Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Acthar for Treatment of Proteinuria in Diabetic Nephropathy Patients

31 oktober 2019 uppdaterad av: Mallinckrodt

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Adaptive Design Pilot Safety and Efficacy Study of H.P. Acthar Gel (Acthar) in Patients With Diabetic Nephropathy and Proteinuria.

This Phase 2A study is an adaptive design pilot study investigating the efficacy and safety of daily Acthar administration in diabetic patients with nephropathy and proteinuria. Patients with type 1 diabetes mellitus (T1DM) or T2DM who currently take insulin will be enrolled and randomized into 6 study groups and will be treated with either Acthar or Placebo for 36 weeks, followed by a 4 week dose taper, and a 12 week observation period. The study will compare three dose regimens of Acthar (8 U [0.1 mL], 16 U [0.2 mL], and 32 U [0.4 mL]) to equivalent volumes of Placebo to ensure the double-blind nature of the study.

Insulin-requiring patients are being enrolled to aid compliance with the daily SC administration of study medication and to allow for ease of blood glucose control by adjustment of current insulin therapy in the event of glycemic excursions. Routine safety measures, including glycemic control, will be monitored throughout the study. The adaptive design component of the study allows for the re-assignment of the high dose group to the mid dose group if unacceptable toxicity is noted as per study protocol in the high dose group. Efficacy will be assessed by monitoring serum creatinine, calculated eGFR, and proteinuria (via urinary protein to creatinine ratio [PCR]). Serum cortisol concentration and additional biomarkers in blood and urine will also be monitored.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Faktisk)

34

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • California
      • Roseville, California, Förenta staterna, 95661
        • Questcor Investigational Site
    • Florida
      • Cooper City, Florida, Förenta staterna, 33024
        • Questcor Investigational Site
      • Miami Springs, Florida, Förenta staterna, 33166
        • Questcor Investigational Site
    • New York
      • Bronx, New York, Förenta staterna, 10461
        • Questcor Investigational Site
    • Ohio
      • Columbus, Ohio, Förenta staterna, 43210
        • Questcor Investigational Site
    • Pennsylvania
      • Bethlehem, Pennsylvania, Förenta staterna, 18017
        • Questcor Investigational Site
    • Tennessee
      • Chattanooga, Tennessee, Förenta staterna, 37408
        • Questcor Investigational Site
    • Texas
      • Greenville, Texas, Förenta staterna, 75402
        • Questcor Investigational Site
      • Houston, Texas, Förenta staterna, 77030
        • Questcor Investigational Site
      • San Antonio, Texas, Förenta staterna, 78229
        • Questcor Investigational Site

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria (numbers 2, 3, 4, 5, 6, and 7 per protocol):

  • Body mass index ≤ 45 kg/m2 at screening.
  • Diagnosis of T1DM or T2DM, with HbA1c ≤ 9.0% at Visit 1A. Diagnosis of T2DM should have been made at > 30 years of age (if diabetes developed at a younger age, C-peptide level may be obtained to confirmed the diagnosis).
  • Currently insulin-requiring

    • Patients on oral hypoglycemic therapy plus insulin are eligible provided that oral hypoglycemic agent(s) administered and the dosing regimen(s) of oral hypoglycemic therapy have been stable for ≥ 12 weeks prior to screening. No changes in oral hypoglycemic therapy should be planned or anticipated during the treatment period.
  • Renal Target Disease Requirements:

    • The average of two eGFR values collected during screening (Visits 1 and 1A) must be between 20-60 mL/min/1.73m2 (calculated using the abbreviated Modification of Diet in Renal Disease [MDRD] equation AND
    • Protein to creatinine ratio (PCR) ≥ 3.0 g/g OR total urine protein ≥ 3.0 g from the 24-hour urine collection returned at Visit 1A.
  • Antihypertensive Therapy:

    • Treatment with an ACEI and/or an ARB for at least 6 weeks prior to screening Visit 1A, with stable maintenance dose for ≥ 14 days prior to screening Visit 1A. No change in ACEI or ARB therapy should be planned or anticipated for the period of the study.
    • If treated with additional antihypertensive therapy(ies), duration of therapy ≥ 30 days prior to screening Visit 1A, with stable maintenance dose for ≥ 14 days prior to screening Visit 1A.
    • If the patient has documented intolerance to ACEI and/or ARB therapy (e.g. angioedema, hyperkalemia), they may be eligible for study entry, but the Medical Monitor must be consulted in these cases prior to randomization.
  • Mean systolic blood pressure ≤ 140 mmHg and diastolic blood pressure ≤ 90 mmHg on ≥ 3 seated readings taken at least 5 minutes apart during the screening period at Visit 1A.

