Proof of Concept (POC) in Patients With Ischaemic Stroke

Terminated

Phase 2 Results

Update History

4 Oct '17
The description was updated.
New
Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability and neurological impairment will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also further characterize the safety, PK, and immunogenicity of GSK249320 will explore pharmacodynamic (PD) markers, and will explore use of actigraphy to measure motor recovery. Subjects will be stratified by gait velocity at baseline for randomization (1:1 allocation) into one of two treatment groups: 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.
Old
Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability and neurological impairment will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also further characterize the safety, PK, and immunogenicity of GSK249320 will explore pharmacodynamic (PD) markers, and will explore use of actigraphy to measure motor recovery. Subjects will be stratified by gait velocity at baseline for randomization (1:1 allocation) into one of two treatment groups: 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.
The gender criteria for eligibility was updated to "All."
The eligibility criteria were updated.
New
Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. A positive hepatitis B or hepatitis C result on the GSK labs drawn at baseline/Study Day 1 do not exclude a subject from continuing in the study unless there are associated clinical signs/symptoms of liver disease; however, the subject should be treated as clinically indicated and the GSK Medical Monitor should be contacted for further discussion. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
Old
Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. A positive hepatitis B or hepatitis C result on the GSK labs drawn at baseline/Study Day 1 do not exclude a subject from continuing in the study unless there are associated clinical signs/symptoms of liver disease; however, the subject should be treated as clinically indicated and the GSK Medical Monitor should be contacted for further discussion. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
24 May '16
Trial name was updated.
New
Proof of Concept (POC) in Patients With Ischaemic Stroke
21 Apr '16
The eligibility criteria were updated.
New
Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. A positive hepatitis B or hepatitis C result on the GSK labs drawn at baseline/Study Day 1 do not exclude a subject from continuing in the study unless there are associated clinical signs/symptoms of liver disease; however, the subject should be treated as clinically indicated and the GSK Medical Monitor should be contacted for further discussion. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
Old
Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. A positive hepatitis B or hepatitis C result on the GSK labs drawn at baseline/Study Day 1 do not exclude a subject from continuing in the study unless there are associated clinical signs/symptoms of liver disease; however, the subject should be treated as clinically indicated and the GSK Medical Monitor should be contacted for further discussion. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
19 Aug '14
A location was updated in Orange.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Jacksonville.
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The overall status was removed for GSK Investigational Site.
A location was updated in Peoria.
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The overall status was removed for GSK Investigational Site.
A location was updated in Lexington.
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The overall status was removed for GSK Investigational Site.
A location was updated in Portland.
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The overall status was removed for GSK Investigational Site.
A location was updated in Nashville.
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The overall status was removed for GSK Investigational Site.
A location was updated in Edmonton.
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The overall status was removed for GSK Investigational Site.
A location was updated in Edmonton.
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The overall status was removed for GSK Investigational Site.
A location was updated in London.
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The overall status was removed for GSK Investigational Site.
A location was updated in Toronto.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Greenfield Park.
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The overall status was removed for GSK Investigational Site.
A location was updated in St-Jerome.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Freiburg.
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The overall status was removed for GSK Investigational Site.
A location was updated in Friedrichshafen.
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The overall status was removed for GSK Investigational Site.
A location was updated in Ulm.
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The overall status was removed for GSK Investigational Site.
A location was updated in Erlangen.
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The overall status was removed for GSK Investigational Site.
A location was updated in Celle.
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The overall status was removed for GSK Investigational Site.
A location was updated in Hannover.
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The overall status was removed for GSK Investigational Site.
A location was updated in Osnabrueck.
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The overall status was removed for GSK Investigational Site.
A location was updated in Essen.
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The overall status was removed for GSK Investigational Site.
A location was updated in Muenster.
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The overall status was removed for GSK Investigational Site.
A location was updated in Leipzig.
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The overall status was removed for GSK Investigational Site.
A location was updated in Bremen.
