Multifocal Motor NeuropathyHYMMNENCT02885259
HyQvia in Multifocal Motor Neuropathy
A study testing rHuPH20 in people with Multifocal Motor Neuropathy, run by UMC Utrecht at 1 site in Netherlands.
Trial summary
Subcutaneous immunoglobulin (SCIG) and recombinant human hyaluronidase (rHuPH20) will be tested in patient witch MMN and currently under maintenance treatment with IVIG for safety, tolerability and efficacy. Read more about this study
- Who is it for?
- Ages 18 to 99 years
- Conditions the study is for
- Multifocal Motor Neuropathy
- What is being tested?
- rHuPH20
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20 participants
- Where
- 1 siteNetherlands
- Study dates
- Sep 2016to Jan 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 99 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age at onset of MMN, 18 - 99 years.
- The presence of asymmetrical limb weakness at onset or motor involvement having a motor nerve distribution in at least two peripheral nerve distributions, predominant upper limb involvement, disabling weakness MRC grade 4 or less in at least one muscle.
- Decreased or absent tendon reflexes in affected limbs.
- Electrophysiological evidence of one site with definite motor conduction block or one site with probable conduction block according to previously defined criteria.
- Response to IVIG according to criteria that were described in previous studies.
- Stable on IVIG maintenance treatment in the year preceding the study.
- Patients have given written informed consent, prior to the study, with the understanding that consent may be withdrawn at any time without prejudice.
Who cannot join
- Bulbar signs or symptoms.
- Upper motor neuron signs (spasticity, hyperreflexia, extensor plantar response).
- Sensory symptoms and signs with sensory deficits on examination (except for vibration sense) and abnormal results of sensory nerve conduction studies
- Other neuropathies (e.g. diabetic, lead, porphyric or vasculitic neuropathy, chronic inflammatory demyelinating polyneuropathy, Lyme neuroborreliosis, post radiation neuropathy, hereditary neuropathy with liability to pressure palsies, Charcot-Marie-Tooth neuropathies, meningeal carcinomatosis).
- Treatment with other immunosuppressive drugs (cyclophosphamide, azathioprine, cyclosporin) in the 6 months preceding the study.
- Female patient who is pregnant or breast-feeding or of childbearing potential.
Show all 11Show fewer
- Confirmation that the patient is not pregnant will be established by a negative b-HCG test within a 7-day period before inclusion in the study. Lack of childbearing potential is met by:
- being post-menopausal,
- being surgically sterile,
- practising contraception with an oral contraceptive, intra-uterine device, diaphragm or condom with spermicide or d) being sexually inactive.
- Age < 18 years.
Trial locations and contacts
1 site in 1 country.
Bas Jongbloed, drs contact
About this study
Official title: Subcutaneous Immunoglobulin With rHuPH20 in Multifocal Motor Neuropathy
Subcutaneous immunoglobulin (SCIG) and recombinant human hyaluronidase (rHuPH20) will be tested in patient witch MMN and currently under maintenance treatment with IVIG for safety, tolerability and efficacy.
Read the detailed description
Multifocal motor neuropathy (MMN) is a chronic immune mediated neuropathy, which affects patients at a relatively young age and necessitates treatment with immunoglobulins (Ig) to improve and maintain muscle strength. Subcutaneous immunoglobulin (SCIG) therapy for MMN is equally efficacious to intravenous immunoglobulin (IVIG), may be self-administered and may induce fewer systemic adverse reactions. However, limited subcutaneous infusion volumes and reduced bioavailability, necessitate multiple infusion sites, more frequent treatment, and dose adjustment to achieve pharmacokinetic equivalence. This is an issue in particular in MMN where relatively high and frequent doses are necessary to maintain long-term improvement of muscle strength. Recombinant human hyaluronidase (rHuPH20) increases subcutaneous tissue permeability and facilitates dispersion and absorption, enabling subcutaneous administration of higher (monthly) doses of Ig. If treatment with HyQvia is at least equally effective and safe as compared with conventional Ig treatment, HyQvia could become the preferred treatment option for patients with MMN as it may have attractive benefits for patients by its mode of administration.
