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 from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 20
- Active, not recruiting: 10
- Completed: 7
- Other: 13
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT01087333 — Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1263 |
| Study Type | OBSERVATIONAL |
| Conditions | Hairy Cell Leukemia (HCL); Chronic Lymphocytic Leukemia (CLL); Non-Hodgkins Lymphoma (NHL); Cutaneous T Cell Lymphoma (CTCL); Adult T Cell Lymphoma (ATL) |
Background:
- Researchers who are studying hairy cell leukemia, and how the disease compares with other disorders, are interested in obtaining additional samples from leukemia patients and healthy volunteers. The investigators are particularly interested in samples from individuals who have diseases that can be treated with a new type of drug called immunotoxin, in which an antibody carrying …
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…
NCT02146170 — Tissue Procurement and Natural History Study of People With Non-Small Cell Lung Cancer, Small Cell Lung Cancer, Extrapulmonary Small Cell Cancer, Pulmonary Neuroendocrine Tumors, and Thymic Epithelial Tumors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Non-Small Cell Lung Cancer; Small Cell Lung Cancer; Extrapulmonary Small Cell Cancer; Pulmonary Neuroendocrine Tumors; Thymic Epithelial Tumors |
Background:
- Lung cancer is the leading cause of cancer-related death worldwide. It causes more than one million deaths every year. Researchers want to gather tissue samples from people with lung and thymic cancers to understand the disease better. This may lead to new ways to diagnose and treat it.
Objective:
- To collect tissue samples for use in the study of lung cancers.
Eligibility:…
NCT03366116 — 5-aza-4’-Thio-2’-Deoxycytidine (Aza-TdC) in People With Advanced Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 65 |
| Study Type | INTERVENTIONAL |
| Conditions | Neoplasms; Solid Tumors |
| Interventions |
Background:
Blood, tissue, and tumor cells contain genes. Genes are made up of DNA. DNA is the “instruction book” for each cell. In some people with cancer, the genes that might have slowed the growth of their tumor were “turned off.” Researchers want to see if a new drug can turn the genes back on and slow the tumor growth. The drug is called Aza-TdC.
Objective:
To test the safety of Aza-Td…
NCT04609072 — Connect for Cancer Prevention Study (Connect)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 200000 |
| Study Type | OBSERVATIONAL |
| Conditions | Cancer; General Research Use |
Background:
The National Cancer Institute, part of the National Institutes of Health, has partnered with nine health care systems across the U.S. to establish the Connect for Cancer Prevention Study. While researchers have made important discoveries, there is more to learn to lower the number of people affected by cancer. By taking part in Connect, participants can help researchers learn how t…
NCT05137054 — A Study to Examine the Effects of Novel Therapy Linvoseltamab in Combination With Other Cancer Treatments for Adult Participants With Multiple Myeloma That is Resistant to Current Standard of Care Treatments
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 317 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma |
| Interventions | ; ; |
This study is researching an experimental drug called linvoseltamab in combination with other drugs for the treatment of a blood cancer called multiple myeloma. Linvoseltamab has previously been studied as a single agent (without other cancer treatments) in participants with multiple myeloma that returned after prior therapies and needed to be treated again.
In the initial study, some particip…
NCT05564390 — MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute Myeloid Leukemia; Acute Myeloid Leukemia Arising From Previous Myelodysplastic/Myeloproliferative Neoplasm; Acute Myeloid Leukemia Post Cytotoxic Therapy; Acute Myeloid Leukemia, Myelodysplasia-Related; Myelodysplastic Syndrome |
| Interventions | ; ; |
This MyeloMATCH Master Screening and Reassessment Protocol (MSRP) evaluates the use of a screening tool and specific laboratory tests to help improve participants’ ability to register to clinical trials throughout the course of their myeloid cancer (acute myeloid leukemia or myelodysplastic syndrome) treatment. This study involves testing patients’ bone marrow and blood for certain biomarkers. …
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
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…
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…
NCT06982521 — Phase 3 Study of RLY-2608 + Fulvestrant vs Capivasertib + Fulvestrant as Treatment for Locally Advanced or Metastatic PIK3CA-mutant HR+/HER2- Breast Cancer
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Relay Therapeutics, Inc. |
| Enrollment | 540 |
| Study Type | INTERVENTIONAL |
| Conditions | PIK3CA Mutation; HER2- Negative Breast Cancer; Hormone Receptor Positive Tumor; Breast Cancer; Metastatic Breast Cancer |
| Interventions | ; ; |
This is a global, multicenter, open-label, randomized Phase 3 study comparing the efficacy and safety of RLY-2608 + fulvestrant to capivasertib + fulvestrant for the treatment of patients with HR+/HER2- ABC with PIK3CA mutation following recurrence or progression on or after treatment with a CDK4/6 inhibitor.
