Nonconforming Lisocabtagene Maraleucel Expanded Access Protocol

Inclusion Criteria:

   1. Subject and/or LAR must understand and voluntarily sign an informed consent form prior
   to any study-related assessments/procedures being conducted.

   2. Subject has relapsed and/or refractory large B-cell lymphoma and is, per the treating
   physician assessment, eligible for treatment with lisocabtagene maraleucel per the
   approved prescribing information.

   3. Subject is ≥ 18 years of age at the time of signing the informed consent form.

   4. Subject had a specific batch of lisocabtagene maraleucel manufactured intended for
   commercial treatment; however, the final manufactured product did not meet commercial
   release criteria.

   5. Remanufacturing (eg, repeat leukapheresis and manufacturing) is deemed not feasible or
   clinically inappropriate per assessment of the treating physician in discussion with
   the subject.

   6. Subject is clinically stable, has recovered from any toxicities prior to receiving
   lymphodepleting chemotherapy, and has adequate bone marrow function to receive
   lymphodepleting chemotherapy. The treating physician is advised to contact Medical
   Monitor in the event there is any concern regarding administration of lymphodepleting
   chemotherapy.

   7. Females of childbearing potential must:

      1. Have a negative pregnancy test as verified by the treating physician within 7
      days prior to the first dose of lymphodepleting chemotherapy following
      institutional testing methodology practices. This applies even if the subject
      practices true abstinence from heterosexual contact.

      2. Either commit to true abstinence from heterosexual contact or agree to use, and
      be able to comply with, effective contraception without interruption.
      Contraception methods must include 1 highly effective method from screening until
      at least 12 months after the nonconforming lisocabtagene maraleucel
      administration.

      3. Agree to abstain from breastfeeding during study participation and for at least
      12 months following nonconforming lisocabtagene maraleucel administration.

      4. There are insufficient exposure data to provide any recommendation concerning the
      duration of contraception and the abstaining from breastfeeding following
      treatment with lisocabtagene maraleucel. Any decision regarding contraception and
      breastfeeding after infusion should be discussed with the treating physician.

   8. Male subjects must:

      1. Practice true abstinence or agree to use a condom during sexual contact with a
      pregnant female or a female of childbearing potential for at least 12 months
      after nonconforming lisocabtagene maraleucel administration even if the subject
      has undergone a successful vasectomy.

      2. There are insufficient exposure data to provide any recommendation concerning the
      duration of contraception following treatment with lisocabtagene maraleucel. Any
      decision regarding contraception after infusion should be discussed with the
      treating physician

   9. Subject must agree to not donate blood, organs, tissue, sperm or semen and egg cells
   for usage in other individuals for at least 1 year following nonconforming
   lisocabtagene maraleucel administration.

Exclusion Criteria:

   1. Subject has a hypersensitivity to the active substance or to any of the excipients.

   2. Subject should not experience a significant worsening in clinical status that would,
   in the opinion of the treating physician, either increase the risk of adverse events
   associated with lymphodepleting chemotherapy, or exclude them from treatment with
   nonconforming lisocabtagene maraleucel.

   3. Subject has any significant medical condition, laboratory abnormality, or psychiatric
   illness, sociologic or geographic condition that would prevent the subject from
   participating in the Expanded Access Protocol complying with protocol requirements in
   the Investigator's judgement.

   4. Subject has any condition and/or laboratory abnormality that places the subject at
   unacceptable risk if he/she were to participate in the Expanded Access Protocol based
   on the Investigator's judgement

   5. Pregnant or nursing women or has intention of becoming pregnant during the study.

   6. Subjects with central nervous system (CNS)-only involvement by malignancy (note:
   subjects with secondary CNS involvement are allowed on study).

   7. Subject has active hepatitis B, hepatitis C, or human immunodeficiency virus (HIV)
   infection at the time of pretreatment evaluation

   8. Subject has uncontrolled systemic fungal, bacterial, viral or other infection despite
   appropriate antibiotics or other treatment at the time of nonconforming lisocabtagene
   maraleucel administration.

   9. Subject has presence of acute or chronic graft-versus-host disease (ie, GVHD)

10. Use of the following:

      1. Therapeutic doses of corticosteroids (defined as > 20 mg/day prednisone or
      equivalent) within 72 hours prior to nonconforming lisocabtagene maraleucel
      administration. Physiologic replacement, topical, and inhaled steroids are
      permitted.

      2. Low dose chemotherapy (eg, vincristine, rituximab, cyclophosphamide ≤ 300
      mg/m2)given after leukapheresis to maintain disease control must be stopped ≥ 7
      days prior to lymphodepleting chemotherapy.

      3. Cytotoxic chemotherapeutic agents that are not considered lymphotoxic (see below)
      within 1 week of LD chemotherapy. Oral chemotherapeutic agents, including
      lenalidomide and ibrutinib, are allowed if at least 3 half-lives have elapsed
      prior to lymphodepleting chemotherapy.

      4. Donor lymphocyte infusions within 6 weeks of nonconforming lisocabtagene
      maraleucel administration.