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 Diseases from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 28
- Active, not recruiting: 5
- Completed: 9
- Other: 8
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001352 — Fungal Infection Susceptibility
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 800 |
| Study Type | OBSERVATIONAL |
| Conditions | Cryptococcal Infection; Cryptococcal Pneumonia; Pulmonary Cryptococcosis; Cryptococcal Meningitis; Cryptococcosis |
The protocol will be carried out in accordance with International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP) and the following United States Code of Federal Regulations (CFR) applicable to clinical studies: 45 CFR Part 46, 21 CFR Part 50, 21 CFR Part 56, 21 CFR Part 312, and/or 21 CFR Part 812.
NIH-funded investigato…
NCT00006150 — Natural History, Management, and Genetics of the Hyperimmunoglobulin E Recurrent Infection Syndrome (HIES)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | Infections; Pneumonia; Immune System Diseases; STAT3 Transcription Factor; Job Syndrome |
The Hyper IgE Syndromes (HIES) are primary immunodeficiencies resulting in eczema and recurrent skin and lung infections. Autosomal dominant Hyper IgE syndrome (AD-HIIES; Job’s syndrome) is caused by STAT3 mutations, and is a multi-system disorder with skeletal, vascular, and connective tissue manifestations. Understanding how STAT3 mutations cause these diverse clinical manifestations is criti…
NCT00077909 — Study of Lung Proteins in Patients With Pneumonia
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 750 |
| Study Type | OBSERVATIONAL |
| Conditions | Pneumonia; Pulmonary Disease; Lung Disease |
This study will examine the different types of proteins present in the lungs of patients with pneumonia to explore the causes of different types of the disease. Pneumonia is a condition that causes lung inflammation AND is often caused by an infection. It is usually diagnosed by lung x-rays and listening to the chest with a stethoscope. This method can diagnose pneumonia, but it does not provid…
NCT00128973 — Evaluation of Patients With Immune Function Abnormalities
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Granulomatous Disease (CGD); X-Linked Severe Combined Immune Deficiency (XSCID); Leukocyte Adhesion Deficiency 1 (LAD); Graft Versus Host Disease (cGvHD) |
This study will evaluate patients with abnormal immune function that results in recurrent or unusual infections or chronic inflammation. This may include inherited conditions, such as X-linked severe combined immunodeficiency (XSCID), chronic granulomatous disease (CGD), and leukocyte adhesion deficiency (LAD), or conditions resulting from outside factors, such as graft-versus-host disease (GVH…
NCT00943514 — Natural History of Bronchiectasis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 900 |
| Study Type | OBSERVATIONAL |
| Conditions | Bronchiectasis; Cystic Fibrosis; Autoimmune Disease; Common Variable Immunodeficiency |
Background:
- Bronchiectasis is a disease characterized by airways that are inflamed, abnormally dilated, and chronically infected. Individuals with bronchiectasis have a history of chronic and recurring respiratory infections. Depending on the underlying cause, these infections may involve the entire respiratory tract, resulting in sinus, ear, and lung disease.
- Bronchiectasis continues to b…
NCT00341237 — Personalized Environment and Genes Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Environmental Health Sciences (NIEHS) |
| Enrollment | 25000 |
| Study Type | OBSERVATIONAL |
| Conditions | Diabetes; Heart Disease; Asthma |
Despite the overwhelming focus on genetic and genomic causes of human disease over the past two decades, it has been estimated that genetics is currently known to explain only 20% and 40% of the etiology of common disease. Thus, it is becoming increasingly apparent that human disease is a consequence of both genetic susceptibility and environmental exposures. Importantly, while individuals cann…
NCT01306084 — Viral Infections in Healthy and Immunocompromised Hosts
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Anogenital Herpes; COVID-19; Herpes Labialis |
Background:
- Viral infections are an important cause of illness and death in hospitalized patients as well as outpatients. New strains of viruses may appear and infect both healthy people and those with weak immune systems. A better understanding of these new virus strains (such as SARS-CoV-2, the virus that causes COVID-19) may help to control and prevent these infections. In particular, so…
NCT01712620 — Spironolactone for Pulmonary Arterial Hypertension
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension |
| Interventions | ; |
Background:
- High blood pressure in the lungs, known as pulmonary arterial hypertension (PAH), is a rare disorder. In spite of recent advances in treatment, the death rate remains unacceptably high. Lung blood vessel function can be harmed by progressive injuries, such as inflammation, leading to worsening of the disease. A drug called spironolactone has been known to improve blood vessel fu…
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:…
NCT04509050 — Study to Evaluate Biological & Clinical Effects of Significantly Corrected CFTR Function in Infants & Young Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sonya Heltshe |
| Enrollment | 210 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis |
| Interventions |
This is a two-part, multi-center, prospective longitudinal, exploratory study of highly effective cystic fibrosis transmembrane conductance regulator (CFTR) modulators and their impact on children with cystic fibrosis (CF).
