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NCT06440954RecruitingPhase 2

Efficacy and Resistance Mechanisms of IP in NSCLC With Leptomeningeal Metastases

To Investigate the Efficacy and Resistance Mechanisms of Intrathecal Pemetrexed in Advanced Non-small Cell Lung Cancer (NSCLC) Patients Harboring Oncogenic Mutations With Leptomeningeal Metastases

Source: ClinicalTrials.gov · Last updated 4 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective interventional study clinical study to investigate the efficacy and resistance mechanisms of intrathecal pemetrexed in patients with driver gene mutations advanced NSCLC with leptomeningeal metastases.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
220 (estimated)
First submitted
23 Apr 2024
Start date
1 May 2024
Primary completion date
31 Dec 2026
Lead sponsor
Hunan Province Tumor Hospital
Diseases
Lung cancer
NCT number
NCT06440954

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 220
  • From 1 May 2024 to the primary completion date, 31 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

  • Previously received intrathecal pemetrexed therapy for locally advanced or metastatic disease.
  • Subjects who have received any of the following treatments must be excluded:
    • Have received radiation within 14 days prior to the first dose or have not recovered from radiation-related toxicity. Chest and extra-brain palliative radiotherapy, stereotactic radiosurgery, and stereotactic body radiotherapy may be performed 7 days prior to the first dose.
  • Adverse events (except alopecia of any degree) of CTCAE \> grade 1 due to prior treatment (e.g., adjuvant chemotherapy, radiotherapy, etc.) prior to the first dose.
  • History of stroke or intracranial hemorrhage within 6 months prior to the first dose.
  • Refractory nausea and vomiting, chronic gastrointestinal disease, difficulty swallowing drugs, or inability to adequately absorb sunvozertinib or anlotinib due to previous bowel resection.
  • Live vaccine was given 2 weeks before the first medication.

Other illness

  • History of other malignant tumors within 2 years.
  • The presence of any severe or poorly controlled systemic disease, including poorly controlled hypertension and active bleeding in the judgment of the investigator.
  • Subjects with persistent or active infection, including but not limited to hepatitis B (HBV), hepatitis C (HCV), human immunodeficiency virus (HIV) and COVID-19 infection.
  • Heart-related diseases or abnormalities
  • Past history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis requiring steroid therapy or interstitial lung disease with active clinical symptoms, immune pneumonia caused by immunotherapy.
  • Hypersensitivity to the test drug and the ingredients.
  • Other conditions assessed by the investigator to be unsuitable for participation in the study.

Other

  • Presence of spinal cord compression or meningeal metastasis.
  • Women who are breastfeeding or pregnant.

Who the study is looking for

  • Age ≥ 18 years.
  • Histopathology or cytology confirmed metastatic non-small cell lung cancer with leptomeningeal metastasis after TKI resistant.
  • EGFR mutant, ALK fusion, ROS1 fusion, and other oncogenic alterations including RET fusion, BRAF mutation, NTRK fusion, KRAS mutation was confirmed by an accredited local laboratory.
  • Adequate bone marrow hematopoiesis and organ function
  • Agree to receive intrathecal pemetrexed
  • ECOG 0 - 2.
  • Predicted survival ≥ 12 weeks.

Age in the registry: 18 years to - · 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
Hunan Cancer Hospital
Coordinator of this site? Confirm its status
ChangshaChinaRecruiting

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