Multiple SclerosisPhase 4ACTHARNCT01838174
A Trial of Neuroprotection With ACTH in Acute Optic Neuritis
A Phase 4 study testing ACTHAR Gel (ACTH) and IV methylprednisolone (steroids) in people with Multiple Sclerosis, run by University of Colorado, Denver at 2 sites in United States.
Trial summary
We hypothesize that the novel melanocortin-mediated anti-inflammatory effects of ACTH will reduce axonal loss following ON by limiting inflammatory optic nerve injury. We will compare the effect of ACTH and intravenous methylprednisolone therapy on axonal injury following ON using OCT, a sensitive, reproducible and… Read more about this study
- Who is it for?
- Ages 18 to 55 years
- Conditions the study is for
- Multiple Sclerosis
- What is being tested?
- ACTHAR Gel (ACTH) and IV methylprednisolone (steroids)
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 37 participants
- Where
- 2 sitesUnited States
- Study dates
- May 2013to 13 Jan 2022
- Phase
- Phase 4
- 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 55 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Ability to provide written informed consent before any study assessment is performed.
- Male and female patients aged between 18 and 55 years, inclusive.
- Diagnosis of clinically unilateral acute demyelinating optic neuritis (ADON)
- Clinical signs and symptoms of ADON starting within the 14 day prior to intended randomization (loss of vision, pain on movement, impairment of color vision).
- The qualifying episode of optic neuritis must be the first clinical episode of optic neuritis in the affected eye.
- Able to undergo treatment with intravenous methylprednisolone or Acthar gel.
Who cannot join
- Functionally or clinically relevant comorbidity of the affected eye (e.g., glaucoma, amblyopia, optic nerve hypoplasia, macular hole, macular edema, vitreomacular traction, uveitis, diabetes, optic neuritis, or other diseases of the optic nerve or a history thereof).
- Bilateral optic neuritis.
- Concurrent functionally or clinically relevant disturbances of the eye not affected by ADON.
- High clinical likelihood of a form of optic neuritis other than ADON (e.g., no pain on movement, no light perception, severe optic disk edema, atrophic optic disk, retinal exudates, or hemorrhages).
- Non-assessable OCT at screening.
- Refractive error greater than ±5 diopters or (pre-surgical value to be used for patients having undergone refractive surgery).
Show all 10Show fewer
- Patients with an immune system disorder other than MS or ADON (e.g. rheumatoid arthritis, scleroderma, Sjogren's syndrome, Crohn's disease, ulcerative colitis, etc.) or with a known immunodeficiency syndrome (AIDS, hereditary immune deficiency, drug-induced immune deficiency). Diagnosis of neuromyelitis optica or MOG-IgG will not exclude a patient from the study but will be accounted for in the data analysis.
- Prior treatment with IVMP or Acthar gel within the past 30 days.
- Treatment with, mitoxantrone, cyclophosphamide, mycophenolate, azathioprine, or other non-approved agents for the treatment of relapsing forms of MS.
- Concurrent use of 4-aminopyridine.
Trial locations and contacts
2 sites in 1 country.
United States2 sites
University of Colorado Denver
Aurora, Colorado, 80045
University of Pennsylvania Scheie Eye Institute
Philadelphia, Pennsylvania, 19104
About this study
Official title: A Phase IV Trial of Neuroprotection With ACTH in Acute Optic Neuritis
We hypothesize that the novel melanocortin-mediated anti-inflammatory effects of ACTH will reduce axonal loss following ON by limiting inflammatory optic nerve injury. We will compare the effect of ACTH and intravenous methylprednisolone therapy on axonal injury following ON using OCT, a sensitive, reproducible and noninvasive tool to measure RNFL thickness.
The primary outcome will be the average RNFL thickness at 6 months. Additional pre-specified statistical analyses will compare the difference in the mean RNFL thickness at 6 months in the affected eye between the IV methylprednisolone- and Acthar-treated groups, and the mean 6-month affected eye RNFL thicknesses adjusted for the baseline unaffected eye RNFL. The secondary outcome measure will examine the frequency of optic nerves with RNFL swelling between the IV methylprednisolone- and Acthar-treated groups at 1 and 3 months. A predefined exploratory outcome will compare the ganglion cell plus inner plexiform layer (GC+IPL) thickness at 6 months between treatment groups. Additional tertiary outcome will be the assessment of changes in fatigue, mood, visual function depression, and quality of life in patients with AON. Assessment will be completed by administration of the following questionnaires: Modified Fatigue Impact Scale, Multiple Sclerosis Quality of Life 54 Instrument, 25-item Visual Function Questionnaire with 10-item supplement, Beck's Depression Inventory. These questionnaires have been validated for the MS (AON) population. Descriptive and correlative analysis will be done at each visit time point to assess for QOL for this study population.