NCT07086105 — A Study to Evaluate Adze1.C in Participants With Metastatic Melanoma
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Adze Biotechnology Australia Pty Ltd |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Melanoma |
| Interventions |
This is Phase I, open label, multi-center clinical trial evaluating an investigational treatment, Adze1.C. Adze1.C is a type of oncolytic virus therapy for adults with advanced Melanoma that have not responded to standard treatments. Oncolytic viruses are designed to infect and destroy cancer cells and have the potential to stimulate the immune system to fight tumors. The purpose of this study …
NCT07264790 — Assessment of Topical Minoxidil on Intraoperative Flap Perfusion and Cutaneous Flap Viability in Breast Recon
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Duke University |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Reconstruction; Perfusion; Complications; High Risk for Breast Cancer; Genetic Predisposition |
| Interventions | ; |
The purpose of the study is to determine whether pharmacologic delay using minoxidil in patients undergoing bilateral risk reducing mastectomy with reconstruction could achieve improvement in flap perfusion and flap viability at the time of surgery. Patients will undergo randomization of their breasts to determine which breast will receive the experimental intervention and which breast will ser…
NCT07690579 — Social, Structural, and Lifestyle Drivers of Prostate Cancer Disparities
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, San Francisco |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Prostate Cancer; Prostate Cancer Recurrent; Prostate Metastases |
| Interventions | ; |
Prostate Cancer (PC) is the most common non-cutaneous malignancy diagnosed and second leading cause of cancer death among men across the United States. PC among Black men accounts for a higher proportion alike of cancer diagnoses and deaths. In the prostate specific antigen (PSA)-based screening era, mortality rates improved at a similar velocity among Black and White men, but the 2- to 3-fold …
NCT07459309 — Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer (Primary and Metastatic); Liver Ablation |
| Interventions |
Clinical Study on the Safety, Efficacy, and Exploration of Immune Mechanisms of a Combined Multimodal Tumor Therapy System for Hepatic Malignancies
NCT07235098 — Effect of a Music Intervention in Reducing Distress and Pain in Patients With Lung Cancer Undergoing Mini-invasive Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Oncology Institute of Southern Switzerland |
| Enrollment | 74 |
| Study Type | INTERVENTIONAL |
| Conditions | Lung Cancer (Suspected or Confirmed) |
| Interventions |
This study aims at evaluating whether music therapy intervention is effective in decreasing psychological (distress) and physical symptoms (pain) in patients with suspected or diagnosed lung cancer undergoing minimally invasive lung surgery.
