Clinical Trials for Bronchial Disorders

Currently registered clinical trials for Bronchial Disorders from ClinicalTrials.gov. 30 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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 Bronchial Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 30
  • Active, not recruiting: 6
  • Completed: 7
  • Other: 7

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

StatusRecruiting
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsCystic 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…

NCT00128973 — Evaluation of Patients With Immune Function Abnormalities

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment3500
Study TypeOBSERVATIONAL
ConditionsChronic 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

StatusRecruiting
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment900
Study TypeOBSERVATIONAL
ConditionsBronchiectasis; 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

StatusRecruiting
PhaseN/A
SponsorNational Institute of Environmental Health Sciences (NIEHS)
Enrollment25000
Study TypeOBSERVATIONAL
ConditionsDiabetes; 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…

NCT01804686 — A Long-term Extension Study of PCI-32765 (Ibrutinib)

StatusRecruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment700
Study TypeINTERVENTIONAL
ConditionsChronic Lymphocytic Leukemia; Small Lymphocytic Lymphoma; Mantle Cell Lymphoma; Follicular Lymphoma; Diffuse Large B-cell Lymphoma
Interventions

The purpose of this study is to collect long-term safety and efficacy data for participants treated with ibrutinib and to provide ongoing access to ibrutinib for participants who are currently enrolled in ibrutinib studies that have been completed according to the parent protocol, are actively receiving treatment with ibrutinib, and who continue to benefit from ibrutinib treatment.

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

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsNon-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:…

NCT03340506 — Dabrafenib and/or Trametinib Rollover Study

StatusRecruiting
PhasePhase 4
SponsorNovartis Pharmaceuticals
Enrollment100
Study TypeINTERVENTIONAL
ConditionsMelanoma; Non Small Cell Lung Cancer; Solid Tumor; Rare Cancers; High Grade Glioma
Interventions;

This study is to provide access for patients who are receiving treatment with dabrafenib and/or trametinib in a Novartis-sponsored Oncology Global Development, Global Medical Affairs or a former GSK-sponsored study who have fulfilled the requirements for the primary objective, and who are judged by the investigator as benefiting from continued treatment in the parent study as judged by the Inve…

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

StatusRecruiting
PhasePhase 1
SponsorBoehringer Ingelheim
Enrollment300
Study TypeINTERVENTIONAL
ConditionsSmall 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…

NCT05543330 — A Phase Ib/II Clinical Trial of M701 in the Treatment of Malignant Pleural Effusions Caused by NSCLC

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorWuhan YZY Biopharma Co., Ltd.
Enrollment116
Study TypeINTERVENTIONAL
ConditionsMalignant 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)

StatusRecruiting
PhaseN/A
SponsorUniversity of California, Davis
Enrollment100
Study TypeINTERVENTIONAL
ConditionsNon-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.

NCT06139627 — Evaluation of Geriatric Assessment and Management for Older Adults With Non-small Cell Lung Cancer Receiving Chemotherapy Radiation Therapy

StatusRecruiting
PhaseN/A
SponsorCity of Hope Medical Center
Enrollment180
Study TypeINTERVENTIONAL
ConditionsLung 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…

NCT06552234 — Phase II Efficacy Study of Repotrectinib in Frail and/or Elderly Patients With ROS1-rearranged Advanced NSCLC

StatusRecruiting
PhasePhase 2
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment30
Study TypeINTERVENTIONAL
ConditionsNSCLC Stage IV; NSCLC, Stage III
Interventions

ROS1 rearrangements are rare, accounting for only 1-2% of NSCLC cases, but have been associated with response to ROS1 inhibitors, such as crizotinib and entrectinib. However, many patients develop resistance to the tyrosine-kinase inhibitors (TKIs), creating a need for new treatments.

Repotrectinib is a new-generation TKI designed against ROS1 or NTRK rearranged malignancies (Drilon 2018). Ear…

NCT06562192 — Phase I Study of [177Lu]Lu-NNS309 in Patients With Pancreatic, Lung, Breast and Colorectal Cancers

StatusRecruiting
PhasePhase 1
SponsorNovartis Pharmaceuticals
Enrollment162
Study TypeINTERVENTIONAL
ConditionsPancreatic 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)

StatusRecruiting
PhasePhase 2
SponsorRegeneron Pharmaceuticals
Enrollment120
Study TypeINTERVENTIONAL
ConditionsNon-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)

StatusRecruiting
PhasePhase 3
SponsorMirati Therapeutics Inc.
Enrollment630
Study TypeINTERVENTIONAL
ConditionsCarcinoma, 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

NCT07690345 — Fungal Status and Prognosis in ABPA

StatusRecruiting
PhaseN/A
SponsorQianfoshan Hospital
Enrollment114
Study TypeOBSERVATIONAL
ConditionsABPA; Allergic Bronchopulmonary Aspergillosis; Allergic Bronchopulmonary Aspergillosis (ABPA); Colonization

This multicenter bidirectional cohort study aims to investigate the clinical characteristics and prognostic outcomes of patients with allergic bronchopulmonary aspergillosis (ABPA) stratified by fungal microbiological status in sputum or bronchoalveolar lavage fluid (BALF).

