Safety Study of Carbamylated Erythropoietin to Treat Patients With the Neurodegenerative Disorder Friedreich's Ataxia

Lundbeck

Status and phase

Completed

Phase 2

Conditions

Friedreich's Ataxia

Treatments

Drug: Placebo

Drug: Lu AA24493

Study type

Interventional

Funder types

Industry

Identifiers

NCT01016366

12631A

2008-003662-25 (EudraCT Number)

Details and patient eligibility

About

The primary purpose of the study is to determine whether carbamylated erythropoietin is a safe treatment for patients who suffer from Friedreich's Ataxia.

Full description

Friedreich's Ataxia (FRDA) is a hereditary, progressive neurodegenerative disorder caused by mutations in the gene encoding frataxin. The mutation results in a severe reduction in levels of the mitochondrial protein, frataxin. A decline in frataxin levels and its associated consequences is believed to be the primary cause of symptoms in FRDA patients. The clinical symptoms of FRDA include progressive gait and limb ataxia, dysarthria, diabetes mellitus and hypertrophic cardiomyopathy. First symptoms usually appear between the age of 5 and 15 years. As the disease progresses the patient becomes confined to a wheel chair and at later stages the patients become increasingly incapacitated. There is currently no effective treatment for FRDA.

The naturally occurring hormone, erythropoietin (EPO), is able to protect various neuronal tissues from ischemic injury. Recombinant human erythropoietin (EPO) increases frataxin expression in lymphocytes from patients with FRDA. Also, EPO treatment of FRDA patients resulted in a favourable outcome compared to baseline as assessed by the levels of frataxin and biomarkers of oxidative stress. In a pilot study with EPO in FRDA patients, the treatment was well tolerated apart from the expected haematological (haematopoietic) side effects. Lu AA24493 (CEPO) is a modified (carbamylated) version of EPO, which is neuroprotective but without the haematopoietic side effects. Lu AA24493 is being developed for treatment of patients with FRDA.

Although the target for the non-haematological effects of Lu AA24493 (and EPO) is currently unknown, Lu AA24493 (CEPO) can protect cells and tissue from various types of injuries. Furthermore, in vitro Lu AA24493 (CEPO) increases the frataxin levels in lymphocytes from FRDA patients as well as from control patients. This study aims to evaluate the safety of 2 weeks treatment (6 doses, 3 doses per week) of CEPO in patients with FRDA and to explore efficacy by using neurological rating scales and by exploring levels of frataxin and biomarkers of oxidative stress.

Enrollment

36 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The patient has been diagnosed with FRDA and has had a genetic test demonstrating >400 GAA nucleotide triplet repeats on the shorter of the two frataxin alleles
The patient has a SARA (Stance) sub-score of <=6
The patient has a SARA (Gait) sub-score of <=6
Man or woman, aged 18 years or over
If female then woman should agree not to try to become pregnant during the study, and use adequate protection/abstinence or not be of child bearing potential

Exclusion criteria

Clinically significant unstable illnesses such as liver, kidney, heart, stomach problems unrelated to their disease of FRDA
Disallowed medications
Serious underlying disease
Clinically significant abnormal vital signs unrelated to the underlying disease of FRDA
Abnormal laboratory blood results considered by the doctor as clinically significant, e.g.anaemia
Treatment with idebenone within 6 weeks prior to screening
Treatment with erythropoietin within 16 weeks prior to screening
Clinically significant abnormal ECG
Received or donated blood within previous 3 months
Participation within another clinical trial within past 30 days
Pregnancy or breast feeding
History of drug allergies or hypersensitivities
Current (or within past 6 months) disorder related to drug or alcohol abuse (as defined DSM-IV-TR)