Title
The Effects of AMPC in the Treatments of Refractory or Relapsed AML
A Phase I Single-arm, Open-label Prospective Study to Evaluate the Efficacy and Safety of Peripheral Blood Derived Autologous Multi-lineage Potential Cells (AMPC) in Relapsed/Refractory Acute Myeloid Leukemia (AMPCAL Study)
Phase
Phase 1Lead Sponsor
Lai Corporation Pty. Ltd.Study Type
InterventionalStatus
Unknown statusIndication/Condition
Acute Myeloid Leukaemia RecurrentIntervention/Treatment
Autologous Multi-lineage Potential Cells (AMPC)Study Participants
10A private trial for evaluating the overall response rate contributed by AMPC in AML in refractory or relapsed AML
After inclusion and exclusion criteria has been determined and approved, written informed consent will be obtained from the candidate. All medical history relevant to the diagnosis of AML will be collected.
Screening period:
The screening period could extend from 0 to 7 days depending on the completion of screening laboratory results as below.
On day -5 (up to day -1), the patient will undergo a screening test for the following test items:
BUN, creatinine, electrolyte, liver function test (LFT)
Full blood count (FBC), including blood smear
Hepatitis B/C
Human T lymphocytic virus type I and II (HTLV-I/II)
HIV1/2
Syphilis serology
Mycoplasma serology For Hepatitis B/C,HTLV-I/II, HIV1/2, Syphilis serology, and Mycoplasma serology, these tests obtained up to 3 months prior to day -5 can be allowed for using as screening result.
Chest X-ray
Bone marrow study including aspiration with wright's stain, biopsy, flow cytometry, and chromosome study (Any molecular testing for AML is optional.).
Bone marrow biopsy can be omitted if the prior study performed within 14 days before day-5 and the available materials (core biopsy and slides) and result can be obtained for pathological review. In this case, only bone marrow aspiration for Wright's stain, flow cytometry, and chromosome study will be performed.
Bone marrow biopsy will be repeated if the previous result has been performed more than 14 days prior to day -5 and/or FBC at day -5 reveals peripheral blast count higher than 10% of total white blood cells.
For chromosome study (cytogenetics), the previous result before the recent line of chemotherapy prior to enrollment can be used for the screening data.
On day 0, peripheral blood will then be collected, ranging from 250mL to 400mL depending on candidate fitness. The blood is collected into a sterile blood bag and sealed. Subsequent processes will be conducted in the blood bag within a closed-system to minimize contamination risks. FBC will be collected in order to determine the disease status. After that, the investigator will consider to prescribe blood transfusion for the candidate.
On day 0 to day 3, the collected blood will be sent to the laboratory for stem cell culture, and a sample of the collected blood will be sent to a third-party laboratory for contamination testing of the following parameters:
Bacterial endotoxin
Total viable aerobic count
Total viable count
Microbial growth
Mycoplasma real-time PCR test
On day 4, the biotest results will be released and the safety profiles of the AMPC product must be completed and passed before the cultured stem cells may be released for treatment
On day 5, candidates will receive an infusion of the cultured stem cells. Prior to the infusion, FBC and blood chemistry (BUN, Cr, electrolyte, LFT) will be collected and the treating doctor will first conduct an allergy skin test to determine suitability for reinfusion. The cultured stem cells are then reinfused intravenously into the candidate in a process that could take up to 2 hours
The candidate participation will take place on day 0 to day 1 or 2 (if blood transfusion is required) and day 5 (period adjusted for blood transfusion if required) for peripheral blood collection and stem cell reinfusion respectively; with 12 month follow up after treatment;
3 days post-treatment follow-up: full blood count test and blood smear, BUN, Cr, electrolyte, LFT
10 days post-treatment follow-up: full blood count test and blood smear, BUN, Cr, electrolyte, LFT
1 month (+/-7 days) post-treatment follow-up: full blood count test and blood smear, BUN, Cr, electrolyte, LFT, bone marrow study
3 month (+/-7 days) post-treatment follow-up: full blood count test and blood smear, BUN, Cr, electrolyte, LFT, bone marrow study
6 month (+/-7 days) post-treatment follow-up: full blood count test with bone marrow study
12 month (+/-7 days) post-treatment follow-up: full blood count test with bone marrow study
Multi-lineage potential cells which were induced to de-differentiate from somatic leukocytes from peripheral blood. Cells are autologous with respect to the patient, and are prepared in a suspension and administered via intravenous infusion. An estimated average of 1 x 10^8 (0.5 to 5.0 x 10^8) cells/per suspension(275 to 450mL) will be infused into the patient via intravenous infusion on day 5. Cell counts depend on yield of initial leukocyte harvest on day 0.
AMPC will be intravenously infused.
Inclusion Criteria: Must be unequivocally diagnosed with AML according to WHO classification with accompanying bone marrow biopsy and blood panel results Must have refractory AML, defined as disease unresponsive to initial treatment; or relapsed AML that re-occured after treatment with conventional high dose chemotherapy Candidates who have no available match-sibling donor for bone marrow transplantation (BMT) or are not suitable for BMT due to any reason. Must have had prior treatment with chemotherapy at least 30 days prior to day 0 of this study and have recovered from treatment-related toxicity of chemotherapeutic agents with the exception of persistent diseases Age 20 to 60 years old Exclusion Criteria: Candidates who received any investigational therapies 4 weeks prior to treatment with this protocol Candidates who received radiotherapy within 4 weeks prior to the treatment of this protocol Candidates who have not recovered from any AE caused by radiotherapy or any agents received 4 weeks earlier Candidates who have had a prior allogeneic stem cell transplant Known case of extramedullary myeloid tumor (myeloid sarcoma) Pregnant or breastfeeding women Hydroxyurea has been prescribed within 10 days prior to day-5 Candidates have any abnormal screening laboratory results as below; Hemoglobin < 9 g/dL Total white blood cells count > 30,000/microL (without ongoing G-CSF therapy) Platelet count < 75,000/microL Creatinine clearance < 30 mL/min/1.73 m2 (by Cockcroft and Gault formula) ALT > 5x upper normal limit Bone marrow study at screening period show blast > 40% of total nucleated cells or severe hypocellularity (defined as < 25% of normal cellularity for corresponding age) with presence of cluster of blasts Candidates have active heart disease including recent or chronic heart failure, unstable angina, recent acute myocardial infarction, or significant arrhythmia within 6 months of recruitment. Candidates have concurrent malignancies unless the candidates has been free of the disease for at least 5 years. Candidates positive for HIV1/2, hepatitis B/C, HTLVI/II, and Syphilis