Read the detailed description
Patients with their first episode of unilateral acute ON will be treated with either 3 days of IV methylprednisolone followed by 11 days of oral prednisone or 15 days of intramuscular or subcutaneous corticotropin (Acthar).
This is a parallel active group, randomized controlled trial in which up to 100 people with clinically unilateral acute optic neuritis (≤ 2 weeks of vision loss; with or without a previous diagnosis of relapsing remitting MS) will be treated with either ACTH or IV methylprednisolone/prednisone for 2 weeks to assess RNFL thickness. The primary, secondary, and tertiary outcomes will be as noted above. Participants will be assessed for inclusion/exclusion criteria by their treating neurologist/ophthalmologist at the University of Colorado Denver (PI- Dr. Jeffrey Bennett) or The University of Pennsylvania Scheie Eye Institute (PI- Dr. Kenneth Shindler). Following informed consent, the University of Colorado will determine patient randomization for both sites per the established randomization scheme. A secured fax or email confirmation regarding randomization will be sent to the University of Pennsylvania research staff and proper pharmacy orders will be placed by the site investigator or designee. We expect to enroll up to 50 subjects per institution.
Following informed consent and randomization, participants will undergo baseline procedures (visit 1) and receive treatment with either high dose methylprednisolone (1000 mg IV qD for 3 days followed by 60 mg oral prednisone daily for 11 days) or Acthar (80 U IM or SC daily for 5 days followed by 40 U IM or SC daily for 10 days). Study follow-up visits will subsequently occur at 1, 3, and 6 months. During each visit, including baseline (visit 1), ETDRS, low contrast acuity (2.5%), and color vision (Farnsworth D-15) will be assessed. OCT evaluations (Optic Disc Cube 200x200 and Macular Cube 512x128) will be performed at baseline, 1, 3 and 6 months using spectral domain OCT (Cirrus OCT; Carl Zeiss Meditec, Dublin, CA, USA). Automated visual fields (Humphrey 30-2 SITA) will be performed at baseline (visit 1) and month 6. Modified Fatigue Impact Scale, Multiple Sclerosis Quality of Life 54 Instrument, 25-item Visual Function Questionnaire with 10-item supplement, Beck's Depression Inventory questionnaires will be assessed at each study visit. The patient's treating physician will perform blood tests and MRI evaluations to exclude other causes of optic neuropathy at the initial study visit as part of their routine care.
RNFL edema will be defined as either average RNFL thickness greater than the 95th percentile of the age matched normal database or a ratio of RNFL thickness (affected/fellow eye) greater than 1.1 in any quadrant.8 The study sites will collect and report data on AEs and SAEs per standard practice.
Detailed Patient Schedule of Assessments:
Baseline, within 2 weeks of onset of vision loss (approximately 2 hours):
- Consent and Discussion of Study Expectations
- Eligibility Checklist
- Review of Medical History \& Demographics
- Record list of Con Meds, Co-Morbidities, and Symptoms at time of Diagnosis
- Obtain Randomization Number
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15], Humphrey's visual fields (HVF).
- Administer Study Medication (either IM or SC Acthar Gel or IV Methylprednisolone with oral taper)
- Labs and MRI, per standard of care
Month 1 +/- 3 days (approximately 1.5 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15]
Month 3 +/- 3 days (approximately 1.5 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15]
Month 6 +/- 3 days (approximately 2 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15], Humphrey's visual fields (HVF)
- Conditions
- Multiple Sclerosis
- Being tested
- ACTHAR Gel (ACTH), IV methylprednisolone (steroids)
- Keywords
- Optic Neuritis
- Medical subject headings
- Multiple Sclerosis, Optic Neuritis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ACTHAR Gel (ACTH)Drug
Also called ACTH
15 days of daily injections
IV methylprednisolone (steroids)Drug
Also called methylprednisolone
3 days of intravenous methylprednisolone followed by 11 days of oral taper
| Study group | Role | What they receive |
|---|---|---|
| Acthar Gel (ACTH) | Experimental | 15 days of intramuscular (IM) or sub-cutaneous corticotropin (SQ) Acthar (ACTH). Receives: Drug: ACTHAR Gel (ACTH) |
| IV methylprednisolone (steroids) | Active comparator | 3 days of IV methylprednisolone (steroids) followed by 11 days of oral prednisone Receives: Drug: IV methylprednisolone (steroids) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Retinal Nerve Fiber Layer (RNFL) thickness
The primary outcome will be the average RNFL thickness at 6 months.
