Natural Killer Cell (CYNK-001) Infusions in Adults With AML

Leukemia Clinical Trial

— CYNK001AML01  

Official title:

A Phase I Multi-dose Study of Human Placental Hematopoietic Stem Cell Derived Natural Killer Cells (CYNK-001) With or Without Recombinant Human Interleukin-2 (rhIL-2) in Adults With Primary or Secondary Acute Myeloid Leukemia (AML) in Morphologic Complete Remission With Minimal Residual Disease (MRD) or Relapsed/Refractory (R/R) AML

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04310592
• Other study ID #: CYNK-001-AML-001
• Status: Recruiting
• Phase: Phase 1
• Start date: March 12, 2020
• Est. completion date: December 3, 2024

Study information

• Verified date: February 2023
• Source: Celularity Incorporated
• Contact: Cherie Daly, MD
• Phone: 908-451-0640
• Email: Cherie.Daly[@]celularity.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will find the maximum tolerated dose or the maximum planned dose of CYNK-001 which contains natural killer (NK) cells derived from human placental CD34+ cells and culture-expanded. CYNK-001 cells will be given after lymphodepleting chemotherapy. The safety of this treatment will be evaluated, and researchers want to learn if NK cells will help in treating acute myeloid leukemia.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 94
• Est. completion date: December 3, 2024
• Est. primary completion date: June 3, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Treatment Eligibility Screening Patient Inclusion Criteria

Patients must satisfy the following criteria to be enrolled in the study:

• Patient has eligible disease status:
• Primary or Secondary acute myeloid leukemia (AML) Patients in first of second Morphological Complete Remission (CR), Morphological Complete Remission with incomplete hematologic recovery (CRi), or Morphologic Leukemia-free State (MLFS) as defined by the European LeukemiaNet (ELN) recommendations for AML Response Criteria (Dohner, 2017).
• R/R diagnosis based on confirmed diagnosis with local pathology report following any reinduction/ salvage therapy ELN guidelines.

1. Relapsed AML are defined as having relapsed after achieving = 1 CR, including relapse after allogeneic stem cell transplantation (= 2 months after transplant).

2. Refractory AML, defined as not achieving CR, CRi, or MLFS after 2 or more cycles of induction therapy (primary refractory) or not achieving CR after treatment for relapsed AML.

3. Secondary AML (MDS transformation): Secondary AML patients are eligible to participate if they have received a minimum of one prior line of treatment for AML.

4. Treatment-related AML: Treatment-related AML patients are eligible to participate if they have received a minimum of one prior line of treatment for AML.

• Patient with prior central nervous system involvement by malignancy are eligible provided that it has been treated and cerebral spinal fluid is clear for at least 2 weeks prior to start of Lymphodepletion Regimen.
• (MRD positive population only): Patient is minimal residual disease (MRD) positive, as assessed on bone marrow aspirate (BMA) by Multiparameter Flow Cytometry (MFC) at time of Treatment Eligibility assessment. For the purposes of this study, MRD positivity is defined as greater than or equal to 0.1% blasts detected by MFC on BMA by the Sponsor-selected Central MRD analysis laboratory, where assay sensitivity allows for a Lower Limit of Detection (LOD) of 1 x 10-4 (0.01%) or lower.
• Patient is = 18 and = 80 years of age at the time of signing the Study informed consent form (ICF).
• Patient understands and voluntarily signs the Study ICF prior to any study-related assessments/procedures are conducted.
• Patient is willing and able to adhere to the study schedule and other protocol requirements.
• Performance status of Eastern Cooperative Oncology Group (ECOG) = 2.
• Ability to be off immunosuppressive drugs for at least 3 days prior to the CYNK-001 infusion. Steroids at the equivalent of no more than 7.5 mg prednisone per day are permissible.
• Female of childbearing potential (FCBP)* must not be pregnant and agree to not becoming pregnant for at least 28 days following the CYNK-001. FCBP must agree to use an adequate method of contraception during the treatment period.
• FCBP is a female who: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).
• Male Patients must agree to use a condom during sexual contact for at least 28 days following the last infusion of CYNK-001, even if he has undergone a successful vasectomy. Treatment Eligibility Screening Patient Exclusion Criteria

The presence of any of the following will exclude the Patient from enrollment:

• Patient has any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the Patient from participating in the study.
• Patient has any condition including the presence of laboratory abnormalities which places the Patient at unacceptable risk if he or she were to participate in the study.
• Patient has any condition that confounds the ability to interpret data from the study.
• Patient has bi-phenotypic acute leukemia.
• Patient has acute promyelocytic leukemia (APL).
• Patient has inadequate organ function as defined below at time of Treatment

Eligibility Period:

1. Patient has aspartate aminotransferase (AST), alanine aminotransferase (ALT), or alkaline phosphatase = 2.5 x the upper limit of normal (ULN).

2. Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2 as calculated using the Modification of Diet in Renal Disease Study equation (Levey, 2006) or history of an abnormal eGFR < 60 and a decline of > 15 mL/min/1.73 m2 below normal in the past year.

3. Patient has a bilirubin level > 2 mg/dL (unless Patient has known Gilbert's disease).

• Patient has had prior treatment with biologic antineoplastic agents less than 7 days before first CYNK-001 infusion and at least 5 half-lives. (Exception will be granted for monoclonal antibodies that are known to have long half-lives, in which case a minimum of 2 weeks from last dose will be required). For agents that have known AEs occurring beyond these specified days after administration, this period must be extended beyond the time during which acute AEs are known to occur. Treating physicians are encouraged to discuss cases with the Medical Monitor.
• Patient is pregnant or breastfeeding.
• Patient has new or progressive pulmonary infiltrates or pleural effusion large enough to be detected by chest x-ray or CT scan within 2 weeks of first CYNK-001 infusion.
• Patient has active autoimmune disease other than controlled connective tissue disorder or those who are not on active therapy.
• Patient has had a Bone Marrow transplant < 60 days prior to screening or plans to have a transplant within the 28 day period following the first CYNK-001 infusion.
• Patient has a history of malignancy other than AML or other underlying hematologic conditions such as myelodysplastic syndromes (MDS) or myeloproliferative neoplasms (MPN) unless the Patient has been free of disease for greater than 3 years prior to

CYNK 001 infusion. Exceptions will include the following malignancies:

1. Basal cell carcinoma of the skin

2. Squamous cell carcinoma of the skin

3. Carcinoma in situ of the cervix

4. Carcinoma in situ of the breast

5. Incidental biological finding of prostate cancer (TNM stage of T1a or T1b)

6. Superficial bladder cancer

7. For patients with therapy-related AML, the underlying malignancy which led to secondary AML must be stabilized (not progressing) and not under active treatment.

• Patient has a history of severe asthma and is presently on chronic medications or has a history of other symptomatic pulmonary disease.
• Patient has the following prior history of GVHD:

Acute GVHD: Subjects with prior history of acute GVHD where signs and/or symptoms did not completely resolve (no clinical signs/symptoms and not on more than 7.5 mg of predinsone per day Chronic GVHD: Subjects with prior history of chronic GVHD where signs and/or symptoms did not completely resolve (no clinical signs/symptoms and not on more than 7.5 mg of prednisone per day) within 90 days of ongoing immunosuppression.

• Patient has an untreated chronic infection or has received treatment of any uncontrolled or progressive infection with systemic antibiotics within 2 weeks prior to first CYNK-001 infusion. Prophylactic antibiotic, antiviral, and antifungal medication are permissible.
• Patient has any other organ dysfunction (CTCAE Version 5.0 Grade 3 or greater) that will interfere with the administration of the therapy according to this protocol.
• Patient has a resting left ventricular ejection fraction (LVEF) of < 40% obtained by echocardiography or multi-gated acquisition scan (MUGA).
• Patient was treated with an investigational product within 28 days of first CYNK-001 infusion. Patient must no longer be a participant in the previous interventional study at the time of CYNK-001 infusion. (Patients who are under survival follow-up or observation associated with a study are permitted, and if treatment information is collected for this period, "Investigational Study" must be used to capture the study treatment.).

Related Conditions & MeSH terms

• Alkylating Agents
• Analgesics
• Analgesics, Non-narcotic
• Anti-infective Agents
• Antimetabolites, Antineoplastic
• Antiviral Agents
• Hematologic Diseases
• Hematologic Neoplasms
• Immunologic Factors
• Immunosuppressive Agents
• Leukemia
• Leukemia in Remission
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute
• Neoplasms
• Neoplasms by Histologic Type
• Peripheral Nervous System Agents
• Physiological Effects of Drugs
• Refractory AML
• Relapsed Adult AML

Intervention

Biological:
• CYNK-001
CYNK-001 is an allogeneic off the shelf cell therapy enriched for CD56+/CD3- NK cells expanded from human placental CD34+ cells.

