Clinical Trials for Non-Small Cell Lung Cancer

A Phase I-II, First-in-Human Study of SKB264 in Patients With Locally Advanced Unresectable /Metastatic Solid Tumors Who Are Refractory to Available Standard Therapies

Active drug

Investigational drug(s) in this trial have shown anticancer activity in clinical trials

High burden on patient

The trial has a high burden on patients. An example would be a phase 1 trial with extra tumor biopsies and frequent pharmacokinetic blood draws.

Started >3 years ago

The trial was activated more than 3 years ago. This is not always bad but can indicate that the trial has less current treatments, or has had trouble getting enough patients to enroll due to other issues.

HealthScout AI summary: The trial investigates SKB264, an antibody-drug conjugate targeting TROP2, in adult patients aged 18-75 with advanced solid tumors unresponsive to standard treatments, including specific interests like triple-negative breast and non-small cell lung cancers. The study aims to determine safety, efficacy, and recommended dosing of SKB264, focusing on cancers where TROP2 is prevalent.

ClinicalTrials.gov ID: NCT04152499

An Open Label, Phase 1, Treatment Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of IDE397 (MAT2A Inhibitor) In Adult Participants With Advanced Solid Tumors

Active drug

Investigational drug(s) in this trial have shown anticancer activity in clinical trials

High burden on patient

The trial has a high burden on patients. An example would be a phase 1 trial with extra tumor biopsies and frequent pharmacokinetic blood draws.

Started >3 years ago

The trial was activated more than 3 years ago. This is not always bad but can indicate that the trial has less current treatments, or has had trouble getting enough patients to enroll due to other issues.

HealthScout AI summary: This trial evaluates the safety and preliminary anti-tumor activity of IDE397, a MAT2A inhibitor, in adult patients with MTAP-deleted advanced solid tumors, either as monotherapy or in combination with docetaxel, paclitaxel, or sacituzumab govitecan. Eligible patients must have advanced or metastatic solid tumors that have failed at least one prior treatment line.

ClinicalTrials.gov ID: NCT04794699

Phase I Study to Evaluate Safety, Tolerability, Pharmacokinetics and Anti-Tumor Activity of WSD0922-FU

Active drug

Investigational drug(s) in this trial have shown anticancer activity in clinical trials

High burden on patient

The trial has a high burden on patients. An example would be a phase 1 trial with extra tumor biopsies and frequent pharmacokinetic blood draws.

Started >3 years ago

The trial was activated more than 3 years ago. This is not always bad but can indicate that the trial has less current treatments, or has had trouble getting enough patients to enroll due to other issues.

HealthScout AI summary: This trial evaluates the safety, tolerability, and anti-tumor activity of WSD0922-FU, an EGFR/EGFRvIII inhibitor, in patients with recurrent glioblastoma, anaplastic astrocytoma, and EGFR-mutant non-small cell lung cancer with CNS metastases. It involves dose-escalation to identify the maximum tolerated dose, focusing on patients with progressive disease and specific inclusion criteria.

ClinicalTrials.gov ID: NCT04197934

A Phase II Study of the Effects of Pembrolizumab on Quality of Life for Patients With Treatment-Naïve, Advanced or Metastatic NSCLC and Poor Performance Status

Moderate burden on patient

The trial has a moderate burden on patients. An example would be a trial testing an IV drug, with scans every 8 weeks which would be more frequent than standard of care.

HealthScout AI summary: This trial evaluates the effects of pembrolizumab on quality of life in treatment-naïve patients with advanced or metastatic NSCLC and poor performance status (ECOG 2 or 3) with a PD-L1 TPS ≥ 1%, who are unsuitable for standard treatments. Pembrolizumab, a PD-1 inhibitor, reactivates T-cells, aiming to improve outcomes and manage toxicity in this specific patient population.

ClinicalTrials.gov ID: NCT05589818

Pragmatica-Lung: A Prospective Randomized Study of Ramucirumab (LY3009806; NSC 749128) Plus Pembrolizumab (MK-3475; NSC 776864) Versus Standard of Care for Participants Previously Treated With Immunotherapy for Stage IV or Recurrent Non-Small Cell Lung Cancer

Moderate burden on patient

The trial has a moderate burden on patients. An example would be a trial testing an IV drug, with scans every 8 weeks which would be more frequent than standard of care.