Patients diagnosed with ABPA according to the ISHAM 2024 criteria will be classified into fungal-positive and fungal-nega…

NCT07201051 — A Study to Assess the Effectiveness and Safety of GSK3862995B in Adults With Bronchiectasis

StatusRecruiting
PhasePhase 2
SponsorGlaxoSmithKline
Enrollment446
Study TypeINTERVENTIONAL
ConditionsBronchiectasis
Interventions;

This study is designed to find out how effective and safe a new drug, GSK3862995B, is for adult participants with bronchiectasis, a chronic lung disease. The study will also test how the body processes the drug and to check for any immune reactions. Participants will be divided into groups randomly to receive either one of two different doses of the study drug or a placebo. The main goal of the…

NCT06066138 — A Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment30
Study TypeINTERVENTIONAL
ConditionsLocally 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

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorPfizer
Enrollment550
Study TypeINTERVENTIONAL
ConditionsSmall 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…

NCT07222566 — Symbiotic-Lung-01 : A Study to Learn About the Study Medicine Called PF-08634404 in Combination With Chemotherapy in Adult Participants With Locally Advanced or Metastatic Non-Small Cell Lung Cancer

StatusRecruiting
PhasePhase 3
SponsorPfizer
Enrollment1410
Study TypeINTERVENTIONAL
ConditionsAdvanced Non-Small Cell Lung Cancer; Non-Small Cell Lung Cancer; Carcinoma, Non-Small-Cell Lung; Carcinoma, Non-Small-Cell Lung (NSCLC); Metastatic Non Small Cell Lung Cancer
Interventions; ;

This study is being done to find out if a new medicine called PF-08634404, when given with chemotherapy, works better than the present standard treatment (pembrolizumab with chemotherapy) for adults with a type of lung cancer called non-small cell lung cancer (NSCLC) that is either locally advanced (spread to nearby tissues) or has spread to other parts of the body.

To join the study, particip…

NCT07227298 — Symbiotic-Lung-20: A Study to Learn About the Study Medicine Called PF-08634404 in Combination With Different Anticancer Agents in Advanced Cancers

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorPfizer
Enrollment162
Study TypeINTERVENTIONAL
ConditionsAdvanced/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)

StatusRecruiting
PhasePhase 2
SponsorRegeneron Pharmaceuticals
Enrollment300
Study TypeINTERVENTIONAL
ConditionsAdvanced/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…

NCT07431827 — MK-3475A±Calderasib (MK-1084) in Completely Resected Stage IIA-IIIB (N2) KRAS G12Cm NSCLC (MK-1084-013)

StatusRecruiting
PhasePhase 3
SponsorMerck Sharp & Dohme LLC
Enrollment400
Study TypeINTERVENTIONAL
ConditionsNon-small Cell Lung Cancer
Interventions; ;

This is a phase 3, randomized, double-blind study of adjuvant calderasib plus subcutaneous pembrolizumab and berahyaluronidase alfa (MK-3475A) versus adjuvant placebo plus MK-3475a in participants with completely resected stage IIA-IIIB (N2), KRAS G12C-mutant non-small cell lung cancer following receipt of either neoadjuvant pembrolizumab plus chemotherapy or adjuvant chemotherapy. The primary …

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

StatusRecruiting
PhaseEarly Phase 1
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Enrollment36
Study TypeINTERVENTIONAL
ConditionsMetastatic 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

StatusRecruiting
PhasePhase 2
SponsorFundación GECP
Enrollment37
Study TypeINTERVENTIONAL
ConditionsLimited-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…

NCT07314216 — Firmonertinib Combined With Definitive Radiotherapy in Stage III Unresectable EGFR Uncommon Mutant Pulmonary Adenocarcinoma

StatusRecruiting
PhasePhase 2
SponsorHunan Cancer Hospital
Enrollment15
Study TypeINTERVENTIONAL
ConditionsNSCLC (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…

NCT07546981 — Efficacy and Safety of CHF 5993 100/6/12.5 μg HFA-152a pMDI in Patients With Asthma Uncontrolled on Medium Doses of Inhaled Corticosteroids in Combination With Long-acting ß2-agonists

StatusRecruiting
PhasePhase 3
SponsorChiesi Farmaceutici S.p.A.
Enrollment554
Study TypeINTERVENTIONAL
ConditionsAsthma
Interventions;

This is a study comparing CHF 5993 pMDI HFA-152a with CHF 1535 pMDI HFA-134a in Chinese patients with asthma uncontrolled on medium doses of ICS+LABA.