Measured: 6 months
Secondary outcomes (1)
Frequency of RNFL swelling
The secondary outcome measure will examine the frequency of optic nerves with RNFL swelling between the IV methylprednisolone- and Acthar-treated groups at 1 and 3 months.
Measured: 1 and 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Apr 2013 (estimated)
- Study startMay 2013
- Primary completion13 Jan 2022
- Study completion13 Jan 2022
Why it stopped: Sponsor requested
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Multiple SclerosisStudies of the same condition, open and under way.
- More trials run by University of Colorado, DenverThe 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 37 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Colorado, Denver
- Sponsor type
- University, hospital or other
- Collaborators
- Mallinckrodt, University of Pennsylvania
- Responsible party
- Sponsor
- Investigators
- Jeffrey Bennett, MD, PhD, Principal investigator, University of Colorado, DenverKenneth Shindler, MD, PhD, Principal investigator, University of Pennsylvania Scheie Eye Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01838174
- Sponsor's protocol ID
- 13-0388
- Acronym
- ACTHAR
- Status last verified
- Apr 2023
- First submitted
- 18 Apr 2013
- Last updated
- 27 Apr 2023
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Publications
Bennett JL, Grove NC, Johnson RK, Mizenko C, DuPont JC, Wagner BD, Lynch AM, Frohman TC, Shindler KS, Frohman EM. A Randomized Prospective Trial Comparing Repository Corticotropin Injection and Intravenous Methylprednisolone for Neuroprotection in Acute Optic Neuritis. J Neuroophthalmol. 2023 Sep 1;43(3):323-329. doi: 10.1097/WNO.0000000000001878. Epub 2023 Jun 1.
PubMed 37261907
Study at a glance
From the registry record, last updated by the sponsor on 27 Apr 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase IV Trial of Neuroprotection With ACTH in Acute Optic Neuritis
- ClinicalTrials.gov ID
- NCT01838174
- Acronym / sponsor ID
- ACTHAR / 13-0388
- Conditions
- Multiple Sclerosis
- Keywords
- Optic Neuritis
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Sponsor requested
- Enrolment
- 37 participants (actual)
- Lead sponsor
- University of Colorado, DenverUniversity, hospital or other
- Collaborators
- Mallinckrodt, University of Pennsylvania
- Study start
- May 2013
- Primary completion
- 13 Jan 2022 (actual)
- Study completion
- 13 Jan 2022 (actual)
- First posted
- 23 Apr 2013 (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.
We hypothesize that the novel melanocortin-mediated anti-inflammatory effects of ACTH will reduce axonal loss following ON by limiting inflammatory optic nerve injury. We will compare the effect of ACTH and intravenous methylprednisolone therapy on axonal injury following ON using OCT, a sensitive, reproducible and noninvasive tool to measure RNFL thickness.
The primary outcome will be the average RNFL thickness at 6 months. Additional pre-specified statistical analyses will compare the difference in the mean RNFL thickness at 6 months in the affected eye between the IV methylprednisolone- and Acthar-treated groups, and the mean 6-month affected eye RNFL thicknesses adjusted for the baseline unaffected eye RNFL. The secondary outcome measure will examine the frequency of optic nerves with RNFL swelling between the IV methylprednisolone- and Acthar-treated groups at 1 and 3 months. A predefined exploratory outcome will compare the ganglion cell plus inner plexiform layer (GC+IPL) thickness at 6 months between treatment groups. Additional tertiary outcome will be the assessment of changes in fatigue, mood, visual function depression, and quality of life in patients with AON. Assessment will be completed by administration of the following questionnaires: Modified Fatigue Impact Scale, Multiple Sclerosis Quality of Life 54 Instrument, 25-item Visual Function Questionnaire with 10-item supplement, Beck's Depression Inventory. These questionnaires have been validated for the MS (AON) population. Descriptive and correlative analysis will be done at each visit time point to assess for QOL for this study population.
