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A Study to Assess the Safety, Tolerability, and Efficacy of BIVV003 for Autologous Hematopoietic Stem Cell Transplantation in Patients With Severe Sickle Cell Disease

Phase 1
Active, not recruiting
Conditions
Sickle Cell Disease
Interventions
Biological: Plerixafor
Genetic: BIVV003
Registration Number
NCT03653247
Lead Sponsor
Sangamo Therapeutics
Brief Summary

This is an open label, multicenter, Phase 1/2 study in approximately eight adults with severe Sickle Cell Disease (SCD). The study will evaluate the safety, tolerability, and efficacy of autologous hematopoietic stem cell transplantation using BIVV003.

Detailed Description

Subject participation in this study will be approximately 136 weeks. Enrolled subjects will be asked to participate in a separate long-term follow-up study to monitor the safety and efficacy of BIVV003 treatment for a total of 15 years post-transplant.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
8
Inclusion Criteria

Not provided

Exclusion Criteria
  • Previous receipt of an autologous or allogeneic HSCT or solid organ transplantation
  • Previous treatment with gene therapy
  • Current enrollment in an interventional study or having received an investigational drug within 30 days of study enrollment
  • Pregnant or breastfeeding female
  • Female or male who plans to become pregnant or impregnate a partner, respectively, during the anticipated study period
  • Contraindication to plerixafor, apheresis, or busulfan
  • Treatment with prohibited medication in previous 30 days
  • Known allergy or hypersensitivity to plerixafor, busulfan, or investigational product excipients
  • History of active malignancy within past 5 years, any history of hematologic malignancy, or a family history of a cancer predisposition syndrome (without negative result of candidate)
  • Current diagnosis of uncontrolled seizures
  • History of significant bleeding disorder
  • Clinically significant infection
  • Any major organ dysfunction involving brain, kidney, liver, lung, or heart (e.g., congestive heart failure, pulmonary hypertension)
  • Corrected QT interval of more than 500 millisecond (ms) based on screening electrocardiogram (ECG)
  • Positive for human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV)
  • Known to have a gamma-globin variant associated with altered oxygen affinity
  • Hereditary persistence of fetal hemoglobin (HPFH) or HbF concentration of more than or equal to 20 percent (%) at screening
  • Absolute Neutrophil Count (ANC) of less than or equal to 1,000 per microliter
  • Platelet count of less than 100,000 per microliter
  • History of platelet alloimmunization (precluding ability to provide transfusion support)
  • Extensive Red Blood Cell (RBC) alloimmunization (precluding ability to provide transfusion support)
  • Judged unsuitable for participation by investigator and/or sponsor

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
BIVV003PlerixaforParticipants will receive plerixafor as subcutaneous (SQ) administration followed by myeloablative conditioning therapy with intravenous (IV) busulfan. BIVV003 will then be administered as a 1-time IV infusion of autologous Cluster of Differentiation 34 + Hematopoietic Stem/Progenitor Cell (CD34+HSPC) transfected ex vivo with zinc finger nuclease (ZFN) messenger ribonucleic acid (mRNAs) targeting the B-cell lymphoma/leukemia 11A (BCL11A) locus.
BIVV003BIVV003Participants will receive plerixafor as subcutaneous (SQ) administration followed by myeloablative conditioning therapy with intravenous (IV) busulfan. BIVV003 will then be administered as a 1-time IV infusion of autologous Cluster of Differentiation 34 + Hematopoietic Stem/Progenitor Cell (CD34+HSPC) transfected ex vivo with zinc finger nuclease (ZFN) messenger ribonucleic acid (mRNAs) targeting the B-cell lymphoma/leukemia 11A (BCL11A) locus.
BIVV003BusulfanParticipants will receive plerixafor as subcutaneous (SQ) administration followed by myeloablative conditioning therapy with intravenous (IV) busulfan. BIVV003 will then be administered as a 1-time IV infusion of autologous Cluster of Differentiation 34 + Hematopoietic Stem/Progenitor Cell (CD34+HSPC) transfected ex vivo with zinc finger nuclease (ZFN) messenger ribonucleic acid (mRNAs) targeting the B-cell lymphoma/leukemia 11A (BCL11A) locus.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants With Successful EngraftmentUp to Day 42

Successful engraftment is defined by absolute neutrophil count (ANC) greater than or equal to \>=500 cells/microliter (mL) for 3 consecutive days.

Number of Participants With Adverse Events (AEs)Up to Week 104

An AE is any untoward medical occurrence in a participant administered a pharmaceutical product that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product.

Number of Participants With Serious Adverse Events (SAEs)Up to Week 104

An SAE is any untoward medical occurrence that at any dose: Results in death, in the view of the Investigator, places the participant at immediate risk of death (a life-threatening event); however, this does not include an event that, had it occurred in a more severe form, might have caused death, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, results in a congenital anomaly/birth defect or is a medically important event.

Percentage of Participants who are Alive at Post-transplantation Day 100Day 100

The percentage of participants who are alive at post-transplantation Day 100 will be calculated using the Kaplan-Meier estimate.

