Phase III Trial Assessing the Efficacy and Safety of PXT3003 in CMT1A Patients

Charcot-Marie-Tooth Disease Clinical Trial

— PREMIER  

Official title:

A Multi-center, Randomized, Double-blind, Placebo Controlled Phase III Study to Assess the Efficacy, Safety, and Tolerability of PXT3003 in Charcot-Marie-Tooth Type 1A (CMT1A)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04762758
• Other study ID #: CLN-PXT3003-06
• Secondary ID: 2020-004805-30
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: March 30, 2021
• Est. completion date: April 19, 2024

Study information

• Verified date: April 2024
• Source: Pharnext S.C.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study will consist of 2 periods: Double-blind Treatment and Open-Label Extension(OLE) Period.

-Double-blind Treatment Period - This will be randomized, double-blind, placebo-controlled part of the study which will be conducted in parallel groups, ie,1 group receiving the active treatment (PXT3003) and the other group receiving placebo.

Primary endpoint of the study will be assessed at Month 15.

-Open-label Extension (OLE) Period - All subjects completing Double-blind Treatment Period will be given an opportunity to enter the OLE Period of the study and receive the active treatment (PXT3003). The duration of the OLE Period will be based on Sponsor discretion, ie, Sponsor intends to keep the study open until the study drug PXT3003 is commercially available.

During this period, the long-term safety and efficacy of PXT3003 will be assessed as an exploratory objective.

Double-blind Treatment Period Objectives:

Primary:

To evaluate the efficacy of treatment with PXT3003 (a fixed-dose combination of [RS]-baclofen, naltrexone hydrochloride [HCl], and D-sorbitol) compared to placebo in subjects with Charcot-Marie-Tooth disease type 1A (CMT1A).

Secondary:

To evaluate the safety and tolerability of PXT3003 treatment in subjects with CMT1A.

Exploratory:

To characterize the relationship between plasma biomarkers and response to PXT3003 treatment.

OLE Period Objective:

Exploratory:

To evaluate the long-term safety and efficacy of PXT3003.

Description:

This is an international, multi-center, randomized, double-blind, placebo-controlled, parallel-group, Phase III study of PXT3003 in subjects with CMT1A. The study will be conducted at approximately 52 sites worldwide.

This study consists of Double-blind Treatment and OLE Periods.

Double-blind Treatment Period:

Eligible subjects will be screened and randomized in a 1:1 ratio to receive either oral PXT3003 or matching placebo, 10 mL, twice daily (BID) for 15 months. In order to maximize the tolerability of (RS)-baclofen for all randomized subjects, treatment will start with a half-dose (5 mL), taken BID (morning and evening with food) during the first 2 weeks, and then will be increased to a full-dose (10 mL), taken BID (morning and evening with food) until completion of the Treatment Period at Month 15.

A total of approximately 350 subjects will be enrolled. Visits will take place at Screening (up to -35 days), Baseline (Day 1), and Months 3, 6, 9, 12, and 15. Telephone contacts will take place at weeks 2 or 3, Month 1 and Month 2, and then monthly between subsequent in-person visits. A genotyping test for the Peripheral Myelin Protein 22 (PMP22) gene duplication will take place at the Screening Visit if it is not already documented for the subject. All subjects completing the Double-blind Treatment Period of the study will be given an opportunity to enter the OLE Period at Month 15 (Visit 6). Subjects not consenting to enter the OLE Period will have their last study visit (ie, Safety Follow-up Visit, Visit 7), 30 days after their last dosing day.

The primary outcome measures modified Overall Neuropathy Limitations Score(mONLS) and the 10-Meter Walk Test (10mWT), along with the Columbia Suicide Severity Rating Scale (C-SSRS) will be evaluated at each post-randomization in-person visit. The other secondary outcome measures, exploratory outcome, and safety/tolerability assessments will be evaluated as per Schedule of Activities (SOA). A Data Safety and Monitoring Board (DSMB) will meet on a scheduled basis throughout the study to review safety data and will reconvene on an ad hoc basis as necessary.

