L-TIL in Patients With Malignancy Resistance to Anti-PD-1 Therapy

Last updated: June 10, 2020
Sponsor: Henan Cancer Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Neoplasms

Treatment

N/A

Clinical Study ID

NCT04268108
Liquid TIL
  • Ages 18-70
  • All Genders

Study Summary

Safety and effectiveness of liquid tumor infiltrating lymphocytes in patients with advanced malignant tumors who have failed to anti-PD-1 therapy

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Expected lifespan is over 3 months

  • malignant tumors diagnosed by pathological examination

  • Imaging examination is at advanced stage with at least one measurable lesion

  • Ineffective or resistant to previous anti-PD-1 therapy

  • ECOG score 0-2

  • Adequate organ function

  • No other serious diseases that conflict with this protocol

  • Women of childbearing age must check for a negative blood pregnancy test within 7days, and subjects of childbearing age must use appropriate contraception during thetest and within 3 months

  • witten informed consent from the patients

Exclusion

Exclusion Criteria:

  • Severe infectious disease within 4 weeks before enrollment

  • Active hepatitis B or C virus or HIV infection

  • Severe autoimmune disease or immunodeficiency disease

  • Severe allergies

  • Severe mental disorder

  • Systematically used a large amount of glucocorticoids within 4 weeks before enrollment

  • With severe heart, liver, kidney insufficiency, diabetes and other diseases

  • Participation in other clinical studies in the past 3 months or having been treatedwith other gene products

Study Design

Total Participants: 30
Study Start date:
April 02, 2020
Estimated Completion Date:
June 19, 2022

Connect with a study center

  • Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital

    Zhengzhou, Henan 450008
    China

    Active - Recruiting

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