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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.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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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

Other trials in United States

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.

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 groups in NCT02486744
Study groupRoleWhat they receive
80 Units of ActharActive comparatorSubjects assigned by random assignment to receive 80 Units of Acthar Gel 2x weekly for 6 months
Receives: Drug: Acthar Gel
40 Units of ActharActive comparatorSubjects 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.

  1. 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)
  1. Hyperparathyroidism

    Change in serum parathyroid hormone levels

    Measured: 6 months

  2. Anemia

    Change in hemoglobin levels

    Measured: 6 months

  3. Inflammatory blood markers

    Change in serum C-Reactive Protein and Creatine Kinase

    Measured: 6 months

  4. Vitamin D uptake

    Change in Vitamin D dosing requirements

    Measured: 6 months

  5. Hypercalcemia

    Change in serum calcium levels

    Measured: 6 months

  6. Phosphate

    Change in serum phosphate levels

    Measured: 6 months

  7. Total Iron Binding Capacity

    Change in Total Iron Binding Capacity in serum

    Measured: 6 months

  8. Epogen Dose

    Change in epogen dosing requirements

    Measured: 6 months

  9. Fall risk

    Timed Up and Go Test will improve

    Measured: 6 months

  10. Walking endurance

    2 minute walk distance

    Measured: 6 months

  11. Gait speed

    10 meter gait speed test

    Measured: 6 months

  12. Mobility disablement risk

    Short Performance Physical Battery

    Measured: 6 months

  13. Habitual Physical Activity

    Physical Activity Scale for the Elderly

    Measured: 6 months

  14. Calf Strength

    Heel Rise Test

    Measured: 6 months

  15. Quality of life

    Medical Outcome Study Short Form 36

    Measured: 6 months

  16. Fear of Falling

    ABC Scale [Activities-specific Balance Confidence Scale-Powell]. Scores to be above 67.

    Measured: 6 months

  17. Self- Report Physical Activity

    RAPA [Rapid Assessment of Physical Activity-Univ of Washington]

    Measured: 6 months

  18. Nutritional Status

    Body Mass Index

    Measured: 6 months

  19. Lean body mass

    Body Composition examination using Noori (2012) regression equation for lean body mass.

    Measured: 6 months

  20. Caloric intake

    Food Frequency Questionnaire (indicator of habitual intake)

    Measured: 6 months

  21. Strength

    Muscle force measures in 8 muscle groups

    Measured: 6 months

  22. 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.

  1. First posted1 Jul 2015 (estimated)
  2. Study startMar 2015
  3. Primary completionJul 2016
  4. Study completionJul 2016

Why it stopped: Recruitment challenges and unforseen costs to continue

Resources

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)
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

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.

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