US Phase I Study of ECT-001-CB in Patients With Sickle-Cell Disease

A Phase I Multicenter Study of Hematopoietic Stem Cell Transplant of ECT-001-Expanded Cord Blood With a Reduced Toxicity Conditioning Regimen in Patients With Severe Sickle Cell Disease

The application of experimental hematopoietic cell transplantation (HCT) therapy in sickle-cell disease (SCD) must strike a balance between the underlying disease severity and the possibility of a direct benefit of the treatment, particularly in pediatric populations. Clinical studies in adults with SCD have focused on interventions that prolong survival and improve the quality of life. Unlike children, adults with SCD are much more likely to have a debilitating complication. As a result, the risk/benefit ratio of HCT is very favorable in adults, particularly if an approach to HCT that defines an acceptable level of toxicity can be established.

Whereas hematopoietic stem cell transplantation (HSCT) remains the only curative treatment currently available for patients with SCD, the morbidity, the frequent irreversible damage in target organs and the mortality reported in the natural course of patients with severe SCD are strong incentives to perform HSCTs in younger age groups. For those who lack a matched related donor, CB transplant is an appealing option, but despite been less problematic, CB accessibility related to cell dose of appropriately matched cord blood unit (CBU) remains a significant issue. Through a 7-day culture process of a CBU's hematopoietic stem cell HSCs with the UM171 compound, the total cell dose is increased mitigating this limitation.

UM171-CB expansion (ECT-001-CB) allows a greater CB accessibility, the selection of better matched cords that might translate into favourable clinical outcomes as reported in previous trials, including a lower risk of graft-versus-host disease. After CB selection and ex-vivo expansion, ECT-001-CB transplant will follow a myeloablative reduced-toxicity conditioning regimen consisting of rATG, busulfan and fludarabine with doses of all agents optimized to the individual using model-based dosing and will be followed by standard supportive care and GVHD prophylaxis consisting of tacrolimus and MMF.

Study Overview

• Status: Withdrawn
• Conditions: Sickle Cell Disease; Umbilical Cord Blood; Hematopoietic Cell Proliferation
• Intervention / Treatment: Biological: ECT-001-CB (UM171-Expanded Cord Blood Transplant)

• Study Type: Interventional
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • California
    • Palo Alto, California, United States, 94304
      • Stanford University School of Medicine
    • San Francisco, California, United States, 94158
      • University of California San Francisco

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 5 years to 30 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Be ≥ 5-30 years of age.
2. Have a diagnosis of SCD, with either βS/βS, βS/β0, βS/β+ or βS/βC genotype and followed at a center of excellence for SCD with at least 2 years of detailed past medical records available.

3. Have severe disease i.e. have experienced one or more of the following SCD related events, in spite of appropriate supportive care measures (e.g. pain management, penicillin prophylaxis):

   1. Recurrent severe vaso-occlusive crisis (VOC) (≥2 episodes/year in the prior 2 years): an episode of pain lasting >2 hours severe enough to require care at a medical facility. Note that priapism that lasts >2 hours and requires care at a medical facility is also considered a VOC. To meet this criterion, subjects must have either experienced hydroxyurea failure at any point in the past (defined as >1 VOC or ≥1 acute chest syndrome (ACS) after taking hydroxyurea for ≥3 months) or must have intolerance to hydroxyurea (defined as inability to be maintained on an adequate dose of hydroxyurea due to marrow suppression or severe drug-induced toxicity [e.g. gastrointestinal distress, fatigue]).
   2. ACS (≥2 total episodes in the prior 2 years, with at least one episode in the past year), defined as an acute event with pneumonia-like symptoms, hypoxemia and the presence of a new pulmonary infiltrate. To meet this criterion, subjects must have either experienced hydroxyurea failure or have intolerance to hydroxyurea, as defined above.
   3. History of an overt stroke, defined as a sudden onset neurologic deficit lasting more than 24 hours that is accompanied by cerebral MRI changes.
   4. patients on chronic transfusions are eligible, provided medical records documenting any of the above severity criteria are available prior to starting the transfusion program.
4. Availability of 1 CB unit ≥ 6/8 HLA match (when A, B, C and DRB1 are performed at the allelic level resolution) with of at least CD34+ cell count 1.5 x 105/kg and total nucleated cells (TNC) 1.5 x 107/kg (pre-freeze)
5. Have adequate organ function to undergo a myeloablative (reduced toxicity conditioning) HSCT.
6. Have a Lansky/Karnofsky performance status of ≥ 80.
7. An appropriate and willing HLA-matched sibling donor is not available.

Exclusion Criteria:

1. Prior HSCT or gene-therapy.
2. Positive for presence of HIV-1 or HIV-2, hepatitis B virus (HBV), or hepatitis C virus (HCV). (Note that patients who have been vaccinated against hepatitis B [hepatitis B surface antibody (HBsAb)-positive] or patients with positive hepatitis B core and/or hepatitis B-e antibodies are also eligible provided viral load is negative by quantitative polymerase chain reaction (qPCR). Patients who are positive for anti-hepatitis C antibody are eligible as long as they have a negative HCV viral load by qPCR). Positive serology for human T-lymphotropic virus-1 (HTLV-1), syphilis (rapid plasma reagin (RPR)), toxoplasmosis.
3. Clinically significant and active bacterial, viral, fungal, or parasitic infection as determined by PI.
4. A white blood cell count <2 × 10e9/L, and/or platelet count <50 × 10e9/L.
5. Any prior or current malignancy or myeloproliferative or a significant coagulation or immunodeficiency disorder.