Detailed description
Patients with their first episode of unilateral acute ON will be treated with either 3 days of IV methylprednisolone followed by 11 days of oral prednisone or 15 days of intramuscular or subcutaneous corticotropin (Acthar).
This is a parallel active group, randomized controlled trial in which up to 100 people with clinically unilateral acute optic neuritis (≤ 2 weeks of vision loss; with or without a previous diagnosis of relapsing remitting MS) will be treated with either ACTH or IV methylprednisolone/prednisone for 2 weeks to assess RNFL thickness. The primary, secondary, and tertiary outcomes will be as noted above. Participants will be assessed for inclusion/exclusion criteria by their treating neurologist/ophthalmologist at the University of Colorado Denver (PI- Dr. Jeffrey Bennett) or The University of Pennsylvania Scheie Eye Institute (PI- Dr. Kenneth Shindler). Following informed consent, the University of Colorado will determine patient randomization for both sites per the established randomization scheme. A secured fax or email confirmation regarding randomization will be sent to the University of Pennsylvania research staff and proper pharmacy orders will be placed by the site investigator or designee. We expect to enroll up to 50 subjects per institution.
Following informed consent and randomization, participants will undergo baseline procedures (visit 1) and receive treatment with either high dose methylprednisolone (1000 mg IV qD for 3 days followed by 60 mg oral prednisone daily for 11 days) or Acthar (80 U IM or SC daily for 5 days followed by 40 U IM or SC daily for 10 days). Study follow-up visits will subsequently occur at 1, 3, and 6 months. During each visit, including baseline (visit 1), ETDRS, low contrast acuity (2.5%), and color vision (Farnsworth D-15) will be assessed. OCT evaluations (Optic Disc Cube 200x200 and Macular Cube 512x128) will be performed at baseline, 1, 3 and 6 months using spectral domain OCT (Cirrus OCT; Carl Zeiss Meditec, Dublin, CA, USA). Automated visual fields (Humphrey 30-2 SITA) will be performed at baseline (visit 1) and month 6. Modified Fatigue Impact Scale, Multiple Sclerosis Quality of Life 54 Instrument, 25-item Visual Function Questionnaire with 10-item supplement, Beck's Depression Inventory questionnaires will be assessed at each study visit. The patient's treating physician will perform blood tests and MRI evaluations to exclude other causes of optic neuropathy at the initial study visit as part of their routine care.
RNFL edema will be defined as either average RNFL thickness greater than the 95th percentile of the age matched normal database or a ratio of RNFL thickness (affected/fellow eye) greater than 1.1 in any quadrant.8 The study sites will collect and report data on AEs and SAEs per standard practice.
Detailed Patient Schedule of Assessments:
Baseline, within 2 weeks of onset of vision loss (approximately 2 hours):
- Consent and Discussion of Study Expectations
- Eligibility Checklist
- Review of Medical History \& Demographics
- Record list of Con Meds, Co-Morbidities, and Symptoms at time of Diagnosis
- Obtain Randomization Number
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15], Humphrey's visual fields (HVF).
- Administer Study Medication (either IM or SC Acthar Gel or IV Methylprednisolone with oral taper)
- Labs and MRI, per standard of care
Month 1 +/- 3 days (approximately 1.5 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15]
Month 3 +/- 3 days (approximately 1.5 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15]
Month 6 +/- 3 days (approximately 2 hours):
- Review of AEs and Con Meds
- Administer MFIS, BDI, VFQ-25 and 10-item supplement, and MSQOL-54 questionnaires
- Eye Testing (OCT - [Optic Disc Cube 200x200 and Macular Cube 512x128], Visual Acuity [High Contrast ETDRS], Low-contrast Letter Acuity [Sloan 2.5% and 1.25% letters], Color Vision [Farnsworth D15], Humphrey's visual fields (HVF)
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Acthar Gel (ACTH) | Experimental | Drug: ACTHAR Gel (ACTH)15 days of intramuscular (IM) or sub-cutaneous corticotropin (SQ) Acthar (ACTH). |
| IV methylprednisolone (steroids) | Active comparator | Drug: IV methylprednisolone (steroids)3 days of IV methylprednisolone (steroids) followed by 11 days of oral prednisone |
Who may qualify
- Ages
- 18 to 55 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- Ability to provide written informed consent before any study assessment is performed.