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The overall status was removed for GSK Investigational Site.
A location was updated in Hamburg.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Hamburg.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Cambridge.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Exeter.
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The overall status was removed for GSK Investigational Site.
A location was updated in Glasgow.
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The overall status was removed for GSK Investigational Site.
A location was updated in Harrow.
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The overall status was removed for GSK Investigational Site.
A location was updated in Liverpool.
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The overall status was removed for GSK Investigational Site.
A location was updated in London.
New
The overall status was removed for GSK Investigational Site.
A location was updated in London.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Newcastle upon Tyne.
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The overall status was removed for GSK Investigational Site.
A location was updated in Romford.
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The overall status was removed for GSK Investigational Site.
A location was updated in Salford.
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The overall status was removed for GSK Investigational Site.
A location was updated in Torquay.
New
The overall status was removed for GSK Investigational Site.
5 Aug '14
A location was updated in Freiburg.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Essen.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Newcastle upon Tyne.
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The overall status was removed for GSK Investigational Site.
29 Jul '14
A location was updated in Lexington.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Nashville.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Edmonton.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Edmonton.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Greenfield Park.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Cambridge.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Exeter.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Harrow.
New
The overall status was removed for GSK Investigational Site.
A location was updated in London.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Salford.
New
The overall status was removed for GSK Investigational Site.
15 Jul '14
A location was updated in Toronto.
New
The overall status was removed for GSK Investigational Site.
A location was updated in St-Jerome.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Glasgow.
New
The overall status was removed for GSK Investigational Site.
1 Jul '14
A location was updated in Erlangen.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Liverpool.
New
The overall status was removed for GSK Investigational Site.
18 Mar '14
A location was updated in London.
New
The overall status was removed for GSK Investigational Site.
11 Mar '14
A location was updated in Friedrichshafen.
New
The overall status was removed for GSK Investigational Site.
5 Mar '14
A location was updated in Peoria.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Osnabrueck.
New
The overall status was removed for GSK Investigational Site.
A location was updated in London.
New
The overall status was removed for GSK Investigational Site.
25 Feb '14
A location was updated in Orange.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Salford.
New
The overall status was removed for GSK Investigational Site.
11 Feb '14
A location was updated in Hamburg.
New
The overall status was removed for GSK Investigational Site.
5 Feb '14
A location was updated in Romford.
New
The overall status was removed for GSK Investigational Site.
29 Jan '14
A location was updated in St-Jerome.
New
The overall status was removed for GSK Investigational Site.
A location was updated in Essen.
New
The overall status was removed for GSK Investigational Site.
4 Jan '14
A location was updated in Greenfield Park.
New
The overall status was removed for GSK Investigational Site.
18 Dec '13
The description was updated.
New
Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability and neurological impairment will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also further characterize the safety, PK, and immunogenicity of GSK249320 will explore pharmacodynamic (PD) markers, and will explore use of actigraphy to measure motor recovery. Subjects will be stratified by gait velocity at baseline for randomization (1:1 allocation) into one of two treatment groups: 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.
Old
Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability and neurological impairment will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also characterize the safety, PK, and immunogenicity profile of GSK249320, and will explore pharmacodynamic markers. Subjects will be stratified by gait velocity at baseline for randomization (1:1 allocation) into one of two treatment groups: 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.
The eligibility criteria were updated.