Planned duration for sites to enroll subjects: approximately 12 months, Subject Screening Period: 35 days, Subject Treatment Period: up to 15 months, Safety Follow-up Period (for subjects not entering the OLE Period): 30 days

OLE Period:

A subject entering the OLE Period (whether the subject was randomized to oral PXT3003 or matching placebo in the Double-blind Treatment Period) will start taking a half-dose of PXT3003 (5 mL) BID (morning and evening with food) during the first 2 weeks, and then a full dose of PXT3003 (10 mL) BID (morning and evening with food) throughout the OLE Period. The visits and assessments during the OLE Period are described in the SOA.

For subjects entering the OLE Period, Screening Day will occur on the same day as Visit 6 (Month 15) of the Double-blind Treatment Period. The duration of the Treatment Period will be based on Sponsor discretion. Sponsor intends to keep the study open until the study drug PXT3003 is commercially available. Safety Follow-up Period: 30 days

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 350
• Est. completion date: April 19, 2024
• Est. primary completion date: April 19, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 65 Years

Eligibility

Double-blind Treatment Period

Inclusion Criteria:

1. Male and non-pregnant female subjects, aged 16 to 65 years with a genetically proven diagnosis of CMT1A. Notes: a) A report of a genetic test confirming PMP22 duplication and therefore a diagnosis of CMT1A must be available in the subject's record at the clinical site. b) In the absence of a report of a genetic test confirming PMP22 duplication in the subject's medical record, a confirmatory genetic test must be conducted via the central laboratory as part of Screening. c) In the exceptional case wherein subject was randomized into the study without meeting(a) or (b), an unscheduled confirmatory genetic test will be performed. In the event of a negative genetic test result, the subject will be withdrawn from the study.

2. Able to provide written informed consent/assent and comply with study procedures.

3. Mild-to-moderate severity assessed by a CMTNS-V2 score >2 and =18.

4. Muscle weakness in at least foot dorsiflexion on clinical assessment.

5. Ulnar nerve motor conduction time of at least 15 m/s.

6. If taking prescribed psychoactive drugs(eg, antidepressants, stimulants, tranquilizers, anti-epileptics) for CMT1A, should be on a stable dose for at least 4 weeks prior to randomization, which is not planned to be changed.

7. If taking prescribed or 'over-the-counter' analgesic medications (eg, paracetamol/acetaminophen, nonsteroidal anti-inflammatory drugs) for CMT1A, should be on a stable dose for at least 2 weeks prior to randomization, which is not planned to be changed.

8. If female, subject must be: (a) surgically sterilized via hysterectomy, bilateral oophorectomy, or bilateral tubal ligation; or (b) of childbearing potential and using a birth control method such as:

• Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation:

• Oral

• Intravaginal

• Transdermal

• Progestogen-only hormonal contraception associated with inhibition of ovulation:

• Oral

• Injectable

• Implantable

• Intrauterine device

• Intrauterine hormone-releasing system

• Bilateral tubal occlusion

• Vasectomized partner

• Sexual abstinence or (c) Of non-childbearing potential (i.e., no menses for = 12 consecutive months without any other underlying medical cause)

9. If male, the subject must have had a vasectomy or must use a reliable method of birth control with their partner or total abstinence from sexual intercourse. The subject must agree to continue using their selected method of birth control with their sexual partner during the study and for 120 days after study completion.

Exclusion Criteria:

1. Subjects previously enrolled in any PXT3003 study.

2. Subjects living in the same household and enrolled in a PXT3003 study (due to potential lack of adequate storage for study material, risk of mixing treatments and potential unblinding).

3. CMT of any subtype other than 1A.

4. ONLS score of 0.

5. Known clinically significant motor or sensory abnormalities secondary to a different neurological cause (eg, diabetes, alcohol, vascular, autoimmune, neoplastic, neurodegenerative, human immunodeficiency virus, etc.). Note: subjects with diagnosis of unilateral carpal tunnel syndrome at least 1 year prior to Screening Visit, that is asymptomatic at the time of Screening Visit, will not be excluded from participating in this study.

6. Subjects who have had any surgery or have a concomitant disorder (eg, severe arthrosis) that reduces the mobility of the ankle or wrist making it, in the opinion of the investigator, difficult to assess the efficacy of the treatment. Note: subjects with surgical repair of unilateral carpel tunnel syndrome will not be excluded from participating in this study.

7. Known peripheral neuropathy, myopathy, or neuromuscular disorder of any other kind. Note: subjects with diagnosis of unilateral carpal tunnel syndrome at least 1year prior to Screening Visit, that is asymptomatic at the time of Screening Visit, will not be excluded from participating in this study.

8. Any other clinically significant and/or uncontrolled medical condition that, in the opinion of the investigator, could be a confound, may increase subject's risk, or may preclude successful participation or completion of the study.

9. Known hypersensitivity or intolerance to PXT3003( or matching placebo), including any of its active ingredients( baclofen, naltrexone, or sorbitol), and/or any of its excipients( acetate buffer, sodium methyl parahydroxybenzoate, sodium propyl parahydroxybenzoate, or isoamyl acetate).

10. Concomitant treatments including but not limited to baclofen, naltrexone, sorbitol (pharmaceutical form), opioids, potent central nervous system depressants (such as barbiturates, long-acting benzodiazepines, and neuroleptics), and potentially neurotoxic drugs such as amiodarone, chloroquine, and chemotherapeutics capable of inducing peripheral neuropathy. Subjects able to stop these medications at least 2 weeks before randomization and for the study duration may be included. Subjects with positive urine drug screen at Baseline Visit will be excluded, except for permitted use of codeine and benzodiazepines.

11. History of porphyria.

12. Diagnosis or history of substance use disorder by Diagnostic and Statistical Manual of Mental Disorders-5th Edition criteria within the past 12 months.

13. Medical or recreational use of marijuana in the 3 months prior to the Screening Visit.

14. Active suicidality (eg, any suicide attempts within the past 12 months or any current suicidal intent, including a plan, as assessed by the C SSRS score of "YES" on questions 4 or 5; and/or based on clinical evaluation by the investigator).

15. Currently active major depression, as determined by a Beck Depression Inventory-II (BDI-II) score =20.

16. Currently lactating, pregnant, or planning on becoming pregnant during the study.

17. Alanine aminotransferase or aspartate aminotransferase levels greater than 2 times the upper limit of normal.

18. Significant renal impairment as determined by glomerular filtration rate of less than 50 mL/min.

19. Subject has participated in an investigational drug or device study within 30 days prior to the Screening Visit or plans to participate in an investigational drug or device study during the course of this study.

20. Subject is a dependent and/or relative of the Sponsor or Principal Investigator.

OLE Period

Inclusion Criteria:

1. Able to provide written informed consent/assent and comply with study procedures.

2. If female, subject must be (a) surgically sterilized via hysterectomy, bilateral oophorectomy, or bilateral tubal ligation; or (b) of childbearing potential and using a birth control method such as:

• Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation:

• Oral

• Intravaginal

• Transdermal

• Progestogen-only hormonal contraception associated with inhibition of ovulation:

• Oral

• Injectable

• Implantable

• IUD

• IUS

• Bilateral tubal occlusion

• Vasectomized partner

• Sexual abstinence or (c) of non-childbearing potential (ie, no menses for =12 consecutive months without any other underlying medical cause).

3. If male, the subject must have had a vasectomy or must use a reliable method of birth control with their partner or total abstinence from sexual intercourse. The subject must agree to continue using their selected method of birth control with their sexual partner during the study and for 120 days after study completion.

Exclusion Criteria:

1. Any clinically significant and/or uncontrolled medical condition that, in the opinion of the investigator, could be a confound factor, may increase subject's risk, or may preclude successful participation or completion of the study.

2. Concomitant treatments including but not limited to baclofen, naltrexone, sorbitol (pharmaceutical form) other than PXT3003 taken in the Double-blind Treatment Period of this study, opioids, potent CNS depressants (such as barbiturates, long-acting benzodiazepines, and neuroleptics), and potentially neurotoxic drugs such as amiodarone, chloroquine, and chemotherapeutics capable of inducing peripheral neuropathy. Subjects able to stop these medications at least 2 weeks before randomization and for the study duration may be included.

3. Diagnosis or history of substance use disorder by Diagnostic and Statistical Manual of Mental Disorders-5?? Edition criteria within the past 12 months.

4. Active suicidality (eg, any suicide attempts within the past 12 months or any current suicidal intent, including a plan, as assessed by the C-SSRS score of "YES" on questions 4 or 5; and/or based on clinical evaluation by the investigator).