NCT07117214 — A Phase I Study of [68Ga]Ga-DWJ155 in Patients With Breast and Lung Cancers

StatusRecruiting
PhasePhase 1
SponsorNovartis Pharmaceuticals
Enrollment36
Study TypeINTERVENTIONAL
ConditionsBreast Neoplasms; Carcinoma, Non-Small-Cell Lung
Interventions

This is a phase I, open label first in human study to evaluate the imaging performance, safety, biodistribution and pharmacokinetics of [68Ga]Ga-DWJ155 in patients ≥ 18 years of age with hormone receptor positive/HER2 negative (HR+/HER2-) and HER2 positive (HER2+) advanced breast cancer (aBC) and advanced Non-Small Cell Lung Cancer (aNSCLC) adenocarcinoma.

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)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsNon-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…

NCT07388524 — Testing the Impact of an Anti-Cancer Drug, Atezolizumab, After Surgery to Prevent Early Stage Non-small Cell Lung Cancer From Returning, AASI-NSCLC Trial

StatusRecruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment336
Study TypeINTERVENTIONAL
ConditionsLung Non-Small Cell Carcinoma
Interventions; ;

This phase III trial compares the effect of atezolizumab (or atezolizumab and recombinant human hyaluronidase) to standard observation for preventing cancer return after surgery (recurrence) in patients who have undergone a complete surgical removal (resection) of stage I non-small cell lung cancer (NSCLC). Patients who have undergone resection for lung cancer are typically followed by observat…

Active, Not Recruiting

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

StatusActive, not recruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment138
Study TypeINTERVENTIONAL
ConditionsMetastatic 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

StatusActive, not recruiting
PhasePhase 1
SponsorMayo Clinic
Enrollment56
Study TypeINTERVENTIONAL
ConditionsAnaplastic 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…

NCT04212416 — Leflunomide in Treating Patients With Steroid Dependent Chronic Graft Versus Host Disease

StatusActive, not recruiting
PhasePhase 1
SponsorCity of Hope Medical Center
Enrollment18
Study TypeINTERVENTIONAL
ConditionsChronic 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…

NCT05003037 — Surufatinib Combined With Toripalimab and Chemotherapy in the Treatment of Non-Small Cell Lung Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorLi Zhang, MD
Enrollment106
Study TypeINTERVENTIONAL
ConditionsNon 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.

NCT05851443 — A Study to Evaluate the Efficacy and Safety Study of Povorcitinib in Participants With Inadequately Controlled Moderate to Severe Asthma

StatusActive, not recruiting
PhasePhase 2
SponsorIncyte Corporation
Enrollment247
Study TypeINTERVENTIONAL
ConditionsModerate to Severe Asthma
Interventions; ;

The study is being conducted to evaluate the effect of 3 dosing regimens of povorcitinib on pulmonary function

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

StatusActive, not recruiting
PhasePhase 3
SponsorSichuan Kelun-Biotech Biopharmaceutical Co., Ltd.
Enrollment432
Study TypeINTERVENTIONAL
ConditionsNon-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

NCT07689786 — Effects of Using Miswak in Addition to Oral Hygiene Products in Patients With Gingivitis

StatusNot yet recruiting
PhaseN/A
SponsorMustafa Kemal University
Enrollment36
Study TypeOBSERVATIONAL
ConditionsGingivitis; Chronic
Interventions;

This pilot study aims to evaluate the effects of miswak use on the oral biological environment by comparing biochemical parameters obtained from saliva and dental plaque samples collected from individuals who use miswak and controls. A total of 36 healthy volunteers will be enrolled in the study, including 18 miswak+rutine oral hygiene products users and 18 rutine oral hygiene products.

Period…

NCT07509034 — Autologous B7-H3 Chimeric Antigen Receptor T Cells in Previously Treated Extensive-Stage Small Cell Lung Cancer With Recurrent or Refractory Disease

StatusNot yet recruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment40
Study TypeINTERVENTIONAL
ConditionsExtensive-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…

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.