HealthScout AI summary: This trial involves patients with stage IV or recurrent non-small cell lung cancer who have progressed despite prior anti-PD-1/PD-L1 therapy and platinum-based chemotherapy, comparing a novel combination of ramucirumab, a VEGFR-2 inhibitor, and pembrolizumab, a PD-1 inhibitor, against standard chemotherapy to evaluate overall survival benefits.

ClinicalTrials.gov ID: NCT05633602

Phase II Trial of Thoracic Radiotherapy for Patients With Metastatic (Stage IV) Non-Small Cell Lung Cancer at High Risk of Symptomatic Progression Within the Thorax

Moderate burden on patient

The trial has a moderate burden on patients. An example would be a trial testing an IV drug, with scans every 8 weeks which would be more frequent than standard of care.

HealthScout AI summary: This trial targets patients with Stage IV NSCLC who have high-risk thoracic lesions and lack targetable mutations such as EGFR or ALK, evaluating the efficacy of prophylactic palliative thoracic radiotherapy in combination with standard systemic therapies like chemotherapy or immunotherapy to prevent symptomatic progression in the thorax.

ClinicalTrials.gov ID: NCT06262321

A Randomized Study of Two Dosing Regimens of Adagrasib in Patients With Previously Treated Non-Small Cell Lung Cancer With KRAS G12C Mutation

Moderate burden on patient

The trial has a moderate burden on patients. An example would be a trial testing an IV drug, with scans every 8 weeks which would be more frequent than standard of care.

HealthScout AI summary: This trial involves adult patients with advanced or metastatic non-small cell lung cancer harboring the KRAS G12C mutation who have previously been treated with platinum-based chemotherapy and immune checkpoint inhibitors, assessing two dosing regimens of adagrasib, an oral covalent inhibitor targeting the KRAS G12C mutation.

ClinicalTrials.gov ID: NCT05853575

A First-in-Human, Multicenter, Open-Label, Phase 1 Dose-Escalation and Cohort Expansion Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TAB004 as Monotherapy and in Combination With Toripalimabin Subjects With Advanced Solid Malignancies Including Lymphoma

Active drug

Investigational drug(s) in this trial have shown anticancer activity in clinical trials

High burden on patient

The trial has a high burden on patients. An example would be a phase 1 trial with extra tumor biopsies and frequent pharmacokinetic blood draws.

Started >3 years ago

The trial was activated more than 3 years ago. This is not always bad but can indicate that the trial has less current treatments, or has had trouble getting enough patients to enroll due to other issues.

HealthScout AI summary: The trial is enrolling adults with advanced, unresectable, or metastatic solid tumors, including lymphoma, who have progressed after prior treatments, to evaluate the safety and tolerability of TAB004, a monoclonal antibody targeting BTLA, as monotherapy and in combination with toripalimab, an anti-PD-1 antibody.

ClinicalTrials.gov ID: NCT04137900

A Phase 1 Study of SGN-B6A in Advanced Solid Tumors

Active drug

Investigational drug(s) in this trial have shown anticancer activity in clinical trials

High burden on patient

The trial has a high burden on patients. An example would be a phase 1 trial with extra tumor biopsies and frequent pharmacokinetic blood draws.

Started >3 years ago

The trial was activated more than 3 years ago. This is not always bad but can indicate that the trial has less current treatments, or has had trouble getting enough patients to enroll due to other issues.

HealthScout AI summary: This trial assesses the safety and efficacy of sigvotatug vedotin, an investigational drug targeting integrin beta-6, alone and combined with pembrolizumab and chemotherapy, in patients with various advanced solid tumors like NSCLC, head and neck cancer, and HER2-negative breast cancer. It includes participants either treatment-naïve or those who have relapsed from standard therapies, in a non-randomized, dose-escalation and expansion design.

ClinicalTrials.gov ID: NCT04389632

A Phase II Trial of Cemiplimab Alone for Untreated Brain Metastases From PD-L1 ≥ 50% Non-Small Cell Lung Cancer

Moderate burden on patient

The trial has a moderate burden on patients. An example would be a trial testing an IV drug, with scans every 8 weeks which would be more frequent than standard of care.

HealthScout AI summary: This trial involves patients aged 18 and older with advanced non-small cell lung cancer (NSCLC) exhibiting PD-L1 expression levels ≥ 50%, who have untreated brain metastases measuring 5-15 mm and no EGFR, ALK, or ROS1 aberrations, and evaluates the efficacy of cemiplimab, a PD-1 blocking monoclonal antibody, administered as monotherapy without upfront radiation.

ClinicalTrials.gov ID: NCT05840770