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An Open-label Study to Assess Safety and Efficacy of SZC in Paediatric Patients With Hyperkalaemia

NCT ID: NCT03813407

Last Updated: 2025-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE3

Total Enrollment

140 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-04-02

Study Completion Date

2026-06-29

Brief Summary

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Sodium zirconium cyclosilicate has been shown to be effective and safe in adults for the treatment of hyperkalaemia, and therefore it is expected to be beneficial in children. This study will evaluate the efficacy, safety and tolerability of sodium zirconium cyclosilicate for the treatment of hyperkalaemia in children \<18 years of age. Approximately 140 participants will enter CP at approximately 46 sites in locations including but not limited to Europe and North America for this study. Treatment will include 3 phases: the CP, MP, and LTMP. Enrolment will start in 2 cohorts, ages 6 to \< 12 years and 12 to \< 18 years. After review of accumulated data, the independent Data Monitoring Committee (iDMC) will recommend whether to open enrolment in the ages 2 to \< 6 years cohort and later in the ages 0 to \< 2 years cohort. All eligible participants with hyperkalaemia will enter an open-label Correction Phase (CP) receiving a fixed dose of SZC three times daily (TID) for up to 3 days until normokalaemia is achieved. Within each age cohorts 2 to \< 18 years, initial participants will be allocated to the dose level (DL) based on body weight equivalent to an adult 5 g TID. After recommendation of higher DLs by the iDMC, subsequent participants may be allocated in the CP to on body weight equivalent to an adult 10 g TID and then potentially on body weight equivalent to an adult 15 g TID. All participants in the ages 0 to \< 2 years cohort will be assigned to the same DL which will be decided based on data from older age cohorts. Participants who successfully achieve normokalaemia in the CP will enter a 28-day open-label Maintenance Phase (MP), which will be initiated with once daily administration of the dose received TID in the CP. During MP, the Investigator is able to titrate the dose up or down in the range 2.5 g to 15 g body weight equivalent to maintain normokalaemia. For participants who, at the end of MP, are normokalaemic or hyperkalaemic without being on maximum dose, the MP is followed by the option to continue the study in a long term maintenance phase (LTMP) where the same titration regimen is used as in MP

Detailed Description

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Protocol title: An open-label study to assess safety and efficacy of SZC in paediatric patients with hyperkalaemia

Rationale: Sodium zirconium cyclosilicate has been shown to be effective and safe in adults for the treatment of hyperkalaemia, and therefore it is expected to be beneficial in children. This study will evaluate the efficacy, safety and tolerability of sodium zirconium cyclosilicate for the treatment of hyperkalaemia in children \<18 years of age

Primary Objective: Correction phase (CP) primary objective:

1. To evaluate the ability to achieve normokalaemia during the CP when initiating treatment with SZC of different dose levels (DLs) in children with hyperkalaemia 28-day Maintenance Phase (MP) primary objective:
2. To evaluate the ability to maintain normokalaemia during the MP when continuing SZC treatment in children achieving normokalaemia

Secondary Objectives: All phases secondary objective:
3. To evaluate the change in S-K+ in children treated with SZC

MP secondary objectives:
4. To evaluate change in serum aldosterone levels in children treated with SZC during the MP
5. To evaluate change in serum electrolytes (including bicarbonate), spot urinary pH and urinary electrolytes levels in children treated with SZC during the MP

Long-term MP (LTMP) secondary objectives:
6. To evaluate the ability of maintaining normokalaemia in children treated with SZC during the LTMP

Safety Objective:
7. To evaluate the safety and tolerability of SZC in the 3 phases (CP, MP, and LTMP)

Tertiary/Exploratory:
8. To evaluate the acceptability and palatability of SZC through the study

Overall design: This is a Phase 3, international, multi-centre, open-label study assessing different doses of SZC. The population to be studied is hyperkalaemic children \< 18 years. Dosing will mirror the regimen approved for adults using body weight equivalent doses. Enrolment will start in 2 cohorts, ages 6 to \< 12 years and 12 to \< 18 years. After review of accumulated data, the independent Data Monitoring Committee (iDMC) will recommend whether to open enrolment in the ages 2 to \< 6 years cohort and later in the ages 0 to \< 2 years cohort.