Percentage of Participants who are Alive at Post-transplantation Week 52Week 52

The percentage of participants who are alive at post-transplantation Week 52 will be calculated using the Kaplan-Meier estimate.

Percentage of Participants who are Alive at Post-transplantation Week 104Week 104

The percentage of participants who are alive at post-transplantation Week 104 will be calculated using the Kaplan-Meier estimate.

Secondary Outcome Measures
NameTimeMethod
CD34 + HSPC Yield from Plerixafor Stem Cell MobilizationApproximately 12 weeks
Proportion of Participants with Sufficient Stem Cell Mobilization for Rescue Aliquot and BIVV003 ProductionApproximately 12 weeks
Yield of Zinc Finger Nuclease (ZFN)-edited Investigational ProductApproximately 12 weeks
Time to Initial Neutrophil Recovery Following BIVV003 InfusionUp to Week 104
Percentage of Participants With Maintenance of Platelet count of >=50,000/mcL to last Participant VisitUp to Week 104

The percentage of participants attaining a post-transplant platelet count of \>=50,000/mcL and maintaining this level through last Participant Visit (Week 104) will be calculated.

Change From Baseline in Peripheral Blood Fetal Hemoglobin (HbF) LevelsBaseline up to Week 104

Change from baseline in HbF up to Week 104 will be assessed.

Change From Baseline in Peripheral Blood Percent (%)F cellsBaseline up to Week 104

Change from baseline in %F cells up to Week 104 will be assessed.

Change From Baseline in Peripheral Blood Sickle Hemoglobin (HbS) LevelsBaseline up to Week 104

Change from baseline in peripheral blood HbS levels up to Week 104 will be assessed.

Change From Baseline in Peripheral blood total hemoglobin (Hb) concentrationBaseline up to Week 104

Change From baseline in peripheral blood total hemoglobin (Hb) concentration up to week 104 will be assessed.

Change From Baseline in Patient-Reported Outcomes Measurement Information System 57 (PROMIS-57) Scale ScoreBaseline up to Week 104

Quality of life (QoL) measures including fatigue will be assessed using PROMIS-57 scale. This is a 57-item questionnaire with 8 questions per domain for assessing physical and mental well-being in participants with SCD. 57 questions are summed into a total score, which is transformed into an age specific normalized t-score with 50 representing normal, and lower scores representing increasing disability.

Number of Participants With Sickle Cell Disease (SCD)-related Clinical EventsBaseline up to Week 104

Number of participants with SCD-related clinical events (including vaso-occlusive crisis \[VOC\], pain episodes etc.) will be reported.

Number of Red Blood Cell (RBC) Transfusions Received During the Post-transplantation Study PeriodUp to Week 104

The number of RBC transfusions received during the Post-Transplantation study period will be reported.

Time to Platelet Recovery Following BIVV003 InfusionUp to Week 104
Percentage of Participants With Maintenance of Absolute Neutrophil Count (ANC) of >=500/mcL to last Participant VisitUp to Week 104

Percentage of participants maintaining ANC of \>=500/mcL to last Participant Visit (Week 104) will be calculated.

Change From Baseline in Serum Bilirubin LevelsBaseline up to Week 104

Change from baseline in serum bilirubin levels up to Week 104 will be assessed.

Change From Baseline in Reticulocyte CountBaseline up to Week 104

Change from baseline in reticulocyte count up to Week 104 will be assessed.

Change From Baseline in Lactate Dehydrogenase (LDH) LevelsBaseline up to Week 104

Change from baseline in LDH levels up to Week 104 will be assessed.

Change From Baseline in Haptoglobin LevelsBaseline up to Week 104

Change from baseline in haptoglobin levels up to Week 104 will be assessed.

Number of SCD Related Clinical Events by SeverityBaseline up to Week 104

Severity will be categorized by toxicity grade according to CTCAE Version 5.0. AEs not listed in the CTCAE Version 5.0 will be evaluated by: Grade 1=Mild, Grade 2=Moderate, Grade 3=Severe or medically significant but not immediately life threatening, Grade 4=Life-threatening consequences; Grade 5=Death.

Participants lymphocyte CountsAt Weeks 13 and 52

Lymphocyte counts will be measured to assess reconstitution of immune function post-BIVV003 transplantation.

Participants Immunoglobulin levelsAt Weeks 13 and 52

Immunoglobulin levels will be measured to assess reconstitution of immune function post-BIVV003 transplantation.

Total Volume of RBC TransfusedUp to Week 104

Total volume of RBC transfused during the Post-Transplantation study period will be reported.

Trial Locations

Locations (5)

UCSF Benioff Children's Hospital

🇺🇸

Oakland, California, United States

Investigational Site Number 101

🇺🇸

Bethesda, Maryland, United States

Karmanos Cancer Institute

🇺🇸

Detroit, Michigan, United States

University of California Davis Comprehensive Cancer Center

🇺🇸

Sacramento, California, United States

Children's Healthcare of Atlanta

🇺🇸

Atlanta, Georgia, United States

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