New
Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. A positive hepatitis B or hepatitis C result on the GSK labs drawn at baseline/Study Day 1 do not exclude a subject from continuing in the study unless there are associated clinical signs/symptoms of liver disease; however, the subject should be treated as clinically indicated and the GSK Medical Monitor should be contacted for further discussion. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
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Inclusion Criteria: - Have a confirmed diagnosis of stroke according to the World Health Organization definition which is, 'a rapid onset event of vascular origin reflecting a focal disturbance of cerebral function, excluding isolated impairments of higher function, and persisting longer than 24 hours [World Health Organization, 1989]. - Stroke onset must be within the last 24-72 hours of the first infusion of Investigational Product. Time of stroke onset is defined at the time at which the patient/relative is first aware of the stroke deficit. For patients who awake with deficits, or who are found unconscious, the time of onset is defined as the time at which they were last known to be symptom free. - Have a stroke that is radiologically confirmed to be ischemic and supratentorial. The diameter of the ischemic lesion is >15mm in any single direction or the volume is >4cc. See the Study Procedures Manual (SPM) for guidance on how to calculate the lesion size. - Have a total NIHSS score of 3-21. - Have a lower limb deficit from the incident stroke which is defined as a score of 1-4 on the NIHSS Motor Leg question (question #6). - Aged 18-90, inclusive. - Expectation the subject will receive standard physical, occupational and speech rehabilitation therapy as indicated for the post stroke deficits. - Male subjects and female subjects of non-child-bearing and child-bearing potential are allowed to participate in this study. See Section 11, Appendix 1 for definitions. Females of child-bearing potential must have a negative pregnancy test prior to enrollment and must agree to use one of the contraceptive methods specified in Section 11, Appendix 1. Exclusion Criteria: - Ability to walk >0.8m/s as measured by the Gait Velocity assessment. - History of a previous symptomatic stroke within 3 months prior to study entry. - Presence of significant disability prior to the current stroke. Significant disability is defined as having a pre-stroke Rankin score of >2. - Subjects who are not alert or are unresponsive as defined by a score of 2 or 3 on the NIHSS Level of Consciousness question (Question 1a). - Presence of significant aphasia likely to confound or interfere with completion of the study assessments. - Presence of a significant pre-existing gait deficit prior to study entry that is likely to confound clinical evaluations - Presence of pre-existing neurologic or psychiatric disease which is active and not adequately controlled such that it interfered with major activities of daily living immediately prior to the current stroke and is likely to interfere with study participation/visits or confound clinical evaluations. - The subject poses a significant suicide risk, in the opinion of the investigator. - Current or chronic history of liver disease, known hepatic or biliary abnormalities (except Gilbert's syndrome or asymptomatic gallstones), or known history of hepatitis B or hepatitis C infection. - Presence of either a central or peripheral demyelinating disease, such as multiple sclerosis or IgM monoclonal gammopathy of unknown significance (MGUS). - Expected death due to the incident stroke, or evidence of a chronic co-morbid condition or unstable acute systemic illness which, in the opinion of the investigator, could shorten the subject's survival such that it would limit his/her ability to complete the study. - Presence of the following ECG values on baseline ECG: QTc > 500 msec (using either Bazett's formula (QTcB) or Fridericia's formula (QTcF)); or uncorrected QT >600msec (machine or manual over-read). If the ECG indicates a prolonged QTc interval value outside these limits, two further ECGs should be performed during the same sitting and the average QTc value of these triplicate ECGs calculated. If the average value exceeds the stated limits, the subject is not eligible. - Participation in any investigational rehabilitation paradigm targeting stroke recovery during the duration of this study. - Have a contraindication to MRI as per local hospital practice/guidelines. - The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer). - Prior treatment with GSK249320. - History of sensitivity to Investigational Product excipients (acetate buffer, polysorbate 80 and sodium chloride) that, in the opinion of the investigator or GSK Medical Monitor, contraindicates the subject's participation. - Pregnant females as determined by positive urine hCG test prior to enrollment. - Lactating females. - Subjects considered unwilling or unable to comply with the procedures and study visit schedule outlined in the protocol.
A location was updated in Freiburg.
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The overall status was removed for GSK Investigational Site.
A location was updated in Ulm.
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The overall status was removed for GSK Investigational Site.
19 Nov '13
A location was updated in Erlangen.
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The overall status was removed for GSK Investigational Site.
13 Nov '13
A location was updated in Exeter.
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The overall status was removed for GSK Investigational Site.
5 Nov '13
A location was updated in Lexington.
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The overall status was removed for GSK Investigational Site.