NCT07545837 — Health and Wellness Coaching to Improve Adherence to Healthy Habits and Treatment Plans in Papillary and Follicular Thyroid Cancer Survivors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Thyroid Gland Follicular Carcinoma; Thyroid Gland Papillary Carcinoma |
| Interventions | ; ; |
This clinical trial evaluates the impact of a patient-centered health and wellness coaching (HWC) intervention on adherence to treatment plans and healthy lifestyle practices in patients with papillary or follicular thyroid cancer. Treatment for thyroid cancer often involves surgery, radioactive iodine and/or lifelong levothyroxine with regular monitoring of thyroid stimulating hormone levels. …
NCT07620951 — Material Balance of [14C]Zorifertinib in Healthy Adult Male Participants in China
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Alpha Biopharma (Jiangsu) Co., Ltd. |
| Enrollment | 8 |
| Study Type | INTERVENTIONAL |
| Conditions | EGFR Mutant Advanced Non-small Cell Lung Cancer; Central Nervous System (CNS) Metastases |
| Interventions |
This is a single-center, single-dose, open-label, Phase I study to evaluate the mass balance, biotransformation, pharmacokinetic characteristics, excretion pathways, and safety of a single oral 200 mg/5 µCi dose of [14C]Zorifertinib in healthy Chinese adult male participants. The study includes a screening period (Day -14 to Day -1) and a dosing and observation period (Day 1 to Day 14). Blood…
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…
NCT07416188 — Novel Indenoisoquinolone CMYC/TOPOISOMERASE 1 Inhibitor (LMP744) in Recurrent Glioblastoma
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Glioblastoma; Glioblastoma IDH (Isocitrate Dehydrogenase) Wildtype; Relapsed Cancer; Recurrent Tumor; Glioblastoma Multiforme |
| Interventions | ; |
Background:
Glioblastoma is a common brain cancer in adults. Treatment includes surgery, radiation, and chemotherapy. But this cancer can return after treatment and is often fatal. Researchers want to know if a study drug (LMP744) can kill glioblastoma tumor cells.
Objective:
To test LMP744 in people with glioblastoma.
Eligibility:
People aged 18 years or older with glioblastoma that retur…
Active, Not Recruiting
NCT00339495 — Prostate Lung Colorectal and Ovarian (PLCO) Cancer Screening Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 154900 |
| Study Type | OBSERVATIONAL |
| Conditions | Cancer; Death |
The Division of Cancer Preventionl (DCP, formerly DCPC), under extramural contracts to 10 U.S. clinical centers, is evaluating the effectiveness of screening for prostate, lung, colorectal and ovarian cancer (The PLCO Trial). In 1996 the NCI Executive Committee approved the expansion of the PLCO Trial to collect additional materials and to conduct additional studies. About, 74,000 men and 74,00…
NCT01582204 — Evaluate The Utility Of 124I-cG250 for The Early Detection Of Response to Therapy In Patients With Metastatic Renal Cell Carcinoma
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 17 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Cancer |
| Interventions |
Usually, doctors monitor kidney cancer with CT scans to measure the size of tumors. Sometimes, even when a drug is working, it can take several months before the effects are seen on a regular CT scan. The purpose of this study is to see if a new kind of scan, called 124I-cG250 PET/CT, can determine response to sunitinib or pazopanib earlier than a regular CT scan.
Research has shown that certa…
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…
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…
NCT04567420 — DNA-guided Second Line Adjuvant Therapy for High Residual Risk, Estrogen Receptor Positive, HER-2 Negative Breast Cancer (DARE)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Criterium, Inc. |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer |
| Interventions | ; ; |
A randomized, Phase II trial of circulating tumor DNA-guided second line Adjuvant therapy for high Residual risk, Estrogen Receptor positive, HER-2 negative breast cancer (DARE)
NCT05038735 — Study to Assess the Efficacy and Safety of Alpelisib Plus Fulvestrant in Participants With HR-positive (HR+), HER2-negative, Advanced Breast Cancer After Treatment With a CDK4/6 Inhibitor and an Aromatase Inhibitor.
