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NCT06607796RecruitingPhase 3

Efficacy and Safety of Intratumoral Toluenesulfonamide (PTS) Injection in Stage IV Driver Gene-Negative NSCLC With/Without Chemoimmunotherapy

A Multicenter Study of the Efficacy and Safety of Intratumoral Injection of Toluenesulfonamide (PTS) in Combination With or Without First-line Chemoimmunotherapy Based on Standard Treatment for Stage IV Driver Gene-negative Non-small Cell Lung Cancer

Source: ClinicalTrials.gov · Last updated 25 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of this study was to evaluate the efficacy and safety of intratumoral injection of toluenesulfonamide(PTS) in combination with or without first-line chemoimmunization based on standard treatment for stage IV driver gene-negative non-small cell lung cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
180 (estimated)
First submitted
18 Sept 2024
Start date
1 Mar 2024
Primary completion date
Dec 2026
Lead sponsor
Zhou Chengzhi
Diseases
Lung cancer
NCT number
NCT06607796

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 180
  • From 1 Mar 2024 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Plans for radiotherapy, surgery, etc. for the lesion after intratumor injection;

Other illness

  • Have severe cardiopulmonary dysfunction, advanced hepatic or renal insufficiency, malignant cardiac arrhythmia, hypertension, etc;
  • Have severe bleeding, clotting disorders, infections, dehydration, etc;
  • Have blood disorders, autoimmune diseases, cirrhosis of the liver, etc;
  • History of severe emphysema and pulmonary alveoli;
  • History of drug allergy or contraindication to toluene sulfonamide;
  • The investigators determined that the patients had other conditions that made them unsuitable for enrollment.

Other

  • Women who are pregnant, breastfeeding, or planning to become pregnant during the study period;

Who the study is looking for

  • Fully understand, be informed about the study and sign the Informed Consent Form (ICF); be willing to follow and be capable of completing all trial procedures;
  • Age ≥18 years and ≤75 years at the time of signing the ICF;
  • Histologically or cytologically confirmed stage IV (AJCC 8th edition) driver gene negative non-small cell lung cancer;
  • At least one measurable target lesion assessed by the investigator according to the requirements of RECIST 1.1 within 4 weeks prior to enrollment, except for lesions proposed for percutaneous PTS local injection;
  • Localized injectable lesions located in a more confined area of the outer lung bands, less than or equal to 5 cm in diameter; these may be primary lesions that are not amenable to surgical resection or localized recurrent lesions after surgical resection and radiotherapy treatment;
  • ECOG PS score of 0 or 1 within 7 days prior to local treatment tolerates PTS intratumoral injections;
  • Patients with localized lesions present and persistently stable (SD evaluated after two courses of treatment) after standard treatment with first-line chemoimmunotherapy;
  • Life expectancy ≥ 3 months;
  • Normal liver, kidney and heart function, normal blood routine, blood biochemistry, coagulation function and electrolytes and other physiological indicators.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.