30 Oct '13
A location was updated in Bremen.
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The overall status was removed for GSK Investigational Site.
A location was updated in Newcastle upon Tyne.
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The overall status was removed for GSK Investigational Site.
A location was updated in Romford.
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The overall status was removed for GSK Investigational Site.
22 Oct '13
A location was updated in Nashville.
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The overall status was removed for GSK Investigational Site.
17 Oct '13
A location was updated in Edmonton.
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The overall status was removed for GSK Investigational Site.
24 Sep '13
A location was updated in Toronto.
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The overall status was removed for GSK Investigational Site.
A location was updated in Muenster.
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The overall status was removed for GSK Investigational Site.
17 Sep '13
A location was updated in Cambridge.
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The overall status was removed for GSK Investigational Site.
4 Sep '13
A location was updated in London.
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The overall status was removed for GSK Investigational Site.
A location was updated in Hamburg.
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The overall status was removed for GSK Investigational Site.
28 Aug '13
A location was updated in Cambridge.
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The overall status was removed for GSK Investigational Site.
20 Aug '13
A location was updated in Cambridge.
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The overall status was removed for GSK Investigational Site.
A location was updated in Glasgow.
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The overall status was removed for GSK Investigational Site.
6 Aug '13
A location was updated in Hannover.
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The overall status was removed for GSK Investigational Site.
30 Jul '13
A location was updated in Jacksonville.
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The overall status was removed for GSK Investigational Site.
A location was updated in London.
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The overall status was removed for GSK Investigational Site.
2 Jul '13
A location was updated in Celle.
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The overall status was removed for GSK Investigational Site.
25 Jun '13
A location was updated in Freiburg.
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The overall status was removed for GSK Investigational Site.
A location was updated in Salford.
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The overall status was removed for GSK Investigational Site.
11 Jun '13
A location was updated in Edmonton.
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The overall status was removed for GSK Investigational Site.
A location was updated in Harrow.
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The overall status was removed for GSK Investigational Site.
2 Apr '13
The description was updated.
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Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability and neurological impairment will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also characterize the safety, PK, and immunogenicity profile of GSK249320, and will explore pharmacodynamic markers. Subjects will be stratified by gait velocity at baseline for randomization (1:1 allocation) into one of two treatment groups: 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.
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Myelin-associated glycoprotein (MAG) is one of the key proteins known to inhibit neuronal regeneration when released from oligodendrocytes in conditions of neuronal injury, such as stroke. GSK249320 is a humanised monoclonal antibody (mAb) that binds with high specificity to MAG and antagonises or neutralises MAG-mediated inhibition and has been shown to improve functional recovery after stroke in pre-clinical models, possibly by promoting neuroregeneration and plasticity. The present study (MAG104615) is designed to establish Proof of Concept (PoC) for GSK249320 in ischemic stroke patients. MAG104615 will be a placebo-controlled, double-blind, multicenter, randomized, repeat dose, Bayesian adaptive design study. PoC will be achieved by demonstrating a clinically meaningful improvement in lower limb motor recovery, specifically by evaluating changes in gait velocity from baseline to Day 90/Month 3. Subjects will also be followed out to Day 180/Month 6 to further evaluate longer term motor recovery and safety. Additional secondary efficacy measures of motor recovery will be evaluated to further demonstrate and characterize the extent and duration of overall motor recovery after treatment with GSK249320. Changes in disability, neurological impairment and activities of daily living will be characterized after treatment with GSK249320 and explored for how they relate to motor recovery. This PoC study will also characterize the safety, PK, and immunogenicity profile of GSK249320, and will explore pharmacodynamic markers as well as the impact of GSK249320 on health related quality of life and health resource utilization. Subjects will be stratified by gait velocity at baseline for randomization (1:1:1 allocation) into one of three treatment groups: 5 mg/kg GSK249320, 15mg/kg GSK249320, or placebo. Each subject will receive 2 repeat IV doses of GSK249320 or placebo.