Treatment Interruption of Natalizumab | NCT01071083 | Trialant
NCT01071083
Sponsor
Biogen
Status
Completed
Last Update Posted
Sep 19, 2013Estimated
Enrollment
175Actual
Phase
Phase 2
Conditions
Relapsing Remitting Multiple Sclerosis
Interventions
natalizumab
interferon beta 1-a
methylprednisolone
IV placebo
glatiramer acetate
Countries
United States
Germany
Spain
Protocol Section
Identification Module
NCT ID
NCT01071083
Obsolete or Duplicate NCT IDs
Not provided
Organization Study
101MS205
Secondary IDs
Not provided
Brief Title
Treatment Interruption of Natalizumab
Official Title
Randomized Treatment Interruption of Natalizumab
Acronym
RESTORE
Organization
BiogenINDUSTRY
Status Module
Record Verification Date
Nov 2012
Overall Recruitment Status or Expanded Access Status
Completed
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Not provided
Expanded Access Info
No
Start Date
Mar 2010
Primary Completion Date
Nov 2011Actual
Completion Date
Nov 2011Actual
First Submitted Date
Feb 17, 2010
First Submission Date that Met QC Criteria
Feb 17, 2010
First Posted Date
Feb 19, 2010Estimated
Results Waived
Not provided
Results First Submitted Date
Oct 25, 2012
Results First Submitted that Met QC Criteria
Dec 20, 2012
Results First Posted Date
Jan 30, 2013Estimated
Certification/Extension (aka Delayed Results) First Submitted Date
Not provided
Certification/Extension First Submitted that Passed QC Review
Not provided
Certification/Extension First Posted Date
Not provided
Last Update Submitted Date
Sep 12, 2013
Last Update Posted Date
Sep 19, 2013Estimated
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
BiogenINDUSTRY
Collaborators
Name
Class
Elan Pharmaceuticals
INDUSTRY
Oversight Module
No data available
No data is available for this block.
Description Module
Brief Summary
This is a randomized, rater blinded trial in patients who interrupt treatment with natalizumab with or without being treated with other immunomodulatory drugs, or continue treatment with natalizumab.
The main purpose of this study is to find out the following, when participants stop taking natalizumab for 24 weeks:
when MS symptoms return, and
if other drugs for MS may help control MS symptoms during the natalizumab-interruption period.
This study will also explore how quickly the effects of natalizumab return after resuming natalizumab dosing.
Detailed Description
Not provided
Conditions Module
Conditions
Relapsing Remitting Multiple Sclerosis
Keywords
MS
Design Module
Study Type
Interventional
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
Not provided
Target Follow-Up Duration
Not provided
Phases
Phase 2
Interventional Study Design
Allocation
Biospecimen
No data available
No data is available for this block.
Enrollment
175Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
natalizumab
Active Comparator
Drug: natalizumab
IV placebo
Placebo Comparator
Other: IV placebo
interferon β-1a, glatiramer acetate, or methylprednisolone
Active Comparator
Drug: interferon beta 1-a
Drug: methylprednisolone
Drug: glatiramer acetate
Interventions
Name
Type
Description
Arm Group Labels
Other Names
natalizumab
Drug
300 mg intravenous every 4 weeks
natalizumab
interferon beta 1-a
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
Time Course to Return of Radiological and/or Clinical Evidence of Multiple Sclerosis Activity, as Measured by the Percentage of Subjects Who Met Magnetic Resonance Imaging (MRI) and/or Clinical Relapse Rescue Criteria.
Rescue criteria were: 1) central reader MRI finding of 1 new gadolinium-enhancing (Gd+) lesion of >0.8 cubic centimeters in volume or 2 or more Gd+ lesions of any size 2) clinical relapse. Clinical relapse was new or recurrent neurological symptoms not associated with fever or infection, lasting at least 24 hours, as defined by: an increase of ≥1 grade in ≥2 functional scales of the Expanded Disability Status Scale (EDSS); an increase of ≥2 grades in 1 functional scale of the EDSS; or an increase of >0.5 in EDSS if the previous EDSS was ≤5.5, or ≥0.5 if the previous EDSS was >5.5
28 Weeks
Secondary Outcomes
Measure
Description
Time Frame
Time Course to Return of Radiological Activity, as Measured by the Percentage of Subjects Who Met Magnetic Resonance Imaging (MRI) Rescue Criteria.
