A Study to Find Out How BIIB141 (Omaveloxolone) is Processed in the Body and to Learn More About Its Safety in Participants With Friedreich's Ataxia Aged 2 to 15 Years Old

NCT ID: NCT06054893

Last Updated: 2026-01-07

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-07-01
• Study Completion Date: 2030-11-22

Brief Summary

In this study, researchers will learn more about BIIB141, also known as omaveloxolone or SKYCLARYS®. This drug has been approved, or made available for doctors to prescribe, for people with Friedrich's Ataxia (FA) who are at least 16 years old. But, it is not yet available for children and teens with FA who are younger than 16 years old. The main objective of this study is to learn how BIIB141 is processed in the body of children and teens who are 2 to 15 years old.

The main question researchers want to answer in this study is:

• How does the body process BIIB141 in children and teens?
• How many participants have medical problems during the study?
• Are there any changes in the participants' overall health during the study?
• Are there any changes in the participants' heart health?
• Are there any changes in how the participants move through puberty? Puberty is the time in someone's life when their body changes from a child to an adult.

This study will be done as follows:

• Participants will be screened to see if they can join the study. The screening period will be up to 14 days, after which participants will check into their study research center.
• There are 2 parts to this study. During Part 1, participants will take a single dose of BIIB141. Participants will be in 1 of 7 different groups based on their age:
• Group A1: 12 to 15 years old, taking 150 milligrams (mg) of BIIB141
• Group A2: 12 to 15 years old, taking a dose of BIIB141 based on the data from Group A1
• Group B1: 7 to 11 years old, taking a dose of BIIB141 based on Group A1 data
• Group C1: 2 to 6 years old, taking a dose of BIIB141 based on Groups A1, A2, and B1 data
• Group A3: 12 to 15 years old, taking a dose of BIIB141 based on Groups A1, A2, and B1 data
• Group B2: 7 to 11 years old, taking a dose of BIIB141 based on Groups A1, A2, and B1 data
• Group C2: 2 to 6 years old, taking a dose of BIIB141 based on Group A1, A2, A3, B1, B2, and C1 data.
• During Part 2, participants from Part 1 will take BIIB141 once in the study research center. Cohort A1 will take 150 mg of BIIB141. Dose of Cohorts A2 and B1 will be based on data from Cohort A1, dose of Cohorts C1, A3 and B2 will be based on data from Cohorts A1, A2 and B1, while Cohort C2's dose will be based on all the other groups. Participants will then take it once a day at home.
• After leaving the study research center in Part 2, participants will return for tests at Week 4, Week 12, Week 24, and then every 24 weeks. Participants will also be contacted by telephone at Week 2, Week 8, and Week 18.
• Participants will be in this study for up to 240 weeks.

Detailed Description

Recruitment will be limited to the U.S. only as participants will be able to remain on Part 2 of the study until they turn 16 and can access commercially-available drug which is FDA approved for age 16 and above. The part 1 primary objective of the study is to evaluate the pharmacokinetics (PK) of omaveloxolone following administration of a single dose in 3 age cohorts (2 to <7 years, 7 to <12 years, and 12 to <16 years) and secondary objective is to evaluate safety and tolerability of drug. The part 2 primary objective is to evaluate long term safety and tolerability of omaveloxolone.

Conditions

Friedreich Ataxia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Part 1 and 2: Cohort A1

Cohort A1 will contain participants 12 to \<16 years of age. Participants will receive a single oral dose of omaveloxolone, 150 milligrams (mg), capsule, on Day 1 of the treatment period of part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian population pharmacokinetics (popPK) analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort A2

Cohort A2 will contain participants 12 to \<16 years of age. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from Cohort A1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort B1

Cohort B1 will contain participants 7 to \<12 years of age and will initiate in parallel with Cohort A2. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from Cohort A1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort C1

Cohort C1 will contain participants 2 to \<7 years of age. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from cohorts A1, A2, and B1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort A3

Cohort A3 will contain participants 12 to \<16 years of age. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from cohorts A1, A2, and B1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort B2

Cohort B2 will contain participants 7 to \<12 years of age and will initiate in parallel with Cohort A3. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from cohorts A1, A2, and B1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Part 1 and 2: Cohort C2

Cohort C2 will contain participants 2 to \<7 years of age. Participants will receive a single oral dose of omaveloxolone, capsule, at a dosage level determined by a Bayesian popPK analysis using the data from Cohorts A1, A2, A3, B1, B2, and C1 to select the dose in part 1, followed by the same dose in part 2 up to week 240 or commercial availability whichever comes first. The dose in part 2 may be adjusted as per additional safety and Bayesian popPK analyses.

Group Type: EXPERIMENTAL

Omaveloxolone

Intervention Type: DRUG

Administered as specified in the treatment arm

Interventions

Omaveloxolone

Administered as specified in the treatment arm

Intervention Type: DRUG

Other Intervention Names

RTA 408; SKYCLARYS; BIIB141

Eligibility Criteria

Inclusion Criteria

• Have genetically confirmed FA.
• Have a left ventricular ejection fraction ≥ 40% (based on ECHO performed at Screening Visit).
• During screening, during the treatment period, and until 28 days following administration of the last dose of omaveloxolone, females of childbearing potential must practice at least 1 of the acceptable methods of birth control.
• During screening, during the treatment period, and until 28 days after the last dose of omaveloxolone, fertile males who have female partners of childbearing potential must practice one of the acceptable methods of birth control.

Exclusion Criteria

• Have uncontrolled diabetes (haemoglobin A1c [HbA1c] >11.0%).
• Have B-type natriuretic peptide (BNP) level >200 picograms per milliliter (pg/mL) at screening.
• Have a history of clinically significant (CS) left-sided heart disease and/or CS cardiac disease, with the exception of mild to moderate cardiomyopathy associated with FA.
• Presence of outflow tract obstruction defined as a peak instantaneous gradient >50 mmHg (based on ECHO performed at screening).
• Have taken any moderate or strong inhibitors and/or inducers of cytochrome P450 3A4 within the 7 days prior to Day 1 or plan to take during study participation (eg, itraconazole, carbamazepine, phenytoin, ciprofloxacin, grapefruit juice, cannabidiol, fluconazole, fluvoxamine, verapamil, diltiazem).
• Have a history of CS liver disease (eg, fibrosis, cirrhosis, hepatitis), or have clinically relevant deviations in laboratory tests at screening
• Plan to or have participated in any other interventional clinical study within the 30 days prior to Day 1.
• Have a cognitive impairment that may preclude ability to comply with study procedures, in the opinion of the investigator.
• Be unable to comply with the requirements of the study protocol or be unsuitable for the study for any reason, in the opinion of the investigator.
• Have previously documented mitochondrial respiratory chain disease.
• Have a history of thromboembolic events within the past 5 years.
• Plan to or have taken anticoagulant therapy within 30 days prior to Day 1 with the exception of a daily low dose aspirin (up to 81 mg).
• Plan to or have scheduled surgical treatment for scoliosis or foot deformity during the study.
• Have had significant suicidal ideation within 30 days prior to Screening Visit, as per investigator judgment, or any history of suicide attempt.
• For females, be pregnant or breastfeeding.

Part 2:

• No discontinuation criteria have been met.
• Safety and tolerability data from Part 1 are supportive of continuation in the judgement of the Investigator.

In the event of intercurrent illness or other change in health status of the participant, additional Part 1 Screening assessments may be repeated prior to initiation of Part 2, based on the judgement of the Investigator in consultation with the Medical Monitor.

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 15 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Biogen

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Biogen

Locations

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

US Biogen Clinical Trial Center

Role: CONTACT

clinicaltrials@biogen.com

866-633-4636

Global Biogen Clinical Trial Center

Role: CONTACT

clinicaltrials@biogen.com

Facility Contacts

Recruiting Coordinator

Role: primary

215-590-2242

Other Identifiers

408-C-2001

Identifier Type: -

Identifier Source: org_study_id