Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| FD-R-004826-01-A2 | Other Identifier | FDA Orphan Products Development Ad Hoc Panel Review |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Funding Source - FDA OOPD
Pioglitazone is currently used in clinical practice to treat diabetes and this study will examine the potential use of a low dose of the same drug for the treatment of polycystic kidney disease. The purpose of this study is to determine whether the diabetes drug pioglitazone (Actos) is a safe and effective treatment of autosomal dominant polycystic kidney disease when treated in its early stages. Pioglitazone is approved by the FDA for the treatment of diabetes. Pre-clinical models of polycystic kidney disease have shown that low dose treatment with pioglitazone decreases the growth of the cysts. The studies also suggest that effective pioglitazone dosing for polycystic kidney disease may be lower than that used to treat diabetes. The purpose of this study is to see if pioglitazone might slow cyst disease in humans.
Patients will be randomize to placebo or 15 mg pioglitazone for 12 months, and then be crossed over to the other arm. Patients will undergo MRI of the liver and kidney and MRspectroscopy of the lumbar spine (if they choose as this is ancillary study) three times during the study. Assessments will be every 3 months and include blood work, blood pressure, and body water assessments.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo Arm | Placebo Comparator | Subject will be on placebo |
|
| Pioglitazone Arm | Active Comparator | Subject will be on pioglitazone |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pioglitazone | Drug | Pioglitazone |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety: Total Body Water | Bioimpedance analysis (BIA)(Ohms); Increase in BIA in Ohms indicates a decrease in total body water | average of 4 measures in each 12 month arm |
| Efficacy: Percent Change in Total Kidney Volume | Change in total kidney volume by Magnetic Resonance Imaging (MRI) from beginning to end of the 12 months | Baseline, end of year 1, and end of year 2 |
| Measure | Description | Time Frame |
|---|---|---|
| Safety: Hypoglycemia | number of patients with blood sugar < 70 mg/dl | measured quarterly for 12 months in pioglitazone and same in placebo |
| Safety: Elevated Liver Function Tests | Number of patients with elevated liver test (ALT or AST) > 2 times upper limit of normal |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Sharon Moe, 317-944-7580 | Indiana University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Indiana University Health | Indianapolis | Indiana | 46202 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39356039 | Derived | St Pierre K, Cashmore BA, Bolignano D, Zoccali C, Ruospo M, Craig JC, Strippoli GF, Mallett AJ, Green SC, Tunnicliffe DJ. Interventions for preventing the progression of autosomal dominant polycystic kidney disease. Cochrane Database Syst Rev. 2024 Oct 2;10(10):CD010294. doi: 10.1002/14651858.CD010294.pub3. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Patients who fulfilled the initial screening underwent further screening with a baseline magnetic resonance imaging (MRI) and randomized to pioglitazone or placebo providing the total kidney volume (TKV) was ≥675 ml (18-25 years old), ≥ 900 ml (26-35 years old), and ≥ 1350 ml (36-55 years old).
Age 18-55 years old, with known autosomal dominant polycystic kidney disease (ADPKD), estimated glomerular filtration rate (eGFR) > 50 ml/min/m2 on recent labs, and no history of diabetes were identified using international disease codes (ICD-9) code for cystic kidney disease by search of electronic medical records or through advertisements and letters sent to Nephrologists.