MRI rescue criteria were the presence of 1 new gadolinium-enhancing (Gd+) lesion of >0.8 cubic centimeters in volume or 2 or more Gd+ lesions of any size, according to the central MRI reader.
28 Weeks
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Major criteria include:
A diagnosis of a relapsing form of MS
Treatment with natalizumab according to locally approved prescribing information
Other protocol defined inclusion/exclusion criteria may apply
Fox RJ, Cree BAC, de Seze J, Gold R, Hartung HP, Jeffery D, Kappos L, Montalban X, Weinstock-Guttman B, Singh CM, Altincatal A, Belviso N, Avila RL, Ho PR, Su R, Engle R, Sangurdekar D, de Moor C, Fisher E, Kieseier BC, Rudick RA. Temporal Relationship Between Serum Neurofilament Light Chain and Radiologic Disease Activity in Patients With Multiple Sclerosis. Neurology. 2024 May 14;102(9):e209357. doi: 10.1212/WNL.0000000000209357. Epub 2024 Apr 22.
interferon β-1a, glatiramer acetate, or methylprednisolone
methylprednisolone
Drug
1000 mg intravenous every 4 weeks
interferon β-1a, glatiramer acetate, or methylprednisolone
IV placebo
Other
placebo intravenous every 4 weeks
IV placebo
glatiramer acetate
Drug
20 mg subcutaneous once daily
interferon β-1a, glatiramer acetate, or methylprednisolone
San Francisco
California
94117
United States
Research Site
Fort Collins
Colorado
United States
Research Site
Pompano Beach
Florida
33060
United States
Research Site
Atlanta
Georgia
30309
United States
Research Site
Atlanta
Georgia
30327
United States
Research Site
Chicago
Illinois
60612
United States
Research Site
Lake Barrington
Illinois
60010
United States
Research Site
Des Moines
Iowa
50314
United States
Research Site
Boston
Massachusetts
2135
United States
Research Site
Boston
Massachusetts
2215
United States
Research Site
Buffalo
New York
14203
United States
Research Site
Latham
New York
12110
United States
Research Site
Patchogue
New York
11772
United States
Research Site
Charlotte
North Carolina
28207
United States
Research Site
Raleigh
North Carolina
27607
United States
Research Site
Cleveland
Ohio
44195
United States
Research Site
Uniontown
Ohio
United States
Research Site
Salt Lake City
Utah
84103
United States
Research Site
Seattle
Washington
98111
United States
Research Site
Freiburg im Breisgau
Baden-Wurttemberg
79106
Germany
Research Site
München
Bavaria
81675
Germany
Research Site
Hennigsdorf
Brandenburg
16761
Germany
Research Site
Hamburg
Free and Hanseatic City of Hamburg
20246
Germany
Research Site
Marburg
Hesse
35039
Germany
Research Site
Bochum
North Rhine-Westphalia
44791
Germany
Research Site
Dresden
Saxony
1307
Germany
Research Site
Barcelona
Barcelona
8035
Spain
Research Site
L'Hospitalet de Llobregat
Barcelona
8907
Spain
Research Site
Málaga
Malaga
29010
Spain
Research Site
El Palmar
Murcia
30120
Spain
Research Site
Valencia
Valencia
46009
Spain
Research Site
Valencia
Valencia
46010
Spain
Derived
Nakamura K, Brown RA, Narayanan S, Collins DL, Arnold DL; Alzheimer's Disease Neuroimaging Initiative. Diurnal fluctuations in brain volume: Statistical analyses of MRI from large populations. Neuroimage. 2015 Sep;118:126-32. doi: 10.1016/j.neuroimage.2015.05.077. Epub 2015 Jun 3.
