RecruitingPhase 3NCT06439082

A Study to Investigate the Efficacy and Safety of Crizanlizumab (5 mg/kg) Compared With Placebo in Adolescent and Adult Sickle Cell Disease Patients Who Experience Frequent Vaso-Occlusive Crises (SPARKLE)

A Phase III, Multicenter, Randomized, Placebo Controlled, Double-blind Study to Assess Efficacy and Safety of Crizanlizumab (5 mg/kg) Versus Placebo, With or Without Hydroxyurea/Hydroxycarbamide Therapy, in Adolescent and Adult Sickle Cell Disease Patients With Frequent Vaso-Occlusive Crises


Sponsor

Novartis Pharmaceuticals

Enrollment

315 participants

Start Date

Oct 24, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

A phase III, multi-center, randomized, placebo-controlled, double-blind study to assess efficacy and safety of crizanlizumab (5 mg/kg) versus placebo, with or without hydroxyurea/hydroxycarbamide therapy, in adolescent and adult Sickle Cell Disease patients with frequent vaso-occlusive crises.


Eligibility

Min Age: 12 YearsMax Age: 100 Years

Inclusion Criteria5

  • Participants must be aged 12 years and older on the day of signing informed consent. Adolescents include participants aged 12 to \<18 years old and adults include participants aged 18 years and older.
  • Confirmed diagnosis of SCD by Hb electrophoresis or high-performance liquid chromatography (HPLC) (performed locally or by central laboratory if not available locally). All SCD genotypes are eligible.
  • Experienced 4 to 12 VOCs (refer to Section 8.3.1 for study definition of VOC) that are HCP-managed (including VOCs leading to management at a health care facility or those managed via remote consultation) within the 12 months prior to the screening visit. Baseline VOCs are determined by medical history and are required to be documented at source.
  • If the participant is on HU/HC, they must be taking it for at least 6 months and at stable dose for at least 3 months prior to the Screening visit and plan to continue taking it at the same dose and schedule until at least the participant has reached 52 weeks of the planned study treatment. Participants who have initiated HU/HC 6-12 months prior to the screening visit must have evidence of insufficient control of acute pain despite initiation. These participants must have a cumulative of 4-12 VOCs in the 12 months prior to the screening period, with at least 2 during the last 6 months while on HU/HC. If receiving erythropoietin stimulating agent, the participant must have been receiving the drug for at least 6 months prior to screening visit and plan to continue taking the drug at the same dose and schedule until the participant has reached 52 weeks of the planned study treatment.
  • Participants who have not been receiving HU/HC, and/or erythropoietin stimulating agent must not have received it for at least 6 months prior to screening visit.

Exclusion Criteria6

  • Fewer than 4 or more than 12 VOCs that are HCP-managed (including VOCs leading to management at a health care facility or those managed via remote consultation) within the 12 months prior to screening visit as determined by medical history and documented at source.
  • History of stem cell transplant and/or gene therapy.
  • Received blood products within 30 days prior to Week 1 Day 1 dosing.
  • Any documented history of a clinical stroke or intracranial hemorrhage, or an uninvestigated neurologic finding within the past 12 months before screening visit. Silent infarct only present on imaging is not excluded.
  • Participating in a chronic transfusion program (pre-planned series of transfusions for prophylactic purposes) and/or planning to undergo an exchange transfusion during the duration of the study; episodic transfusion in response to worsened anemia or VOC is permitted.
  • Contraindication or hypersensitivity to any drug or metabolites from similar class as study drug or to any excipients of the study drug formulation. History of severe hypersensitivity reaction to other monoclonal antibodies, which in the opinion of the investigator may pose an increased risk of serious infusion reaction.

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Interventions

BIOLOGICALCrizanlizumab

Crizanlizumab is supplied in single use 10 mL glass vials at a concentration of 10 mg/mL. One vial contains 100 mg of crizanlizumab. This is a concentrate for solution for IV infusion.

DRUGPlacebo

Placebo is supplied in single use 10 mL glass vials at a concentration of 0 mg/mL. This is a concentrate for solution for IV infusion.


Locations(30)

University Of Alabama

Birmingham, Alabama, United States

Childrens National Hospital

Washington D.C., District of Columbia, United States

University of Florida

Jacksonville, Florida, United States

Augusta University Georgia

Augusta, Georgia, United States

WCG Sonar Clinical Research

Riverdale, Georgia, United States

Norton Children s Hospital

Louisville, Kentucky, United States

The Johns Hopkins University School of Medicine

Baltimore, Maryland, United States

Southern Specialty Research

Flowood, Mississippi, United States

Childrens Hospital at Montefiore

The Bronx, New York, United States

East Carolina University

Greenville, North Carolina, United States

Wake Forest University Baptist Medical Center

Winston-Salem, North Carolina, United States

Spoknwrdclinicaltrials

Easton, Pennsylvania, United States

U of TX Health Science Ct

Houston, Texas, United States

Novartis Investigative Site

Salvador, Estado de Bahia, Brazil

Novartis Investigative Site

São Luís, Maranhão, Brazil

Novartis Investigative Site

Campinas, São Paulo, Brazil

Novartis Investigative Site

Ribeirão Preto, São Paulo, Brazil

Novartis Investigative Site

Sao Jose Rio Preto, São Paulo, Brazil

Novartis Investigative Site

São Paulo, São Paulo, Brazil

Novartis Investigative Site

São Paulo, São Paulo, Brazil

Novartis Investigative Site

Medellín, Antioquia, Colombia

Novartis Investigative Site

Cali, Valle del Cauca Department, Colombia

Novartis Investigative Site

Cali, Valle del Cauca Department, Colombia

Novartis Investigative Site

Montería, Colombia

Novartis Investigative Site

Ahero, Kisumu County, Kenya

Novartis Investigative Site

Kisumu, Kenya

Novartis Investigative Site

Kisumu, Kenya

Novartis Investigative Site

Siaya, Kenya

Novartis Investigative Site

Kampala, Uganda

Novartis Investigative Site

Tororo, Uganda

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NCT06439082


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