in treating patients with high-risk stage III-IV head and neck cancer the begins in the thin, flat cells (squamous cell). Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells a…
NCT04847063 — Individual Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Treatment of Peritoneal Carcinomatosis From Peritoneal Mesothelioma or Atypical Mesothelial Proliferation or From Ovarian, Colorectal, or Appendiceal Histologies
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Peritoneal Mesothelioma; Peritoneal Carcinomatosis; Ovarian Cancer; Gastrointestinal Cancer; Appendiceal Cancer |
| Interventions | ; ; |
Background:
Cytoreductive surgery (CRS) removes tumors in the abdomen. HIPEC is hyperthermic (heated) chemotherapy that washes the inside of the abdomen. CRS with HIPEC may help people with peritoneal carcinomatosis. These are tumors that have spread to the lining of the abdomen from other cancers. Researchers think they can improve the results of CRS with HIPEC treatment on these tumors by ch…
NCT05001880 — Chemotherapy With or Without Immunotherapy for Peritoneal Mesothelioma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Peritoneal Malignant Mesothelioma |
| Interventions | ; ; |
This phase II trial compares the usual treatment alone (carboplatin, pemetrexed, and bevacizumab) to using immunotherapy (atezolizumab) plus the usual treatment in treating patients with peritoneal mesothelioma. The usual treatment consists of surgery or chemotherapy. Carboplatin is in a class of medications known as platinum-containing compounds. It works in a way similar to the anticancer dru…
NCT05058651 — Evaluating the Addition of the Immunotherapy Drug Atezolizumab to Standard Chemotherapy Treatment for Advanced or Metastatic Neuroendocrine Carcinomas That Originate Outside the Lung
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 189 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Extrapulmonary Neuroendocrine Carcinoma; Metastatic Extrapulmonary Neuroendocrine Carcinoma; Recurrent Extrapulmonary Neuroendocrine Carcinoma; Unresectable Extrapulmonary Neuroendocrine Carcinoma |
| Interventions | ; ; |
This phase II/III trial compares the effect of immunotherapy with atezolizumab in combination with standard chemotherapy with a platinum drug (cisplatin or carboplatin) and etoposide versus standard therapy alone for the treatment of poorly differentiated extrapulmonary (originated outside the lung) neuroendocrine cancer that may have spread from where it first started to nearby tissue, lymph n…
NCT05691478 — A Study to Test the Addition of the Drug Cabozantinib to Chemotherapy in Patients With Newly Diagnosed Osteosarcoma
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1122 |
| Study Type | INTERVENTIONAL |
| Conditions | High Grade Osteosarcoma; Localized Osteosarcoma; Metastatic Osteosarcoma; Secondary Osteosarcoma |
| Interventions | ; ; |
This phase II/III trial tests the safety, side effects, and best dose of the drug cabozantinib in combination with standard chemotherapy, and to compare the effect of adding cabozantinib to standard chemotherapy alone in treating patients with newly diagnosed osteosarcoma. Cabozantinib is in a class of medications called kinase inhibitors which block protein signals affecting new blood vessel f…
NCT06058377 — Adding an Immunotherapy Drug, MEDI4736 (Durvalumab), to the Usual Chemotherapy Treatment (Paclitaxel, Cyclophosphamide, and Doxorubicin) for Stage II-III Breast Cancer
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 3680 |
| Study Type | INTERVENTIONAL |
| Conditions | Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; HER2-Negative Breast Carcinoma; Hormone Receptor-Positive Breast Carcinoma |
| Interventions | ; ; |
This phase III trial compares the addition of an immunotherapy drug (durvalumab) to usual chemotherapy versus usual chemotherapy alone in treating patients with MammaPrint High 2 Risk (MP2) stage II-III hormone receptor positive, HER2 negative breast cancer. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body’s immune system attack the cancer, and may interfere with …
NCT06091865 — A Study to Compare How Well Odronextamab Combined With Chemotherapy Works and How Safe it is Against Rituximab Combined With Chemotherapy, in Adult Patients With Previously Untreated Diffuse Large B-cell Lymphoma
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 904 |
| Study Type | INTERVENTIONAL |
| Conditions | Diffuse Large B-cell Lymphoma (DLBCL) |
| Interventions | ; ; |
This study is researching an experimental drug called odronextamab, referred to as study drug, when used in combination with chemotherapy. The study is focused on patients with Diffuse Large B-cell Lymphoma (DLBCL) that have not been treated before (called “previously untreated”). Patients with DLBCL that have come back after treatment (called “relapsed”), or have not responded to treatment (ca…
NCT06172296 — Dinutuximab With Chemotherapy, Surgery and Stem Cell Transplantation for the Treatment of Children With Newly Diagnosed High Risk Neuroblastoma
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 478 |
| Study Type | INTERVENTIONAL |
| Conditions | Ganglioneuroblastoma, Nodular; Neuroblastoma |
| Interventions | ; ; |
This phase III trial tests how well the addition of dinutuximab to Induction chemotherapy along with standard of care surgical resection of the primary tumor, radiation, stem cell transplantation, and immunotherapy works for treating children with newly diagnosed high-risk neuroblastoma. Dinutuximab is a monoclonal antibody that binds to a molecule called GD2, which is found on the surface of n…
NCT06139627 — Evaluation of Geriatric Assessment and Management for Older Adults With Non-small Cell Lung Cancer Receiving Chemotherapy Radiation Therapy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Lung Non-Small Cell Carcinoma; Stage III Lung Cancer AJCC v8 |
| Interventions | ; ; |
This clinical trial tests how well a geriatric assessment (GA) with GA-directed treatment recommendations, compared to GA with usual care, works in identifying risk factors, reducing chemotherapy radiation toxicity and functional decline, and improving the overall quality of life in older patients with non-small cell lung cancer (NSCLC). Older patients with lung cancer undergoing chemotherapy a…
NCT06465329 — A Study of Cemiplimab Plus Chemotherapy Versus Cemiplimab Plus Chemotherapy Plus Other Cancer Treatments for Adult Patients With Operable Non-Small Cell Lung Cancer (NSCLC)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-Small Cell Lung Cancer |
| Interventions | ; ; |
This study will enroll adult participants with early-stage (stage II-IIIB) non-small cell lung cancer for whom surgery is planned.
The aim is to find out whether an investigational treatment (consisting of the immunotherapy drug cemiplimab plus chemotherapy plus a third drug) works better than cemiplimab plus chemotherapy without the additional drug.
The study is also looking at several other…
NCT06875310 — A Study of Adagrasib Plus Pembrolizumab Plus Chemotherapy vs. Placebo Plus Pembrolizumab Plus Chemotherapy in Participants With Previously Untreated Non-squamous Non-small Cell Lung Cancer With KRAS G12C Mutation (KRYSTAL-4)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Mirati Therapeutics Inc. |
| Enrollment | 630 |
| Study Type | INTERVENTIONAL |
| Conditions | Carcinoma, Non-Small-Cell Lung |
| Interventions | ; ; |
This is a trial to evaluate the efficacy, safety, and tolerability of adagrasib plus pembrolizumab plus platinum-doublet chemotherapy versus placebo plus pembrolizumab plus platinum-doublet chemotherapy in participants with previously untreated, locally advanced or metastatic NSCLC with KRAS G12C mutation
NCT06351046 — Preventive Interventions for Chronic Pain Worsening
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Rigshospitalet, Denmark |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Non-Cancer Pain |
| Interventions |
This is an open label randomized controlled trial (RCT), which will be conducted with patients of the Copenhagen Wound Healing Center at Bispebjerg Hospital in Copenhagen (DK). The trial has two arms (1:1): A Virtual Reality based Pain Self-management (VRPS) program group, and a control group (usual care). Included will be 44 patients at least 18 years old; fluent in the Danish language; compla…
NCT06989489 — Implementation of an Oral Chemotherapy Adherence Intervention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | UNC Lineberger Comprehensive Cancer Center |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Solid Tumor; Hematologic Malignancy |
| Interventions |
The goal of this study is to evaluate the effectiveness and usability of a newly developed oral anticancer agent adherence program implemented across 6 cancer clinics (two academic, two urban, and two rural). The study will include 160 adult participants with either solid tumors or hematologic malignancies who have been taking oral anticancer agents for at least six months.
