Study of STX-100 in Renal Transplant Patients With Interstitial Fibrosis and Tubular Atrophy (IF/TA)

Chronic Allograft Dysfunction Clinical Trial

Official title:

Randomized Double-Blind, Placebo-Controlled, Single and Multiple Dose, Dose-Escalation Study of STX 100 in Renal Transplant Patients With Biopsy Proven Interstitial Fibrosis and Tubular Atrophy (IF/TA)

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00878761
• Other study ID #: STX-002
• Status: Withdrawn
• Phase: Phase 2
• First received: April 6, 2009
• Last updated: May 20, 2011
• Start date: September 2010
• Est. completion date: December 2011

Study information

• Verified date: May 2011
• Source: Stromedix, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This Phase 2 study is a multi-center, randomized, double-blind, placebo-controlled, single followed by multiple dose, dose escalation study designed to evaluate the safety, tolerability, pharmacokinetics, immunogenicity, and impact of STX-100 on gene and protein expression for αvβ6 related and TGF-β-inducible genes (including tubulointerstitial injury, epithelial function, and IF/TA related genes) in renal transplant patients with biopsy.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 48
• Est. completion date: December 2011
• Est. primary completion date: October 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Consenting adult patients, 18 (or the legal age of consent) to 65 years old, male or female.

• eGFR = 25 ml/min (Cockcroft-Gault formula).

• Six to 60 months post renal transplant at the initiation of screening.

• Qualifying renal biopsy obtained within 8 weeks prior to randomization with histologic evidence of = Grade 2 IF/TA (Banff score) without morphologic evidence of a treatable etiology (e.g., BK virus nephropathy, chronic obstruction).

• Adequate bone marrow and liver function

• Weight between 40-110 kg.

• Female patients must be surgically sterile, postmenopausal (minimum 1 year without menses and verified by follicular-stimulating hormone [FSH] levels), or agree to use contraception from the time of signing the informed consent form through 16 weeks following the last injection of study medication. Male patients must also agree to use birth control for either themselves or their partner, as appropriate, from the time of signing the informed consent form through 16 weeks following the last injection of study medication.

Exclusion Criteria:

• Recipient of a multi-organ transplant.

• History of T-cell mediated rejection (TCMR) within 3 months prior to randomization.

• Patients who are receiving high dose corticosteroids at the time of screening.

• Histologic evidence of acute TCMR (= Banff Grade 1A) on a qualifying renal biopsy for this study. Patients with 'borderline' changes (Banff criteria) on a qualifying renal biopsy are eligible for this study if the Principal Investigator believes treatment for TCMR is not warranted.

• Prior or current histologic evidence of polyomavirus BK virus nephropathy.

• Any histologic finding on the qualifying renal biopsy that the Investigator believes warrants modifying the patient's current therapy.

• Evidence of active tissue invasive cytomegalovirus or Epstein-Barr virus infection.

• History of malignancy, including carcinoma or post-transplant lymphoproliferative disorder.

• History of chronic pulmonary disease or smoker within the past 5 years or more than 15 pack-years exposure.

• Serious local infection or systemic infection within 3 months prior to screening.

• Surgery within 3 months prior to Day 1 (other than minor cosmetic surgery, minor dental procedures, or percutaneous kidney transplant biopsy).

• Positive test for HBsAg, HCV, or HIV antibody at screening.

• Treatment with another investigational drug, investigational device, or approved therapy for investigational use within 1 month prior to dosing.

Study Design

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

Related Conditions & MeSH terms

• Chronic Allograft Dysfunction
• Lung Diseases, Interstitial

Intervention

Biological:
• STX-100
SC, single dose followed by multiple dose

Locations

Country	Name	City	State
United States	Stromedix Investigative Site	Cambridge	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Stromedix, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety as measured by adverse events		25 weeks from first dosing (per cohort)	Yes