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 210 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer |
| Interventions | ; ; |
The purpose of this study is to complement Study CBYL719C2301 (SOLAR-1) and obtain more comprehensive data on the efficacy and safety of alpelisib (BYL719) in combination with fulvestrant compared with placebo plus fulvestrant in men or postmenopausal women with HR-positive, HER2-negative advanced breast cancer with a PIK3CA mutation who progressed or relapsed on or after treatment with an AI p…
NCT05409066 — Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Follicular Lymphoma
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Genmab |
| Enrollment | 549 |
| Study Type | INTERVENTIONAL |
| Conditions | Follicular Lymphoma (FL) |
| Interventions | ; ; |
Follicular Lymphoma (FL) is the second most common B-cell cancer and the most common type of cancer of lymphocytes. Unfortunately, this disease is incurable with conventional treatment and the disease recurs in almost all patients. This study will assess how safe and effective epcoritamab is in combination with lenalidomide and rituximab (R2) in treating adult participants with relapsed or refr…
NCT06909357 — Creation of an Infrastructure to Support Delivery of mHealth Interventions for Cancer Patients
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | H. Lee Moffitt Cancer Center and Research Institute |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Smoking Cessation |
| Interventions | ; |
Despite the deleterious impact of smoking upon cancer treatment outcomes, smoking prevalence remains alarmingly high among cancer patients. Thus, reducing smoking by cancer patients is a public health priority, but treatments to date have demonstrated limited efficacy. Mobile health (mHealth) interventions have the potential to improve treatment efficacy while also greatly extending reach. The …
NCT06933251 — PCSK9 Inhibitor and PD-1 Inhibitor Combined With Neoadjuvant Chemoradiotherapy for pMMR/MSS Locally Advanced Rectal Cancer
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Guangdong Provincial People’s Hospital |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Rectal Cancer (LARC) |
| Interventions |
This is a single-center, open-label, single-arm clinical study aimed at conducting a preliminary evaluation of the efficacy and safety of combining PCSK9 inhibitors and PD-1 inhibitors (dual inhibitors) with neoadjuvant chemoradiotherapy in patients with pMMR/MSS locally advanced rectal cancer.
NCT06676033 — Epcoritamab in Chronic Lymphocytic Leukemia and Richter Syndrome
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Leukemia, Chronic Lymphocytic; Richter Syndrome |
| Interventions |
This correlative study aims to understand the pharmacodynamic effects and clonal dynamics in response to epcoritamab by obtaining and analyzing lymph node, bone marrow, and blood samples from subjects enrolled in GCT3013-03 trial sponsored by Genmab at NIH. Samples will be collected before and at multiple time points during treatment with epcoritamab. National Heart, Lung, and Blood Institute (…
Not Yet Recruiting
NCT07691255 — MELanoma Brain Metastasis Treated With CYberknife
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | European Institute of Oncology |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Melanoma (Skin Cancer) |
Melanoma is a type of cancer that can spread to the brain, making the disease harder to treat and worsening both survival and quality of life.
In recent years, treatments have improved significantly thanks to advances in surgery, radiotherapy, immunotherapy, and targeted therapy. These new treatments have greatly increased survival rates for patients with metastatic melanoma.
This study focus…
NCT07685548 — AI-Driven Tumor Response Evaluation for Solid Tumors
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Shanghai Zhongshan Hospital |
| Enrollment | 6120 |
| Study Type | OBSERVATIONAL |
| Conditions | Solid Tumor Cancer; Neoplasms; Hepatocellular Carcinoma |
| Interventions |
Purpose: This study is developing and validating an artificial intelligence (AI)-driven system to evaluate tumor response using changes in total tumor volume. The goal is to determine whether this AI-based approach can better predict patient survival compared with the current standard method (RECIST), which relies on linear measurements of a few selected tumors.
