Cancer Lung

5

Review clinical trials related to Cancer Lung. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Feasibility Study of Personalized Ultra-fractionated Stereotactic Ablative Radiotherapy (PULSAR) for Cancers of the Central Lung

The objective of this study is to enhance the safety profile of SAbR in ultra-central tumors of the lung (primary or metastatic) without compromising its effectiveness.

Participants needed: 30
Trial details
Phase: Early Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years of age. [+8]

Prior radiotherapy to the region of the study cancer that would result in overla... [+3]

Status: Recruiting

A Phase 1 Study of CPO301 in Adult Patients With Advanced or Metastatic Solid Tumors

The goal of this clinical trial is to test CPO301, a type of drug called an antibody drug conjugate in adult patients with advanced or metastatic solid tumors. The main questions it aims to answer are: * To assess the safety and tolerability of CPO301 at increasing doses and determine the dose to be used in the second part of the study (Part A) * To assess the safety and tolerability of CPO301 at the dose determined to be safe and tolerable in Part A in patients with Non-Small Cell Lung Cancer and potentially other tumor types (Part B) * To evaluate how quickly CPO301 is metabolized by the body (pharmacokinetics or PK) * To evaluate if antibodies to the study drug develop (immunogenicity) * To evaluate preliminary efficacy to the drug * To correlate preliminary efficacy with mutations in a biomarker called EGFR Participants will: * Provide written informed consent * Undergo screening tests to ensure they are eligible for study treatment * Attend all required study visits and receive CPO301 by intravenous injection every 3 weeks until the study doctor determines study treatment should be stopped, based on how well a participant is doing on treatment * Be followed for progression every 3 months for up to 2 years

Participants needed: 132
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Conjupro Biotherapeutics, Inc.Updated: Mar 20, 2026Locations: 14
Eligibility criteria

Age ≥18 years [+6]

Known, active, or uncontrolled central nervous system (CNS) metastasis or carcin... [+5]

Status: Recruiting

Precision Lung Cancer Survivorship Care Intervention

The overarching goal of the Kentucky LEADS Collaborative Lung Cancer Survivorship Care program is to reduce the burden of lung cancer by offering an innovative survivorship care approach that improves lung cancer quality of life, overcomes lung cancer stigma, and helps survivors engage with care. The project involves a two-group parallel randomized clinical trial comparing the impact of the Kentucky LEADS Collaborative Lung Cancer Survivorship Care program (KLCLCSC) among lung cancer survivors (N=300) against an enhanced usual care condition (bibliotherapy+assessment) on quality of life outcomes.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Jerod L Stapleton, PhDUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Have been diagnosed with lung cancer [+3]

Have significant psychiatric disturbance that requires a higher level of care [+3]

Status: Recruiting

Exploration of Circulating microRNAs as Biomarkers of Chemo-induced Peripheral Neuropathy: a Study in Cancer Patients

This study aims to find out whether certain molecules in the blood, called microRNAs, are linked to how often and how severely people develop nerve damage from chemotherapy. The investigators will look at patients receiving cancer drugs known to affect the nerves, such as paclitaxel (used for lung cancer) and oxaliplatin (used for colorectal cancer).

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, Clermont-FerrandUpdated: Feb 23, 2026Locations: 1
Eligibility criteria

Patient treated for colorectal cancer and scheduled to receive oxaliplatin-based... [+1]

Neurodegenerative disease (e.g., Parkinson's, Alzheimer's, etc.), [+5]

Status: Recruiting

SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry

International registry for cancer patients evaluating the feasibility and clinical utility of an Artificial Intelligence-based precision oncology clinical trial matching tool, powered by a virtual tumor boards (VTB) program, and its clinical impact on pts with advanced cancer to facilitate clinical trial enrollment (CTE), as well as the financial impact, and potential outcomes of the intervention.

Participants needed: 50,000
Trial details
Biological sex: AllType: ObservationalSponsor: Massive Bio, Inc.Updated: Oct 28, 2025Locations: 68Duration: 36 Months
Eligibility criteria

Pts with solid and hematological malignancies; [+2]

ECOG PS > 2; [+2]