Objective:
The primary objective is to study the safety and tolerability of HyQvia in patients with
MMN as compared with conventional intravenous, by documenting:
- Side effects by using a diary and a 10 cm visual analogue scale (VAS) scales to measure headache and nausea.
- Biochemical tests (Hemoglobin, haptoglobin, reticulocyte counts, lactate dehydrogenase, bilirubin, DAT) for haemolytic anemia 3-7 days after the last IVIG/SCIG infusion, during the enrolment period and 3-7 days after the last HyQvia infusion during the treatment period.
- Anti- hyaluronidase antibody titer before and after/during the HyQvia treatment. Together with the above mentioned test parameters in point 2, each time 30ml (equal to three tubes) will be drawn.
- Patient satisfaction of product on a 10 cm VAS scale.
The secondary objective is to determine the efficacy of treatment with HyQvia in patients with MMN on:
- Disability, measured by Guy's Neurological Disability Scale and the self-evaluation scale;
- Function, measured by a nine hole peg test (9-HPT) and a 40 meter walk test (40-MWT);
- Muscle strength, measured by manual muscle testing and hand-held dynamometry.
Study design:
HyQvia in MMN will be studied in a prospective, uncontrolled single-blind open-label study of 20 patients on IVIG with a duration of 48 to 60 weeks consisting of:
- Enrolment period of 12 to 24 weeks' duration in which patients will be treated according to their regular maintenance treatment regimen with IVIG, and visit the outpatient clinic every 6 weeks.
- Treatment period of 9 months' duration in which patients will be treated with HyQvia, using the same dose as during the enrolment period and visit the outpatient clinic at start and after 6, 12, 24 and 36 weeks.
- During the study, the dose may be increased if patients' functioning in daily life is worsening: the score of either the upper or lower limb score of the Guy's Neurological Disability Scale or the score of at least two motor activities on the self- evaluation scale have increased with 1 point or muscle strength on hand-held dynamometry has worsened by 50% or more in at least two clinically affected muscles or muscle groups. If patients do not improve on increased Ig dose during the treatment period the investigator can decide to stop maintenance treatment with HyQvia and restart the previous treatment after a period of minimal 3 months.
HyQvia will be administrated in patients' routine setting -at home or in the hospital- with help of a nurse who is trained in using HyQvia. The patients are carefully monitored for potential adverse signs throughout the study period as well as anti- hyaluronidase antibody induction.
Study population:
From the outpatient clinic at the UMC Utrecht, 20 patients with MMN and currently under maintenance treatment with IVIG will be selected to study the safety, tolerability and efficacy of HyQvia.
Intervention: 20 MMN patients, currently under maintenance treatment with IVIG, will be will be treated with HyQvia during a 9 months' period using the same dose as IVIG during the enrolment period.
Main study parameters/endpoints:
The following main study parameters will be used to assess tolerability and efficacy of HyQvia in MMN patients:
- Disability using the Guy's Neurologic Disability Scale and the self- evaluation scale.
- Function will be evaluated with a 9-HPT and a 40 MWT.
- Muscle strength will be measured with manual muscle testing using the Medical Research Council scale (MRC). Hand-held dynamometry will be performed in a selection of those muscles or muscle groups with an MRC score < 5 at any time. Grip strength of the hands will be measured using a hand-held dynamometer.
- Adverse events by using 10 cm long VAS analogue scales for headache and nausea as well as a diary, which will be provided to the patient at each visit in the clinic.
- IgM anti-GM1 ganglioside antibody titers at the enrolment visit and at the final visit.
Biochemical tests for haemolytic anemia 3-7 days after the last IVIG/SCIG infusion during the enrolment period and 3-7 days after the last HyQvia infusion during the treatment period.
- Anti-hyaluronidase antibody titer 12 weeks before and at 3 and 9 months during HyQvia treatment. Together with the above mentioned test parameters in point 5, each time 30ml (equal to three tubes) will be drawn.
