Principal Investigator
Enrollment Status
Clinical Trial ID
Clinical Trial Summary
The purpose of this study is to test the safety and efficacy of AUTO3, a CAR T cell treatment
targeting CD19 and CD22 followed by limited duration of anti-PD1 antibody in patients with
DLBCL
Phase
Phase 1/Phase 2
Funding Agency/Sponsor
Industrial
Disease
Lymphoma
Enrollment Eligibility
Inclusion Criteria:
1. Male or female, aged ≥18 years.
2. Willing and able to give written, informed consent.
3. Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 1.
4. Histologically confirmed DLBCL and large B cell lymphoma (at last relapse) subsets,
including:
Phase I and Phase II Cohort 1:
1. DLBCL, not otherwise specified (NOS), per World Health Organisation
classification and DLBCL with MYC and BCL2 and/or BCL6 rearrangements
(double/triple hit).
2. Transformed DLBCL from FL.
3. High-grade B cell lymphoma with MYC expression (excluding Burkitt's lymphoma)
Phase I and Phase II Cohort 2:
4. Transformed DLBCL from other indolent lymphomas (excluding Richter's
transformation).
5. Primary mediastinal large B cell lymphoma.
5. Chemotherapy-refractory disease, defined as one or more of the following:
1. Stable disease (≤12 months) or progressive disease as best response to most
recent chemotherapy containing regimen. Refractory disease after frontline
chemo-immunotherapy is allowed.
2. Disease progression or recurrence in ≤12 months of prior autologous
haematopoietic stem cells transplantation (ASCT).
OR
6. Relapse after ≥two lines of therapy or after ASCT. At a minimum:
1. Patients must have received rituximab or another anti-CD20 monoclonal antibody
(unless Investigator determines that tumour is CD20-negative) and an
anthracycline-containing chemotherapy regimen.
2. Patients must have either failed ASCT, or be ineligible for or not consenting to
ASCT.
3. Patients with transformed DLBCL must have received at least one line of therapy
after transformation to DLBCL.
7. PET-positive disease per Lugano classification.
8. For females of childbearing potential, a negative serum or urine pregnancy test must
be documented at screening, prior to pre-conditioning and confirmed before receiving
the first dose of study treatment.
For females who are not postmenopausal or surgically sterile, highly effective methods
of contraception must be used during the treatment period and for at least 12 months
after the last dose of study treatment.
9. For males, it must be agreed that that two acceptable methods of contraception are
used.
10. Adequate renal, hepatic, pulmonary, and cardiac function defined as:
1. Creatinine clearance ≥40 cc/min.
2. Serum alanine aminotransferase / aspartate aminotransferase ≤2.5 x ULN.
3. Total bilirubin ≤1.5 x ULN, except in subjects with Gilbert's syndrome.
4. LVEF ≥50% (by ECHO or MUGA) unless the institutional lower limit of normal is
lower.
5. Baseline oxygen saturation >92% on room air and ≤Grade 1 dyspnoea.
11. Patient has adequate BM function without requiring ongoing blood product or
granulocyte-colony stimulating factor support and meets the following criteria:
1. Absolute neutrophil count ≥1.0 × 109/L.
2. Absolute lymphocyte count ≥0.3 × 109/L (at enrolment and prior to leukapheresis).
3. Haemoglobin ≥80 g/L.
4. Platelets ≥75 × 109/L
12. No contra-indications for leukapheresis.
Exclusion Criteria:
1. Prior allogeneic haematopoietic stem cell transplant.
2. Females who are pregnant or lactating.
3. History or presence of clinically relevant CNS pathology such as epilepsy, paresis,
aphasia, stroke within prior 3 months, severe brain injuries, dementia, Parkinson's
disease, cerebellar disease, organic brain syndrome, uncontrolled mental illness, or
psychosis.
4. Patients with active CNS involvement by malignancy. Patients with history of CNS
involvement with malignancy may be eligible if CNS disease has been effectively
treated and provided treatment was at least 4 weeks prior to enrolment (at least 8
weeks prior to AUTO3 infusion).
5. Clinically significant, uncontrolled heart disease or a recent (within 12 months)
cardiac event.