Exclusion Criteria (numbers 2, 3, 4, 5, 7, and 11 per protocol):

  • Therapies and/or Medications:

    • History of prior sensitivity to Acthar or other porcine protein products.
    • Chronic systemic corticosteroid use, defined as ≥ 20 mg of prednisone or equivalent systemic corticosteroid taken for more than 4 consecutive weeks within 6 months prior to randomization. Topical, inhaled, or intra-articular corticosteroids are allowed.
    • Planned treatment with live or live attenuated vaccines once enrolled in the study.
    • Previous treatment on a drug being investigated for the treatment of diabetic nephropathy within 6 months prior to randomization.
  • Contraindication to Acthar per Prescribing Information Section 4: scleroderma, osteoporosis, systemic fungal infections, ocular herpes simplex, recent surgery, history of or the presence of peptic ulcer, congestive heart failure, uncontrolled hypertension, primary adrenocortical insufficiency, or adrenal cortical hyperfunction.

    • For the purpose of this study, history of peptic ulcer is defined as ≤ 6 months prior to Visit 1A.
  • Diabetes Target Disease Exceptions:

    • Severely uncontrolled diabetes mellitus as judged by the Principal Investigator
    • HbA1c > 9% at screening Visit 1A.
    • Fasting serum glucose > 230 mg/dL at BOTH screening Visits 1 and 1A.
    • History of diabetic ketoacidosis or non-ketotic hyperosmolar coma within 6 months of screening.
    • History of ocular laser photocoagulation therapy within 6 months of screening OR diabetic retinopathy, diabetic macular edema, or cataracts associated with impairment of visual acuity that will affect adherence with the dosing or administration of SC injections.
    • Patients unwilling to titrate insulin for blood glucose control if adjustment of hypoglycemic therapy is required during the study.
  • Renal Target Disease Exceptions:

    • History of clinical or renal biopsy evidence of non-diabetic renal disease
    • Patients requiring diagnostic or interventional procedure requiring an intravenous contrast agent must delay screening/randomization for at least 14 days
  • Tuberculosis: Any patient with a positive Interferon-gamma release assay, OR signs and symptoms concerning for active tuberculosis.
  • Cardiovascular:

    • History of congestive heart failure (NYHA Functional Class III-IV).
    • History of dilated cardiomyopathy with ejection fraction < 40%.

      1. Exceptions require approval by the Medical Monitor.

    • Patient has had any of the following within 3 months of screening:

      1. Unstable angina
      2. Myocardial infarction
      3. Coronary artery bypass graft or percutaneous transluminal coronary angioplasty
      4. Transient ischemic attack or cerebrovascular accident
      5. Unstable arrhythmia