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | PIO Then PLACEBO | Sequence Pioglitazone then Placebo |
| FG001 | Placebo Then PIO | sequence placebo then pioglitazone |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
18 patients randomized to either pioglitazone for 12 months and then placebo for 12 months and then cross over to the other arm. So baseline data represents both arms
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | All Study Participants | at randomization to sequence 1 (pioglitazone 15 mg) or placebo for cross over study |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| 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 | Safety: Total Body Water | Bioimpedance analysis (BIA)(Ohms); Increase in BIA in Ohms indicates a decrease in total body water | All patients randomized | Posted | Mean | 95% Confidence Interval | Ohms | average of 4 measures in each 12 month arm |
|
|
2 years
Not provided
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Pioglitazone | 15 mg po daily | 0 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| hospitalization | Hepatobiliary disorders | Non-systematic Assessment | pancreatitis |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| headache | Nervous system disorders | Non-systematic Assessment |
The major limitation is the small sample size.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Sharon Moe | Indiana University School of Medicine | 317 278 2868 | smoe@iu.edu |
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | May 31, 2017 | Nov 18, 2019 | ICF_000.pdf |
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Aug 20, 2018 | Oct 15, 2020 | Prot_SAP_001.pdf |
Not provided
| ID | Term |
|---|---|
| D007690 | Polycystic Kidney Diseases |
| ID | Term |
|---|---|
| D052177 | Kidney Diseases, Cystic |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| D000077205 | Pioglitazone |
| ID | Term |
|---|---|
| D045162 | Thiazolidinediones |
| D013844 | Thiazoles |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Placebo | Drug | Placebo |
|
| measured quarterly over 12 months for each arm |
| Efficacy: Glomerular Filtration Rate | average estimated glomerular filtration rate by chronic kidney disease (CKD) epidemiologic (epi) formula measured quarterly | average of 4 values over 12 months |
| Efficacy Blood Pressure | mean systolic and diastolic blood pressure | average of 4 measures over 12 months |
| Bone Marrow Fat | We will assess change in bone marrow fat by MR spectroscopy as an ancillary study to be done at the same time as MRI; will not be done due to person leaving institution. | Baseline, end of year 1, and end of year 2 |
| Participants |
|
| Age, Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| estimated glomerular filtration rate (eGFR) by CKD-epi | Mean | Standard Deviation | ml/min/m2 |
|
| right kidney volume | Mean | Standard Deviation | ml |
|
| left kidney volume | Mean | Standard Deviation | ml |
|
| Participants |
|
|
|
| Primary | Efficacy: Percent Change in Total Kidney Volume | Change in total kidney volume by Magnetic Resonance Imaging (MRI) from beginning to end of the 12 months | Those who completed both arms | Posted | Mean | 95% Confidence Interval | percentage of change | Baseline, end of year 1, and end of year 2 |
|
|
|
|
| Secondary | Safety: Hypoglycemia | number of patients with blood sugar < 70 mg/dl | All randomized participants | Posted | Count of Participants | Participants | measured quarterly for 12 months in pioglitazone and same in placebo |
|
|
|
| Secondary | Safety: Elevated Liver Function Tests | Number of patients with elevated liver test (ALT or AST) > 2 times upper limit of normal | All patients who were randomized, regardless of whether they completed both arms | Posted | Count of Participants | Participants | measured quarterly over 12 months for each arm |
|
|
|
|
| Secondary | Efficacy: Glomerular Filtration Rate | average estimated glomerular filtration rate by chronic kidney disease (CKD) epidemiologic (epi) formula measured quarterly | All patients that completed both arms. | Posted | Mean | 95% Confidence Interval | ml/min/m2 | average of 4 values over 12 months |
|
|
|
|
| Secondary | Efficacy Blood Pressure | mean systolic and diastolic blood pressure | All patients that completed both arms | Posted | Mean | 95% Confidence Interval | mmHg | average of 4 measures over 12 months |
|
|
|
|
| Secondary | Bone Marrow Fat | We will assess change in bone marrow fat by MR spectroscopy as an ancillary study to be done at the same time as MRI; will not be done due to person leaving institution. | The MRIs were done, but could not be analyzed as requires special expertise and software. | Posted | Baseline, end of year 1, and end of year 2 |
|
|
| 18 |
| 0 |
| 18 |
| 13 |
| 18 |
| EG001 | Placebo | Over encapsulated (identical appearing) placebo | 0 | 18 | 3 | 18 | 15 | 18 |
| pyelonephritis | Infections and infestations | Non-systematic Assessment |
|
| surgery | Gastrointestinal disorders | Non-systematic Assessment | elective surgery/gastric banding |
|
| dizziness | Nervous system disorders | Non-systematic Assessment |
|
| infection | Infections and infestations | Non-systematic Assessment |
|
| gastrointestinal symptom | Gastrointestinal disorders | Non-systematic Assessment |
|
| musculoskeletal pain | Musculoskeletal and connective tissue disorders | Non-systematic Assessment |
|
| urinary tract infection or pain | General disorders | Non-systematic Assessment | or cyst rupture |
|
Not provided
Not provided
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D000015 | Abnormalities, Multiple |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D000072661 | Ciliopathies |
| D030342 | Genetic Diseases, Inborn |
| D001393 |
| Azoles |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |