6-Month Safety And Efficacy Study Of TTP488 In Patients With Type 2 Diabetes And Persistent Albuminuria

Diabetic Nephropathy Clinical Trial

Official title:

Double-Blind, Randomized, Placebo-Controlled, Phase IIa, Multicenter Study In Patients With Type 2 Diabetes And Persistent Albuminuria To Evaluate The Safety And Efficacy Of A Six Month Regimen Of Orally-Administered TTP488

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00287183
• Other study ID #: B0341001
• Secondary ID: TTP488-202
• Status: Completed
• Phase: Phase 2
• First received: January 20, 2006
• Last updated: September 30, 2009
• Start date: February 2006
• Est. completion date: August 2009

Study information

• Verified date: September 2009
• Source: Pfizer
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

Current research indicates that TTP488 may be a viable agent for the treatment of diabetic nephropathy. The purpose of this study is to determine the safety and efficacy of a six-month regimen of daily orally-administered TTP488 to patients with diabetic nephropathy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 110
• Est. completion date: August 2009
• Est. primary completion date: August 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 31 Years and older

Eligibility

Inclusion Criteria:

• Male or female outpatients 31 years of age or older.

• Females must no longer be of child-bearing potential, must have a negative serum pregnancy test, and cannot be breast-feeding.

• Non-vasectomized male must be willing to abstain from sexual intercourse or willing to use a condom in addition to having their female partner use another form of contraception.

• Diagnosis of probable Type 2 diabetes after the age of 30 and for at least 6 months prior to the screening visit and: not requiring insulin within first year of diagnosis; no history of diabetic ketoacidosis (DKA); body mass index (BMI) of 40 or less at the screening visit

• Presence of persistent albuminuria with a UACR of 6.7 - 203 mg/mmol Must be taking the highest tolerated dose of an angiotensin converting enzyme (ACE) inhibitor or an angiotensin II receptor blocker (ARB) and have been maintained on that dose for at least 3 months prior to the Baseline visit

• Blood pressure(BP) must be stable and well controlled by the judgement of the investigator (goal of the control of BP is 130/80 or less). If required, the use of anti-hypertensives in addition to an ACE inhibitor or an ARB is acceptable.

• Patients with a calculated creatinine clearance of greater than or equal to 30 mL/min and without the presence of clinically significant hematuria or red or white cell casts can be included in the study.

Exclusion Criteria:

• Diagnosis of Type 1 diabetes

• Hemoglobin A1c (HbA1c) >10%

• Females cannot be breast-feeding

• Known renal artery stenosis

• Calculated creatinine clearance <30 mL/min or the presence of clinically significant hematuria of red or white cell casts

• Chronic use of NSAIDs or more than 1 g/day of aspirin

• QTc >450 msec for females or >430 msec for males (a measure of the time between the start of the Q wave and the end of the T wave in the heart's electrical cycle)

• Known family history of prolonged QT syndrome

• History of symptomatic congestive heart failure within the last 2 years

• History of syncope in the lst 2 years or recurrent hypokalemia, including that caused by diuretics

• Myocardial infarction or signs or symptoms of unstable coronary artery disease with the last year

• Pulmonary disease or evidence of clinically significant pulmonary symptoms.

• Active neoplastic disease. (Excised cutaneous basal cell carcinomas are not excluded). Patients with stable prostate cancer may be included at the discretion of the Medical Monitor.

• Any clinically significant hematologic or coagulation disorder

• Any clinically significant hepatic disease

• Use of excluded medications: drugs known to significantly increase QTc and/or have increased risk of torsades de point, immunosuppressive agents, cancer chemotherapeutic agents, oral corticosteroids other than maintenance doses equivalent to 7.5 mg prednisone per day, and radiotherapy

• Use of an investigational drug within 30 days or within 5 half-lives of the investigational agent, whichever is longer, or use of an investigational medical device within 2 weeks before or after the study

• Any other disease or condition that, in the opinion of the investigator, makes the patient unsuitable to participate in this study

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Albuminuria
• Diabetic Nephropathies
• Diabetic Nephropathy

Intervention

Drug:
• PF-04494700 (TTP488)
60 mg/day for 6 days followed by 20 mg/day for 175 days vs placebo, oral medication

Other:
• Placebo
Placebo

Locations

Country	Name	City	State
Canada	Pfizer Investigational Site	Burlington	Ontario
Canada	Pfizer Investigational Site	Courtice	Ontario
Canada	Pfizer Investigational Site	Fort Erie	Ontario
Canada	Pfizer Investigational Site	Hamilton	Ontario
Canada	Pfizer Investigational Site	Kitchener	Ontario
Canada	Pfizer Investigational Site	Kitchener	Ontario
Canada	Pfizer Investigational Site	Millon	Ontario
Canada	Pfizer Investigational Site	North Bay	Ontario
Canada	Pfizer Investigational Site	Oakville	Ontario
Canada	Pfizer Investigational Site	Penticton	British Columbia
Canada	Pfizer Investigational Site	Red Deer	Alberta
Canada	Pfizer Investigational Site	Saint Catherines	Ontario
Canada	Pfizer Investigational Site	Saskatoon	Saskatchewan
Canada	Pfizer Investigational Site	Scarborough	Ontario
Canada	Pfizer Investigational Site	Smith Falls	Ontario
Canada	Pfizer Investigational Site	Thornhill	Ontario
Canada	Pfizer Investigational Site	Toronto	Ontario
Canada	Pfizer Investigational Site	Toronto	Ontario
Canada	Pfizer Investigational Site	Vancouver	British Columbia

Sponsors (1)

Lead Sponsor	Collaborator
Pfizer

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary endpoint of efficacy will be assessed by comparing the treatment groups based on the change in urinary albumin-creatinine ratio (UACR)		from baseline to end of treatment (Month 6).	No
Secondary	To evaluate treatment on estimated GFR and serum creatinine		evaluated for change from baseline to months 3 & 6	No
Secondary	To evaluate the effects of TTP488 on other relevant biomarkers		evaluated at months 1, 3 & 6	No
Secondary	To evaluate the safety of TTP488		Ongoing	Yes
Secondary	To evaluate the PK profile of oral TTP488.		Ongoing	No
Secondary	To evaluate the effect of treatment with TTP488 on UACR		evaluated from baseline to month 3 visit	No

External Links

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