1. Uncontrolled cardiac arrhythmia (patients with rate-controlled atrial
fibrillation are not excluded).
2. Evidence of pericardial effusion
6. Patients with a history (within 3 months) or evidence of deep vein thrombosis or
pulmonary embolism requiring ongoing therapeutic anticoagulation at the time of
pre-conditioning.
7. Patients with active gastrointestinal bleeding.
8. Patients with any major surgical intervention in the last 3 months.
9. Active bacterial, viral or fungal infection requiring systemic treatment. Active or
latent hepatitis B infection or hepatitis C infection. Testing positive for human
immunodeficiency virus, human T cell lymphotropic virus (HTLV1 and 2) or syphilis.
10. History of autoimmune disease resulting in end organ injury or requiring systemic
immunosuppression/systemic disease modifying agents within the last 24 months.
11. Patients with a known history or prior diagnosis of optic neuritis or other
immunologic or inflammatory disease affecting the CNS.
12. Evidence of active pneumonitis on chest computed tomography (CT) scan at screening or
history of drug-induced pneumonitis, idiopathic pulmonary fibrosis, organising
pneumonia, or idiopathic pneumonitis.
13. History of other malignant neoplasms unless disease free for at least 24 months
(carcinoma in situ, non-melanoma skin cancer, breast or prostate cancer on hormonal
therapy allowed).
14. Prior treatment with PD1, PD-L1, or cytotoxic T lymphocyte-associated
protein-4-targeted therapy, or tumour necrosis factor (TNF) receptor superfamily
agonists within 6 weeks prior to AUTO3 infusion.
15. Prior treatment with investigational or approved gene therapy or cell therapy products
until a dose level has treated at least three patients and has been declared safe.
16. Prior CD19 or CD22 targeted therapy.
17. The following medications are excluded:
1. Steroids: Therapeutic doses of corticosteroids within 7 days of leukapheresis or
72 hours prior to AUTO3 administration. However, physiological replacement,
topical, and inhaled steroids are permitted.
2. Immunosuppression: Immunosuppressive medication must be stopped ≥2 weeks prior to
leukapheresis or AUTO3 infusion.
3. Cytotoxic chemotherapies within 2 weeks of AUTO3 infusion and 1 week prior to
leukapheresis (2 weeks for lymphodepleting chemotherapy).
4. Antibody therapy use including anti-CD20 therapy within 2 weeks prior to AUTO3
infusion, or 5 half-lives of the respective antibody, whichever is shorter.
5. Granulocyte-colony stimulating factor less than 10 days prior to leukapheresis.
6. Live vaccine ≤4 weeks prior to enrolment.
7. Prophylactic intrathecal therapy: Methotrexate within 4 weeks and other
intrathecal chemotherapy (e.g. Ara-C) within 2 weeks prior to starting
pre-conditioning chemotherapy.
18. Prior limited radiation therapy within 4 weeks of AUTO3 infusion or within 24 weeks
for definitive radiation to chest.
19. Research participants receiving any other investigational agents, or concurrent
biological, chemotherapy, or radiation therapy.
20. Known allergy to albumin, dimethyl sulphoxide (DMSO), cyclophosphamide or fludarabine,
pembrolizumab or tocilizumab.
21. Any contraindications to receive anti-PD1 antibody pembrolizumab will be excluded from
cohorts requiring administration of pembrolizumab.
22. Patients, who in the opinion of the Investigator, may not be able to understand or
comply with the safety monitoring requirements of the study.
23. Any other condition that in the Investigator's opinion would make the patient
unsuitable for the clinical trial.
Phase I outpatient cohort:
24. Subjects who do not have caregiver support (in line with institutional outpatient
transplant guidelines) for outpatient/ambulatory care setting.
25. Subjects who are staying greater than 60 minutes (or whatever is permissible per
institutional outpatient transplant guidelines) from the clinical trial site at the
time of treatment.
For AUTO3 Infusion: Patients meeting any of the following exclusion criteria must not be
treated with AUTO3 or have treatment delayed until they no longer meet these criteria:
1. Severe intercurrent infection.
2. Requirement for supplementary oxygen or active pulmonary infiltrates.
3. Clinical deterioration of organ function (renal and hepatic) exceeding the criteria
set at study entry.