- Male and female patients aged between 18 and 55 years, inclusive.
- Diagnosis of clinically unilateral acute demyelinating optic neuritis (ADON)
- Clinical signs and symptoms of ADON starting within the 14 day prior to intended randomization (loss of vision, pain on movement, impairment of color vision).
- The qualifying episode of optic neuritis must be the first clinical episode of optic neuritis in the affected eye.
Key exclusion criteria (10 listed)
- Functionally or clinically relevant comorbidity of the affected eye (e.g., glaucoma, amblyopia, optic nerve hypoplasia, macular hole, macular edema, vitreomacular traction, uveitis, diabetes, optic neuritis, or other diseases of the optic nerve or a history thereof).
- Bilateral optic neuritis.
- Concurrent functionally or clinically relevant disturbances of the eye not affected by ADON.
- High clinical likelihood of a form of optic neuritis other than ADON (e.g., no pain on movement, no light perception, severe optic disk edema, atrophic optic disk, retinal exudates, or hemorrhages).
- Non-assessable OCT at screening.
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 |
|---|---|---|
| ACTHAR Gel (ACTH)Also: ACTH15 days of daily injections | Drug | Acthar Gel (ACTH) |
| IV methylprednisolone (steroids)Also: methylprednisolone3 days of intravenous methylprednisolone followed by 11 days of oral taper | Drug | IV methylprednisolone (steroids) |
Primary outcome
Retinal Nerve Fiber Layer (RNFL) thickness
Time frame: 6 months
The primary outcome will be the average RNFL thickness at 6 months.
1 secondary outcome
Frequency of RNFL swelling
Time frame: 1 and 3 months
Results and safety
The study was stopped early (reason given: Sponsor requested). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Apr 2023.
- Derived from this study: PubMed 37261907Bennett JL, Grove NC, Johnson RK, Mizenko C, DuPont JC, Wagner BD, Lynch AM, Frohman TC, Shindler KS, Frohman EM. A Randomized Prospective Trial Comparing Repository Corticotropin Injection and Intravenous Methylprednisolone for Neuroprotection in Acute Optic Neuritis. J Neuroophthalmol. 2023 Sep 1;43(3):323-329. doi: 10.1097/WNO.0000000000001878. Epub 2023 Jun 1.
- Individual participant dataSharing planned: No
Related trials for Multiple Sclerosis
RecruitingPhase 2
Metformin as an add-on or Monotherapy in Treatment of Aging People With Multiple Sclerosis (MS)
Multiple Sclerosis
RecruitingObservational study
Pain Phenotypes in Individuals With Multiple Sclerosis
Multiple Sclerosis, Chronic Pain
Not yet recruiting
Evaluating the Effect of the Zeen Mobility Device on Clinical Practicality, Safety, and Impact (Via Assessments of Walking, Standing Tolerance, Balance, Endurance, Effort, and Participation in Daily Tasks) in an Outpatient Rehabilitation Setting for Individuals With Mobility Impairments.
Stroke, Parkinson's Disease (PD)
RecruitingPhase 3
Dalfampridine Combined With Physical Therapy for Mobility Impairment in Multiple Sclerosis
Multiple Sclerosis
RecruitingPhase 2
Targeting Agonists of Glucagon-like Peptide-1 Receptor for Multiple Sclerosis
Multiple Sclerosis
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.
Jeffrey Bennett, MD, PhD principal investigator
University of Colorado, Denver
Kenneth Shindler, MD, PhD principal investigator
University of Pennsylvania Scheie Eye Institute
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing ACTHAR Gel (ACTH) and IV methylprednisolone (steroids) in people with Multiple Sclerosis, run by University of Colorado, Denver at 2 sites in United States.
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 6 inclusion and 10 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: stopped early, as of the sponsor's last update on 27 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Sponsor requested). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Retinal Nerve Fiber Layer (RNFL) thickness (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01838174, which also lists 1 linked publication.
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 27 Apr 2023.