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NCT04846634Not yet recruitingPhase 2

Penpulimab-based Combination Neoadjuvant/Adjuvant Therapy for Patients With Resectable Locally Advanced Non-small Cell Lung Cancer: a Phase II Clinical Study (ALTER-L043)

Source: ClinicalTrials.gov · Last updated 15 Apr 2021 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a multicenter, randomized, open label, phase II study.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
First submitted
14 Apr 2021
Start date
Aug 2021
Primary completion date
Mar 2023
Lead sponsor
Tianjin Medical University Cancer Institute and Hospital
Diseases
Lung cancer
NCT number
NCT04846634

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 90
  • From Aug 2021 to the primary completion date, Mar 2023
  • 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

  • Prior treatment with local radiotherapy.
  • Prior treatment with any drug that targets T cell co-stimulations pathways (such as checkpoint inhibitors).
  • Prior treatment with antilotinib and other antiangiogenic drugs.
  • Patients with multiple factors affecting oral medication (e.g. inability to swallow, chronic diarrhea, and intestinal obstruction, etc.).

Other illness

  • Large cell carcinoma and mixed cell lung cancer.
  • Any systemic anti-cancer treatment for NSCLC, including cytotoxic drug therapy, immunotherapy, experimental treatment.
  • History of hypersensitivity to any active or inactive ingredient of Penpulimab, Anlotinib or chemotherapy.
  • Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis that required steroid treatment, or any evidence of clinically active interstitial lung disease.
  • Patients whose tumor has invaded important blood vessels or whose tumor is likely to invade important blood vessels and cause fatal massive hemorrhage during follow-up study.
  • Patients who have had arteriovenous thrombosis events within 6 months, such as cerebrovascular accident (including transient ischemic attack), deep venous thrombosis and pulmonary embolism.
  • History of neurological or mental disorders, including epilepsy or dementia.

Other

  • Pregnant or lactating women.

Who the study is looking for

  • Early stage IIB-IIIB (N2), operable non-small cell lung cancer, confirmed in tissue.
  • Epidermal growth factor receptor/anaplastic lymphoma kinase/ROS1 gene fusions mutation was negative in primary tumor or lymph node metastasis.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1 with no deterioration over the previous 2 weeks and a minimum life expectancy of 12 weeks.
  • Lung function capacity capable of tolerating the proposed lung surgery.
  • Patients had never received surgery, chemotherapy, radiotherapy or biotherapy.

Age in the registry: 18 years to 70 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 NanChang University
Coordinator of this site? Confirm its status
NanchangChinaUnknown status

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