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 Lung Cancer from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 27
- Active, not recruiting: 8
- Completed: 4
- Other: 11
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001532 — Role of Genetic Factors in the Development of Lung Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; Pulmonary Fibrosis; Tuberous Sclerosis; Asthma; Pulmonary Sarcoidosis |
This study is designed to evaluate the genetics involved in the development of lung disease by surveying genes involved in the process of breathing and examining the genes in lung cells of patients with lung disease.
The study will focus on defining the distribution of abnormal genes responsible for processes directly involved in different diseases affecting the lungs of patients and healthy v…
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:…
NCT04429087 — A Study to Test Different Doses of Obrixtamig in Patients With Small Cell Lung Cancer and Other Neuroendocrine Tumours That Are Positive for DLL3
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Boehringer Ingelheim |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Small Cell Lung Carcinoma and Other Neuroendocrine Neoplasms Expressing DLL3 |
| Interventions | ; |
This study is open to adults with small cell lung cancer and other neuroendocrine cancers that are positive for the tumour marker delta-like 3 (DLL3). The study is in people with advanced cancer for whom previous treatment was not successful or no standard treatment exists.
The purpose of this study is to find out the highest dose of obrixtamig and the best treatment schedule that people can t…
NCT04181060 — Osimertinib With or Without Bevacizumab as Initial Treatment for Patients With EGFR-Mutant Lung Cancer
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lung Non-Squamous Non-Small Cell Carcinoma; Metastatic Lung Non-Squamous Non-Small Cell Carcinoma; Recurrent Lung Non-Squamous Non-Small Cell Carcinoma; Stage IIIB Lung Cancer AJCC v8; Stage IV Lung Cancer AJCC v8 |
| Interventions | ; ; |
This phase III trial compares the effect of bevacizumab and osimertinib combination vs. osimertinib alone for the treatment of non-small cell lung cancer that has spread outside of the lungs (stage IIIB-IV) and has a change (mutation) in a gene called EGFR. The EGFR protein is involved in cell signaling pathways that control cell division and survival. Sometimes, mutations in the EGFR gene caus…
NCT05543330 — A Phase Ib/II Clinical Trial of M701 in the Treatment of Malignant Pleural Effusions Caused by NSCLC
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Wuhan YZY Biopharma Co., Ltd. |
| Enrollment | 116 |
| Study Type | INTERVENTIONAL |
| Conditions | Malignant Pleural Effusions; NSCLC Stage IV |
| Interventions | ; ; |
This is a phase 1/phase 2, multicenter, open-label study to evaluate the safety, tolerability, PK, PD, immunogenicity and preliminary efficacy of M701 in patients with treatment of malignant pleural effusions caused by NSCLC.
NCT06103682 — LOcally ABLatIve ThErapy for OligopRogressive Lung And Thoracic MalignanciEs (OBLITERATE)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, Davis |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-small Cell Lung Cancer; Oligoprogressive; Small-cell Lung Cancer |
| Interventions |
This is a phase 2 pragmatic study that evaluates the clinical benefit of continuing systemic therapy with the addition of locally ablative therapies for oligo-progressive solid tumors as the primary objective. The primary outcome measure is the time to treatment failure (defined as time to change in systemic failure or permanent discontinuation of therapy) following locally ablative therapy.
NCT06547710 — Primary Tumor Resection for M1a Stage Lung Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fudan University |
| Enrollment | 66 |
| Study Type | OBSERVATIONAL |
| Conditions | Lung Cancer Metastatic; Surgical Resection |
This is a clinical trial from Eastern Cooperative Thoracic Oncology Project (ECTOP), numbered as ECTOP-1023. This study aims to explore the safety and efficacy of primary lesion resection in the treatment of M1a stage lung cancer with pleural dissemination found during surgery, and to more accurately evaluate whether primary lesion resection can improve the OS and quality of life of the corresp…
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…
NCT06562192 — Phase I Study of [177Lu]Lu-NNS309 in Patients With Pancreatic, Lung, Breast and Colorectal Cancers
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 162 |
| Study Type | INTERVENTIONAL |
| Conditions | Pancreatic Ductal Adenocarcinoma; Non-small Cell Lung Cancer; HR+/HER2- Ductal and Lobular Breast Cancer; Triple Negative Breast Cancer; Colorectal Cancer |
| Interventions | ; |
The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of [177Lu]Lu-NNS309 and the safety and imaging properties of [68Ga]Ga-NNS309 in patients aged ≥ 18 years with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC), non-small cell lung cancer (NSCLC), HR+/HER2- ductal and lobular breast cancer (BC), triple negative breast c…
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
NCT07066813 — Staging Strategies and Their Association With Prognosis and Therapy in Lung Cancer With Cystic Airspaces
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Central South University |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Lung Cancer Associated With Cystic Airspaces |
The goal of this observational study is to determine the most accurate tumor size measurement method for T-staging and prognostic assessment in lung cancer with cystic airspaces (LCCA). The main questions it aims to answer are:
- What is the optimal T-staging approach for accurately classifying lung cancer with cystic airspaces (LCCA) and predicting patient outcomes?