- Patient satisfaction of product on a 10 cm VAS scale.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
The risks are negligible and the burden minimal for patients enrolled in this study, assessing tolerability and efficacy of HyQvia in MMN patients. Patients participating in the study, will be assigned 6 grouped evaluations at fixed intervals: filling out a diary, evaluation scales, 3 blood samples, visit the outpatient clinic and are also evaluated with routine physical examinations. The two components of HyQvia, Subcutaneous immunoglobulin (SCIG) and recombinant human hyaluronidase (rHuPH20), are known to be safe and are already applied in primary and secondary immunodeficiency disorders, multiple myeloma and chronic lymphatic leukemia. SCIG therapy for MMN, is safe and equally efficacious to intravenous immunoglobulin (IVIG). Furthermore, it may be self-administered and may induce fewer systemic adverse reactions than IVIG. Recombinant human hyaluronidase (rHuPH20), increases subcutaneous tissue absorption and enables higher doses of subcutaneous administration Ig, which will decrease the number of infusion sites, resulting in less frequent treatment and dose adjustments.
- Conditions
- Multifocal Motor Neuropathy
- Being tested
- rHuPH20
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
rHuPH20Drug
Also called HyQvia
human immunoglobulin and one vial of recombinant human hyaluronidase
| Study group | Role | What they receive |
|---|---|---|
| HyQvia | Experimental | human immunoglobulin and one vial of recombinant human hyaluronidase (rHuPH20 Receives: Drug: rHuPH20 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Safety measured by anamnesis
presence of headache, gastrointestinal complaints, fatigue, flue-like symptoms
Measured: 1 year
Secondary outcomes (4)
Quality of life (QoL) measured by a VAS questionnaire
VAS questionnaire every visit at the outpatient clinic.
Measured: 1 year
Stability of muscle strength
Every visit at the outpatient clinic a Guy's neurologic disability scale (GNDS) and MRC sum score are obtained
Measured: 1 year
Safety measured by questionnaire
QoL questionnaire measured in a VAS number
Measured: 1 year
Safety measured by blood test
Liver tests and blood counts
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Aug 2016 (estimated)
- Study startSep 2016
- Primary completionDec 2017 (estimated)
- Study completionJan 2018 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Multifocal Motor NeuropathyStudies of the same condition, open and under way.
- More trials run by UMC UtrechtThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- UMC Utrecht
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, L.H. van den Berg, UMC Utrecht
- Investigators
- Leonard van den Berg, prof, Principal investigator, UMCU
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02885259
- Sponsor's protocol ID
- NL52642.041.15
- Acronym
- HYMMNE
- Status last verified
- Aug 2016
- First submitted
- 25 Jan 2016
- Last updated
- 31 Aug 2016
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Aug 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Subcutaneous Immunoglobulin With rHuPH20 in Multifocal Motor Neuropathy
- ClinicalTrials.gov ID
- NCT02885259
- Acronym / sponsor ID
- HYMMNE / NL52642.041.15
- Conditions
- Multifocal Motor Neuropathy
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- UMC UtrechtUniversity, hospital or other
- Study start
- Sep 2016
- Primary completion
- Dec 2017 (estimated)
- Study completion
- Jan 2018 (estimated)
- First posted
- 31 Aug 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Subcutaneous immunoglobulin (SCIG) and recombinant human hyaluronidase (rHuPH20) will be tested in patient witch MMN and currently under maintenance treatment with IVIG for safety, tolerability and efficacy.