The study will be conducted in approximately 11 countries and 46 sites. All eligible participants with hyperkalaemia will enter an open-label Correction Phase (CP) receiving a fixed dose of SZC three times daily (TID) for up to 3 days until normokalaemia is achieved. Within each age cohorts 2 to \< 18 years, initial participants will be allocated to the dose level (DL) based on body weight equivalent to an adult 5 g TID. After recommendation of higher DLs by the iDMC, subsequent participants may be allocated in the CP to on body weight equivalent to an adult 10 g TID and then potentially on body weight equivalent to an adult 15 g TID. All participants in the ages 0 to \< 2 years cohort will be assigned to the same DL which will be decided based on data from older age cohorts.

Participants who successfully achieve normokalaemia in the CP will enter a 28-day open-label Maintenance Phase (MP), which will be initiated with once daily administration of the dose received TID in the CP. During MP, the Investigator is able to titrate the dose up or down in the range 2.5 g to 15 g body weight equivalent to maintain normokalaemia. The MP is followed by the option for participants to continue the study in a long-term maintenance phase (LTMP) where the same titration regimen is used as in MP, but with monthly visits.

Study period: Estimated date of first participant enter the CP Q4 2018. Estimated date of last participant completed 27 December 2024.

Number of participants: This study aims to enter into CP a total of approximately 140 participants with hyperkalaemia. Of these, approximately 85 participants are expected to have moderate to severe hyperkalaemia. Enrolment will continue until at least 54 participants with moderate to severe hyperkalaemia have entered the MP and 45 participants with moderate to severe hyperkalaemia have completed the MP. A maximum of 55 participants with mild hyperkalaemia will enter the CP. In addition, there are minimum requirements for participants in each age cohort

Duration: Study duration is approximately 28 weeks including up to 3 days of correction treatment, followed by maintenance treatment for 28 days, a LTMP for up to 22 weeks, and a safety follow-up visit 1 week after the last dose.

Treatments and treatment duration:

Treatment will include 3 phases: the CP, MP, and LTMP. All age cohorts are eligible to participate in all phases of the study. The 3 treatment phases are specified below:

Correction phase (CP): All eligible participants with hyperkalaemia will enter an open-label Correction Phase (CP) receiving a fixed dose of SZC three times daily (TID) for up to 3 days until normokalaemia is achieved. Within each age cohorts 2 to \< 18 years, initial participants will be allocated to the dose level (DL) 5 g TID. After recommendation of higher DLs by the iDMC, subsequent participants may be allocated in the CP to 10 g TID and then potentially 15 g TID. All participants in the ages 0 to \< 2 years cohort will be assigned to the same DL which will be decided based on data from older age cohorts.

Maintenance phase (MP): Participants who successfully achieve normokalaemia in the CP will enter a 28-day open-label Maintenance Phase (MP), which will be initiated with once daily administration of the dose received TID in the CP. During MP, the Investigator is able to titrate the dose up or down in the range 2.5 g to 15 g body weight equivalent to maintain normokalaemia.

Long term Maintenance Phase (LTMP): For participants who, at the end of MP, are normokalaemic or hyperkalaemic without being on maximum dose, the MP is followed by the option to continue the study in a long term maintenance phase (LTMP) where the same titration regimen is used as in MP.

Data Monitoring Committee:

The iDMC will recommend on the opening of dose levels during the CP after reviewing all available data. Additionally, iDMC will recommend whether and when enrolment in the ages 0 to \< 6 years cohorts will begin, and will also evaluate emerging safety data during all phases of the study.

Statistical methods: Objectives will be evaluated based on analysis populations corresponding to each study phase. Analysis sets are defined for each phase as the set of all participants who transitioned from previous phase and who received at least one dose of SZC during the phase. Primary assessments of the primary objectives, the probability to achieve and maintain normokalaemia when treated with SZC, will be based on point estimates together with 95% confidence intervals (CIs) from generalised linear models (repeated measures model for the MP). The secondary objective of change in S-K+ over time will be evaluated using a repeated measures linear model. Additional analyses, including analyses for other secondary objectives, will be done descriptively. In general, data will be analysed in the total analysis population, within each age cohort and, for the CP, within adult body weight equivalent dose-level, as appropriate. An interim read-out may be conducted.