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.
NCT06000761 — Frequent Standardized Oral Care Using Human Milk in the Neonatal Intensive Care Unit
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Florida |
| Enrollment | 218 |
| Study Type | INTERVENTIONAL |
| Conditions | Ventilator Associated Pneumonia; Bronchopulmonary Dysplasia; Respiratory Disease |
| Interventions |
Premature infants are susceptible to complications related to infrequent and non-standardized oral care. Although the benefits of frequent standardized oral care are known to reduce oral dysbiosis (increased level of potentially pathogenic bacteria) and its associated complications in critically ill adults leading to established evidence-based guidelines, no such information exists for VLBW inf…
NCT06087315 — Evaluation of a Multi-country Medical Oxygen Program
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Murdoch Childrens Research Institute |
| Enrollment | 1200 |
| Study Type | OBSERVATIONAL |
| Conditions | Hypoxemia; Neonatal Disease; Pneumonia; Sepsis; Morality |
| Interventions |
REAL-MOXY is a set of 5 mixed methods studies designed to understand how oxygen and pulse oximetry are used (or not used) at a facility level, to identify opportunities and barriers for strengthening oxygen systems for beneficiaries, users and managers.
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…
NCT06588634 — The PERSEVERE Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Inari Medical |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Embolism; Pulmonary Thromboembolism |
| Interventions | ; |
Randomized Controlled Trial of High-Risk Pulmonary Embolism Comparing FlowTriever System vs. Standard of Care
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
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…
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.
NCT07450547 — Phase 2 Study to Assess the Safety and Efficacy of ANG003
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Anagram Therapeutics, Inc. |
| Enrollment | 113 |
| Study Type | INTERVENTIONAL |
| Conditions | Exocrine Pancreatic Insufficiency (EPI); Cystic Fibrosis (CF) |
| Interventions | ; ; |
In this study, ANG003, a pancreatic enzyme replacement therapy (PERT; commonly called “enzymes”), is being investigated as a potential treatment for exocrine pancreatic insufficiency (EPI). People with EPI due to Cystic Fibrosis (CF) may be eligible to participate in this study. The primary objective of this study is to evaluate the safety of ANG003 and see if it works as well compared to Creon…
NCT07530146 — Comparative Efficacy and Safety of Propofol-Ketamine Combination Versus Propofol Monotherapy in Geriatric Patients Under Invasive Ventilation
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Helwan University |
| Enrollment | 41 |
| Study Type | INTERVENTIONAL |
| Conditions | The Critically Ill Patient is Requiring Intubation; Septic Shock; Pneumonia |
| Interventions | ; |
The study is a prospective randomized controlled trial comparing the efficacy and safety of propofol-ketamine (“Ketofol”) versus propofol monotherapy in geriatric ICU patients. Eligible participants are critically ill elderly patients with a history of cardiac disease who require endotracheal intubation and have not yet received sedation. The investigators focus on a specific population in whic…
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…
NCT07670494 — Mechanical Power During Different Ventilation Modes in Laparoscopic Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Laparoscopic Cholecystectomy; Mechanical Ventilation; Ventilator-Induced Lung Injury |
| Interventions | ; |
This study investigates how different breathing machine (ventilator) settings affect the energy delivered to the lungs during surgery. Mechanical power is a measure of this energy, and high levels can sometimes lead to lung irritation. In clinical practice, a mode called Pressure-Regulated Volume Control (PRVC) is often used because it lowers the “peak” pressure in the airways, which is general…
NCT07522346 — deMISTify: The Impact of Ventilator Pressure Levels During Minimally Invasive Surfactant Therapy on Lung Aeration in Preterm Infants
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Murdoch Childrens Research Institute |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Surfactant Deficiency Syndrome Neonatal |
| Interventions | ; |
Infants born preterm (before 36 weeks’ gestation age) have immature lungs and struggle to breathe on their own. They are supported via respiratory machines like ventilators, as well as pharmaceutical aids like surfactant replacement therapy. Surfactant replacement therapy is an established therapy for the treatment of respiratory distress syndrome, which is a common illness in infants born pret…
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
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…
NCT03256773 — High Resolution Micro OCT Imaging
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 160 |
| Study Type | OBSERVATIONAL |
| Conditions | Cystic Fibrosis; COPD; PCD - Primary Ciliary Dyskinesia; Covid19; Sinusitis |
The purpose of this study is to learn about using the imaging to make images of the lungs and nose with the long-term goal of the research leading to potential treatments and new therapies for patients with cystic fibrosis.
NCT04212416 — Leflunomide in Treating Patients With Steroid Dependent Chronic Graft Versus Host Disease
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | City of Hope Medical Center |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Graft Versus Host Disease; Steroid Refractory Graft Versus Host Disease |
| Interventions |
This phase I trial studies the side effects of leflunomide in treating patients with steroid dependent chronic graft versus host disease (cGVHD). cGVHD is a common complication of bone marrow transplant. GVHD occurs when immune cells transplanted from a donor (the graft) recognize the transplant recipient (the host) as foreign, and cause damage to the skin, gastrointestinal tract or other organ…
NCT04212962 — Transitional Care Model Evaluation 2020
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Mathematica Policy Research, Inc. |
| Enrollment | 962 |
| Study Type | INTERVENTIONAL |
| Conditions | CHF - Congestive Heart Failure; COPD; Pneumonia |
| Interventions | ; |
The study is a randomized controlled trial to estimate the effects of the transitional care model (TCM) on hospital admissions and patients’ experience during the year following the patient’s qualifying discharge. The University of Pennsylvania, where TCM was developed, will be the coordinating center for the implementation. The study will be conducted in three large health systems spread throu…
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.
Not Yet Recruiting
NCT07613099 — Fibrotic Disease Activity in Cardiopulmonary Disorders Using 18F-Fibroblast Activation Protein Inhibitor (18F-FAPI-74) PET/CT Imaging
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 210 |
| Study Type | INTERVENTIONAL |
| Conditions | Allogeneic Stem Cell Transplantation; Lung Allograft Transplantation; Interstitial Lung Disease; Acute Lung Injury; Pulmonary Arterial Hypertension |
| Interventions | ; |
Background:
Injury or diseases of the heart and lung can sometimes cause scar tissue (fibrosis) to build up in those organs. Current imaging scans can see this scar tissue once it has formed, but researchers want to find a way to detect the fibrosis in its earliest stages, while there might still be time to prevent serious damage. A new tracer (a radioactive substance injected during imaging s…
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…
NCT06602557 — " Study of the Benefit of Nebulized Amikacin in the Treatment of Gram-negative Bacillus Pneumonia Acquired During Mechanical Ventilation in Patients Receiving Extracorporeal Membrane Veno-arterial Oxygenation “
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | Pneumonia, Bacterial; Extracorporeal Membrane Oxygenation |
| Interventions | ; |
Pneumonia are the most frequent infectious complication in patients on Extracorporeal Membrane Oxygenation Veno-arterial (ECMO-VA), with a treatment failure rate of around 40%, even though antibiotic therapy is tailored to the germs identified. One hypothesis to explain this particularly high failure rate is the reduced pulmonary blood flow associated with ECMO offloading of the heart. Although…
NCT04231760 — The Effect of Inhaled Nitric Oxide on Pulmonary Gas-exchange in COPD
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | University of Alberta |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease |
| Interventions | ; |
Chronic Obstructive Pulmonary Disease (COPD) is a lung disorder commonly caused by smoking, which makes breathing more difficult. When COPD patients exercise, they are not efficient breathers and this leads to serious breathing difficulties, which often causes these patients to stop exercise at low intensities. Even though patients with a mild form of COPD have relatively well preserved lung fu…
Enrolling by Invitation
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…
NCT05350774 — Immunotherapy for Neurological Post-Acute Sequelae of SARS-CoV-2
| Status | Enrolling by invitation |
| Phase | Phase 2 |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Inflammation; Neuroinflammation; Microvascular Thrombosis |
| Interventions | ; |
Background:
COVID-19 can cause problems in different parts of the body. For most people, it causes fevers or trouble breathing. Some people might not recover all the way. Researchers want to see if a treatment can help with people who have recovered from COVID-19 but still have symptoms (“Long COVID”).