Detailed description
Multifocal motor neuropathy (MMN) is a chronic immune mediated neuropathy, which affects patients at a relatively young age and necessitates treatment with immunoglobulins (Ig) to improve and maintain muscle strength. Subcutaneous immunoglobulin (SCIG) therapy for MMN is equally efficacious to intravenous immunoglobulin (IVIG), may be self-administered and may induce fewer systemic adverse reactions. However, limited subcutaneous infusion volumes and reduced bioavailability, necessitate multiple infusion sites, more frequent treatment, and dose adjustment to achieve pharmacokinetic equivalence. This is an issue in particular in MMN where relatively high and frequent doses are necessary to maintain long-term improvement of muscle strength. Recombinant human hyaluronidase (rHuPH20) increases subcutaneous tissue permeability and facilitates dispersion and absorption, enabling subcutaneous administration of higher (monthly) doses of Ig. If treatment with HyQvia is at least equally effective and safe as compared with conventional Ig treatment, HyQvia could become the preferred treatment option for patients with MMN as it may have attractive benefits for patients by its mode of administration.
Objective:
The primary objective is to study the safety and tolerability of HyQvia in patients with
MMN as compared with conventional intravenous, by documenting:
- Side effects by using a diary and a 10 cm visual analogue scale (VAS) scales to measure headache and nausea.
- Biochemical tests (Hemoglobin, haptoglobin, reticulocyte counts, lactate dehydrogenase, bilirubin, DAT) for haemolytic anemia 3-7 days after the last IVIG/SCIG infusion, during the enrolment period and 3-7 days after the last HyQvia infusion during the treatment period.
- Anti- hyaluronidase antibody titer before and after/during the HyQvia treatment. Together with the above mentioned test parameters in point 2, each time 30ml (equal to three tubes) will be drawn.
- Patient satisfaction of product on a 10 cm VAS scale.
The secondary objective is to determine the efficacy of treatment with HyQvia in patients with MMN on:
- Disability, measured by Guy's Neurological Disability Scale and the self-evaluation scale;
- Function, measured by a nine hole peg test (9-HPT) and a 40 meter walk test (40-MWT);
- Muscle strength, measured by manual muscle testing and hand-held dynamometry.
Study design:
HyQvia in MMN will be studied in a prospective, uncontrolled single-blind open-label study of 20 patients on IVIG with a duration of 48 to 60 weeks consisting of:
- Enrolment period of 12 to 24 weeks' duration in which patients will be treated according to their regular maintenance treatment regimen with IVIG, and visit the outpatient clinic every 6 weeks.
- Treatment period of 9 months' duration in which patients will be treated with HyQvia, using the same dose as during the enrolment period and visit the outpatient clinic at start and after 6, 12, 24 and 36 weeks.
- During the study, the dose may be increased if patients' functioning in daily life is worsening: the score of either the upper or lower limb score of the Guy's Neurological Disability Scale or the score of at least two motor activities on the self- evaluation scale have increased with 1 point or muscle strength on hand-held dynamometry has worsened by 50% or more in at least two clinically affected muscles or muscle groups. If patients do not improve on increased Ig dose during the treatment period the investigator can decide to stop maintenance treatment with HyQvia and restart the previous treatment after a period of minimal 3 months.
HyQvia will be administrated in patients' routine setting -at home or in the hospital- with help of a nurse who is trained in using HyQvia. The patients are carefully monitored for potential adverse signs throughout the study period as well as anti- hyaluronidase antibody induction.
Study population:
From the outpatient clinic at the UMC Utrecht, 20 patients with MMN and currently under maintenance treatment with IVIG will be selected to study the safety, tolerability and efficacy of HyQvia.
Intervention: 20 MMN patients, currently under maintenance treatment with IVIG, will be will be treated with HyQvia during a 9 months' period using the same dose as IVIG during the enrolment period.
Main study parameters/endpoints:
The following main study parameters will be used to assess tolerability and efficacy of HyQvia in MMN patients:
- Disability using the Guy's Neurologic Disability Scale and the self- evaluation scale.
- Function will be evaluated with a 9-HPT and a 40 MWT.
- Muscle strength will be measured with manual muscle testing using the Medical Research Council scale (MRC). Hand-held dynamometry will be performed in a selection of those muscles or muscle groups with an MRC score < 5 at any time. Grip strength of the hands will be measured using a hand-held dynamometer.