FG002
Interferon β-1a
30 ug intramuscular once per week
FG003
Glatiramer Acetate
20 mg subcutaneous once daily
FG004
Methylprednisolone
1000 mg intravenous every 4 weeks
FG00042 subjects
FG00145 subjects
FG00217 subjects
FG00317 subjects
FG00454 subjects
COMPLETED
FG00035 subjects
FG00143 subjects
FG00212 subjects
FG00315 subjects
FG00446 subjects
NOT COMPLETED
FG0007 subjects
FG0012 subjects
FG0025 subjects
FG0032 subjects
FG0048 subjects
Type
Comment
Reasons
Adverse Event
FG0001 subjects
FG0010 subjects
FG0021 subjects
FG0030 subjects
FG0041 subjects
Withdrawal by Subject
FG0003 subjects
FG0010 subjects
FG0022 subjects
FG0030 subjects
FG004
Physician Decision
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0031 subjects
FG004
Early Rescue
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Subject Moved
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG004
Images Not Usable (Motion)
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG004
Did Not Meet Eligibility Criteria
FG0000 subjects
FG0010 subjects
FG0021 subjects
FG0031 subjects
FG004
Did Not Want Per Protocol Treatment
FG0000 subjects
FG0010 subjects
FG0021 subjects
FG0030 subjects
FG004
Subject Refused to Continue
FG0001 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
Natalizumab
300 mg intravenous every 4 weeks
BG001
Intravenous Placebo
placebo matching natalizumab, intravenous every 4 weeks
BG002
Interferon β-1a
30 ug intramuscular once per week
BG003
Glatiramer Acetate
20 mg subcutaneous once daily
BG004
Methylprednisolone
1000 mg intravenous every 4 weeks
BG005
Total
Total of all reporting groups
Denominators
Units
Counts
Participants
BG00045
BG00142
BG00217
BG00317
BG00454
BG005175
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age Continuous
Mean
Standard Deviation
Years
Title
Denominators
Categories
Title
Measurements
BG00041.2± 9.70
BG00140.0± 10.36
BG00245.1± 9.92
BG003
Sex: Female, Male
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Female
BG00037
BG00131
BG002
Type
Title
Description
Population Description
Reporting Status
Anticipated Posting Date
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Time Frame
Units Analyzed
Denominator Units Selected
Arm/Group Information
Denominators
Classes
Analyses
Primary
Time Course to Return of Radiological and/or Clinical Evidence of Multiple Sclerosis Activity, as Measured by the Percentage of Subjects Who Met Magnetic Resonance Imaging (MRI) and/or Clinical Relapse Rescue Criteria.
Rescue criteria were: 1) central reader MRI finding of 1 new gadolinium-enhancing (Gd+) lesion of >0.8 cubic centimeters in volume or 2 or more Gd+ lesions of any size 2) clinical relapse. Clinical relapse was new or recurrent neurological symptoms not associated with fever or infection, lasting at least 24 hours, as defined by: an increase of ≥1 grade in ≥2 functional scales of the Expanded Disability Status Scale (EDSS); an increase of ≥2 grades in 1 functional scale of the EDSS; or an increase of >0.5 in EDSS if the previous EDSS was ≤5.5, or ≥0.5 if the previous EDSS was >5.5
Of the randomized subjects, data from 167 subjects were used in efficacy analyses. Eight subjects were excluded from the analyses: 3 subjects had major protocol deviations and 5 subjects discontinued study participation prior to Week 4 Visit.
Posted
Nov 2012
Number
Percentage of subjects meeting criteria
28 Weeks
ID
Title
Description
OG000
Natalizumab
300 mg intravenous every 4 weeks
OG001
Intravenous Placebo
placebo matching natalizumab, intravenous every 4 weeks
OG002
Interferon β-1a
30 ug intramuscular once per week
OG003
Glatiramer Acetate
20 mg subcutaneous once daily
OG004
Methylprednisolone
1000 mg intravenous every 4 weeks
Units
Counts
Participants
OG00045
OG00141
OG00214
OG003
Title
Denominators
Categories
Title
Measurements
OG0004.7
OG00160.5
OG00228.6
OG003
Secondary
Time Course to Return of Radiological Activity, as Measured by the Percentage of Subjects Who Met Magnetic Resonance Imaging (MRI) Rescue Criteria.
MRI rescue criteria were the presence of 1 new gadolinium-enhancing (Gd+) lesion of >0.8 cubic centimeters in volume or 2 or more Gd+ lesions of any size, according to the central MRI reader.
Of the randomized subjects, data from 167 subjects were used in efficacy analyses. Eight subjects were excluded from the analyses: 3 subjects had major protocol deviations and 5 subjects discontinued study participation prior to Week 4 Visit.
