Overview

Study of XL784 in Patients With Albuminuria Due to Diabetic Nephropathy

Status:
Completed
Trial end date:
2007-12-01
Target enrollment:
0
Participant gender:
All
Summary
This clinical study is being conducted at multiple sites to determine the activity, safety and tolerability of XL784 when given daily to patients with albuminuria due to diabetic nephropathy. XL784 is a small molecule reno-protective metalloproteinase inhibitor, inhibiting both ADAMs (including ADAM10, a target of significant interest because of its important role in blood vessel formation and cell proliferation, and ADAM17/TACE, activation of which has been associated with renal deterioration) and MMPs (including MMP-2 and MMP-9). XL784 was specifically optimized to be MMP-1 sparing, which may be clinically significant because inhibition of MMP-1 has been hypothesized to be associated with musculoskeletal toxicity.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Symphony Evolution, Inc.
Criteria
Inclusion Criteria:

- Type 1 or Type 2 diabetes mellitus with albuminuria, observed within 3 months of
screening

- Prior to randomization, subject has a glomerular filtration rate (GFR) >/= 40 mL/min

- Prior to randomization, the subject has albuminuria defined as ACR >/= 500 mg/g

- Stable seated blood pressure at the screening visit and prior to randomization

- Subject has been on a stable dose and schedule of an angiotension converting enzyme
(ACE) inhibitor and/or an angiotension receptor blocker (ARB) for at least 3 months
before first dose of study drug

- If on antidiabetic medication, subject has been on a stable dose and schedule for at
least 3 months prior to first dose of study drug

- Sexually active subjects must use an accepted method of contraception during the
course of the study and for 3 months after

- Signed informed consent

Exclusion Criteria:

- Subject has participated in an investigational study and received an investigational
drug within 30 days of the first dose of XL784

- Hemoglobin A1c (HbA1c) value of >10% at screening

- Subject has had either organ transplantation or is currently on immunosuppressive
therapy

- Non-steroidal anti-inflammatory drugs (NSAIDs) within 5 days of urine screening
assessments

- Current diagnosis of one or more of the following conditions: 1) infection requiring
parenteral antibiotics, 2) urinary tract infection, 3) hepatic dysfunction or disease,
4) symptomatic congestive heart failure, 5) unstable angina pectoris, 5) serious
cardiac arrhythmia

- Clinically evident diabetic gastroparesis or motility disturbance

- Proteinuria not due to diabetic nephropathy

- Diltiazem or verapamil

- Ongoing condition where treatment with NSAIDs is anticipated (aspirin is allowed)

- Recent history of drug or alcohol abuse

- Pregnant or breastfeeding female subjects

- Known HIV and/or receiving anti-retroviral therapy

- Known allergy or hypersensitivity to any component of XL784 formulation