- Adverse events by using 10 cm long VAS analogue scales for headache and nausea as well as a diary, which will be provided to the patient at each visit in the clinic.
- IgM anti-GM1 ganglioside antibody titers at the enrolment visit and at the final visit.
Biochemical tests for haemolytic anemia 3-7 days after the last IVIG/SCIG infusion during the enrolment period and 3-7 days after the last HyQvia infusion during the treatment period.
- Anti-hyaluronidase antibody titer 12 weeks before and at 3 and 9 months during HyQvia treatment. Together with the above mentioned test parameters in point 5, each time 30ml (equal to three tubes) will be drawn.
- Patient satisfaction of product on a 10 cm VAS scale.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
The risks are negligible and the burden minimal for patients enrolled in this study, assessing tolerability and efficacy of HyQvia in MMN patients. Patients participating in the study, will be assigned 6 grouped evaluations at fixed intervals: filling out a diary, evaluation scales, 3 blood samples, visit the outpatient clinic and are also evaluated with routine physical examinations. The two components of HyQvia, Subcutaneous immunoglobulin (SCIG) and recombinant human hyaluronidase (rHuPH20), are known to be safe and are already applied in primary and secondary immunodeficiency disorders, multiple myeloma and chronic lymphatic leukemia. SCIG therapy for MMN, is safe and equally efficacious to intravenous immunoglobulin (IVIG). Furthermore, it may be self-administered and may induce fewer systemic adverse reactions than IVIG. Recombinant human hyaluronidase (rHuPH20), increases subcutaneous tissue absorption and enables higher doses of subcutaneous administration Ig, which will decrease the number of infusion sites, resulting in less frequent treatment and dose adjustments.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| HyQvia | Experimental | Drug: rHuPH20human immunoglobulin and one vial of recombinant human hyaluronidase (rHuPH20 |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Age at onset of MMN, 18 - 99 years.
- The presence of asymmetrical limb weakness at onset or motor involvement having a motor nerve distribution in at least two peripheral nerve distributions, predominant upper limb involvement, disabling weakness MRC grade 4 or less in at least one muscle.
- Decreased or absent tendon reflexes in affected limbs.
- Electrophysiological evidence of one site with definite motor conduction block or one site with probable conduction block according to previously defined criteria.
- Response to IVIG according to criteria that were described in previous studies.
Key exclusion criteria (11 listed)
- Bulbar signs or symptoms.
- Upper motor neuron signs (spasticity, hyperreflexia, extensor plantar response).
- Sensory symptoms and signs with sensory deficits on examination (except for vibration sense) and abnormal results of sensory nerve conduction studies
- Other neuropathies (e.g. diabetic, lead, porphyric or vasculitic neuropathy, chronic inflammatory demyelinating polyneuropathy, Lyme neuroborreliosis, post radiation neuropathy, hereditary neuropathy with liability to pressure palsies, Charcot-Marie-Tooth neuropathies, meningeal carcinomatosis).
- Treatment with other immunosuppressive drugs (cyclophosphamide, azathioprine, cyclosporin) in the 6 months preceding the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| rHuPH20Also: HyQviahuman immunoglobulin and one vial of recombinant human hyaluronidase | Drug | HyQvia |
Primary outcome
Safety measured by anamnesis
Time frame: 1 year
presence of headache, gastrointestinal complaints, fatigue, flue-like symptoms
4 secondary outcomes
Quality of life (QoL) measured by a VAS questionnaire
Time frame: 1 year
Stability of muscle strength
Time frame: 1 year
Safety measured by questionnaire
Time frame: 1 year
Safety measured by blood test
Time frame: 1 year
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2016.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Bas Jongbloed, drs contact
Leonard van den Berg, prof principal investigator
UMCU
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing rHuPH20 in people with Multifocal Motor Neuropathy, run by UMC Utrecht at 1 site in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 31 Aug 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Bas Jongbloed, drs (b.a.jongbloed-2@umcutrecht.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Safety measured by anamnesis (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2016.