Participants: The study include…
NCT07691281 — Disparities in Mental Health Screening and Support
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | European Institute of Oncology |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Mental Health; Cancer |
To develop and administer online surveys to cancer patients and their families across diverse regions within the EU to detect possible disparities in their access to mental health screening and psychological-cognitive support
NCT07437963 — Testing the Addition of Iberdomide to Therapy in People With Neuroblastoma That Has Come Back, Not Responded to Treatment, or Gotten Worse
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 76 |
| Study Type | INTERVENTIONAL |
| Conditions | Recurrent Ganglioneuroblastoma; Recurrent Neuroblastoma; Refractory Ganglioneuroblastoma; Refractory Neuroblastoma |
| Interventions | ; ; |
This phase I/II trial studies the side effects and best dose of iberdomide when given together with chemoimmunotherapy drugs and to see how well it works in treating patients with neuroblastoma that has come back after a period of improvement (relapsed), that does not respond to treatment (refractory), or that is growing, spreading, or getting worse (progressive) following prior chemoimmunother…
NCT07690293 — Traditional Chinese Medicine Patch for Cancer-Related Fatigue During Radiotherapy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | China Medical University Hospital |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Cancer-related Fatigue |
| Interventions | ; |
This randomized, double-blind, parallel-group controlled clinical trial aims to evaluate the effects of traditional Chinese medicine patch application at the Shenque (RN8) acupoint on cancer-related fatigue in adult cancer patients scheduled to undergo radiotherapy. Eligible participants will be randomly assigned to receive either a traditional Chinese medicine patch or a sham patch at the same…
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
NCT07691008 — Wearable Data for Personalized Prognostication in Cancer: A Registry Protocol
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | City of Hope Medical Center |
| Enrollment | 1200 |
| Study Type | OBSERVATIONAL |
| Conditions | Hematopoietic Neoplasm; Malignant Solid Neoplasm; Lymphatic System Neoplasm; Hematopoietic and Lymphatic System Neoplasm |
| Interventions |
This study receives physiological and lifestyle-related data from mobile phones to create an institutional database.
Enrolling by Invitation
NCT00923065 — Data Collection, Clinical Care and Interventions in CCR, NCI
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 10000 |
| Study Type | OBSERVATIONAL |
| Conditions | Neoplasms; Cancer |
This study provides cancer care through the National Cancer Institute’s Medical Oncology Branch (MOB) to patients who are not enrolled in an active treatment research protocol. Patients receive standard treatments only; no investigational therapies are provided on this protocol.
Patients 18 years of age and older may be eligible for this protocol. Candidates are patients for whom an NCI invest…
NCT02154022 — Collection of Pharmacokinetic Samples From People With Unanticipated Response, Significant Toxicity or Concern of Future Toxicity
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Cancer; Solid Tumors; Neoplasm |
Background:
- Certain drugs - even when they are meant to help people - cause side effects. These are unwanted effects of the drug. There are many reasons why a drug might cause side effects in one person and not in another. It may be because of how much of the drug is in the person s blood at one time. Researchers want to study the blood of people having drug side effects to better understan…
NCT05369611 — COVID-19 Experiences in the SELF Cohort
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Institute of Environmental Health Sciences (NIEHS) |
| Enrollment | 1668 |
| Study Type | OBSERVATIONAL |
| Conditions | COVID-19 |
Background:
COVID-19 affected African Americans more than Whites. African Americans, especially women, have had higher rates of COVID-19 infections compared to Whites. They are also more likely to go to the hospital or die of this disease. Many researchers who looked into these issues lacked background data on the people they studied. SELF is a 10-year study of fibroids in African American wom…
Completed Trials
NCT00342888 — Case-Control Study of Pesticides and Childhood Leukemia
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 629 |
| Study Type | OBSERVATIONAL |
| Conditions | Leukemia |
Childhood leukemia is the most common type of childhood cancer and its etiology is largely unknown. Most case-control studies of childhood leukemia have reported elevated risks among children whose parents were occupationally exposed to pesticides or who used pesticides in the home or garden. Investigators at the University of California at Berkeley (UCB) conducted a case-control study of child…
NCT01352962 — Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Neoplasms; Neoplasms, Urethral; Cancer of the Urethra; Urethral Cancer |
| Interventions | ; ; |
Background:
- Gemcitabine and carboplatin are chemotherapy drugs used to treat several types of cancer, including cancer of the pancreas, bladder, ovaries, and lung. Lenalidomide, a drug that prevents the growth of new blood vessels in tumors, has been approved for treatment of certain blood cancers, but it has not yet been approved for use in combination with gemcitabine and carboplatin. Res…
NCT01387555 — A Phase 2b Study of Modified Vaccinia Virus to Treat Patients Advanced Liver Cancer Who Failed Sorafenib
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Jennerex Biotherapeutics |
| Enrollment | 129 |
| Study Type | INTERVENTIONAL |
| Conditions | Hepatocellular Carcinoma; Liver Cancer; HCC |
| Interventions | ; |
This study is to determine whether JX-594 (Pexa-Vec) plus best supportive care is more effective in improving survival than best supportive care in patients with advanced Hepatocellular Carcinoma (HCC) who have failed sorafenib.