Objective:
To learn if human immunoglobulin (IVIG) will help with neurological symptoms of…
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
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…
NCT04069312 — Roflumilast or Azithromycin to Prevent COPD Exacerbations Trial
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Johns Hopkins University |
| Enrollment | 1032 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Obstructive Pulmonary Disease Severe; Chronic Bronchitis |
| Interventions | ; |
A multi-center, randomized, 72-month, parallel- group, non-inferiority, phase III study to compare the effectiveness of roflumilast (Daliresp, 500 mcg quaque die (QD) or alternate regimen) therapy versus azithromycin (250 mg QD, 500 mg QD three times per week, or alternate regimen) to prevent hospitalization or death in a patients at high risk for COPD exacerbations.
NCT05548803 — COVID-19 Citizen Science Expansion Project
| Status | Completed |
| Phase | N/A |
| Sponsor | University of California, San Francisco |
| Enrollment | 52351 |
| Study Type | OBSERVATIONAL |
| Conditions | Covid19 |
COVID-19 Citizen Science (CCS), launched in March 2020, supports collaborative research on symptoms, risk factors, surveillance, biomarkers and testing for COVID-19 using the Eureka Research Platform. CCS maintains IRB approval with UCSF’s IRB (UCSF IRB# 17-21879).
This CCS Expansion Project, which is funded jointly by the National Institutes of Health (NIH), the Patient-Centered Outcomes Rese…
NCT04315948 — Trial of Treatments for COVID-19 in Hospitalized Adults
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France |
| Enrollment | 1552 |
| Study Type | INTERVENTIONAL |
| Conditions | Corona Virus Infection |
| Interventions | ; ; |
DisCoVeRy is a randomized controlled trial among adults (≥18-year-old) hospitalized for COVID-19. This study is an adaptive, randomized, open or blinded, depending on the drug to be evaluated, clinical trial to evaluate the safety and efficacy of possible therapeutic agents in hospitalized adult patients diagnosed with COVID-19. The study is a multi-centre/country trial that will be conducted i…
NCT05074758 — Characterization of the microVAScular Dysfunction in Covid-19 ARDS
| Status | Completed |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 39 |
| Study Type | OBSERVATIONAL |
| Conditions | ARDS, Human; COVID-19 Acute Respiratory Distress Syndrome |
| Interventions | ; ; |
The primary endpoint of this research is to establish that the alveolar dead space is significantly higher in patients with COVID-19 ARDS, compared to patients with non-COVID-19 ARDS.
Secondarily, the investigators want to establish the prognostic value of the alveolar-dead space (measured iteratively) in patients with COVID-19 and non-COVID-19 ARDS, to establish the respective influences of t…
NCT05221502 — Safety and Efficacy Evaluation of 4-month Regimen of OPC-167832, Delamanid and Bedaquiline in Participants With Drug-Susceptible Pulmonary TB
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Otsuka Pharmaceutical Development & Commercialization, Inc. |
| Enrollment | 122 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary TB |
| Interventions | ; ; |
This trial will assess the safety and efficacy of OPC-167832 combined with delamanid and bedaquiline in participants with drug-susceptible tuberculosis (DS-TB) administered for 17 weeks compared to rifampin, isoniazid, ethambutol, pyrazinamide (RHEZ) administered for 26 weeks.
NCT07690943 — Evaluation of the Safety and Efficacy of Autologous COVID-19 Antigen Specific T Cell in Prolonged SARS-CoV-2 Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | LucasBio |
| Enrollment | 13 |
| Study Type | INTERVENTIONAL |
| Conditions | COVID-19; COVID-19 (SARS-CoV-2 Infection) |
| Interventions |
The goal of this clinical study is to evaluate the safety and efficacy of autologous COVID-19 antigen specific T cell (LB-DTK-COV19) treatment in prolonged SARS-CoV-2 infected patients. The main questions it aims to answer are:
- What adverse events occur after the infusion of LB-DTK-COV19?
- Is there a clinically significant improvement in clinical symptoms within 4 weeks after the infusion? …
NCT06404060 — RECOVER-ENERGIZE Platform Protocol_Appendix A (Exercise Intolerance)
| Status | Completed |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 360 |
| Study Type | INTERVENTIONAL |
| Conditions | Long COVID; Long Covid19; Long Covid-19 |
| Interventions | ; |
This is a platform protocol designed to be flexible so that it is suitable for a range of interventions and settings within diverse health care systems and community settings with incorporation into clinical COVID-19 management programs and treatment plans if results achieve key study outcomes.
This protocol is a prospective, multi-center, multi-arm, randomized, controlled platform trial evalu…
NCT06495996 — The Protrieve PROTECTOR Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Inari Medical |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Venous Thromboembolism; Deep Venous Thrombosis |
| Interventions |
The Protrieve PROTECTOR Study is a prospective, single-arm, multicenter study of the Protrieve Sheath.
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…