- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT06775041
Undersøgelse for at bestemme optimal dosis og evaluere sikkerhed, tolerabilitet og farmakokinetik af progerinin hos patienter med Hutchinson-Gilford Progeria syndrom (HGPS)
Et fase 2a, randomiseret, åbent studie til at bestemme den optimale dosis og evaluere sikkerheden, tolerabiliteten og farmakokinetikken af progerinin hos patienter med Hutchinson-Gilford Progeria syndrom (HGPS)
Researchers will compare treatment with progerinin plus lonafarnib vs lonafarnib alone to assess optimal dosing, safety, tolerability, and pharmacokinetics in patients with Hutchinson-Gilford Progeria Syndrome (HGPS). Subjects in the randomized study arms will continue to take the standard of care (SOC), lonafarnib, and will be randomized to either take SOC alone or in combination with progerinin.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
During this trial, a total of 10 subjects will be randomized in a 4:1 ratio to receive treatment with progerinin plus lonafarnib vs lonafarnib alone. Dose escalation will occur through intra-subject dose titration. Two ascending doses of progerinin will be assessed. The dose levels proposed in this study were determined using body weight based on adult doses assessed in previously completed studies, and on a simulated population pharmacokinetic (PK) model. If systemic exposures of Progerinin in pediatric patients are lower than those in adults, a dose escalation may be added at the end of the study.
Progerinin will be administered, with food. The study treatment is available in sachets of 250 mg or 350 mg and the doses in the study range from 500 to 1500 mg daily, dosed BID (twice a day).
Lonafarnib is considered as the standard of care (SOC) and all subjects in the randomized study arms will continue taking lonafarnib for the duration of the study. Subjects who are not already taking lonafarnib will also have the opportunity to initiate lonafarnib on this study as part of the lonafarnib naïve arm (separate from the randomized study arms).
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 2
Kontakter og lokationer
Studiesteder
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02115
- Boston Children's Hospital
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
Subjects will be eligible for enrollment in the study only if they meet ALL the following criteria at time of Screening:
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Subjects ≥ 1 year of age and weight ≥ 17.6 lb (8 kg).
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Subject must have confirmatory mutational analysis showing the classic HGPS mutation (c. 1824 C>T), nonclassic HGPS, Zmpset24 gene mutation, or other LMNA mutation (all subjects will havedocumentation of genetic testing prior to enrollment). *Only subjects with progerin producing mutations will be eligible for randomization. Other PL are eligible to enroll as naïve subjects (see note for criterion #5).
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Subject must display clinical signs of Progeria as per the clinical trial team.
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Subject must be willing and able to come to Boston for appropriate assessments and examinations.
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Subject must be taking lonafarnib for at least 4 months prior to enrollment and have no history of grade 3 or 4 side effects that can be probably or possibly attributed to lonafarnib for at least 2 months prior to enrollment.
Note: Subjects with no prior treatment (i.e., no commercial or managed access program source) with lonafarnib may be enrolled to initiate treatment with lonafarnib monotherapy. These subjects will initiate lonafarnib therapy in preparation for an upcoming phase of the study following the completion of phase 2a. These subjects will be excluded from the analysis of this phase 2a study. These subjects must be at least 12 months of age per lonafarnib package insert.
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Subjects must have had no recent fractures or major surgery (within four weeks).
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Subject must have adequate organ and marrow function as defined by the following parameters:
- Blood: APC (ANC + bands + monocytes) >1,000/µL, platelets >75,000/µL (transfusion independent); hemoglobin >9 g/dL.
- Renal: creatinine ≤ 1.5 times normal for age or Glomerular Filtration Rate (GFR) >70 mL/min/1.73m2.
- Hepatic: bilirubin ≤1.5x upper limit of normal for age; Serum Glutamic Pyruvic Transaminase (SGPT) (Alanine Transaminase, [ALT]) < and Serum Glutamic-Oxaloacetic Transaminase (SGOT) (Aspartate Aminotransferase, [AST]) ≤ 2.5x normal range for age.
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The subject is willing to provide written informed assent form, when possible, to participate in the study after reading the informed assent form and the information provided and has had the opportunity to discuss the study with the investigator or designee. Additionally, the subject's legally authorized guardian (LAR) is willing to provide written informed consent.
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The subject is able to communicate satisfactorily with the investigator and to participate in, and comply with, the requirements of the study.
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The subject (or LAR) is able to understand the nature of the study and any potential hazards associated with participating in it.
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Negative pregnancy test for female subjects of childbearing potential and those who have not been surgically sterilized or who do not have verbal or laboratory confirmation of two years postmenopausal status. Women of childbearing potential (WOCBP) and Women of non-childbearing potential are eligible to participate. Women of childbearing potential should use an acceptable method of birth control and agree to continue to use this method for the duration of the study and for 90 days after taking the last dose of Progerinin.
Acceptable methods of contraception include abstinence, female subject/partner's use of hormonal contraceptive (oral, implanted, or injected) in conjunction with a barrier method (WOCBP only) (e.g., diaphragm, cervical cap, male condom, and female condom and spermicidal foam, sponges, and film), female subject/partner's use of an intrauterine device (IUD), or if the female subject/partner is surgically sterile (e.g., bilateral tubal ligation, hysterectomy) or two years postmenopausal at time of screening. All male subjects/partners (excluding men who have been sterilized) must agree to consistently and correctly use a condom for the duration of the study and for 90 days after taking the study drug. In addition, subjects may not donate sperm for the duration of the study and for 90 days after taking study drug.
Exclusion Criteria:
Subjects meeting ANY of the following criteria at time of Screening will be excluded from enrollment:
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Other than the drugs used in this protocol, other drugs targeted to treat Progeria are excluded. Drugs to treat symptoms of Progeria are permitted.
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Subjects are taking medications that significantly affect the metabolism of Progerinin.
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Subjects with an active bleeding diathesis or on oral anti-vitamin K medication (except low dose coumadin).
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Subjects who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study such as:
- known severely impaired lung function
- active (acute or chronic) or uncontrolled severe infections.
- liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis.
- history of hepatitis B or hepatitis C documented by history and confirmed by serology if positive for history.
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Other concurrent severe and/or uncontrolled medical disease that could compromise participation in the study (i.e., uncontrolled diabetes, uncontrolled hypertension, severe infection, severe malnutrition, chronic liver or renal disease, active upper GI tract ulceration).
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A known history of Human Immunodeficiency Virus (HIV) seropositivity or known immunodeficiency.
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Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of Progerinin (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection). A nasogastric tube (NG tube) or gastric tube (G tube) is allowed.
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Subjects who have known or suspected hypersensitivity to any of the excipients included in the formulation should not be treated.
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Subjects who have used marijuana or other (Tetrahydrocannabinol) THC containing products either recreationally or for medical purposes within three months prior to entering the study.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Progerinin + Lonafarnib
Subjects who have successfully completed the Screening phase will enter the treatment phase of the study and be randomized to a treatment arm. Subjects randomized to the progerinin + lonafarnib arm will take progerinin at a dose dependent on their body weight and will continue taking lonafarnib per the package insert. For each dose cohort, subjects will complete a 28-day treatment period of toxicity assessment, and a minimum four-month treatment period for plasma progerin evaluation. After the last subject completes the toxicity assessment period, the independent Data Monitoring Committee (iDMC) will meet to confirm that subjects can be escalated to the next dose. All subjects will remain on the current dose until the iDMC decision is confirmed. Each subject will only be escalated to the next dose after their 4-month (±2 weeks) plasma progerin sample is collected. |
Dosing will be determined based on body weight. Dosing ranges from 500mg to 1500mg daily. Progerinin is available in sachets of 250 mg or 350 mg for oral use. Lonafarnib is considered as the standard of care (SOC). Subjects in the randomized arms will continue taking lonafarnib per the package insert. Subjects in the lonafarnib naïve arm will initiate lonafarnib as per FDA-approved study 07-01-7505. |
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Andet: Lonafarnib Naïve
Subjects with no prior treatment with lonafarnib (i.e., no commercial or managed access program source) may be enrolled to initiate treatment with lonafarnib monotherapy. These subjects will initiate lonafarnib therapy in preparation for an upcoming phase of the study following the completion of phase 2a. These subjects will be excluded from the analysis of this phase 2a study. They will come to the study site for a baseline visit and at one year for assessment as described later in this protocol. |
Lonafarnib is considered as the standard of care (SOC). Subjects in the randomized arms will continue taking lonafarnib per the package insert. Subjects in the lonafarnib naïve arm will initiate lonafarnib as per FDA-approved study 07-01-7505. |
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Aktiv komparator: Lonafarnib
Subjects in the main study arms (Progerinin + Lonafarnib and non-naïve Lonafarnib) will continue taking lonafarnib per the package insert. Subjects randomized to the lonafarnib alone arm will not take progerinin during this study. |
Lonafarnib is considered as the standard of care (SOC). Subjects in the randomized arms will continue taking lonafarnib per the package insert. Subjects in the lonafarnib naïve arm will initiate lonafarnib as per FDA-approved study 07-01-7505. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Ændring fra baseline i plasmaprogerinkoncentration
Tidsramme: Baseline og måned 4 for hver kohorte
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Baseline og måned 4 for hver kohorte
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Maksimal observeret plasma-lægemiddelkoncentration (Cmax)
Tidsramme: Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Kovariater: Alder
Tidsramme: Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Kovariater: Kropsvægt
Tidsramme: Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Baseline og før-dosis (0 timer) og 2-5 timer efter dosis ved måned 4 i hver kohorte
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Forekomst af doseringsbegrænsende toksiciteter (DLTs)
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Forekomst og sværhedsgrad af behandlingsrelaterede bivirkninger (TEAEs)
Tidsramme: Fra baseline til opfølgning (cirka 13 måneder)
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Fra baseline til opfølgning (cirka 13 måneder)
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Hyppighed af tilbagetrækninger på grund af bivirkninger (AEs)
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Forekomst af behandlingsrelaterede bivirkninger
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Forekomst af alvorlige bivirkninger (SAE'er)
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændringer/ændringer i laboratorieværdier fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i blodtryk fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i hjertefrekvens fra udgangspunktet
Tidsramme: Fra baseline til opfølgning (cirka 13 måneder)
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Fra baseline til opfølgning (cirka 13 måneder)
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Ændring i respirationsfrekvens fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i temperatur fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i elektrokardiogram (EKG) parameter, ventrikulær frekvens (slag pr. minut), fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i elektrokardiogram (EKG) parameter, PR-interval (ms), fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i elektrokardiogram (EKG)-parameter, QRS-interval (ms), fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Ændring i elektrokardiogram (EKG) parameter, QT-interval (msek), fra baseline
Tidsramme: Fra baseline til opfølgning (cirka 13 måneder)
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Fra baseline til opfølgning (cirka 13 måneder)
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Ændring i elektrokardiogram (EKG) parameter, QTc-interval (msek), fra baseline
Tidsramme: Fra baseline til opfølgning (ca. 13 måneder)
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Fra baseline til opfølgning (ca. 13 måneder)
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Tilsyneladende terminal eliminationshalveringstid (t1/2)
Tidsramme: Baseline og før dosis (0 time) samt 2-5 timer efter dosis ved måned 4 i kohorte 1 og kohorte 2
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Baseline og før dosis (0 time) samt 2-5 timer efter dosis ved måned 4 i kohorte 1 og kohorte 2
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Tid til maksimal observeret plasmakoncentration af lægemiddel (Tmax)
Tidsramme: Baseline og præ-dose (0 timer) og 2-5 timer post-dose i måned 4 for kohorte 1 & kohorte 2
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Baseline og præ-dose (0 timer) og 2-5 timer post-dose i måned 4 for kohorte 1 & kohorte 2
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Areal under plasmakoncentrations-tidskurven (AUC) fra tid 0 til slutningen af doseringsperioden (AUC0-τ)
Tidsramme: Baseline, og før dosering (0 time) og 2-5 timer efter dosering ved måned 4 for kohorte 1 & kohorte 2
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Baseline, og før dosering (0 time) og 2-5 timer efter dosering ved måned 4 for kohorte 1 & kohorte 2
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Clearance (CL)
Tidsramme: Baseline og før dosis (0 time) samt 2-5 timer efter dosis i måned 4 for kohorte 1 & kohorte 2
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Baseline og før dosis (0 time) samt 2-5 timer efter dosis i måned 4 for kohorte 1 & kohorte 2
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Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- PRG-PRO-005
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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