NCT03251989 — Rare CNS Tumors Outcomes &Risk
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 326 |
| Study Type | OBSERVATIONAL |
| Conditions | High Grade Meningioma; Ependymoma; Medulloblastoma; PNET; Primary CNS Sarcoma |
Background:
Primary tumors of the brain and spine are those that start in the brain or spine. These tumors are rare, accounting for <2% of all cancers diagnosed in the United States. Some of these tumors occur in less than 2,000 people per year. Researchers want to study a large group of people with this kind of tumor. They want to learn more about the tumors, including the risk factors relat…
NCT05142592 — Phase1/2a Study for IPG7236 in Patients With Advanced Solid Tumors
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Nanjing Immunophage Biotech Co., Ltd |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Safety Issues; Tolerability; Pharmacokinetics |
| Interventions |
This is a Phase 1/2a first-in-human, multi-center, non-randomized, open-label study to assess the safety, tolerability, pharmacokinetics profile, and preliminary anti-tumor activity of IPG7236 administered orally as a single agent to patients with advanced solid tumors.
The study will include a dose escalation phase (Phase 1) and a dose expansion phase (Phase 2a).
Each part will consist of a …
NCT05565534 — Diabetes Care for Breast Cancer Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Weill Medical College of Cornell University |
| Enrollment | 74 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer; PreDiabetes; Type 2 Diabetes |
| Interventions |
The goal of this study is to find a new way to make diabetes care better for patients with breast cancer and diabetes who are currently receiving cancer treatment. We will have two groups, the researchers will decide who is in which group. One group will be working with a nurse who is trained in diabetes care while the other does not. This will allow the investigators to see if having a trained…
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 (Withdrawn)
NCT02432378 — Intensive Locoregional Chemoimmunotherapy for Recurrent Ovarian Cancer Plus Intranodal DC Vaccines
| Status | Withdrawn |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Roswell Park Cancer Institute |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Cancer of Ovary; Cancer of the Ovary; Neoplasms, Ovarian; Ovarian Cancer; Ovary Cancer |
| Interventions | ; |
This study will evaluate the immunologic and potential clinical effectiveness of intensive locoregional sequential intraperitoneal (IP) cisplatin (IPC) with intravenous (iv) paclitaxel followed by peritoneal infusion of a chemokine modulatory (CKM) regimen composed of a cocktail of IP rintatolimod and interferon-alpha (IFNα) for patients with advanced stage ovarian cancer (III-IV) at primary ne…
Other (Terminated)
NCT04251533 — Study Assessing the Efficacy and Safety of Alpelisib + Nab-paclitaxel in Subjects With Advanced TNBC Who Carry Either a PIK3CA Mutation or Have PTEN Loss
| Status | Terminated |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 137 |
| Study Type | INTERVENTIONAL |
| Conditions | Triple Negative Breast Neoplasms |
| Interventions | ; ; |
The purpose of this study was to determine whether treatment with alpelisib in combination with nab-paclitaxel is safe and effective in subjects with advanced triple negative breast cancer (aTNBC) who carry either a PIK3CA mutation (Study Part A) or have PTEN loss (Study Part B1) or PTEN loss without PIK3CA mutation (Study Part B2)
Other (Suspended)
NCT06557733 — An Investigational Drug (TPST-1495) in Patients With Familial Adenomatous Polyposis
| Status | Suspended |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Colorectal Carcinoma; Familial Adenomatous Polyposis |
| Interventions | ; ; |
This open-label phase II trial tests how well TPST-1495 works in reducing the number of polyps in the small bowel and colon in patients with familial adenomatous polyposis (FAP). FAP is an inherited condition in which numerous polyps (growths that protrude from mucous membranes) form on the inside walls of the colon and rectum. It increases the risk for colon cancer. TPST-1495 binds to specific…