Overview
TCR Modified T Cells MDG1011 in High Risk Myeloid and Lymphoid Neoplasms
Status:
Recruiting
Recruiting
Trial end date:
2024-04-01
2024-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a multicentre, non-randomized, open-label, Phase I/II clinical trial of MDG1011, an investigational medicinal product (IMP), consisting of patient-derived autologous T cells, persistently transduced with a Preferentially Expressed Antigen in Melanoma (PRAME)-specific human leukocyte antigen (HLA)-A*02:01-restricted T cell receptor (TCR).Phase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Medigene AG
Criteria
INCLUSION CRITERIA:1. Signed written informed consent prior to any clinical trial-related activities
2. Documented diagnosis with the last disease staging within the last 4 weeks prior to
screening
3. Human leukocyte antigen (HLA):
1. Phase I and Phase II (treatment group): Subjects positive for HLA-A*02:01
according to genotyping results
2. Phase II (concurrent control group): Subjects negative for HLA-A*02:01 according
to genotyping results
4. Age ≥ 18 years
5. Life expectancy of at least 4 months.
6. Eastern Cooperative Oncology Group (ECOG) performance status 0-2
7. Subjects not planned for allogeneic HSCT (e.g. based on disease characteristics or
subject characteristics). Bridging to an allogeneic HSCT will be allowed.
8. Females of childbearing potential must have a negative serum beta human chorionic
gonadotropin (β-hCG) pregnancy test result before leukapheresis and before
administration of lymphodepleting chemotherapy. Females of non-childbearing potential
are those who are postmenopausal greater than 2 years or who have had a bilateral
tubal ligation or hysterectomy.
9. Females of childbearing potential and males who have partners of childbearing
potential must agree to use an effective contraception method during the clinical
trial and for 6 months following the last dose of IMP.
Effective birth control includes:
1. intrauterine device plus 1 barrier method; or (b) 2 barrier methods. Effective barrier
methods are male or female condoms, diaphragms, and spermicides (creams or gels that
contain a chemical to kill sperm).
AML-SPECIFIC INCLUSION CRITERIA:
1. No Complete remission/response (CR) or Complete remission with incomplete
hematologic recovery (CRi) after completion of at least 2 cycles of intensive
induction chemotherapy or 1 cycle of intensive induction and consolidation
(intermediate or high dose cytarabine) chemotherapy each and/or
2. No CR or no CRi after completion of at least 1 cycle of intensive induction
chemotherapy including at least 5 days of cytarabine 100-200 mg/m^2 continuously
or an equivalent regimen with cytarabine with total dose not less than 500 mg/m^2
per cycle and at least 2 days of an anthracycline (e.g. daunorubicine,
idarubicin), unable to undergo allogeneic HSCT and/or
3. Refractory disease (including stable disease [SD], progressive disease [PD]) or
relapsed disease after hypomethylating agent therapy (e.g. azacitidine,
decitabine) and/or
4. Any SD, partial response (PR), CRi, CR obtained after re-induction or
salvage-therapy and/or
5. Relapsed AML patients unable to undergo allogeneic HSCT and/or
6. Relapsed AML after allogeneic HSCT
1. at least 100 days after transplant
2. no evidence of active acute or chronic GvHD at enrolment
3. in case of history of acute (> overall grade 1) or chronic GvHD
(moderate/severe) requiring immunosuppression treatment, no
immunosuppression within the last 3 months
4. no immunosuppression (with the exception of low dose steroids <= 10 mg
prednisone or equivalent) 4 weeks before enrolment and ongoing and
7. Myeloid blasts must positively express PRAME
MDS-SPECIFIC INCLUSION CRITERIA:
1. IPSS INT-2 or High Grade MDS Excess Blasts-2 (EB-2) not responding to at least 6
courses of azacitidine or 4 courses of decitabine and/or
2. IPSS INT-1, INT-2 or High Grade MDS with recurrence after initial response and
3. Blasts must positively express PRAME
MM-SPECIFIC INCLUSION CRITERIA:
1. Relapsed and refractory multiple myeloma:
• Progressive MM, also defined as relapsed disease, defined as:
1. A 25% increase from baseline in the serum M-protein (absolute increase
- 0.5 g/dL), urine M-protein (absolute increase > 200 mg/day), and/or the
difference between involved and uninvolved free light chain levels
(absolute increase ≥ 10 mg/dL).
2. The presence of definite new bone lesions and/or soft tissue plasmacytomas
with a clear increase in the size of existing plasmacytomas, or
hypercalcemia, that cannot be attributed to another cause. • Relapsed and
refractory MM is defined as disease progression within 60 days of a
patient's last treatment where at least a minimal response was achieved. •
Primary refractory MM is defined as disease that fails to achieve at least a
minimal response with any therapy. and
2. At least 3 previous therapy lines with at least one proteasome inhibitor and one
immunomodulatory derivate (IMiDs). Induction with or without hematopoietic stem
cell transplant and with or without maintenance therapy is considered a single
regimen. and
3. Myeloma cells must positively express PRAME
CRITERIA FOR PRE-EMPTIVE LEUKAPHERESIS PROCEDURE
• subject is positive for HLA-A*02:01 and their blasts/myeloma cells express
PRAME
• subject fulfills at least some inclusion criteria and, based on the judgement
of the investigator, have a likelihood of being eligible for IMP administration
in the further course of the subjects disease
- subject does not fulfill any exclusion criterion that would be considered
permanent (i.e.
irreversible organ function impairment) and therefore would certainly preclude
the subject from receiving the IMP in the future
EXCLUSION CRITERIA:
1. Subjects with acute promyelocytic leukemia exhibiting t(15;17)(q22;q12);
PML-RARA, or with variant translocations
2. Pregnant or lactating women
3. Known positive for HIV, active hepatitis B virus (HBV) or hepatitis C virus (HCV)
infection
4. Any clinically significant, advanced or unstable disease or inadequate main organ
function that may put the subject at special risk, such as: a. creatinine > 2.0
times the upper normal serum level b. total bilirubin, ALT, AST >3 times the
upper normal serum level c. cardiac left ventricular ejection fraction < 40% at
rest d. severe restrictive or obstructive lung disease
5. History of haploidentical allogeneic stem cell transplantation
6. Subjects both with urinary outflow obstructions and on dialysis or subjects for
whom cyclophosphamide is contraindicated for other reasons
7. Clinical significant and ongoing immune suppression including, but not limited
to: immunosuppressive agents such as cyclosporine or corticosteroids (at an
equivalent dose of >= 10 mg prednisone per day). Inhaled steroid and
physiological replacement for adrenal insufficiency is allowed.
8. Subjects with currently active autoimmune disease.
9. Subjects with a history of primary immunodeficiency.
10. Subjects with a currently active second malignancy other than non- melanoma skin
cancers or subjects with history of prior malignancy and previously treated with
a curative intent therapy less than 1 year ago
11. Known or suspected hypersensitivity or intolerance to IMP, cyclophosphamide,
fludarabine and/or tocilizumab or to any of the excipients
12. Participation in any clinical trial < 60 days prior to first IMP administration
in case of antibodies and < 14 days for all other IMPs
13. Vulnerable subjects and/or subjects unwilling or unable to comply with procedures
required in this clinical trial protocol
MM-SPECIFIC EXCLUSION CRITERIA FOR PHASE I AND PHASE II (TREATMENT GROUP):
1. Prior therapy with IMiDs within 14 days prior to leukapheresis and/or infusion of
IMP
2. Prior therapy with corticosteroids within 7 days prior to leukapheresis or 7 days
prior to infusion of IMP
EXCLUSION CRITERIA FOR TREATMENT WITH IMP IN PHASE I AND PHASE II (TREATMENT GROUP):
1. Uncontrolled central nervous system (CNS) disease
2. Uncontrolled infections or uncontrolled disseminated intravascular coagulation;
however, if these problems resolve, the start of treatment can be initiated on a
delayed schedule
3. Ongoing 3 grade cardiac, renal, pulmonary, gastrointestinal or hepatic toxicities
according to CTCAE v4.03; however, if these problems resolve, the start of
treatment can be initiated on a delayed schedule
4. Evidence of acute or chronic GvHD