Posted
Nov 2012
Number
Percentage of subjects meeting criteria
28 Weeks
ID
Title
Description
OG000
Natalizumab
300 mg intravenous every 4 weeks
OG001
Intravenous Placebo
placebo matching natalizumab, intravenous every 4 weeks
OG002
Interferon β-1a
30 ug intramuscular once per week
OG003
Glatiramer Acetate
20 mg subcutaneous once daily
Time Frame
Not provided
Description
Not provided
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
Intravenous Placebo
placebo matching natalizumab, intravenous every 4 weeks
1
35
EG001
Natalizumab
300 mg intravenous every 4 weeks
1
38
EG002
Interferon β-1a
30 ug intramuscular once per week
1
15
EG003
Glatiramer Acetate
20 mg subcutaneous once daily
1
15
EG004
Methylprednisolone
1000 mg intravenous every 4 weeks
1
42
Serious Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Chest Pain
General disorders
Systematic Assessment
EG0000 events0 affected42 at risk
EG0011 events1 affected45 at risk
EG0020 events0 affected17 at risk
EG0030 events0 affected17 at risk
EG0040 events0 affected54 at risk
Multiple Sclerosis
Nervous system disorders
Systematic Assessment
EG0001 events1 affected42 at risk
EG0010 events0 affected45 at risk
EG0020 events0 affected17 at risk
EG003
Multiple Sclerosis Relapse
Nervous system disorders
Systematic Assessment
EG0000 events0 affected42 at risk
EG0010 events0 affected45 at risk
EG0020 events0 affected17 at risk
EG003
Brain Abscess
Infections and infestations
Systematic Assessment
EG0000 events0 affected42 at risk
EG0010 events0 affected45 at risk
EG0020 events0 affected17 at risk
EG003
Syncope
Nervous system disorders
Systematic Assessment
EG0000 events0 affected42 at risk
EG0010 events0 affected45 at risk
EG0021 events1 affected17 at risk
EG003
Presyncope
Nervous system disorders
Systematic Assessment
EG0000 events0 affected42 at risk
EG0010 events0 affected45 at risk
EG0022 events1 affected17 at risk
EG003
Other Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
INCISION SITE PAIN
Injury, poisoning and procedural complications
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG0030 affected17 at risk
EG0040 affected54 at risk
BACK PAIN
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0001 affected42 at risk
EG0012 affected45 at risk
EG0020 affected17 at risk
EG003
SYNCOPE
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
MEMORY IMPAIRMENT
Nervous system disorders
Systematic Assessment
EG0002 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
FOLATE DEFICIENCY
Metabolism and nutrition disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
BLOOD GLUCOSE INCREASED
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
MUSCLE SPASMS
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0022 affected17 at risk
EG003
HYPERTENSION
Vascular disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
HYPOAESTHESIA
Nervous system disorders
Systematic Assessment
EG0002 affected42 at risk
EG0013 affected45 at risk
EG0021 affected17 at risk
EG003
POST LUMBAR PUNCTURE SYNDROME
Injury, poisoning and procedural complications
Systematic Assessment
EG0001 affected42 at risk
EG0010 affected45 at risk
EG0022 affected17 at risk
EG003
DRUG SPECIFIC ANTIBODY PRESENT
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
CONCUSSION
Injury, poisoning and procedural complications
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
HYPERREFLEXIA
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
URINARY TRACT INFECTION
Infections and infestations
Systematic Assessment
EG0005 affected42 at risk
EG0011 affected45 at risk
EG0022 affected17 at risk
EG003
PROTEIN URINE PRESENT
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0020 affected17 at risk
EG003
SLEEP DISORDER
Psychiatric disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
DRUG HYPERSENSITIVITY
Immune system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
RASH
Skin and subcutaneous tissue disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
INFLUENZA LIKE ILLNESS
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0025 affected17 at risk
EG003
ECZEMA
Skin and subcutaneous tissue disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
COGNITIVE DISORDER
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
ALANINE AMINOTRANSFERASE INCREASED
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
DYSPNOEA
Respiratory, thoracic and mediastinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
ANTICHOLINERGIC SYNDROME
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
BREAST CYST
Reproductive system and breast disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
MULTIPLE SCLEROSIS RELAPSE
Nervous system disorders
Systematic Assessment
EG0008 affected42 at risk
EG0012 affected45 at risk
EG0024 affected17 at risk
EG003
HALLUCINATION, VISUAL
Psychiatric disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
GAMMA-GLUTAMYLTRANSFERASE INCREASED
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
NEURALGIA
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
INFLUENZA
Infections and infestations
Systematic Assessment
EG0001 affected42 at risk
EG0011 affected45 at risk
EG0020 affected17 at risk
EG003
PANIC ATTACK
Psychiatric disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
TONGUE CYST
Gastrointestinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
SKIN LESION
Skin and subcutaneous tissue disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
MUSCULAR WEAKNESS
