Status:

UNKNOWN

MIDRIX4-LUNG Dendritic Cell Vaccine in Patients With Metastatic Non-small Cell Lung Cancer

Lead Sponsor:

University Hospital, Ghent

Collaborating Sponsors:

University Ghent

Kom Op Tegen Kanker

Conditions:

Non-small Cell Lung Cancer Metastatic

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

MIDRIX4-LUNG is a novel tetravalent autologous dendritic cell vaccine in metastatic non-small cell lung cancer patients. This first-in-human study aims to primarily establish maximal tolerated dose of...

Detailed Description

Immunotherapy, in the shape of immune checkpoint inhibitors, is transforming the therapeutic landscape of non-small cell lung cancer. Checkpoint inhibitors can deliver durable tumor regressions, howev...

Eligibility Criteria

Inclusion

  • Male and female patients older than 18 years with histologically or cytologically proven diagnosis of non-small cell lung cancer, newly diagnosed or recurrent stage IV, or stage IIIB not amenable to radical chemoradiotherapy (TNM 8th Edition), and for which no standard-of-care therapy is applicable or available at the time of enrollment
  • Documented brain metastasis must be either asymptomatic or stabilized after adequate radiotherapeutic treatment as per institutional practice
  • WHO-ECOG performance status 0 to 2 and absence of any persisting and assessable toxicity \> CTC grade 2 due to a previous therapy (e.g. brain radiotherapy)
  • Before patient registration and screening, written informed consent must be given for the interventional study and for the "Prelevation and storage of human tissues and cells" according to ICH/GCP and institutional practice.
  • Adequate organ function, including:
  • Adequate bone marrow reserve: absolute neutrophil count \> 1.5\*10E9/L, platelet count \> 100\*10E9/L, and Hb \> 9.0 g/dL
  • Sufficient renal function as defined by eGFR \> 40 ml/min
  • Sufficient hepatic function as defined by total bilirubin ≤1.5× ULN OR direct bilirubin within normal limits for participants with total bilirubin levels \>1.5× ULN; AST and ALT ≤ 2.5x ULN
  • Having passed all tests defined in the institutional Leukapheresis Donor Fitness Screening, including:
  • Adequate peripheral vein access to perform leukapheresis
  • Adequate coagulation function defined as international normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN and activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless the participant is receiving anticoagulant therapy
  • Negative test results for HBs-antigen, anti-HBc-serology, anti-HCV serology, anti-HIV1-2 serology, anti-CMV IgM, anti-Syphilis (Treponema pallidum) serology
  • Negative test results for Epstein-Barr virus (IgG and IgM) and for toxoplasmosis (IgG and IgM)
  • For female participants: a negative serum beta-HCG test result less than 1 week before the day of leukapheresis
  • For female participants with child-bearing potential, the willingness to follow contraceptive guidance and pregnancy testing during the projected duration of the trial (see Appendix B for Contraceptive Guidance and Pregnancy Testing)
  • For male participants having a partner with child-bearing potential: agreement to use contraception during the projected duration of the trial, starting with the screening visit through 90 days after the last dose of trial treatment. Sperm donation must have been performed before anti-cancer treatment as per standard practice

Exclusion

  • Presence of oncogenic driver genomic alterations for which a targeted therapy is available
  • Concomitant participation in another clinical interventional trial
  • Prior treatment with autologous or allogeneic dendritic cell-based vaccines
  • NSCLC with large-cell neuro-endocrine or sarcomatoid histology
  • Prior malignancy, except for adequately treated basal cell, superficial or in situ cancer of the bladder or the cervix, or other cancer for which the patient has been disease-free for at least five years.
  • Dermatological pathology interfering with the in vivo immunomonitoring readout (DTH skin test)
  • Untreated brain metastases with neurological symptoms or brain metastasis requiring a daily intake of steroids of \> 10 mg oral prednisolone or equivalent.
  • Disease requiring chronic treatment with systemic glucocorticosteroids with a daily dose \> 10 mg oral prednisolone or equivalent, or other immunosuppressive drugs. Inhaled corticosteroids and topical corticosteroids on skin sites other than those used for DTH are allowed.
  • Chronic or active concomitant infection requiring active therapy, including including HIV, viral hepatitis (HBV, HCV), CMV or fungal infection
  • Autoimmune disease requiring active treatment at the time of the study
  • Organ allograft
  • Chronic comorbidity (such as asthma, COPD, heart failure, renal failure, arterial hypertension or diabetes mellitus) that is uncontrolled or not stabilized under medication at the time of study enrollment, OR stable yet severe enough to constitute an unwarranted high risk for the investigational cellular therapy.
  • For female participants: pregnancy or lactation, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 90 days after the last dose of trial treatment
  • Any organic brain syndrome or other significant psychiatric abnormality which would comprise the ability to give informed consent and preclude participation in the full protocol and follow-up.
  • Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.

Key Trial Info

Start Date :

August 26 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 31 2021

Estimated Enrollment :

7 Patients enrolled

Trial Details

Trial ID

NCT04082182

Start Date

August 26 2019

End Date

December 31 2021

Last Update

March 30 2021

Active Locations (1)

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1

Ghent University Hospital

Ghent, Belgium, B-9000