This study will hav…
NCT06124157 — A Study Testing the Combination of Dasatinib or Imatinib to Chemotherapy Treatment With Blinatumomab for Children, Adolescents, and Young Adults With Philadelphia Chromosome Positive (Ph+) or ABL-Class Philadelphia Chromosome-Like (Ph-Like) B-cell Acute Lymphoblastic Leukemia (B-ALL)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 222 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia |
| Interventions | ; ; |
This pilot trial assesses the effect of the combination of blinatumomab with dasatinib or imatinib and standard chemotherapy for treating patients with Philadelphia chromosome positive (Ph+) or ABL-class Philadelphia chromosome-like (Ph-like) B-Cell acute lymphoblastic leukemia (B-ALL). Blinatumomab is a bispecific antibody that binds to two different proteins-one on the surface of cancer cells…
NCT06317662 — Testing the Addition of the Anti-cancer Drug Venetoclax and/or the Anti-cancer Immunotherapy Blinatumomab to the Usual Chemotherapy Treatment for Infants With Newly Diagnosed KMT2A-rearranged or KMT2A-non-rearranged Leukemia
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 153 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Leukemia of Ambiguous Lineage; B Acute Lymphoblastic Leukemia |
| Interventions | ; ; |
This phase II trial tests the addition of venetoclax and/or blinatumomab to usual chemotherapy for treating infants with newly diagnosed acute lymphoblastic leukemia (ALL) with a KMT2A gene rearrangement (KMT2A-rearranged [R]) or without a KMT2A gene rearrangement (KMT2A-germline [G]). Venetoclax is in a class of medications called B-cell lymphoma-2 (Bcl-2) inhibitors. It may stop the growt…
NCT06696768 — Clinical Trial of an Anti-cancer Drug, CA-4948 (Emavusertib), in Combination With Chemotherapy Treatment (FOLFOX Plus Bevacizumab) in Metastatic Colorectal Cancer
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Colorectal Adenocarcinoma; Stage III Colorectal Cancer AJCC v8; Stage IV Colorectal Cancer AJCC v8; Unresectable Colorectal Adenocarcinoma |
| Interventions | ; ; |
This phase I trial studies the side effects and best dose of CA-4948 when given together with fluorouracil, leucovorin, oxaliplatin (FOLFOX) plus bevacizumab in treating patients with colorectal cancer that has spread from where it first started (primary site) to other places in the body (metastatic). CA-4948 may stop the growth of tumor cells by blocking some of the enzymes needed for cell gro…
NCT07017673 — Phase II Trial of Ivonescimab in Combination With Carboplatin + Docetaxel in Patients With Early-Stage Triple Negative Breast Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Cedars-Sinai Medical Center |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | TNBC; TNBC - Triple-Negative Breast Cancer; Early Stage Triple-Negative Breast Carcinoma |
| Interventions | ; ; |
This is a single arm phase II trial combination of ivonescimab and carbo-docetaxel every 3 weeks for 6 cycles in patients with early-stage triple negative breast cancer. The trial is designed to test the safety and efficacy of adding ivonescimab in patients with early TNBC undergoing neoadjuvant chemotherapy with carboplatin and docetaxel. Patients will receive ivonescimab 20 mg/kg IV on Day 1 …
NCT07226999 — Symbiotic-Lung-04: A Study to Learn About the Study Medicine Called PF-08634404 in Combination With Chemotherapy in Adult Participants With Extensive-Stage Small Cell Lung Cancer
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Pfizer |
| Enrollment | 550 |
| Study Type | INTERVENTIONAL |
| Conditions | Small Cell Lung Cancer (SCLC) |
| Interventions | ; ; |
This study is being done to learn more about a new medicine called PF-08634404 and how well it works when given with chemotherapy to adults with extensive-stage small cell lung cancer (ES-SCLC), a fast-growing type of lung cancer that has spread widely in the body.
To join the study, participants must meet the following conditions:
- Be 18 years or older.