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0004 affected42 at risk
EG0012 affected45 at risk
EG0020 affected17 at risk
EG003
VULVOVAGINAL CANDIDIASIS
Infections and infestations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
CONSTIPATION
Gastrointestinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
HYPOTENSION
Vascular disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
GAIT DISTURBANCE
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
DIZZINESS
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0013 affected45 at risk
EG0020 affected17 at risk
EG003
OROPHARYNGEAL PAIN
Respiratory, thoracic and mediastinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
LACERATION
Injury, poisoning and procedural complications
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
PAIN IN EXTREMITY
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0001 affected42 at risk
EG0013 affected45 at risk
EG0020 affected17 at risk
EG003
INJECTION SITE HAEMATOMA
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
UPPER RESPIRATORY TRACT INFECTION
Infections and infestations
Systematic Assessment
EG0006 affected42 at risk
EG0013 affected45 at risk
EG0020 affected17 at risk
EG003
WHITE BLOOD CELLS URINE POSITIVE
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
IRON DEFICIENCY
Metabolism and nutrition disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
LYMPHOCYTE MORPHOLOGY ABNORMAL
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
NASOPHARYNGITIS
Infections and infestations
Systematic Assessment
EG0005 affected42 at risk
EG00111 affected45 at risk
EG0024 affected17 at risk
EG003
MIGRAINE
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
INCREASED UPPER AIRWAY SECRETION
Respiratory, thoracic and mediastinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
LHERMITTE'S SIGN
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
ANXIETY
Psychiatric disorders
Systematic Assessment
EG0002 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
FALL
Injury, poisoning and procedural complications
Systematic Assessment
EG0002 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
EOSINOPHIL COUNT INCREASED
Investigations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
BURNING FEET SYNDROME
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
SINUS CONGESTION
Respiratory, thoracic and mediastinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
LYMPHADENOPATHY
Blood and lymphatic system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0013 affected45 at risk
EG0020 affected17 at risk
EG003
CONTUSION
Injury, poisoning and procedural complications
Systematic Assessment
EG0001 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
VITAMIN D DEFICIENCY
Metabolism and nutrition disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
ARTHRALGIA
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0002 affected42 at risk
EG0011 affected45 at risk
EG0020 affected17 at risk
EG003
ASTHENIA
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0022 affected17 at risk
EG003
HEADACHE
Nervous system disorders
Systematic Assessment
EG0003 affected42 at risk
EG0018 affected45 at risk
EG0021 affected17 at risk
EG003
JOINT STIFFNESS
Musculoskeletal and connective tissue disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
INJECTION SITE URTICARIA
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
DEPRESSION
Psychiatric disorders
Systematic Assessment
EG0002 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
FATIGUE
General disorders
Systematic Assessment
EG0006 affected42 at risk
EG0012 affected45 at risk
EG0021 affected17 at risk
EG003
INJECTION SITE PAIN
General disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
PRESYNCOPE
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
FUNGAL SKIN INFECTION
Infections and infestations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
DYSGEUSIA
Nervous system disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
PARAESTHESIA
Nervous system disorders
Systematic Assessment
EG0003 affected42 at risk
EG0013 affected45 at risk
EG0020 affected17 at risk
EG003
DEHYDRATION
Metabolism and nutrition disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0020 affected17 at risk
EG003
PYELONEPHRITIS
Infections and infestations
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
BALANCE DISORDER
Nervous system disorders
Systematic Assessment
EG0001 affected42 at risk
EG0010 affected45 at risk
EG0020 affected17 at risk
EG003
PRODUCTIVE COUGH
Respiratory, thoracic and mediastinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0010 affected45 at risk
EG0021 affected17 at risk
EG003
NAUSEA
Gastrointestinal disorders
Systematic Assessment
EG0000 affected42 at risk
EG0011 affected45 at risk
EG0021 affected17 at risk
EG003
Certain Agreements
Are all PI(s) employees of the sponsor?
No
Restriction Type
OTHER
Results Disclosure Restriction on PI(s)?
Yes
Other Details
The provisions of our agreement are subject to confidentiality but generally the PI can publish, for noncommercial purposes only, results and methods of the trial, but no other Sponsor Confidential Information. PI must give Sponsor no less than 60 days to review any manuscript for a proposed publication and must delay publication for up to 90 days thereafter if Sponsor needs to file any patent application to protect any of Sponsor's intellectual property contained in the proposed publication.