End Stage Renal DiseasePhase 1NCT02486744
Safety and Efficacy of Acthar Gel in an Outpatient Dialysis Population
A Phase 1 study testing Acthar Gel in people with End Stage Renal Disease, run by Youngstown State University at 1 site in United States.
Trial summary
This will be a prospective observational study of Acthar Gel in Non-Diabetic Hemodialysis [NDHD] patients receiving dialysis for ≤ 2 years. The project will aimed at providing proof-of-concept data that 80 U two times [2x] week Acthar for 6 months is a safe and effective therapy for NDHD. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- End Stage Renal Disease
- What is being tested?
- Acthar Gel
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 9 participants
- Where
- 1 siteUnited States
- Study dates
- Mar 2015to Jul 2016
- Phase
- Phase 1
- 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 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Inclusion criteria will be individuals requiring dialysis for treatment of ESRD who have had poor response to immunosuppressive strategies.
- Non-Diabetic
- Adults age 18-80
Who cannot join
- receiving hemodialysis for > 5 years
- diabetic, less than 18 years of age
- are pregnant
- have a history of cancer in the last 5 years
- have an active infection
- have recently had a myocardial infarction (within 6 weeks)
Show all 14Show fewer
- have malignant arrhythmias, unstable angina, uncontrolled hypertension (SBP> 180 and/or DBP > 105)
- recent hospitalization (< 30 days),
- ocular disease,
- accelerated osteoporosis,
- gastrointestinal diseases (ulcerative colitis, diverticulitis, myasthenia gravis)
- any disorder that may be exacerbated by short periods of activity.
- cognitive dysfunction
- neurological deficits leading to limited ambulation.
Trial locations and contacts
1 site in 1 country.
United States1 site
Center for Dialysis Care 3695 Stutz Drive
Canfield, Ohio, 44406
About this study
This will be a prospective observational study of Acthar Gel in Non-Diabetic Hemodialysis [NDHD] patients receiving dialysis for ≤ 2 years. The project will aimed at providing proof-of-concept data that 80 U two times [2x] week Acthar for 6 months is a safe and effective therapy for NDHD. Effectiveness of lower dose 40 U 2X week will also be determined. Therefore the study will be a repeated measures design (Time x condition) comparison of improvement in renal function, nutritional status, quality of life and physical performance resulting from Acthar therapy.
Read the detailed description
Recent reports demonstrated Acthar gel is effective to induce remission of proteinuria in the Nephrotic Syndrome patients (Bomback 2011, 2012). There are limited published reports documenting the clinical response (creatinine, proteinuria, serum albumin and cholesterol) to ACTHAR therapy in a non-diabetic hemodialysis population. In addition to renal dysfunction and high risk for mortality, individuals who receive dialysis also have decreased strength, low exercise capacity, poor physical functioning, and a low quality of life (Edgell 1996, Johansen, 2001). Strength deficits are well documented in those with End Stage Renal Disease [ESRD] (Cheema 2010, Yoda 2012). There are several reports documenting an association between strength and gait deficits and other measures of physical performance in persons with ESRD (Bohannon 1994, Fitts 1997, Segura-Orti 2011). It is well known that measures of physical performance may predict risk for fall and hospitalization in older individuals (Guralnik JM, 2000).
Deficits to physical performance may be further compounded by poor nutritional status. Persons with chronic renal disease, particularly in the context of hemodialysis or chronic renal replacement therapy, are often malnourished and/or are affected by abnormal micronutrient status (McMahon 2012). Furthermore, previous studies have shown that more than a third of acute-care, nephrology-related admissions are characterized by malnutrition (Lim 2012), and that it affects from 23% - 76% of all patients receiving hemodialysis (including outpatients)(Blumenkrantz 1980, Ikizler 1996, Pecoits-Filho 2002).
Decreased functional status and concomitant malnutrition contribute to increased hospital readmissions, prolonged length of stay (and inevitably, increased medical costs), and increased morbidity and mortality patients (Isabel 2003, Lim 2012). Given the high prevalence of these characteristics in persons with renal disease, it is important to prioritize identification of novel and effective means by which to sustain and improve the functional capability of these patients, and to maintain their nutritional status and attenuate malnutrition.
To date, there are no reports of the impact of Acthar gel therapy on renal function, strength, physical performance, nutritional status and quality of life in NDHD patients. This study will determine if Acthar gel therapy will maintain or improve overall kidney function as measured with 24 hour urine study at baseline and at the end of study period. In addition this study will determine if Acthar gel therapy will improve nutritional, physical and biochemical status in an outpatient non-diabetic hemodialysis population.