StatusNot yet recruiting
PhaseN/A
SponsorNatera, Inc.
Enrollment920
Study TypeINTERVENTIONAL
ConditionsNSCLC (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

StatusNot yet recruiting
PhaseN/A
SponsorAlireza Mansouri
Enrollment77
Study TypeINTERVENTIONAL
ConditionsLeptomeningeal 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…

Completed Trials

NCT00001888 — Sample Collections From the Airways of Asthmatic Patients

StatusCompleted
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment574
Study TypeOBSERVATIONAL
ConditionsAsthma

Fiberoptic bronchoscopy is a procedure which involves passing a pencil-thin tube into the lung in order to collect fluid and cells from the airways. Fiberoptic bronchoscopy can collect cells from the walls of airways by gently brushing them (bronchial brushing). In addition, squirting small amounts of sterile water in to the airway and gently suctioning it back into the bronchoscope (bronchoalv…

NCT00720785 — Natural Killer Cells and Bortezomib to Treat Cancer

StatusCompleted
PhasePhase 1
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment35
Study TypeINTERVENTIONAL
ConditionsChronic 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

NCT01264055 — Cross-sectional Characterization of Idiopathic Bronchiectasis

StatusCompleted
PhaseN/A
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment275
Study TypeOBSERVATIONAL
ConditionsInfection; Bronchial Diseases; Respiratory Tract Diseases

Background:

- Bronchiectasis is a type of lung condition in which the lungs airways are abnormally stretched and widened. This stretching and widening makes it difficult for mucus and other substances to move out of the lungs, encouraging the growth of bacteria and leading to breathing problems or infection. Bronchiectasis can be caused by genetic disorders or diseases such as tuberculosis or…

NCT01352962 — Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors

StatusCompleted
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment18
Study TypeINTERVENTIONAL
ConditionsUrethral 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

StatusCompleted
PhasePhase 3
SponsorJohns Hopkins University
Enrollment1032
Study TypeINTERVENTIONAL
ConditionsChronic 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.

NCT04487756 — Combination of Atezolizumab With Dendritic Cell Vaccine in Patients With Lung Cancer

StatusCompleted
PhasePhase 1 / Phase 2
SponsorInstituto Oncológico Dr Rosell
Enrollment20
Study TypeINTERVENTIONAL
ConditionsExtensive-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…

NCT04905316 — A Study of Canakinumab With Chemotherapy, Radiation Therapy, and Durvalumab in People With Lung Cancer

StatusCompleted
PhasePhase 2
SponsorMemorial Sloan Kettering Cancer Center
Enrollment41
Study TypeINTERVENTIONAL
ConditionsNon-small Cell Lung Cancer
Interventions; ;

The researchers are doing this study to find out whether canakinumab in combination with chemoradiation and durvalumab is an effective and safe treatment for people with locally advanced non-small cell lung cancer (NSCLC).

Other (Suspended)

NCT04585477 — Adjuvant ctDNA-Adapted Personalized Treatment in Early Stage NSCLC (ADAPT-E)

StatusSuspended
PhasePhase 2
SponsorStanford University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsNon-small Cell Lung Cancer; Non-small Cell Lung Cancer Stage I; Non-small Cell Lung Cancer Stage II; Non-small Cell Lung Cancer Stage III
Interventions; ;

In this study circulating tumor DNA (ctDNA) blood testing is used to detect the residual blood cancer. If residual cancer using this blood test is detected there may be at higher risk of having the cancer return. The study is going to test whether or not the number of circulating cancer cells detected in the blood can be reduced by administration durvalumab after the standard treatment if you a…

Other (Terminated)

NCT06466187 — A Study of SGN-MesoC2 in Advanced Solid Tumors

StatusTerminated
PhasePhase 1
SponsorSeagen, a wholly owned subsidiary of Pfizer
Enrollment19
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Non-Small-Cell Lung; Ovarian Neoplasms; Pancreatic Adenocarcinoma; Colorectal Neoplasms; Mesothelioma
Interventions

This clinical trial is studying advanced solid tumors. Solid tumors are cancers that start in a part of your body like your lungs or liver instead of your blood. Once tumors have grown bigger in one place but haven’t spread, they’re called locally advanced. If your cancer has spread to other parts of your body, it’s called metastatic. When a cancer has gotten so big it can’t easily be removed o…

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

StatusSuspended
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment30
Study TypeINTERVENTIONAL
ConditionsNon-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…