- Have extensive-stage small cell lun…
NCT07198074 — Testing the Addition of an Antiangiogenic Drug (Bevacizumab) to Chemotherapy (Carboplatin and Paclitaxel) Combined With Immunotherapy (Pembrolizumab) for pMMR, TP53 Mutated Endometrial Cancer
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 255 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Endometrial Carcinoma; Recurrent Endometrial Carcinoma |
| Interventions | ; ; |
This phase III trial compares the effect of bevacizumab in combination with carboplatin, paclitaxel and pembrolizumab to the usual treatments of carboplatin and paclitaxel with or without pembrolizumab in treating patients with stage III, IVA or IVB mismatch repair protein proficient (pMMR) and TP53 mutated endometrial cancer that may have spread from where it first started to nearby tissue, ly…
NCT07195734 — Testing the Addition of Chemotherapy or Chemo-Immunotherapy to the Usual Surgery for Advanced Head and Neck Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Locally Recurrent Head and Neck Squamous Cell Carcinoma; Locally Recurrent Hypopharyngeal Squamous Cell Carcinoma; Locally Recurrent Laryngeal Squamous Cell Carcinoma |
| Interventions | ; ; |
This phase II trial tests the addition of chemotherapy, with carboplatin and paclitaxel, or chemo-immunotherapy, with carboplatin, paclitaxel and cemiplimab to standard salvage surgery followed by post operative radiation therapy and cisplatin for high risk patients, for the treatment of patients with PD-L1 positive head and neck squamous cell carcinoma that has come back and spread to nearby t…
NCT07242547 — Study of Tarlatamab as Maintenance Treatment After Chemo-radiotherapy for Limited Stage SCLC Patients
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Fundación GECP |
| Enrollment | 37 |
| Study Type | INTERVENTIONAL |
| Conditions | Limited-stage Small-cell Lung Cancer; Carcinoma, Small Cell Lung; Respiratory Tract Neoplasms; Thoracic Neoplasms |
| Interventions |
This is an open-label, phase II, exploratory and multi-centre clinical trial. 37 Limited stage SCLC patients not eligible for concurrent chemo-radiotherapy will be enroll.
Patients will be enrolled in the trial after receiving sequential chemo-radiotherapy, if there is no progression disease, patients will be treated with maintenance Tarlatamab.
Patients will receive maintenance with Tarlatam…
NCT07621718 — Study of Zoldonrasib + Chemo of Investigator’s Choice vs Placebo + Chemo of Investigator’s Choice as First-line Treatment in Metastatic KRAS G12D-mutated Pancreatic Adenocarcinoma ( RASolute 305 )
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Revolution Medicines, Inc. |
| Enrollment | 670 |
| Study Type | INTERVENTIONAL |
| Conditions | Pancreatic Cancer; Pancreatic Cancer Metastatic; PDAC; PDAC - Pancreatic Ductal Adenocarcinoma; Pancreatic Ductal Adenocarcinoma (PDAC) |
| Interventions | ; ; |
The purpose of this study is to evaluate the efficacy of an investigational RAS(ON) inhibitor administered in combination with chemotherapy compared to placebo in combination with chemotherapy.
NCT07665515 — Study of CryptiVax-1001 in Maintenance Setting for Advanced Serous Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Epitopea Ltd |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Ovarian Cancer; HGSOC; HGS Ovarian, Fallopian Tube or Primary Peritoneal Cancer |
| Interventions |
Ovarian, fallopian tube, or primary peritoneal cancer, collectively referred to as ovarian cancer, remains the deadliest type of gynaecological cancer. The most common and aggressive form is called high-grade serous ovarian cancer.
The main purpose of this study is to understand whether an experimental study vaccine, CryptiVax-1001, is safe when administered to patients with high-grade serous …
NCT07689851 — Chemoradiotherapy and SHR-1701 in Patients With Unresectable Gastric Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Cancer Institute and Hospital, Chinese Academy of Medical Sciences |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Gastric Cancer (GC); Gastroesophageal Junction Adenocarcinoma |
| Interventions | ; ; |
