BridgeMD
New treatment option for Non Small Cell Lung Cancer
Official title Immuno-effect of Tα1 for Stage I NSCLC
ClinicalTrials.gov ID: NCT06598839
What this study is testing
What is Thymosin Alpha1?
Thymosin Alpha1 is an investigational medicine, given as an injection under the skin, being studied as a potential treatment for non small cell lung cancer.
Also referred to as Tα1, Thymalfasin.
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
- To explore the effect of thymosin alpha 1 (Tα1) on postoperative peripheral blood circulating tumor cells and immunosenescence in patients with early-stage non-small cell lung cancer (NSCLC).
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 75
You may be able to join if
- Pathologically confirmed stage I (per AJCC 8th edition) invasive NSCLC
- Resectable tumor
- undergoing lobectomy and systemic lymph node dessection
- Without a previous history of malignant tumors or other concurrent malignancies
- Naïve to any anticancer therapies or other immunostimulatory agents
You likely can't join if
- With a pathologically confirmed non-invasive NSCLC, including preinvasive lesions, small cell lung cancer, and benign lesions
- Post-diagnostic use of immunosuppressive medications or other immunostimulatory agents
- With known or suspected active autoimmune disease
- Allergic to thymopeptides
- With other uncontrolled serious illnesses or having acute or chronic conditions that may confound test outcomes, including active severe clinical...
See the full eligibility criteria
- Pathologically confirmed stage I (per AJCC 8th edition) invasive NSCLC
- Resectable tumor
- undergoing lobectomy and systemic lymph node dessection
- Without a previous history of malignant tumors or other concurrent malignancies
- Naïve to any anticancer therapies or other immunostimulatory agents
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) score 0-1, with cardiac, pulmonary, hepatic, cerebral, and renal functions capable of withstanding surgery
- Aged ≥18 years and ≤75 years
- Having signed written informed consent and capable of adhering to the visit schedule and related procedures outlined in the study protocol
- With a pathologically confirmed non-invasive NSCLC, including preinvasive lesions, small cell lung cancer, and benign lesions
- Post-diagnostic use of immunosuppressive medications or other immunostimulatory agents
- With known or suspected active autoimmune disease
- Allergic to thymopeptides
- With other uncontrolled serious illnesses or having acute or chronic conditions that may confound test outcomes, including active severe clinical infections ( \>NCI-CTCAE grade 2 infection); diagnosed with epilepsy...
The study team makes the final eligibility decision.
Where it's taking place
- Beijing, Beijing Municipality, 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 to 75 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Beijing, Beijing Municipality, 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.