Conditions

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Hyperkalaemia

Keywords

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sodium zirconium cyclosilicate Hyperkalaemia in children

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Treatment includes 3phases:CP,MP,LTMP Eligible participants with hyperkalaemia will enter CP receiving fixed dose of SZC three times daily(TID) for up to 3days until normokalaemia.Within each cohort 2 to\<18 years,initial participants will be allocated to dose level (DL)5g TID.After recommendation of higher DLs by iDMC,subsequent participants may be allocated in the CP to 10g TID and potentially 15g TID.Participants in 0 to\<2 years cohort will be assigned to the same DL decided based on data from older cohorts.Those who achieve normokalaemia in the CP will enter a 28-day MP,which starts with once daily administration of the dose received TID in the CP.During MP,the Investigator is able to titrate the dose up or down in the range 2.5gto15g body weight equivalent to maintain normokalaemia.For participants who,at the end of MP,are normokalaemic/hyperkalaemic without being on maximum dose,the MP is followed by option to continue in an LTMP where the same titration regimen is used as in MP.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

All phases in the study are open-label

Study Groups

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Active Arm ( Sodium Zirconium Cyclosilicate SZC)

Dosage formulation: 5 g sachets 2.5 g sachets 0.25 g sprinkle capsules 0.125 g sprinkle capsules (can be manufactured to support participants \<2 years of age) Route of administration: Oral Dosing instructions: SZC is provided as a powder. At the time of dosing SZC is mixed with a quantity of water or sprinkled onto semi-solid food (eg, milk, baby food, yogurt, or ice cream) within an hour of drug administration. Packaging and labelling: Study treatment will be provided in sachets packed in cartons or sprinkle capsules in high density polyethylene bottles, as appropriate for the dose. Each carton of sachets, individual sachets, and bottle of capsules will be labelled in accordance with Good Manufacturing Practice Annex 13 and per country regulatory requirement. Participant-specific dosing cards (diary) will be provided.

Group Type EXPERIMENTAL

Sodium Zirconium Cyclosilicate (SZC) Reduced Dose Level

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Dose: Paediatric dose based on body weight equivalent to an adult 2.5 g

Sodium Zirconium Cyclosilicate (SZC) Dose Level 1 (DL1)

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC)Paediatric dose based on body weight equivalent to an adult 5 g

Sodium Zirconium Cyclosilicate (SZC) Dose Level 2 (DL2)

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Paediatric dose based on body weight equivalent to an adult 10 g

Sodium Zirconium Cyclosilicate (SZC) Dose Level 3 (DL3)

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Paediatric dose based on body weight equivalent to an adult 15 g

Sodium Zirconium Cyclosilicate (SZC) Dose During 28 Day Maintenance Phase

Intervention Type DRUG

A 28-day period during which SZC is administered orally once daily (QD) to maintain normokalaemia. A dose titration regimen starting with QD administration of the dose of SZC the participants received TID in the CP will be studied in the MP and continued in the LTMP. The maximum dose that can be used is the calculated body weight equivalent to the 15 g adult dose

Interventions

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Sodium Zirconium Cyclosilicate (SZC) Reduced Dose Level

Sodium Zirconium Cyclosilicate (SZC) Dose: Paediatric dose based on body weight equivalent to an adult 2.5 g

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Dose Level 1 (DL1)

Sodium Zirconium Cyclosilicate (SZC)Paediatric dose based on body weight equivalent to an adult 5 g

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Dose Level 2 (DL2)

Sodium Zirconium Cyclosilicate (SZC) Paediatric dose based on body weight equivalent to an adult 10 g

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Dose Level 3 (DL3)

Sodium Zirconium Cyclosilicate (SZC) Paediatric dose based on body weight equivalent to an adult 15 g

Intervention Type DRUG

Sodium Zirconium Cyclosilicate (SZC) Dose During 28 Day Maintenance Phase

A 28-day period during which SZC is administered orally once daily (QD) to maintain normokalaemia. A dose titration regimen starting with QD administration of the dose of SZC the participants received TID in the CP will be studied in the MP and continued in the LTMP. The maximum dose that can be used is the calculated body weight equivalent to the 15 g adult dose

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Provision of written informed consent of the participant or legal representative, and informed assent from the participant (as appropriate)
2. Female or male from birth to \< 18 years of age (for the study duration).
3. Participants (including those receiving a stable peritoneal dialysis regimen for a minimum of 2 months) requiring long-term treatment of hyperkalaemia (chronic hyperkalaemia) in the age cohort ≥ 2 years, and participants requiring either short- or long-term treatment for hyperkalaemia (acute and chronic hyperkalaemia) in the age cohort \< 2 years.
4. Participants must meet the following criteria for hyperkalaemia: Please refer to the Table 6 in the protocol.
5. Using digital ECG, QT interval corrected by Bazett's method (QTcB) must meet the age-appropriate parameters at Screening: a. For participants aged 0 to ≤ 3 days after birth: \< 450 ms b. For participants aged \>3 days to \< 12 years: \< 440 ms c. For participants aged ≥ 12 to \< 18 years: \< 450 ms (male), \< 460 ms (female) All QTcB values outside the reference values specified in the protocol should be manually re-measured and re-calculated, and if there is a difference in measurement between the automatic and manual ECG, the manual measurement should always be considered correct.
6. Ability to have repeated blood draws or effective venous catheterisation.
7. Females of childbearing potential (defined as a female with potential of becoming pregnant who has experienced her menarche) must have a negative pregnancy test within one day prior to the first dose of SZC on CP Study Day 1 and sexually active females of childbearing potential must be using 2 forms of medically acceptable contraception with at least one being a barrier method
8. Optional open-label, LTMP only:

1. Provision of written informed consent of the participant or legal representative, and informed assent from the participant (as appropriate) to take part in the LTMP.
2. Participants who are normokalaemic at the end of MP or hyperkalaemic and not on maximum dose.
3. Participants who would benefit from long-term treatment for their hyperkalaemia, as judged by the Investigator.

Exclusion Criteria

1. Neonates with a gestational age \< 37 weeks at birth or a birth weight \< 2500 g.
2. Term and preterm neonates with suspected conditions predisposing them to intestinal ischaemia (eg, perinatal hypoxia or sepsis).
3. Participants with pseudohyperkalaemia caused by excessive fist clenching to enable venepuncture, by haemolysed blood specimens, or by severe leukocytosis or thrombocytosis.
4. Participants with hyperkalaemia due to soft-tissue damage from crush injury or burns. 5. Participants with hyperkalaemia due to a secondary cause, such as dehydration, excessive use of K+ supplements, or drug use (eg, beta-adrenergic antagonists) and that would be more appropriately treated with other interventions (eg, fluid resuscitation, dose adjustments of medications).

6\. Participants with transient iatrogenic hyperkalaemia (eg, due to treatment with tacrolimus).

7\. Participants treated with lactulose, rifaximin (XIFAXAN™), or other nonabsorbed antibiotics for hyperammonaemia within the last 7 days.

8\. Participants treated with CPS, sodium polystyrene sulfonate (eg, KAYEXALATE™), or patiromer within the last 4 days prior to first dose of study treatment.

9\. Participants with a life expectancy of less than 3 months. 10. Participants who are known to have tested Human Immunodeficiency Virus (HIV) positive.

11\. Presence of any condition which, in the opinion of the Investigator, places the participant at undue risk or potentially jeopardises the quality of the data to be generated. 12. Known hypersensitivity or previous anaphylaxis to SZC or to components thereof.

13\. Participants with cardiac arrhythmias that require immediate treatment. 14. Participants with a family history of long QT syndrome. 15. Participants on haemodialysis. 16. Participants with a history of bowel obstruction. 17. Participants with severe gastrointestinal disorder or major gastrointestinal surgery (eg, large bowel resection).

18\. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site).

19\. Previous treatment with SZC. 20. Treatment with a drug or device within the last 30 days prior to first dose of study treatment that has not received regulatory approval at the time of study entry.

21\. Previous enrolment in the present study. 22. Females who are pregnant, breastfeeding, or planning to become pregnant. 23. Judgement by the Investigator that the participant should not participate in the study if the participant is unlikely to comply with study procedures, restrictions, and requirements. 24. If the participant has evidence of Coronavirus disease 2019 (COVID-19) within 2 weeks prior to enrolment (a positive COVID-19 test or suspicion of COVID-19 infection) the participant cannot be enrolled in the study.
Minimum Eligible Age

0 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Research Site

Birmingham, Alabama, United States

Site Status RECRUITING

Research Site

Atlanta, Georgia, United States

Site Status WITHDRAWN

Research Site

Baltimore, Maryland, United States

Site Status RECRUITING

Research Site

Grand Rapids, Michigan, United States

Site Status NOT_YET_RECRUITING

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St Louis, Missouri, United States