Locations

Country	Name	City	State
United States	Roswell Park Comprehensive Cancer Center	Buffalo	New York
United States	University of Chicago	Chicago	Illinois
United States	Colorado Blood Cancer Institute	Denver	Colorado
United States	Hackensack University Medical Center	Hackensack	New Jersey
United States	MD Anderson Cancer Center	Houston	Texas
United States	Tennessee Oncology	Nashville	Tennessee
United States	Columbia University and New York Presbyterian Hospital	New York	New York
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	Swedish Health Services	Seattle	Washington
United States	Westchester Medical Center	Valhalla	New York

Sponsors (1)

Lead Sponsor	Collaborator
Celularity Incorporated

Country where clinical trial is conducted

United States, 

References & Publications (2)

Dohner H, Estey E, Grimwade D, Amadori S, Appelbaum FR, Buchner T, Dombret H, Ebert BL, Fenaux P, Larson RA, Levine RL, Lo-Coco F, Naoe T, Niederwieser D, Ossenkoppele GJ, Sanz M, Sierra J, Tallman MS, Tien HF, Wei AH, Lowenberg B, Bloomfield CD. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Blood. 2017 Jan 26;129(4):424-447. doi: 10.1182/blood-2016-08-733196. Epub 2016 Nov 28. — View Citation

Levey AS, Coresh J, Greene T, Stevens LA, Zhang YL, Hendriksen S, Kusek JW, Van Lente F; Chronic Kidney Disease Epidemiology Collaboration. Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate. Ann Intern Med. 2006 Aug 15;145(4):247-54. doi: 10.7326/0003-4819-145-4-200608150-00004. Erratum In: Ann Intern Med. 2008 Oct 7;149(7):519. Ann Intern Med. 2021 Apr;174(4):584. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants who experience a Dose-limiting Toxicity (DLT) in MRD positive AML patients	The number of participants who experience a DLT will be measured.	Day +28
Primary	Number of Participants who experience a Dose-limiting Toxicity (DLT) in Relapsed/Refractory AML patients	The number of participants who experience a DLT will be measured.	Day +28
Primary	Determine the Maximum Tolerated Dose (MTD) or Maximum Planned Dose (MPD) of CYNK-001 in MRD positive AML patients	The maximum dose safely administered for the treatment of patients with AML.	up to 28 days
Primary	Determine the Maximum Tolerated Dose (MTD) or Maximum Planned Dose (MPD) of CYNK-001 in Relapsed/Refractory AML patients	The maximum dose safely administered for the treatment of patients with AML.	up to 28 days
Primary	Frequency and Severity of Adverse Events (AEs)	Frequency and severity of Adverse Events will be evaluated.	up to 12 months
Secondary	Number Participants who experience Minimal Residual Disease (MRD) Response	The number of participants who convert from MRD positive to MRD negative in the MRD positive arm.	up to 12 months
Secondary	Time to MRD Response	The time it takes to convert from MRD positive to MRD negative in the MRD positive arm.	up to 12 months
Secondary	Duration of MRD Response	The measure of how long participants remain MRD negative in the MRD positive arm.	up to 12 months
Secondary	Progression-free Survival (PFS)	Date of first CYNK-001 infusion to date of disease progression in the MRD positive arm.	up to 12 months
Secondary	Time to Progression (TTP)	Date of first CYNK-001 infusion to date of disease progression in the MRD positive arm.	up to 12 months
Secondary	Duration of Morphologic Complete Remission (CR)	Duration from first Morphologic CR observation to time of disease progression in the MRD positive arm.	up to 12 months
Secondary	Overall Survival (OS)	Date of first CYNK-001 infusion to date of death.	up to 12 months
Secondary	Overall Response Rate (ORR)	Defined as achievement of Complete Remission (CR), Complete Remission with incomplete (CRi) hematologic recovery, or Morphologic leukemic-free state (MLFS) in the Relapsed/Refractory AML arm.	up to 12 months
Secondary	Duration of Response (DoR)	Duration of best response in the Relapsed/Refractory AML arm.	up to 12 months