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Acthar 8 U (0.1 mL) daily
Repository Corticotropin Injection
H.P. Acthar Gel (repository corticotropin injection) is administered via daily SC injection for 36 weeks in the three dose groups [8 U (0.1 mL), 16 U (0.2 mL), or 32 U (0.4 mL)].
Andra namn:
  • ACTH
  • Acthar
  • ACTH Gel
  • H.P. Acthar Gel (repository corticotropin injection)
Placebo-jämförare: Placebo (0.1 mL) daily
Placebo
Placebo contains the same inactive ingredients as H.P. Acthar Gel without the active pharmaceutical ingredient (API). Placebo is administered via daily SC injection for 36 weeks in equal volumes as the Acthar comparator volumes.
Experimentell: Acthar 16 U (0.2 mL) daily
Repository Corticotropin Injection
H.P. Acthar Gel (repository corticotropin injection) is administered via daily SC injection for 36 weeks in the three dose groups [8 U (0.1 mL), 16 U (0.2 mL), or 32 U (0.4 mL)].
Andra namn:
  • ACTH
  • Acthar
  • ACTH Gel
  • H.P. Acthar Gel (repository corticotropin injection)
Placebo-jämförare: Placebo (0.2 mL) daily
Placebo
Placebo contains the same inactive ingredients as H.P. Acthar Gel without the active pharmaceutical ingredient (API). Placebo is administered via daily SC injection for 36 weeks in equal volumes as the Acthar comparator volumes.
Experimentell: Acthar 32 U (0.4 mL) daily
Repository Corticotropin Injection
H.P. Acthar Gel (repository corticotropin injection) is administered via daily SC injection for 36 weeks in the three dose groups [8 U (0.1 mL), 16 U (0.2 mL), or 32 U (0.4 mL)].
Andra namn:
  • ACTH
  • Acthar
  • ACTH Gel
  • H.P. Acthar Gel (repository corticotropin injection)
Placebo-jämförare: Placebo (0.4 mL) daily
Placebo
Placebo contains the same inactive ingredients as H.P. Acthar Gel without the active pharmaceutical ingredient (API). Placebo is administered via daily SC injection for 36 weeks in equal volumes as the Acthar comparator volumes.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Percent Change in Estimated Glomerular Filtration Rate (eGFR) at Visit 12
Tidsram: Visit 12 (Week 36)
Percent change in eGFR at Visit 12 (Week 36) compared to average baseline eGFR obtained during screening
Visit 12 (Week 36)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Percent Change in eGFR at Visit 17
Tidsram: Visit 17 (Week 52)
Percent change in eGFR at Visit 17 (Week 52) compared to baseline eGFR obtained during screening
Visit 17 (Week 52)
Frequency of Patients With a Doubling of Serum Creatinine, Progression to End-stage Renal Disease (ESRD), or Death
Tidsram: Visit 12 (Week 36) and Visit 17 (Week 52)
Visit 12 (Week 36) and Visit 17 (Week 52)
Complete or Partial Remission of Proteinuria
Tidsram: Visit 12 (Week 36) and Visit 17 (Week 52)
Proportion of patients with complete remission (PCR 0.5 g/g) or partial remission (reduction in PCR of >50% from baseline, plus PCR≤2.5 g/g but >0.5 g/g) of proteinuria at Visit 12 (Week 36) and/or at Visit 17 (Week 52)
Visit 12 (Week 36) and Visit 17 (Week 52)
Percent Change in eGFR Calculated Using Cystatin C
Tidsram: Visit 12 (Week 36) and Visit 17 (Week 52)
Percent change in eGFR calculated using cystatin C compared to baseline obtained at Visit 2.
Visit 12 (Week 36) and Visit 17 (Week 52)
Percent Change From Baseline in eGFR by Visit
Tidsram: Visit 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17
Percent change from baseline in eGFR by visit
Visit 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17
Percent Change From Baseline in Protein to Creatinine Ratio (PCR)
Tidsram: Visits 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17
Percent change from baseline in PCR
Visits 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17
Proportion of Subjects Whose Best Response Was Complete or Partial Remission of Proteinuria
Tidsram: Visit 12 (Week 36) and Visit 17 (Week 52)
Proportion of subjects whose best response was complete remission (PCR 0.5 g/g) or partial remission (reduction in PCR of >50% from baseline, plus PCR≤2.5 g/g but >0.5 g/g) of proteinuria
Visit 12 (Week 36) and Visit 17 (Week 52)
Percent Change From Baseline of Serum Total Cholesterol, Triglycerides, LDL, HDL, Lp(a), Albumin, and Cortisol
Tidsram: Visit 6, 9, 12, and 17
Percent change from baseline of serum total cholesterol, triglycerides, LDL, HDL, Lp(a), albumin, and cortisol
Visit 6, 9, 12, and 17

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Mean HbA1c
Tidsram: Week 36
Change from baseline mean HbA1c (%) to Week 36
Week 36

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 maj 2012

Primärt slutförande (Faktisk)

1 januari 2016

Avslutad studie (Faktisk)

1 mars 2016

Studieregistreringsdatum

Först inskickad

15 maj 2012

Först inskickad som uppfyllde QC-kriterierna

16 maj 2012

Första postat (Uppskatta)

17 maj 2012

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

18 november 2019

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

31 oktober 2019

Senast verifierad

1 juli 2017

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera