Ulipristal Acetate In Disease Charcot-Marie-Tooth Type of 1A

CMT1A Clinical Trial

— UPACOMT  

Official title:

LONG-TERM EFFECTS TOLERANCE AND THE Ulipristal Acetate IN DISEASE Charcot-MARIE-TOOTH TYPE OF 1A

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02600286
• Other study ID #: 6100
• Status: Terminated
• Phase: Phase 2
• Start date: October 23, 2015
• Est. completion date: November 2, 2017

Study information

• Verified date: July 2022
• Source: University Hospital, Strasbourg, France
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The disease Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited peripheral neuropathy, for which no treatment has proved its effectiveness. It is autosomal dominant, associated with a duplication of the chromosome 17p11.2 region which leads to overexpression of the gene and the protein-peripheral myelin protein-22 (PMP22), a major component of peripheral myelin. In animals and humans, PMP22 mRNA level of glutathione S-transferase theta 2 and Cathepsin A (markers of oxidative stress), detected in a skin biopsy are markers that may play a role in the prognosis evolution of the disease. Furthermore, several studies have shown that the administration of progesterone increased the expression of PMP22 gene (measured in a skin biopsy) and worsening symptoms. In contrast, anti-progestins reduce the synthesis of PMP22 and improve symptoms in rat CMT1A. The long-term safety of anti-progesterone was evaluated for mifepristone (RU486) ulipristal acetate and (EllaOne®). Few side effects have been reported including a few cases of endometrial hyperplasia reversible upon discontinuation of treatment. With the RU486, rare cases of adrenal androgen and failure have been observed. However, EllaOne® has low antagonistic action on the glucocorticoid receptor and no action on androgen receptors. The investigators therefore believe that it will be well tolerated in humans and will reduce the synthesis of PMP22 and the action of oxidative stress by improving disability of patients.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 23
• Est. completion date: November 2, 2017
• Est. primary completion date: November 2017
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Male 18-70 years
• CMT1A proven genetically (17p11.2 duplication)
• symptomatic CMT1A (MRC score <5 in at least one muscle group)
• Non severe axonal impairment (amplitude of the motor evoked potential on the median nerve and / or ulnar than 50% of normal)
• Subject contacted with a valid phone number
• Subject affiliated to a social security scheme
• Subject has been informed of the results of the medical examination prior

Exclusion Criteria:

• Another cause of neuropathy: Chronic alcohol intoxication, chemotherapy, diabetes, kidney failure, monoclonal gammopathy, cryoglobulin, B12 deficiency, hepatitis B / C, HIV, Lyme or poliomyelitis
• Liver failure
• Lapp lactase deficiency, malabsoprtion syndrome glucose / galactose
• Support long-term drug interacting with the CYP3A4
• Patients with indication against xylocaine adrenaline
• In the biopsy site: surgery, skin disease or local infection
• Immunosuppression innate or acquired
• Hypersensitivity to the active substance / excipient
• uncontrolled severe asthma
• Treatment with vitamin C or vitamin B3 in the four weeks preceding randomization
• Orthopaedic surgery of the lower limbs in the 6 months prior to randomization or planned
• Against indication xylocaine adrenaline
• Malfunction of the innate or acquired coagulation

Related Conditions & MeSH terms

• Charcot-Marie-Tooth Disease
• CMT1A
• Hereditary Sensory and Motor Neuropathy
• Nerve Compression Syndromes

Intervention

Drug:
• EllaOne
5 mg/per os of EllaOne every day through 12 months. 10 mg/per os of EllaOne every day through 12 months. EllaOne placebo/per os every day through 12 months.
• EllaOne placebo
5 mg/per os of EllaOne every day through 12 months. 10 mg/per os of EllaOne every day through 12 months. EllaOne placebo/per os every day through 12 months.

Locations

Country	Name	City	State
France	Service d'Explorations et pathologies neuro- musculaires	Besançon
France	Département de Neurologie	Dijon
France	Département de Neurologie	Nancy
France	Unité de pathologie neuro-musculaire	Paris
France	Département de Neurologie Centre de Référence des Maladies Neuromusculaires Grand Est (CERNEST) Hôpital de Hautepierre	Strasbourg

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Analysis of the effectiveness of Ellaone. This will be assessed by the production of RNA PMP22 using skin biopsy.		12 months after treatment with EllaOne