- Conditions
- End Stage Renal Disease
- Being tested
- Acthar Gel
- Keywords
- Acthar, Dialysis, Kidney, Non-Diabetic
- Medical subject headings
- Kidney Failure, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Acthar GelDrug
Also called repository corticotropin injection
Subjects will be given an injection subcutaneously 2x week for 6 months. Dosing will be randomly assigned as either 80 U or 40 U
| Study group | Role | What they receive |
|---|---|---|
| 80 Units of Acthar | Active comparator | Subjects assigned by random assignment to receive 80 Units of Acthar Gel 2x weekly for 6 months Receives: Drug: Acthar Gel |
| 40 Units of Acthar | Active comparator | Subjects assigned by random assignment to receive 40 Units of Acthar Gel 2x weekly for 6 months Receives: Drug: Acthar Gel |
What is being measured
The primary outcome is the main question the study is designed to answer.
Renal Function
Maintain or improve renal function [Creatinine clearance and Proteinuria] by ≥ 20% , as measured by eGFR or 24 hour urine study.
Measured: 6 months
Secondary outcomes (22)
Hyperparathyroidism
Change in serum parathyroid hormone levels
Measured: 6 months
Anemia
Change in hemoglobin levels
Measured: 6 months
Inflammatory blood markers
Change in serum C-Reactive Protein and Creatine Kinase
Measured: 6 months
Vitamin D uptake
Change in Vitamin D dosing requirements
Measured: 6 months
Hypercalcemia
Change in serum calcium levels
Measured: 6 months
Phosphate
Change in serum phosphate levels
Measured: 6 months
Total Iron Binding Capacity
Change in Total Iron Binding Capacity in serum
Measured: 6 months
Epogen Dose
Change in epogen dosing requirements
Measured: 6 months
Fall risk
Timed Up and Go Test will improve
Measured: 6 months
Walking endurance
2 minute walk distance
Measured: 6 months
Gait speed
10 meter gait speed test
Measured: 6 months
Mobility disablement risk
Short Performance Physical Battery
Measured: 6 months
Habitual Physical Activity
Physical Activity Scale for the Elderly
Measured: 6 months
Calf Strength
Heel Rise Test
Measured: 6 months
Quality of life
Medical Outcome Study Short Form 36
Measured: 6 months
Fear of Falling
ABC Scale [Activities-specific Balance Confidence Scale-Powell]. Scores to be above 67.
Measured: 6 months
Self- Report Physical Activity
RAPA [Rapid Assessment of Physical Activity-Univ of Washington]
Measured: 6 months
Nutritional Status
Body Mass Index
Measured: 6 months
Lean body mass
Body Composition examination using Noori (2012) regression equation for lean body mass.
Measured: 6 months
Caloric intake
Food Frequency Questionnaire (indicator of habitual intake)
Measured: 6 months
Strength
Muscle force measures in 8 muscle groups
Measured: 6 months
Nutritional Indices
Pre-Albumin
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Jul 2015 (estimated)
- Study startMar 2015
- Primary completionJul 2016
- Study completionJul 2016
Why it stopped: Recruitment challenges and unforseen costs to continue
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for End Stage Renal DiseaseStudies of the same condition, open and under way.
- 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 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 9 participants (actual)
Sponsor and investigators
- Lead sponsor
- Youngstown State University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Erdal Sarac, MD, Principal investigator, Renal Group
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02486744
- Sponsor's protocol ID
- 014-2015
- Status last verified
- Feb 2017
- First submitted
- 8 Jun 2015
- Last updated
- 10 Feb 2017
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Feb 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Safety and Efficacy of Acthar Gel in an Outpatient Dialysis Population
- ClinicalTrials.gov ID
- NCT02486744
- Acronym / sponsor ID
- 014-2015
- Conditions
- End Stage Renal Disease
- Keywords
- Acthar, Dialysis, Kidney, Non-Diabetic
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Recruitment challenges and unforseen costs to continue
- Enrolment
- 9 participants (actual)
- Lead sponsor
- Youngstown State UniversityUniversity, hospital or other
- Study start
- Mar 2015
- Primary completion
- Jul 2016 (actual)
- Study completion
- Jul 2016 (actual)
- First posted
- 1 Jul 2015 (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.
This will be a prospective observational study of Acthar Gel in Non-Diabetic Hemodialysis [NDHD] patients receiving dialysis for ≤ 2 years. The project will aimed at providing proof-of-concept data that 80 U two times [2x] week Acthar for 6 months is a safe and effective therapy for NDHD. Effectiveness of lower dose 40 U 2X week will also be determined. Therefore the study will be a repeated measures design (Time x condition) comparison of improvement in renal function, nutritional status, quality of life and physical performance resulting from Acthar therapy.