6. Advanced liver disease, defined as:

   1. Persistent aspartate transaminase, alanine transaminase, or direct bilirubin value >5 times the upper limit of normal (ULN); or
   2. Cirrhosis or bridging fibrosis; or
   3. Baseline prothrombin time or partial thromboplastin time > 1.5 x ULN; or
   4. in chronically transfused patients a liver iron concentration (LIC) of ≥ 15 mg/g on T2* Magnetic Resonance Imaging [MRI] of liver.
7. Left ventricular ejection fraction (LVEF) <45% and for patients on chronic transfusions a cardiac T2* < 10 ms by MRI.
8. Baseline estimated glomerular filtration rate < 60 mL/min/1.73 m2.
9. Baseline oxygen saturation < 85% without supplemental oxygen (excluding periods of SCD crisis or infection).
10. Diffusion capacity of carbon monoxide (DLCO) <50% of predicted (corrected for hemoglobin and/or alveolar volume).
11. Any contraindication to general anaesthesia.
12. Participation in another clinical study with an investigational drug within 30 days of Screening.
13. Diagnosis of a significant psychiatric disorder as deemed as the PI that could seriously impede the subject's ability to participate in the study.
14. Pregnancy or breastfeeding in a postpartum female or absence of adequate contraception for fertile patients. Females of child bearing potential are required to use effective contraception from enrollment through at least 6 months after drug product infusion. Male patients are required to use effective contraception from enrollment through at least 6 months after drug product infusion.
15. An assessment by the PI that the subject would not comply with the study procedures outlined in the protocol.
16. Any abnormal condition or laboratory result that is considered by the PI capable of altering patient condition or study outcome.

Note: should a patient be out of range for any numerical exclusion criteria, the PI is allowed to repeat the dosage once during the screening period to definitely determine eligibility

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: ECT-001-CB; An Umbilical Cord Blood for transplant will undergo CD34+ selection and expansion. The CD34- fraction is infused on Day +1 post-transplant.; Patients will receive standard supportive care and GVHD prophylaxis	Biological: ECT-001-CB (UM171-Expanded Cord Blood Transplant); Single ECT-001-CB transplant (CD34+: 2 to 5.75x10E5/kg, CD3+ >1x10E6/kg)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Evaluate feasibility of finding a suitable ECT-001-CB graft for transplantation in the context of SCD.	Calculate the proportion of recruited SCD patients for whom a suitable CBU (i.e., ≥ 6/8 human leukocyte antigen (HLA) with an appropriate cell dose) is identified.	Up to 24-months
Evaluate feasibility of a successfully performing ECT-001-CB transplantation in the context of SCD.	Calculate the percentage of selected grafts that will be successfully expanded and transplanted with absence of technical hurdles	During accrual (up to 24-months)
Evaluate the Safety of ECT-001-CB by evaluating tri-lineage hematopoietic reconstitution	Measure the time required to achieve neutrophil and platelet engraftment	Up to 12-Months
Evaluate the Safety of ECT-001-CB by calculating incidence of acute and chronic GvHD	Calculate incidence of Acute GVHD and Chronic GVHD as per NIH criteria	Up to 12-Months
Evaluate the Safety of ECT-001-CB by evaluating adverse events	Calculate the Incidence of Adverse Events from the beginning of the conditioning regimen up to 12 months after ECT-001-CB transplant	Up to 12-Months
Evaluate the Safety of ECT-001-CB by evaluating incidence of transplant related mortality (TRM)	Calculate incidence of any mortality related to the investigational product until the end of evaluation period.	Up to 12-Months
Evaluate the Safety of ECT-001-CB by incidence of graft failure	Calculate the incidence of primary and late graft failure	Up to 100 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Determine the pharmacologic effect of ECT-001-CB by evaluating donor chimerism	The percentage of hematopoietic chimerism, based on DNA polymorphisms, will be measured and compared to baseline.	Up to 12-Months post treatment
Determine the pharmacologic effect of ECT-001-CB by measuring sickle hemoglobin (HbS) in peripheral blood.	The concentration of the Sickle Hemoglobin (HbS) will be compared to baseline.	Up to 12-Months post treatment
Evaluate impact of ECT-001-CB on SCD-related events during the study period.	The incidence of SCD-related adverse events will be compared to internal controls	Up to 12-Months post treatment

Collaborators and Investigators

• Sponsor: ExCellThera inc.
• Collaborators: California Institute for Regenerative Medicine (CIRM)
• Investigators: Study Director: Medical Monitor, ExCellThera inc.

Study record dates

Study Major Dates

• Study Start (Actual): July 13, 2021
• Primary Completion (Anticipated): September 1, 2023
• Study Completion (Anticipated): February 2, 2024

Study Registration Dates

• First Submitted: September 28, 2020
• First Submitted That Met QC Criteria: October 18, 2020
• First Posted (Actual): October 20, 2020

Study Record Updates

• Last Update Posted (Actual): July 5, 2022
• Last Update Submitted That Met QC Criteria: June 29, 2022
• Last Verified: June 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Hematologic Diseases; Genetic Diseases, Inborn; Anemia; Anemia, Hemolytic, Congenital; Anemia, Hemolytic; Hemoglobinopathies; Anemia, Sickle Cell
• Other Study ID Numbers: ECT-001.CB.005

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No