Site Status RECRUITING

Research Site

Hackensack, New Jersey, United States

Site Status COMPLETED

Research Site

New York, New York, United States

Site Status WITHDRAWN

Research Site

Stony Brook, New York, United States

Site Status WITHDRAWN

Research Site

Charlotte, North Carolina, United States

Site Status WITHDRAWN

Research Site

Winston-Salem, North Carolina, United States

Site Status WITHDRAWN

Research Site

Akron, Ohio, United States

Site Status COMPLETED

Research Site

Cincinnati, Ohio, United States

Site Status RECRUITING

Research Site

Columbia, South Carolina, United States

Site Status RECRUITING

Research Site

Morgantown, West Virginia, United States

Site Status RECRUITING

Research Site

Campinas, , Brazil

Site Status RECRUITING

Research Site

São Paulo, , Brazil

Site Status RECRUITING

Research Site

São Paulo, , Brazil

Site Status RECRUITING

Research Site

Calgary, Alberta, Canada

Site Status RECRUITING

Research Site

Edmonton, Alberta, Canada

Site Status WITHDRAWN

Research Site

Vancouver, British Columbia, Canada

Site Status WITHDRAWN

Research Site

Montreal, Quebec, Canada

Site Status RECRUITING

Research Site

Beijing, , China

Site Status RECRUITING

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Beijing, , China

Site Status RECRUITING

Research Site

Changsha, , China

Site Status RECRUITING

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Chengdu, , China

Site Status RECRUITING

Research Site

Chengdu, , China

Site Status RECRUITING

Research Site

Chongqing, , China

Site Status RECRUITING

Research Site

Hangzhou, , China

Site Status RECRUITING

Research Site

Hefei, , China

Site Status WITHDRAWN

Research Site

Shanghai, , China

Site Status RECRUITING

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Shanghai, , China

Site Status RECRUITING

Research Site

Berlin, , Germany

Site Status WITHDRAWN

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Essen, , Germany

Site Status RECRUITING

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Heidelberg, , Germany

Site Status RECRUITING

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Bhubaneshwar, , India

Site Status RECRUITING

Research Site

Gurgaon, , India

Site Status NOT_YET_RECRUITING

Research Site

New Delhi, , India

Site Status WITHDRAWN

Research Site

Bunkyō City, , Japan

Site Status RECRUITING

Research Site

Fuchu-shi, , Japan

Site Status RECRUITING

Research Site

Fukuoka, , Japan

Site Status RECRUITING

Research Site

Kawasaki-shi, , Japan

Site Status RECRUITING

Research Site

Kobe, , Japan

Site Status RECRUITING

Research Site

Matsumoto-shi, , Japan

Site Status RECRUITING

Research Site

Nakagami-gun, , Japan

Site Status RECRUITING

Research Site

Saitama-Shi, , Japan

Site Status RECRUITING

Research Site

Sendai, , Japan

Site Status RECRUITING

Research Site

Shizuoka, , Japan

Site Status RECRUITING

Research Site

Bialystok, , Poland

Site Status COMPLETED

Research Site

Krakow, , Poland

Site Status WITHDRAWN

Research Site

Lodz, , Poland

Site Status COMPLETED

Research Site

Warsaw, , Poland

Site Status RECRUITING

Research Site

Bucharest, , Romania

Site Status RECRUITING

Research Site

Bucharest, , Romania

Site Status WITHDRAWN

Research Site

Cluj-Napoca, , Romania

Site Status RECRUITING

Research Site

Târgu Mureş, , Romania

Site Status RECRUITING

Research Site

Timișoara, , Romania

Site Status RECRUITING

Research Site

Samara, , Russia

Site Status WITHDRAWN

Research Site

Esplugues de Llobregat, , Spain

Site Status RECRUITING

Research Site

Madrid, , Spain

Site Status RECRUITING

Research Site

Dnipropetrovsk, , Ukraine

Site Status SUSPENDED

Research Site

Kharkiv Region, , Ukraine

Site Status SUSPENDED

Research Site

Kyiv, , Ukraine

Site Status SUSPENDED

Research Site

Odesa, , Ukraine

Site Status WITHDRAWN

Research Site

Sumy, , Ukraine

Site Status SUSPENDED

Research Site

Zaporizhzhia, , Ukraine

Site Status TERMINATED

Research Site

Glasgow, , United Kingdom

Site Status RECRUITING

Research Site

Hampshire, , United Kingdom

Site Status RECRUITING

Research Site

Manchester, , United Kingdom

Site Status COMPLETED

Research Site

Nottingham, , United Kingdom

Site Status TERMINATED

Countries

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Italy United States Brazil Canada China Germany India Japan Poland Romania Russia Spain Ukraine United Kingdom

Central Contacts

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AstraZeneca Clinical Study Information Center

Role: CONTACT

Phone: 1-877-240-9479

Email: [email protected]

Other Identifiers

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2023-508455-38-00

Identifier Type: REGISTRY

Identifier Source: secondary_id

2018-001331-48

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

D9481C00001

Identifier Type: -

Identifier Source: org_study_id