5. Currently active major depression, as determined by a BDI-II score =20.

6. Currently lactating, pregnant, or planning on becoming pregnant during the study.

7. ALT or AST levels greater than 2 × ULN relative to Baseline.

8. Estimated GFR of less than 50 mL/min.

Note: PXT3003 will be dispensed to all subjects before laboratory results are available, and if the laboratory results are out of range, ie, subject meeting the exclusion criteria, the subject will be called immediately to stop taking PXT3003. One retest within 4 weeks may be performed in consultation with the Medical Monitor if any of the above laboratory abnormalities are found. In case of eligibility determination after the retest, subjects will restart taking 2 weeks of half dose of PXT3003.

Related Conditions & MeSH terms

• Charcot-Marie-Tooth Disease
• Hereditary Sensory and Motor Neuropathy
• Nerve Compression Syndromes
• Tooth Diseases

Intervention

Drug:
• (RS)-baclofen, naltrexone hydrochloride and D-sorbitol
oral fixed dose combination
• Placebo
liquid oral solution

Locations

Country	Name	City	State
Belgium	Universitaire Ziekenhuizen Leuven	Leuven
Canada	CIUSS de Saguenay-Lac-Saint-Jean Centre d'etudes Cliniques	Chicoutimi	Quebec
Canada	Montreal Neurological Institute and Hospital-Clinical Research Unit	Montréal	Quebec
Canada	Ottawa Hospital Research Institute- Neuromuscular Research Centre	Ottawa	Ontario
Canada	CHU de Quebec-Universite Laval- Hopital Enfant-Jesus	Québec	Quebec
Canada	UHN Toronto General Hospital Krembil Neuroscience Centre	Toronto	Ontario
Denmark	Rigshospitalet, University of Copenhagen Copenhagen Neuromuscular Center	Copenhagen
France	Centre de Reference des Maladies Neuromusculaires AOC Service de Neurologie, CHU d'Angers	Angers
France	Centre de reference des maladies neuromusculaires AOC Hopital Pellegrin CHU de Bordeaux	Bordeaux
France	CHU de Lille Hôpital Salengro	Lille
France	Service de Neurologie et Maladies Neuromusculaires, CHU de Marseille - Hopital La Timone	Marseille
France	Association lnstitut de Myologie Hopital Pitie-Salpetriere Service de Neuro-Myologie	Paris
France	Centre d'investigation Clinique CHU de Strasbourg Hopital de Hautepierre	Strasbourg
Germany	University Hospital RWTH Aachen, Department of Neurology and Institute for Neuropathology	Aachen
Germany	University Medical Centre Goettingen, Dept. of Clinical Neurology	Göttingen
Germany	Friedrich-Baur-Institut, Neurologische Klinik und Poliklinik Ludwig-Maximilians-Universität	München
Germany	University Hospital Muenster UKM Department of Neurology	Münster
Germany	Universitätsklinikum Tübingen Crona Kliniken Neuromuskuläres Zentrum	Tübingen
Israel	Hadassah Ein Kerem University Medical Center Department of Neurology	Jerusalem
Israel	Sheba Medical Center	Ramat Gan
Israel	Tel Aviv Sourasky Medical Center	Tel Aviv
Italy	Azienda Ospedaliera Universitaria San Martino Universita Degli Studi di Genova Clinica Neurologica	Genova
Italy	Azienda Ospedaliera Universitaria Policlinico "G. Martino" di Messina	Messina
Italy	University of Naples Federico II	Naples
Italy	Tor Vergata University of Rome	Rome
Italy	University Hospital GB Rossi UOC Neurologia B, AOUI Verona Department of Neuroscience, Biomedicine and Movement Sciences	Verona
Spain	Hospital Universitario Clinico San Carlos	Madrid
Spain	Complejo Hospitalario Universitario de Santiago	Santiago De Compostela
Spain	Hospital Universitario Virgen del Rocío	Sevilla
Spain	Hospital Universitario y Politécnico La Fé	Valencia
United States	National Neuromuscular Research Institute	Austin	Texas
United States	Massachusetts General Hospital Neuromuscular Diagnostic Center	Boston	Massachusetts
United States	UNC Department of Neurology Peripheral Neuropathy Center	Chapel Hill	North Carolina
United States	Atrium Health Neurosciences Institute	Charlotte	North Carolina
United States	MU Health Care Neurology and Sleep Disorders Clinic	Columbia	Missouri
United States	The Ohio State University Wexner Medical Center	Columbus	Ohio
United States	University of Kansas Medical Center Research Institute	Fairway	Kansas
United States	University of Florida Clinical Research Center	Gainesville	Florida
United States	Hackensack Meridian Health Hackensack University Medical Center	Hackensack	New Jersey
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	UCLA Department of Psychiatry and Biobehavioral Sciences	Los Angeles	California
United States	University of Miami Leonard M. Miller School of Medicine	Miami	Florida
United States	University of Minnesota Health	Minneapolis	Minnesota
United States	Hospital for Special Care	New Britain	Connecticut
United States	Colombia University Department of Neurology	New York	New York
United States	Advent Health Medical Group Neurology Orlando	Orlando	Florida
United States	UC Davis Health Department of Physical Medicine and Rehabilitation	Sacramento	California
United States	Neurology Clinic at University of Washington Medical Center	Seattle	Washington
United States	Providence St. Luke's Rehabilitation Medical Center	Spokane	Washington
United States	Oregon Neurology	Springfield	Oregon

Sponsors (2)

Lead Sponsor	Collaborator
Pharnext S.C.A.	Worldwide Clinical Trials

Countries where clinical trial is conducted

United States,  Belgium,  Canada,  Denmark,  France,  Germany,  Israel,  Italy,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	modified Overall Neuropathy Limitation Scale (mONLS)	The modified ONLS is a disability scale that was derived and improved from the Overall Disability Sum Score to measure limitations in the everyday activities of the upper limbs (rated on 5 points) and the lower limbs (rated on 7 points).38 The total score goes from 0 (no disability) to 12 (maximum disability). Lower values in the ONLS indicate a better clinical condition.	From Baseline to Month 15
Secondary	10-Meter Walk Test	The 10mWT is simple to administer, standardized, and valid performance evaluation of functional mobility and gait that has been proven reliable in neurologic disorders, including CMT. Results recorded are the time to walk 10 meters and the number of steps performed.	From Baseline to Month 15
Secondary	Quantified Muscular Testing (QMT) (bilateral foot dorsiflexion dynamometry)	QMT is used to evaluate motor strength in CMT1A.The following muscles will be evaluated: tibialis anterior (right and left). The best value on three consecutive and reproducible tests will be collected in the electronic Case Record Form (eCRF) for each muscle.	From Baseline to Month 15
Secondary	Patient Global Impression of Severity (PGI-S)	The PGI-S is a validated tool that is used to rate the severity of a specific condition. Subjects will rate their health status over the past week. The PGI-S is a 1-item questionnaire on a 5-point scale and subjects will be asked to rate the severity of their condition from "None" (Score = 1) to "Very Severe" (Score = 5). Assessments obtained over the course of the study will be compared to baseline, prior to initiation of treatment.	From Baseline to Month 15
Secondary	Patient Global Impression of Change (PGI-C)	The PGI-C scale is a validated generic tool for assessment of overall change in the severity of illness following treatment. Subjects will rate how they feel now compared with how they felt before receiving study drug on a 7-point scale where 1 is "Very much improved" and 7 is "Very much worse".	From Baseline to Month 15
Secondary	CMTNS-V2	CMTNS is a specific scale designed to assess severity of impairment in CMT disease. Although not completely validated, it provides a single and reliable measure of CMT severity. It is a 36-point scale based on 9 items: 5 of them quantify impairment (sensory symptoms, pin sensibility, vibration, arm, and leg strength), 2 activity limitations (motor symptoms arms and legs) and 2 electrophysiological data (amplitudes of ulnar compound muscle action potential and sensory nerve action potential). Increased scores indicate a worsening of the function: the scores categorize a disability as mild (0 to10), moderate (11 to 20) and severe (21 to 36).; A modified version 2 (CMTNS-V2) was issued in 2011 to attempt to reduce floor and ceiling effects and to standardize patient assessment.	From Baseline to Month 15
Secondary	QMT (hand grip)	QMT is used to evaluate motor strength in CMT1A. The following muscles will be evaluated: hand grip (right and left). The best value on three consecutive and reproducible tests will be collected in the eCRF for each muscle.	From Baseline to Month 15