Gastric Cancer is one of the leading causes of cancer-related death worldwide, and patients with unresectable locally advanced or metastatic disease have a poor prognosis. This study aims to evaluate the safety and efficacy of radiotherapy combined with CAPOX and SHR-1701, a PD-L1/TGF-β bispecific antibody, in patients with unresectable locally advanced or metastatic gastric or gastroesophageal…
NCT06694454 — Neoadjuvant Inhaled Azacytidine With Platinum-Based Chemotherapy and Durvalumab (MEDI4736) - a Combined Epigenetic-Immunotherapy (AZA-AEGEAN) Regimen for Operable Early-Stage Non-Small Cell Lung Cancer (NSCLC)
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-small Cell Lung Cancer (NSCLC); Carcinoma, Non-Small Cell Lung; Non-Small Cell Lung Carcinoma; Non Small Cell Lung Cancer; Non Small Cell Lung Carcinoma |
| Interventions | ; ; |
Background:
Lung cancer is the leading cause of cancer-related death worldwide. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. Surgery to remove the tumors is the standard treatment for people diagnosed with early stages of NSCLC. Despite complete removal of these tumors, many recur (happen again). An FDA-approved drug combination to treat early-stage NSCLC prior to…
Active, Not Recruiting
NCT01081262 — Carboplatin and Paclitaxel or Oxaliplatin and Capecitabine With or Without Bevacizumab as First-Line Therapy in Treating Patients With Newly Diagnosed Stage II-IV or Recurrent Stage I Epithelial Ovarian or Fallopian Tube Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Borderline Ovarian Mucinous Tumor; Ovarian Mucinous Cystadenocarcinoma; Recurrent Fallopian Tube Carcinoma; Recurrent Ovarian Carcinoma; Stage IA Fallopian Tube Cancer AJCC v6 and v7 |
| Interventions | ; ; |
This randomized phase III trial studies carboplatin given together with paclitaxel with or without bevacizumab to see how well it works compared with oxaliplatin given together with capecitabine with or without bevacizumab as first-line therapy in treating patients with newly diagnosed stage II-IV, or recurrent (has come back) stage I epithelial ovarian or fallopian tube cancer. Drugs used in c…
NCT02445391 — Platinum in Treating Patients With Residual Triple-Negative Breast Cancer Following Neoadjuvant Chemotherapy
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | ECOG-ACRIN Cancer Research Group |
| Enrollment | 415 |
| Study Type | INTERVENTIONAL |
| Conditions | Estrogen Receptor Negative; HER2/Neu Negative; Invasive Breast Carcinoma; Progesterone Receptor Negative; Stage II Breast Cancer |
| Interventions | ; ; |
This randomized phase III trial studies how well cisplatin or carboplatin (platinum based chemotherapy) works compared to capecitabine in treating patients with remaining (residual) basal-like triple-negative breast cancer following chemotherapy after surgery (neoadjuvant). Drugs used in chemotherapy, such as cisplatin, carboplatin and capecitabine, work in different ways to stop the growth of …
NCT02997228 — Testing the Addition of Atezolizumab to Combination Chemotherapy or Atezolizumab Alone for Metastatic Colon or Rectal Cancer, the COMMIT Study
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Colorectal Adenocarcinoma; Stage IV Colorectal Cancer AJCC v7 |
| Interventions | ; ; |
This phase III trial studies how well combination chemotherapy, bevacizumab, and/or atezolizumab work in treating patients with deficient deoxyribonucleic acid (DNA) mismatch repair colorectal cancer that has spread from where it first started (primary site) to other places in the body (metastatic). Chemotherapy drugs, such as fluorouracil, oxaliplatin, and leucovorin calcium, work in different…
NCT03269669 — Obinutuzumab With or Without Umbralisib, Lenalidomide, or Combination Chemotherapy in Treating Patients With Relapsed or Refractory Grade I-IIIa Follicular Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 73 |
| Study Type | INTERVENTIONAL |
| Conditions | Grade 1 Follicular Lymphoma; Grade 2 Follicular Lymphoma; Grade 3a Follicular Lymphoma; Recurrent Follicular Lymphoma; Refractory Follicular Lymphoma |
| Interventions | ; ; |
This phase II trial studies how well obinutuzumab with or without umbralisib, lenalidomide, or combination chemotherapy work in treating patients with grade I-IIIa follicular lymphoma that has come back (relapsed) or does not respond to treatment (refractory). Immunotherapy with obinutuzumab, may induce changes in body’s immune system and may interfere with the ability of tumor cells to grow an…
