Sirolimus for Leigh Syndrome

Official title

A Pilot Phase 2 Study With Long-Term Extension to Assess the Safety and Efficacy of Sirolimus in Patients With Leigh Syndrome Caused by Genetically-Confirmed Mitochondrial Respiratory Chain Deficiency

Overview

The purpose of this study is to evaluate the safety and efficacy of the drug Sirolimus in participants with Leigh syndrome.

Detailed description

This is a pilot phase 2 study with long-term extension to evaluate the safety and efficacy of enteral sirolimus in patients with genetically-confirmed Leigh syndrome.

Sirolimus will be given daily at a starting dose of 0.8 to 1.3 mg/m2 depending on subject age, weight, and BSA (body surface area). Dosage will be adjusted as needed based on sirolimus trough level to maintain patients within a range of 5 to10 ng/mL, a level lower than what is targeted in renal transplant recipients. Patients will be followed through this study for up to 24 weeks in the active phase. Participants who are eligible for the long-term extension may choose to stay on drug for up to 2 years thereafter

Interventions

• Drug Sirolimus
  Sirolimus will be given at a starting dose of 0.8 to 1.3 mg/m2 twice daily, depending on subject age and weight.

Primary outcome measures

• Rate of Adverse Events [Time frame: Up to 2.5 years]
• Rate of Intercurrent Infection and Hospitalization [Time frame: Up to 2.5 years]
• Incidence of abnormal safety lab values [Time frame: Up to 2.5 years]
• Sirolimus Trough Level [Time frame: Up to 2.5 years]

Secondary outcome measures (12)

• Change in MM-COAST Score [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in GMFM (Gross Motor Function Measure) Score [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in Movement Disorder-Childhood Rating Score (MDCRS) [Time frame: Baseline up to end of study (up to 2.5 years)]
• CGI Scale [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in Barry-Albright Dystonia Scale (BADS) [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in Scale for the Assessment and Rating of Ataxia (SARA) [Time frame: Baseline up to end of study (up to 2.5 years)]
• Newcastle Pediatric Mitochondrial Disease Scale (NPMDS) [Time frame: Baseline up to end of study (up to 2.5 years)]
• Newcastle Adult Mitochondrial Disease Scale (NMDAS) [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in PEDI-CAT Score [Time frame: Baseline up to end of study (up to 2.5 years)]
• Patient Global Impression of Change (PGIC) [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in PedsQL [Time frame: Baseline up to end of study (up to 2.5 years)]
• Change in Karnofsky-Lansky [Time frame: Baseline up to end of study (up to 2.5 years)]

Eligibility criteria

Inclusion criteria

• Genetically-confirmed diagnosis of Leigh syndrome with neurodevelopmental manifestations, which include documented developmental delay, developmental regression, or abnormal neurologic exam findings including but not limited to hypotonia, hypertonia, dystonia, chorea, nystagmus, ataxia, dysmetria, tremor or muscle weakness.
• Age 6 months to 55 years at the time of enrollment.
• Weight ≥ 5 kg at the time of enrollment.
• Adequate liver function as evidenced by total bilirubin < 1.5x upper limit of normal (ULN) and liver function tests, alanine transaminase (ALT) and aspartate aminotransferase (AST), < 3x ULN.
• Adequate renal function as evidenced by glomerular filtration rate (GFR) > 60 mL/min/1.73m2 (cystatin C for pediatric population).
• Normal hematologic parameters as defined as:

• Absolute neutrophil count (ANC) ≥ 1.0 x 109/L
• Platelet count ≥ 100,000/mm3 (100 x 109/L)
• Hemoglobin ≥ 9 g/dL
• Non-fasting serum triglycerides and cholesterol < 300 mg/dL.
• Serum amylase and lipase < 2x ULN.
• Adequate immunoglobulin levels as outlined below that, in the opinion of the investigator, will not place the patient at increased risk of infection.

• Immunoglobulin G (IgG) ≥ 200 mg/dL
• Immunoglobulin M (IgM) ≥ 30 mg/dL
• Immunoglobulin A (IgA) ≥ 10 mg/dL
• All sexually active participants must agree to use effective contraception:

• Females of child-bearing potential must agree to use effective contraception without interruption from 28 days prior to starting Investigational Product (IP) throughout 3 months after last dose of IP and have a negative urine pregnancy test result at screening and agree to ongoing pregnancy testing during the course of the study.
• Male patients must practice abstinence or agree to use a condom during sexual contact with a pregnant female or a female of childbearing potential while participating in the study and throughout 3 months after the last dose of investigational drug.
• The patient or parent(s)/legal guardian(s) is/are willing and able to comply with the study visit schedule and other protocol requirements, in the opinion of the investigator.
• The patient or the patient's parent(s)/legal guardian(s) understand(s) and voluntarily sign(s) the informed consent documents(s) prior to any study-related assessments/procedures being conducted.

Exclusion criteria

• Cardiac ejection fraction ≤ 50 %, shortening fraction ≤ 25% on cardiac echocardiogram within one year of screening and/or severe end-organ hypo-perfusion syndrome (secondary to cardiac failure) resulting in lactic acidosis.
• Patients with implanted cardiac assist/medical devices (including pacemakers), unless device was implanted prophylactically, and the patient is clinically asymptomatic.
• In the opinion of the investigator, clinically significant ECG and/or echocardiogram alterations at the time of screening.
• Myocardial infarction within 6 months prior to enrollment.
• Symptomatic congestive heart failure (CHF), unstable angina pectoris, cardiac arrhythmia, uncontrolled hypertension, or unstable coronary artery disease.
• Prior history of hypersensitivity to sirolimus or other mTOR (Mechanistic Target of Rapamycin inhibitors).
• Prior history of angioedema requiring treatment or cessation of a presumed causative agent.
• Planned surgical procedure during the study period.
• Confirmed or highly suspected immunodeficiency disorder(s), including but not limited to, common variable immune deficiency (CVID), complement deficiency, etc.
• Clinically significant proteinuria that requires ongoing medical therapy.
• Any uncontrolled psychiatric or medical condition which, in the opinion of the investigator, would interfere with the patient's participation in the study.
• Patients who are breastfeeding or are pregnant.
• History of solid organ transplant (kidney, liver, heart, lung) or bone marrow transplant.
• Treatment with any investigational drug (i.e., a drug for which there is no approved indication), including an investigational drug for mitochondrial disease within 1 month prior to receiving the first dose of study drug (or within 3 months for a trial with an investigational biologic).
• Patients with confirmed or suspected increased intracranial pressure, pseudotumor cerebri (PTC)/idiopathic intracranial hypertension, and or papilledema.
• Currently active malignancy (other than adequately treated non-melanoma skin cancers \[i.e., squamous cell and/or basal cell carcinoma\], carcinoma in situ of the cervix, or other adequately treated carcinoma in situ) and/or ongoing treatment for malignancy are ineligible. Patients are not considered to have a currently active malignancy if they have completed therapy and are free of disease for ≥ 1 year.
• Recent infection requiring systemic anti-infective treatment that was completed ≤ 14 days prior to enrollment.
• Uncontrolled diabetes mellitus, as defined by HbA1c > 8%, despite adequate therapy.
• History of interstitial lung disease and/or pneumonitis.
• Use of strong inhibitors and/or inducers of cytochrome P450 (CYP) 3A4 (CYP3A4) and/or p-glycoprotein (p-GP) within the 14 days prior to receiving the first dose of study drug. Additionally, use of any known CYP3A4 substrates with a narrow therapeutic window (e.g., fentanyl, alfentanil, astemizole, cisapride, dihydroergotamine, pimozide, quinidine, terfenadine) within the 14 days prior to receiving the first dose of study drug.
• Use of medications with a high risk of angioedema
• Known human immunodeficiency virus (HIV), active hepatitis B or hepatitis C infection(s).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

United States · 1 center

• Children's Hospital of Philadelphia — Philadelphia

Publications

• Johnson SC, Yanos ME, Kayser EB, Quintana A, Sangesland M, Castanza A, Uhde L, Hui J, Wall VZ, Gagnidze A, Oh K, Wasko BM, Ramos FJ, Palmiter RD, Rabinovitch PS, Morgan PG, Sedensky MM, Kaeberlein M. mTOR inhibition alleviates mitochondrial disease in a mouse model of Leigh syndrome. Science. 2013 Dec 20;342(6165):1524-8. doi: 10.1126/science.1244360. Epub 2013 Nov 14. PMID 24231806
• Johnson SC, Yanos ME, Bitto A, Castanza A, Gagnidze A, Gonzalez B, Gupta K, Hui J, Jarvie C, Johnson BM, Letexier N, McCanta L, Sangesland M, Tamis O, Uhde L, Van Den Ende A, Rabinovitch PS, Suh Y, Kaeberlein M. Dose-dependent effects of mTOR inhibition on weight and mitochondrial disease in mice. Front Genet. 2015 Jul 22;6:247. doi: 10.3389/fgene.2015.00247. eCollection 2015. PMID 26257774
• Tinker RJ, Falk MJ, Goldstein A, George-Sankoh I, Xiao R, Adang L, Ganetzky R. Early developmental delay in Leigh syndrome spectrum disorders is associated with poor clinical prognosis. Mol Genet Metab. 2022 Apr;135(4):342-349. doi: 10.1016/j.ymgme.2022.02.006. Epub 2022 Feb 19. PMID 35216885
• Zheng X, Boyer L, Jin M, Kim Y, Fan W, Bardy C, Berggren T, Evans RM, Gage FH, Hunter T. Alleviation of neuronal energy deficiency by mTOR inhibition as a treatment for mitochondria-related neurodegeneration. Elife. 2016 Mar 23;5:e13378. doi: 10.7554/eLife.13378. PMID 27008180

Identifiers

NCT: NCT06843811 · 24-022433

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