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A Phase 1b Study Evaluating the Safety, Tolerability and Preliminary Anti-tumor Activity of NT-I7 (Efineptakin Alfa) a Long-acting Human IL-7, Post-Kymriah® (Tisagenlecleucel), Post-Yescarta® (Axicabtagene Ciloleucel), or Post-Breyanzi® (Lisocabtagene Maraleucel) in Subjects With Relapsed/Refractory Large B-cell Lymphoma

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Trial Profile

A Phase 1b Study Evaluating the Safety, Tolerability and Preliminary Anti-tumor Activity of NT-I7 (Efineptakin Alfa) a Long-acting Human IL-7, Post-Kymriah® (Tisagenlecleucel), Post-Yescarta® (Axicabtagene Ciloleucel), or Post-Breyanzi® (Lisocabtagene Maraleucel) in Subjects With Relapsed/Refractory Large B-cell Lymphoma

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 03 Jan 2025

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At a glance

  • Drugs Efineptakin alfa (Primary) ; Axicabtagene ciloleucel; Lisocabtagene-maraleucel; Tisagenlecleucel
  • Indications B-cell lymphoma; Diffuse large B cell lymphoma
  • Focus Adverse reactions
  • Sponsors NeoImmuneTech

    • Most Recent Events

    • 09 Sep 2024 Interim results presented in a NeoImmuneTech media release.
    • 09 Sep 2024 According to a NeoImmuneTech media release, the company will present interim results present at the European Society for Medical Oncology (ESMO) in Barcelona, Spain, from September 13 to 17.
    • 07 Apr 2023 Primary end-points have been updated to remove efficacy end-points, thus safety or "AR" remains the only trial focus.

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