Recruiting PHASE2 Non-Small Cell Lung Cancer(NSCLC)

New treatment option for Non-Small Cell Lung Cancer(NSCLC)

Official title Neoadjuvant WX-0593 in Resectable ALK-positive or ROS1-positive Non-small Cell Lung Cancer

ClinicalTrials.gov ID: NCT05765877

What this study is testing

What is WX-0593 Tablets?

WX-0593 Tablets is an investigational medicine, given as an once-daily pill taken by mouth, being studied as a potential treatment for non-small cell lung cancer(nsclc).

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This is a single-arm, exploratory trial to evaluate the efficacy and safety of neoadjuvant WX-0593 in patients with resectable ALK-positive or ROS1- positive non-small cell lung cancer(NSCLC).
  • Phase 2: a mid-size study of how well it works

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Histologically confirmed non-small cell lung cancer (NSCLC).
  • ALK-positive or ROS1-positive NSCLC in Stage IB-IIIA (according to the 8th American Joint Committee on Cancer TNM edition), as assessed by...
  • Complete surgical resection of the primary NSCLC must be deemed achievable, as assessed by a MDT evaluation (which should include a thoracic surgeon...
  • ECOG Performance Status of 0-1.
  • At least one measurable lesion according to RECIST 1.1.

You likely can't join if

  • Prior treatment with any systemic anti-cancer therapy for NSCLC including chemotherapy, biologic therapy, immunotherapy, or any investigational drug.
  • Prior treatment with ALK TKI or ROS1 TKI.
  • Prior treatment with local radiotherapy.
  • Mixed small cell and NSCLC histology.
  • Patients who are candidates to undergo only segmentectomies or wedge resections.
See the full eligibility criteria
Who can join
  • Histologically confirmed non-small cell lung cancer (NSCLC).
  • ALK-positive or ROS1-positive NSCLC in Stage IB-IIIA (according to the 8th American Joint Committee on Cancer TNM edition), as assessed by investigator.
  • Complete surgical resection of the primary NSCLC must be deemed achievable, as assessed by a MDT evaluation (which should include a thoracic surgeon, specialized in oncologic procedures).
  • ECOG Performance Status of 0-1.
  • At least one measurable lesion according to RECIST 1.1.
  • Adequate organ and marrow function.
What rules you out
  • Prior treatment with any systemic anti-cancer therapy for NSCLC including chemotherapy, biologic therapy, immunotherapy, or any investigational drug.
  • Prior treatment with ALK TKI or ROS1 TKI.
  • Prior treatment with local radiotherapy.
  • Mixed small cell and NSCLC histology.
  • Patients who are candidates to undergo only segmentectomies or wedge resections.

The study team makes the final eligibility decision.

Where it's taking place

  • Jinan, Shandong, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Jinan, Shandong, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.