NCT03914625 — A Study to Investigate Blinatumomab in Combination With Chemotherapy in Patients With Newly Diagnosed B-Lymphoblastic Leukemia
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6720 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia; B Lymphoblastic Lymphoma; Down Syndrome |
| Interventions | ; ; |
This phase III trial studies how well blinatumomab works in combination with chemotherapy in treating patients with newly diagnosed, standard risk B-lymphoblastic leukemia or B-lymphoblastic lymphoma with or without Down syndrome. Monoclonal antibodies, such as blinatumomab, may induce changes in the body’s immune system and may interfere with the ability of cancer cells to grow and spread. Che…
NCT03984448 — Testing the Addition of a New Anti-cancer Drug, Venetoclax, to Usual Chemotherapy for High Grade B-cell Lymphomas
| Status | Active, not recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 363 |
| Study Type | INTERVENTIONAL |
| Conditions | Diffuse Large B-Cell Lymphoma; Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; Double-Expressor Lymphoma; EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified; High Grade B-Cell Lymphoma With MYC and BCL2 or BCL6 Rearrangements |
| Interventions | ; ; |
This phase II/III trial tests whether it is possible to decrease the chance of high-grade B-cell lymphomas returning or getting worse by adding a new drug, venetoclax to the usual combination of drugs used for treatment. Venetoclax may stop the growth of cancer cells by blocking a protein called Bcl-2. Drugs used in usual chemotherapy, such as rituximab, cyclophosphamide, doxorubicin, vincristi…
NCT04530565 — Testing the Use of Steroids and Tyrosine Kinase Inhibitors With Blinatumomab or Chemotherapy for Newly Diagnosed BCR-ABL-Positive Acute Lymphoblastic Leukemia in Adults
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 348 |
| Study Type | INTERVENTIONAL |
| Conditions | B Acute Lymphoblastic Leukemia With t(9;22)(q34.1;q11.2); BCR-ABL1 |
| Interventions | ; ; |
This phase III trial compares the effect of usual treatment of chemotherapy and steroids and a tyrosine kinase inhibitor (TKI) to the same treatment plus blinatumomab. Blinatumomab is a Bi-specific T-Cell Engager (‘BiTE’) that may interfere with the ability of cancer cells to grow and spread. The information gained from this study may help researchers determine if combination therapy with stero…
NCT04799275 — Testing CC-486 (Oral Azacitidine) Plus the Standard Drug Therapy in Patients 75 Years or Older With Newly Diagnosed Diffuse Large B Cell Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 422 |
| Study Type | INTERVENTIONAL |
| Conditions | Ann Arbor Stage III Diffuse Large B-Cell Lymphoma; Ann Arbor Stage IIX (Bulky) Diffuse Large B-Cell Lymphoma; Ann Arbor Stage IV Diffuse Large B-Cell Lymphoma; Diffuse Large B-Cell Lymphoma Activated B-Cell Type; Diffuse Large B-Cell Lymphoma Associated With Chronic Inflammation |
| Interventions | ; ; |
This phase II/III trial compares the side effects and activity of oral azacitidine in combination with the standard drug therapy (reduced dose rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone [R-miniCHOP]) versus R-miniCHOP alone in treating patients 75 years or older with newly diagnosed diffuse large B cell lymphoma. R-miniCHOP includes a monoclonal antibody (a type of p…
NCT05003037 — Surufatinib Combined With Toripalimab and Chemotherapy in the Treatment of Non-Small Cell Lung Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Li Zhang, MD |
| Enrollment | 106 |
| Study Type | INTERVENTIONAL |
| Conditions | Non Small Cell Lung Cancer |
| Interventions |
A phase II study to assess the efficacy and safety of Surufatinib Combined With Toripalimab and Chemotherapy in patients with advanced non-squamous non-small cell lung cancer.
NCT05357469 — Innovative Treatment of Chemotherapy-Induced Painful Peripheral Neuropathy in Adolescents and Young Adults With Cancer: A Two Arm Pilot Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Peripheral Neuropathy |
| Interventions | ; |
To evaluate the efficacy and safety of Scrambler therapy (ST) for chemotherapy-induced painful peripheral neuropathy (CIPN), and the impact of ST on physical functioning and quality of life (QoL) in adolescents and young adults (AYA) cancer patients.
