Evaluation of Long-term Efficacy of Treatment With Lamazym

Alpha-Mannosidosis Clinical Trial

— rhLAMAN-10  

Official title:

A Single Center, Open Label Clinical Trial Investigating the Long-term Efficacy of rhLAMAN (Recombinant Human Alpha-mannosidase or Lamazym) Treatment in Subjects With Alpha-Mannosidosis Who Previously Participated in Lamazym Trials

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02478840
• Other study ID #: rhLAMAN-10
• Status: Completed
• Phase: Phase 3
• Start date: February 2015
• Est. completion date: June 2015

Study information

• Verified date: November 2020
• Source: Chiesi Farmaceutici S.p.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The overall objective is to evaluate the long-term efficacy of Lamazym i.v. treatment in patients with alpha-Mannosidosis previously enrolled in Lamazym trials and currently receiving the treatment according to the AfterCare Program.

Description:

The primary objective of the trial is to evaluate the impact of the long-term treatment with Lamazym upon the level of biomarker oligosaccharides in serum and upon the endurance as measured by the change from baseline in the number of steps climbed in 3 minutes (3MSCT). As secondary objectives, the long term efficacy of Lamazym will be investigated upon endurance as measured by the change from baseline in the number of meters walked in six minutes (6MWT), upon pulmonary function, motor proficiency by BOT-2 and hearing capability by audiometry. In addition, cognitive development will be assessed by Leiter-R test. CNS involvement will be evaluated with MRI/MRS (for patients who previously participated in rhLAMAN-02 trial), CSF biomarkers (Tau, NFL, GFAp) and CSF biomarkers oligosaccharides. Clearance of oligosaccharides in urine will be measured. Long-term safety and Pharmaco-Kinetic (PK) profile after long-term treatment as measured by rhLAMAN levels in plasma will be assessed as well. Quality of life will be assessed by questionnaires (CHAQ and EQ-5D-5L).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: June 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. The subject must have participated in the phase 1 trial (EudraCT number:

2010-022084-36), phase 2a trial (EudraCT number: 2010-022085-26), phase 2b trial (EudraCT number: 2011-004355-40) or phase 3 trial (EudraCT number: 2012-000979-17)

2. The subject must still be receiving weekly intravenous infusions of Lamazym according to the AfterCare Program

3. The Subject or subjects legally authorized guardian(s) must provide signed, informed consent prior to performing any trial-related activities

4. The subject and his/her guardian(s) must have the ability to comply with the protocol

Exclusion Criteria:

1. History of bone marrow transplantation

2. Presence of known clinically significant cardiovascular, hepatic, pulmonary or renal disease or other medical conditions that, in the opinion of the Investigator, would preclude participation in the trial. Subjects unable to perform the motor tests independently from support are permitted to participate in the trial and will be evaluated for the remnant non motor endpoints

3. Any other medical condition or serious intercurrent illness, or extenuating circumstance that, in the opinion of the investigator, would preclude participation in the trial

4. Pregnant and/or lactating women cannot participate in the trial. Concerning women of child bearing potential (WOCBP), the investigators will decide whether or not there is a need for contraception. This assessment will be done through interviews with the patient and parents.

5. Participation in other interventional trials testing IMP, including rhLAMAN-07 (EudraCT number: 2013-000336-97) and rhLAMAN-09 (EudraCT number: 2013-000321-31) trials with Lamazym

6. Pause of the IMP for 2 consecutive weeks during the last month. Subjects are allowed to be re-screened

Related Conditions & MeSH terms

• Alpha-Mannosidosis

Intervention

Drug:
• Lamazym
recombinant human alpha-mannosidase

Locations

Country	Name	City	State
Denmark	Center for Metabolic Diseases, Department of Clinical Genetics, Juliane Marie Centre, Copenhagen University Hospital, Blegdamsvej 9	Copenhagen

Sponsors (1)

Lead Sponsor	Collaborator
Zymenex A/S

Country where clinical trial is conducted

Denmark, 

References & Publications (4)

Borgwardt L, Guffon N, Amraoui Y, Jones SA, De Meirleir L, Lund AM, Gil-Campos M, Van den Hout JMP, Tylki-Szymanska A, Geraci S, Ardigò D, Cattaneo F, Harmatz P, Phillips D. Health Related Quality of Life, Disability, and Pain in Alpha Mannosidosis: Long-Term Data of Enzyme Replacement Therapy With Velmanase Alfa (Human Recombinant Alpha Mannosidase). Journal of Inborn Errors of Metabolism & Screening 2018, Volume 6: 1-12