- How do imaging features …
NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 24000 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma |
| Interventions | ; ; |
The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…
NCT06066138 — A Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced Alveolar Soft Part Sarcoma; Metastatic Alveolar Soft Part Sarcoma; Locally Advanced Non Small Cell Lung Cancer; Metastatic Non Small Cell Lung Cancer; Locally Advanced Small Cell Lung Cancer |
| Interventions |
Background:
A type of drug called monoclonal antibody immune checkpoint inhibitors are often used in cancer treatment. These drugs help the body s immune system fight cancer by blocking proteins that cause cancer cells to grow. One of these drugs (atezolizumab) is approved to treat certain cancers. Researchers want to find out if lower doses of this drug might provide the same benefit with few…
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…
NCT07227298 — Symbiotic-Lung-20: A Study to Learn About the Study Medicine Called PF-08634404 in Combination With Different Anticancer Agents in Advanced Cancers
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Pfizer |
| Enrollment | 162 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced/Metastatic Non-Small Cell Lung Cancer; Carcinoma, Non-Small Cell Lung; Non-Small Cell Lung Cancer |
| Interventions | ; ; |
This study is being done to learn more about a new medicine called PF-08634404 and how it works when used with other cancer medicines in people who have advanced solid tumors. An advanced solid tumor is a type of cancer that has spread beyond its original location and cannot be removed by surgery or cured with standard treatments.
To join in the study, participants must:
- Be 18 years or olde…
NCT07367529 — A Clinical Trial on the Efficacy and Safety of TQB6411 for Injection
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. |
| Enrollment | 465 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lung Cancer |
| Interventions |
To evaluate the efficacy and safety of TQB6411 for Injection in subjects with advanced lung cancer
NCT07277413 — A Study of IDE892 as Monotherapy and Combination in MTAP-deleted Advanced Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | IDEAYA Biosciences |
| Enrollment | 260 |
| Study Type | INTERVENTIONAL |
| Conditions | NSCLC Adenocarcinoma; Gastroesophageal Cancer (GC); Gastric Adenocarcinoma; Adenocarcinoma of Esophagus; Squamous Cell Car. - Esophagus |
| Interventions | ; |
This is a multicenter clinical study to evaluate the safety, efficacy, and Pharmacokinetics (PK) of IDE892 as monotherapy and in combination with other agents including IDE397 in participants with methylthioadenosine phosphorylase (MTAP)-deleted advanced solid tumors within indications of interest.
NCT07154290 — A Study to Investigate Ubamatamab With and Without REGN7075 in Adult Participants With Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced/Metastatic Non-Small Cell Lung Cancer |
| Interventions | ; ; |
This study will evaluate two study drugs called ubamatamab and REGN7075, to see if they can help treat advanced or metastatic Non-Small Cell Lung Cancer (NSCLC), and sarilumab, to evaluate to see if it can help with immune-related side effects from ubamatamab.
The study is looking at:
- How well ubamatamab and REGN7075 works
- The side effects that ubamatamab and REGN7075 might cause
- How mu…
NCT07296887 — CARE Tool Study Aim 3
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Washington University School of Medicine |
| Enrollment | 430 |
| Study Type | INTERVENTIONAL |
| Conditions | Gynecologic Cancer; Prostate Cancer; Lung Cancer; Colorectal Cancer |
| Interventions | ; ; |
This study is a multi-site randomized trial to study the implementation of the CARE Tool and evaluate the CARE Tool. The CARE Tool is a web-based tool that gives people information about cancer care costs, health insurance, and resources to help with costs. Overall, the study aims to help patients with cancer overcome barriers they face navigating insurance and accessing financial resources.
NCT07416695 — A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of HLX3901 in Patients With Advanced SCLC or NEC
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Shanghai Henlius Biotech |
| Enrollment | 138 |
| Study Type | INTERVENTIONAL |
| Conditions | SCLC; NEC |
| Interventions |
This study is an open-label first-in-human phase I clinical study to evaluate the safety, tolerability, and pharmacokinetic characteristics of HLX3901 in patients with Advanced Small Cell Lung Cancer or Neuroendocrine Carcinoma.
NCT07689643 — Safety and Preliminary Efficacy of [177Lu]Lu-RTX-2358 Combined With Immune Checkpoint Inhibitors in Patients With FAP-positive Metastatic Non-Small Cell Lung Cancer
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Union Hospital, Tongji Medical College, Huazhong University of Science and Technology |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Non-small Cell Lung Cancer |
| Interventions |
This is a prospective, single-center, open-label investigator-initiated study designed to evaluate the safety, tolerability, radiation dosimetry, biodistribution, and preliminary antitumor activity of [177Lu]Lu-RTX-2358 in combination with immune checkpoint inhibitors (ICIs) in patients with fibroblast activation protein (FAP)-positive metastatic non-small cell lung cancer (NSCLC). Eligible p…
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…
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.
NCT07314216 — Firmonertinib Combined With Definitive Radiotherapy in Stage III Unresectable EGFR Uncommon Mutant Pulmonary Adenocarcinoma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hunan Cancer Hospital |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | NSCLC (Non-small Cell Lung Carcinoma); Stage III; EGFR Uncommon Mutations |
| Interventions | ; |
This is a prospective, single-arm, Phase II clinical study aimed at evaluating the efficacy and safety of 160mg fimonertinib in combination with definitive radiotherapy for patients with EGFR uncommon driver mutation-positive, Stage III unresectable lung adenocarcinoma. The primary endpoint is Progression-Free Survival (PFS), assessed by the investigator according to RECIST 1.1 criteria, define…
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…
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…
NCT02484404 — Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can…
| Status | Active, not recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 268 |
| Study Type | INTERVENTIONAL |
| Conditions | Colorectal Neoplasms; Breast Neoplasms |
| Interventions | ; ; |
Background:
- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the co…
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT02496663 — Osimertinib and Necitumumab in Treating Patients With EGFR-Mutant Stage IV or Recurrent Non-small Cell Lung Cancer Who Have Progressed on a Previous EGFR Tyrosine Kinase Inhibitor
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 138 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Lung Non-Small Cell Carcinoma; Recurrent Lung Non-Small Cell Carcinoma; Stage IV Lung Cancer AJCC v8 |
| Interventions | ; ; |
This phase I trial studies the safety, side effects and best dose of necitumumab when given together with osimertinib in treating patients with EGFR-mutant non-small cell lung cancer that is stage IV or has come back after a period of improvement (recurrent) and who have progressed on a previous EGFR tyrosine kinase inhibitor. Immunotherapy with monoclonal antibodies, such as necitumumab, may i…
NCT04197934 — WSD0922-FU for the Treatment of Glioblastoma, Anaplastic Astrocytoma, or Non-small Cell Lung Cancer With Central Nervous System Metastases
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Mayo Clinic |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Anaplastic Astrocytoma, IDH-Wildtype; Glioblastoma, IDH-Wildtype; Metastatic Lung Non-Small Cell Carcinoma; Metastatic Malignant Neoplasm in the Central Nervous System; Stage IV Lung Cancer AJCC v8 |
| Interventions | ; ; |
This phase I trial studies the side effects and best dose of WSD0922-FU for the treatment of glioblastoma, anaplastic astrocytoma, or non-small cell lung cancer that has spread to the central nervous system (central nervous system metastases). WSD0922-FU is a targeted treatment which blocks the EGFR protein - a strategy that has led to a lot of benefit in patients with many different cancers. W…
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.
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
NCT07676383 — Precision Navigation to Improve Community Cancer Screening Participation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Hunan Cancer Hospital |
| Enrollment | 1500 |
| Study Type | INTERVENTIONAL |
| Conditions | Cancer Screening; Lung Cancer; Breast Cancer; Colorectal Cancer; Upper Gastrointestinal Cancer |
| Interventions | ; |
This study will evaluate whether a precision navigation intervention can help community residents at high risk for cancer complete recommended cancer screening. The study will be conducted in communities participating in an urban cancer screening program in China.
Eligible participants will be adults aged 45 to 74 years who are permanent residents of participating communities and have been ide…
NCT07509034 — Autologous B7-H3 Chimeric Antigen Receptor T Cells in Previously Treated Extensive-Stage Small Cell Lung Cancer With Recurrent or Refractory Disease
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Extensive-Stage Small Cell Lung Cancer; Extrapulmonary Neuroendocrine Carcinoma; Recurrent or Refractory; Solid Tumors |
| Interventions | ; ; |
Background:
Small cell lung cancer (SCLC) is the deadliest form of lung cancer. Extrapulmonary neuroendocrine cancer (EPNEC) is a similar type of cancer that develops anywhere other than the lungs. EPNEC is also deadly. B7-H3 is a protein often found in SCLC and EPNEC tumor cells. Researchers can modify a person s own T cells, or immune cells, to target B7-H3. When these modified T cells are r…
NCT07005297 — Clinical Genetics Branch Eligibility Screening Survey
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Melanoma; Li-Fraumeni Syndrome; Pulmonary Blastoma; Chordoma; Congenital Bone Marrow Failure Syndromes |
Background:
Clinical Genetics Branch (CGB) researchers study individuals and populations at high genetic risk of cancer in order to improve our understanding of cancer and to improve cancer care. There are currently 6 open clinical genetics studies at the CGB eligible for this screening process.
- 02C0052: Etiologic Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndr…
NCT07689968 — A Pilot Study of the VosCryoTM Breathalyser in Lung Cancer
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sheffield Teaching Hospitals NHS Foundation Trust |
| Enrollment | 24 |
| Study Type | OBSERVATIONAL |
| Conditions | Advanced Lung Cancer |
| Interventions |
CryoPilot is a single-centre pilot study being conducted at Weston Park Cancer Centre in Sheffield, UK. The goal of this pilot study is to determine whether small-volume exhaled breath condensate sample (EBC) obtained via a VosCryo™ breath sample collection device can provide quantifiable and analysable cellular material, including epithelial cells, leukocytes, or exfoliated tumour cells, in pa…
NCT07689812 — A Multicenter Randomized Open-Label Trial Evaluating MRD-Guided Interruption Versus Standard of Care Immune-Checkpoint Inhibitor (ICI) Therapy In Patients With Advanced / Metastatic Solid Tumors.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Natera, Inc. |
| Enrollment | 920 |
| Study Type | INTERVENTIONAL |
| Conditions | NSCLC (Advanced Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Carcinoma); NSCLC; Melanoma (Skin Cancer) |
| Interventions |
This is an open-label, randomized study evaluating whether MRD-guided intermittent ICI therapy provides comparable survival to SOC continuous ICI therapy in subjects with histologically confirmed advanced / metastatic NSCLC, melanoma, MSI-High/dMMR CRC, RCC and other solid tumors. This study will be conducted in up to 100 sites.
NCT07689721 — ctDNA-Guided Intraventricular Therapy for CNS Malignancies
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Alireza Mansouri |
| Enrollment | 77 |
| Study Type | INTERVENTIONAL |
| Conditions | Leptomeningeal Disease; Glioblastoma; Brain Metastases; Non-Small Cell Lung Cancer; Breast Cancer |
| Interventions |
This prospective, single-center study will evaluate whether cerebrospinal fluid (CSF) circulating tumor DNA (ctDNA) testing using the Belay Summit assay can improve the clinical management of patients with malignant gliomas or brain metastases from non-small cell lung cancer (NSCLC) or breast cancer who are suspected of having central nervous system (CNS) disease. Patients undergoing clinically…
Enrolling by Invitation
NCT00001620 — Screening for Hematology Branch Protocols
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 10000 |
| Study Type | OBSERVATIONAL |
| Conditions | Hematologic Disease and Disorders; Donors; Healthy Volunteer |
This study allows the evaluation of subjects in order to determine their ability to safely participate in other active research studies.
After subjects complete the screening process, they will be offered the opportunity to participate in an active research study, or if no appropriate studies are available information and recommendations will be provided for other treatment options….
NCT04450927 — Data Collection of Standard Care and Evaluation of NHLBI Patients and Donors
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 10000 |
| Study Type | OBSERVATIONAL |
| Conditions | Wide Spectrum of Diseases; Hematologic Diseases |
Background:
Researchers seek ways to study people s medical problems in order to teach and further general knowledge. The ability to assess and treat people with a wide range of diseases is critical to training people to be good doctors. It is also needed to keep medical staff up to date. In this study, researchers want to study the course of some illnesses to learn more about them. To do this…
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
NCT00720785 — Natural Killer Cells and Bortezomib to Treat Cancer
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Myeloid Leukemia (CML); Pancreatic Ca; Colon/Rectal Ca; Multiple Myeloma; Carcinoma, Non-Small -Cell Lung |
| Interventions | ; |
Natural killer (NK) cells are white blood cells that have a limited ability to kill cancer cells. This ability might be enhanced if they are given 24 hours after an injection of the drug bortezomib. This study will determine the following:
- What dose of NK cells can be given safely to subjects with metastatic solid tumors or leukemia.
- The effectiveness and side effects of NK cell therapy
- …
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…
NCT06049966 — Atezolizumab in Large Cell Neuroendocrine Carcinoma
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Oncology Center of Biochemical Education And Research |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Large Cell Neuroendocrine Carcinoma of the Lung |
| Interventions | ; ; |
Large-cell neuroendocrine carcinoma (LCNEC) of the lung is a rare and aggressive malignancy with limited prospective evidence to guide systemic treatment. This prospective, non-randomized, real-world study evaluated the effectiveness and safety of atezolizumab in combination with platinum-etoposide chemotherapy in treatment-naïve patients with metastatic lung-derived LCNEC.
Patients who receiv…
NCT04487756 — Combination of Atezolizumab With Dendritic Cell Vaccine in Patients With Lung Cancer
| Status | Completed |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Instituto Oncológico Dr Rosell |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Extensive-stage Small Cell Lung Cancer |
| Interventions | ; ; |
This is a single-arm Phase Ib/II multicenter open-label study, with translational sub-study, of atezolizumab plus autologous dendritic cell vaccine as maintenance treatment in extensive-stage small cell lung cancer (ES-SCLC). It is expected that three Spanish sites will include patients in this study.
Patients will receive standard treatment with carboplatin and etoposide, plus atezolizumab fo…
Other (Terminated)
NCT06585488 — A First-in-human Study of BGB-53038, a Pan-KRAS Inhibitor, Alone or in Combinations in Participants With Advanced or Metastatic Solid Tumors With KRAS Mutations or Amplification
| Status | Terminated |
| Phase | Phase 1 |
| Sponsor | BeOne Medicines |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Solid Tumors; Advanced Non-squamous Non-small-cell Lung Cancer; Advanced Colorectal Cancer; Advanced Pancreatic Ductal Adenocarcinoma; Advanced Gastric Cancer |
| Interventions | ; ; |
This is a first-in-human (FIH), open-label, multicenter, dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BGB-53038 as monotherapy in participants with advanced or metastatic solid tumors harboring KRAS mutations or amplification, as well as when used in combination with tislelizumab (al…
Other (Suspended)
NCT05642195 — Evaluation of a Cancer Lysate Vaccine and Montanide (Registered Trademark) ISA-51 VG With or Without the IL-15 Super-Agonist N-803 as Adjuvant Therapy for PD-L1 Negative Non-Small Cell Lung Cancer
| Status | Suspended |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-Small Cell Lung Cancer; Non-Small Cell Lung Carcinoma; Carcinoma, Non-Small-Cell Lung; Carcinomas |
| Interventions | ; ; |
Background:
Surgery is the primary treatment for non-small cell lung cancer (NSCLC) that is diagnosed in its earlier stages. But the tumors often return. Radiation and chemotherapy can improve survival in some people who have had surgery for NSCLC, but these treatments also cause serious side effects. A new approach, called immunotherapy, may be a better way to stop NSCLC tumors from coming ba…