Detailed description
Recent reports demonstrated Acthar gel is effective to induce remission of proteinuria in the Nephrotic Syndrome patients (Bomback 2011, 2012). There are limited published reports documenting the clinical response (creatinine, proteinuria, serum albumin and cholesterol) to ACTHAR therapy in a non-diabetic hemodialysis population. In addition to renal dysfunction and high risk for mortality, individuals who receive dialysis also have decreased strength, low exercise capacity, poor physical functioning, and a low quality of life (Edgell 1996, Johansen, 2001). Strength deficits are well documented in those with End Stage Renal Disease [ESRD] (Cheema 2010, Yoda 2012). There are several reports documenting an association between strength and gait deficits and other measures of physical performance in persons with ESRD (Bohannon 1994, Fitts 1997, Segura-Orti 2011). It is well known that measures of physical performance may predict risk for fall and hospitalization in older individuals (Guralnik JM, 2000).
Deficits to physical performance may be further compounded by poor nutritional status. Persons with chronic renal disease, particularly in the context of hemodialysis or chronic renal replacement therapy, are often malnourished and/or are affected by abnormal micronutrient status (McMahon 2012). Furthermore, previous studies have shown that more than a third of acute-care, nephrology-related admissions are characterized by malnutrition (Lim 2012), and that it affects from 23% - 76% of all patients receiving hemodialysis (including outpatients)(Blumenkrantz 1980, Ikizler 1996, Pecoits-Filho 2002).
Decreased functional status and concomitant malnutrition contribute to increased hospital readmissions, prolonged length of stay (and inevitably, increased medical costs), and increased morbidity and mortality patients (Isabel 2003, Lim 2012). Given the high prevalence of these characteristics in persons with renal disease, it is important to prioritize identification of novel and effective means by which to sustain and improve the functional capability of these patients, and to maintain their nutritional status and attenuate malnutrition.
To date, there are no reports of the impact of Acthar gel therapy on renal function, strength, physical performance, nutritional status and quality of life in NDHD patients. This study will determine if Acthar gel therapy will maintain or improve overall kidney function as measured with 24 hour urine study at baseline and at the end of study period. In addition this study will determine if Acthar gel therapy will improve nutritional, physical and biochemical status in an outpatient non-diabetic hemodialysis population.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 80 Units of Acthar | Active comparator | Drug: Acthar GelSubjects assigned by random assignment to receive 80 Units of Acthar Gel 2x weekly for 6 months |
| 40 Units of Acthar | Active comparator | Drug: Acthar GelSubjects assigned by random assignment to receive 40 Units of Acthar Gel 2x weekly for 6 months |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Inclusion criteria will be individuals requiring dialysis for treatment of ESRD who have had poor response to immunosuppressive strategies.
- Non-Diabetic
- Adults age 18-80
Key exclusion criteria (14 listed)
- receiving hemodialysis for > 5 years
- diabetic, less than 18 years of age
- are pregnant
- have a history of cancer in the last 5 years
- have an active infection
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 GelAlso: repository corticotropin injectionSubjects will be given an injection subcutaneously 2x week for 6 months. Dosing will be randomly assigned as either 80 U or 40 U | Drug | 40 Units of Acthar, 80 Units of Acthar |
Primary outcome
Renal Function
Time frame: 6 months
Maintain or improve renal function [Creatinine clearance and Proteinuria] by ≥ 20% , as measured by eGFR or 24 hour urine study.
22 secondary outcomes
Hyperparathyroidism
Time frame: 6 months
Anemia
Time frame: 6 months
Inflammatory blood markers
Time frame: 6 months
Vitamin D uptake
Time frame: 6 months
Hypercalcemia
Time frame: 6 months
Phosphate
Time frame: 6 months
Total Iron Binding Capacity
Time frame: 6 months
Epogen Dose
Time frame: 6 months
Fall risk
Time frame: 6 months
Walking endurance
Time frame: 6 months
Gait speed
Time frame: 6 months
Mobility disablement risk
Time frame: 6 months
Habitual Physical Activity
Time frame: 6 months
Calf Strength
Time frame: 6 months
Quality of life
Time frame: 6 months
Fear of Falling
Time frame: 6 months
Self- Report Physical Activity
Time frame: 6 months
Nutritional Status
Time frame: 6 months
Lean body mass
Time frame: 6 months
Caloric intake
Time frame: 6 months
Strength
Time frame: 6 months
Nutritional Indices
Time frame: 6 months
Results and safety
The study was stopped early (reason given: Recruitment challenges and unforseen costs to continue). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Feb 2017.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Erdal Sarac, MD principal investigator
Renal Group
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing Acthar Gel in people with End Stage Renal Disease, run by Youngstown State University at 1 site 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 3 inclusion and 14 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 10 Feb 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in 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 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
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: Recruitment challenges and unforseen costs to continue). 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?
Renal Function (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2017.