Harmatz P, Cattaneo F, Ardigò D, Geraci S, Hennermann JB, Guffon N, Lund A, Hendriksz CJ, Borgwardt L. Enzyme replacement therapy with velmanase alfa (human recombinant alpha-mannosidase): Novel global treatment response model and outcomes in patients wit — View Citation

Lund AM, Borgwardt L, Cattaneo F, Ardigò D, Geraci S, Gil-Campos M, De Meirleir L, Laroche C, Dolhem P, Cole D, Tylki-Szymanska A, Lopez-Rodriguez M, Guillén-Navarro E, Dali CI, Héron B, Fogh J, Muschol N, Phillips D, Van den Hout JMH, Jones SA, Amraoui Y — View Citation

Phillips D, Hennermann JB, Tylki-Szymanska A, Borgwardt L, Gil-Campos M, Guffon N, Amraoui Y, Geraci S, Ardigò D, Cattaneo F, Lund AM. Use of the Bruininks-Oseretsky test of motor proficiency (BOT-2) to assess efficacy of velmanase alfa as enzyme therapy for alpha-mannosidosis. Mol Genet Metab Rep. 2020 Apr 8;23:100586. doi: 10.1016/j.ymgmr.2020.100586. eCollection 2020 Jun. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Quality of life based on questionnaires	filled by the subject's guardian, will be evaluated by Childhood Health Assessment Questionnaire (CHAQ) questionnaires filled in by the subject's guardian, will be evaluated by CHAQ and EQ-5D-5L	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Other	Quality of life based on questionnaires	filled by the subject's guardian, will be evaluated by Health Questionnaire (EQ-5D-5L) questionnaires filled in by the subject's guardian, will be evaluated by CHAQ and EQ-5D-5L	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Other	Development of adverse events	Safety endpoint assessed from signing of the Informed Consent Form (ICF)	1 week
Other	Development of clinically significant changes in vital signs and change in physical examination	Safety endpoint assessed throughout the trial	1 week
Other	Development of clinically significant changes in the clinical laboratory Parameters: Hematology	Safety endpoint assessed throughout the trial	1 week
Other	Development of clinically significant changes in the clinical laboratory Parameters: Biochemistry	Safety endpoint assessed throughout the trial	1 week
Other	Development of clinically significant changes in the clinical laboratory Parameters: Urinalysis	Safety endpoint assessed throughout the trial	1 week
Other	Development of rhLAMAN antibodies	Safety endpoint assessed throughout the trial	1 week
Other	Development of rhLAMAN neutralizing/inhibitory antibodies	Safety endpoint assessed throughout the trial	1 week
Primary	Change from baseline in reduction of oligosaccharides in serum	Primary Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Primary	Change from baseline in 3 Minutes Stair Climb Test (3MSCT)	Primary Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	6 Minute Walk Test (6MWT)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Pulmonary function: Forced Vital Capacity (FVC)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Pulmonary function: Forced Expiratory Volume during first second (FEV1)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Pulmonary function: Peak Expiratory Flow Rate (PEF)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Functional capacity according to Bruininks-Oseretsky test of Motor Proficiency (BOT-2)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Pure Tone Audiometry (PTA)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Equivalence age measured by Leiter International Performance Scale-Revised (Leiter-R)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Assessment of mannose-rich oligosaccharides in brain tissue as measured by Magnetic Resonance Spectroscopy (MRS) visual score (for patients who previously participated in rhLAMAN-02)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Assessment of mannose-rich oligosaccharides in brain tissue as measured by Magnetic Resonance Imaging (MRI) diffusion coefficient (for patients who previously participated in rhLAMAN-02)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Cerebrospinal fluid biomarkers: Oligosaccharides in Cerebrospinal Fluid (CSF)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Cerebrospinal fluid neuro-degeneration biomarkers: Tau Protein (Tau) in Cerebrospinal Fluid (CSF)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Cerebrospinal fluid neuro-degeneration biomarkers: Neurofilament Protein Light (NFL) in Cerebrospinal Fluid (CSF)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Cerebrospinal fluid neuro-degeneration biomarkers: Glial Fibrillary Acidic protein (GFAp) in Cerebrospinal Fluid (CSF)	Endpoint evaluation as change	Baseline evaluation prior to first dose compared to evaluation after one, two or four years of treatment
Secondary	Drug exposure by Pharmaco Kinetic (PK) sampling profile on plasma	Evaluation of steady state Pharmaco Kinetics	1 week
Secondary	Measurement of in vivo biological activity of Lamazym in blood before and after Infusion of Lamazym	Comparing with Anti Body (AB) and PK measurements. Measuring unit is mU/mL	1 week
Secondary	Oligosaccharides in urine	Evaluation of steady state	1 week

External Links

•   Study Record on EU Clinical Trials Register including results