In this proposed study, we will conduct a two-arm prospective, randomized wait-list controlled clinical trial to investigate the effectiveness of…
NCT05211323 — A Study to Determine Whether Chemotherapy and Atezolizumab is Better Than Chemotherapy, Bevacizumab and Atezolizumab in Patients With Advanced Liver Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Combined Hepatocellular Carcinoma and Cholangiocarcinoma; Stage III Liver Cancer; Stage IV Liver Cancer |
| Interventions | ; ; |
This phase II trial compares the effect of adding bevacizumab and atezolizumab to gemcitabine and cisplatin (chemotherapy) versus chemotherapy and atezolizumab in treating patients with liver cancer that cannot be removed by surgery (unresectable) or that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monocl…
NCT05063552 — Testing the Use of Investigational Drugs Atezolizumab and/or Bevacizumab With or Without Standard Chemotherapy in the Second-Line Treatment of Advanced-Stage Head and Neck Cancers
| Status | Active, not recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 430 |
| Study Type | INTERVENTIONAL |
| Conditions | Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Metastatic Head and Neck Squamous Cell Carcinoma; Metastatic Hypopharyngeal Squamous Cell Carcinoma; Metastatic Laryngeal Squamous Cell Carcinoma; Metastatic Lip and Oral Cavity Carcinoma |
| Interventions | ; ; |
This phase II/III compares the standard therapy (chemotherapy plus cetuximab) versus adding bevacizumab to standard chemotherapy, versus combination of just bevacizumab and atezolizumab in treating patients with head and neck cancer that has spread to other places in the body (metastatic or advanced stage) or has come back after prior treatment (recurrent). Immunotherapy with monoclonal antibod…
NCT05813626 — Neoadjuvant Chemotherapy Plus Toripalimab in Patients With Locoregionally Advanced Nasopharyngeal Carcinoma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Zhejiang Cancer Hospital |
| Enrollment | 89 |
| Study Type | INTERVENTIONAL |
| Conditions | Nasopharyngeal Carcinoma |
| Interventions | ; ; |
Neoadjuvant chemotherapy plus toripalimab in patients with locoregionally advanced nasopharyngeal carcinoma
NCT06711900 — A Study of SKB264 in Combination With Pembrolizumab Versus Chemotherapy in Combination With Pembrolizumab as First-Line Treatment for PD-L1 Negative Patients With Locally Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. |
| Enrollment | 432 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-Small Cell Lung Cancer |
| Interventions | ; ; |
The study aims to evaluate the efficacy and safety of SKB264 in combination with pembrolizumab versus chemotherapy in combination with pembrolizumab in the first-line treatment of patients with locally advanced or metastatic non-squamous NSCLC with PD-L1 negative.
NCT06939595 — A Study to Compare Effects and Safety of CT-P51 and Keytruda in Patients With Previously Untreated Metastatic Lung Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Celltrion |
| Enrollment | 225 |
| Study Type | INTERVENTIONAL |
| Conditions | Non Squamous Non Small Cell Lung Cancer |
| Interventions | ; |
The goal of this Phase 3 clinical trial is to compare efficacy and safety of CT-P51 and European Union (EU) approved Keytruda in combination with platinum pemetrexed chemotherapy in patients with previously untreated metastatic nsNSCLC.
Not Yet Recruiting
NCT07667400 — Docetaxel and SX-682 in Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma, Salivary Gland Carcinoma, and Advanced Prostate Cancer
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Head and Neck Cancer; Head and Neck Squamous Cell Carcinoma; Paranasal Sinus Neoplasms; Nasopharyngeal Carcinoma; Oropharyngeal Squamous Cell Carcinoma |
| Interventions | ; |
Background:
Head and neck cancers (HNCs) account for about 5% of all cancers worldwide. They grow in the mouth, throat, nasal cavity, or salivary glands. Prostate cancer is the most common cancer in men in the United States. Survival rates for these cancers are lower than 50% if they spread to other parts of the body or return after treatment. Better treatments are needed.
Objective:
To test…
NCT07444710 — Testing the Addition of an Anti-Cancer Drug, Glofitamab, to the Usual Chemotherapy Treatment (Alternating R-CHOP/R-DHAP) for Previously Untreated Mantle Cell Lymphoma
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Ann Arbor Stage II Mantle Cell Lymphoma; Ann Arbor Stage III Mantle Cell Lymphoma; Ann Arbor Stage IV Mantle Cell Lymphoma |
| Interventions | ; ; |
This phase I trial tests the safety, side effects and best dose of glofitamab given with alternating cycles of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP)/ rituximab, dexamethasone, cytarabine, and cisplatin (R-DHAP) for the treatment of mantle cell lymphoma. Glofitamab is a monoclonal antibody that may interfere with the ability of cancer cells to grow and sp…
NCT07689539 — Trial of DN022150 Versus Chemotherapy in Previously Treated Advanced Pancreatic Cancer With KRAS G12D Mutation
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Jiangxi Kvvit Pharmaceutical Co., Ltd. |
| Enrollment | 360 |
| Study Type | INTERVENTIONAL |
| Conditions | Pancreatic Cancer |
| Interventions | ; |
This study plans to enroll participants with previously treated advanced pancreatic cancer and harbor centrally confirmed KRAS G12D mutation. Eligible participants will be randomized 1:1 to DN022150 Monotherapy or Investigator’s Choice Chemotherapy
NCT07504588 — Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 87 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Primary Peritoneal Endometrioid Adenocarcinoma |
| Interventions | ; ; |
This phase II trial compares the effect of sacituzumab govitecan and bevacizumab to standard care (carboplatin, pegylated liposomal doxorubicin, and bevacizumab) in patients with ovarian cancer that has come back after an initial response to platinum therapy (platinum-sensitive), that has progressed after poly (adenosine diphosphate-ribose) polymerase (PARP) inhibitor maintenance therapy (recur…
NCT07572123 — Evaluating the Addition of Maintenance Immunotherapy Compared to the Usual Treatment of Chemotherapy and Autologous Stem Cell Transplant Alone for High-risk Patients With Relapsed or Refractory Hodgkin Lymphoma
| Status | Not yet recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 374 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Classic Hodgkin Lymphoma; Refractory Classic Hodgkin Lymphoma |
| Interventions | ; ; |
This phase II trial compares the impact of brentuximab vedotin and nivolumab after radiation to standard of care high dose chemotherapy (HDT)-autologous stem cell transplant (ASCT) in standard-risk patients with classic Hodgkin lymphoma that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory). In addition, the phase III trial will …
Enrolling by Invitation
NCT07149428 — Longitudinal Deep Phenotyping of Central Mechanisms in Dysosmia: A Pilot Study Using Electrobulbogram (EBG), Functional MRI (fMRI), and Diffusion-Weighted Imaging (DWI)
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Institute on Deafness and Other Communication Disorders (NIDCD) |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Respiratory Tract Infection; Smell Disorder; Influenza; Rhinosinusitis; COVID-19 |
Background:
Loss of the sense of smell can seriously affect a person’s quality of life. The ability to smell can be damaged by many factors, including illnesses, injuries, and exposure to toxic chemicals. The effects can vary, including complete loss of smell, partial loss, and parosomia, which is when things smell differently than they should.
Objective:
To study how brain function changes …
Completed Trials
NCT03879109 — Chemotherapy Followed by Pelvic Reirradiation Versus Chemotherapy Alone as Pre-operative Treatment for Locally Recurrent Rectal Cancer
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Rectal Cancer |
| Interventions | ; ; |
GRECCAR 15 is focused on Locally Recurrent Rectal Cancer (LRRC) for patients with previous pelvic radiotherapy for the primary rectal cancer. This situation leads to a 20% higher risk of non-curative resection for the LRRC management (R1 status) impacting significantly the overall survival. The widespread use of neoadjuvant radiotherapy for primary rectal cancer introduces this new problem: the…
NCT04905316 — A Study of Canakinumab With Chemotherapy, Radiation Therapy, and Durvalumab in People With Lung Cancer
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 41 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-small Cell Lung Cancer |
| Interventions | ; ; |
The researchers are doing this study to find out whether canakinumab in combination with chemoradiation and durvalumab is an effective and safe treatment for people with locally advanced non-small cell lung cancer (NSCLC).
NCT06636591 — Pilot Study of Neoadjuvant Chemotherapy Combined With Immunotherapy and Multimodal Thermal Therapy for HER2-negative Breast Cancer
| Status | Completed |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 14 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer Female; HER2-negative Breast Cancer |
| Interventions | ; |
In this study, breast cancer (BC) patients eligible for inclusion will be divided into two groups according to molecular typing and subtyping, which combined immunotherapy and multimodal thermal therapy with conventional neoadjuvant chemotherapy, to explore methods of immune induction for BC, enhance the efficacy of immunotherapy, and accumulate data for subsequent stages of clinical study.
Other (Terminated)
NCT04527900 — The UPPROACH (Upfront Intensity Modulated Proton Beam Therapy) Approach
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | University of Maryland, Baltimore |
| Enrollment | 2 |
| Study Type | INTERVENTIONAL |
| Conditions | Endometrial Cancer |
| Interventions | ; |
A phase 2 study with the primary objective of testing treatment compliance of Upfront Intensity Modulated Proton Beam Therapy (IMPT) and Concurrent Chemotherapy (UPPROACH) for Post-operative Treatment in Loco-regionally Advanced Endometrial Cancer is non-inferior to the historic compliance rate of the chemoradiation arm of GOG 258 study