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Observational Study of Kibow Biotics in Chronic Kidney Failure Patients

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2012 by Kibow Biotech Inc..
Recruitment status was:  Recruiting
Thomas Jefferson University
Information provided by (Responsible Party):
Kibow Biotech Inc. Identifier:
First received: September 26, 2011
Last updated: May 2, 2012
Last verified: May 2012
A specifically formulated probiotic product comprised of defined and tested microbial strains may afford renoprotection in what has been generally called "Enteric DialysisTM". However, it is also referred to as enteric toxin reduction technology. Our hypothesis is to assess the potential benefits in devising a bowel-based probiotic formulation (Kibow® Biotics/RenadylTM) as a dietary supplement product for patients undergoing standardized care of treatment for their CKD stage 3 and stage 4 conditions.

Condition Intervention
Chronic Kidney Failure
Dietary Supplement: Kibow Biotics/Renadyl

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Observational Clinical Trials of Kibow Biotics (a Patented and Proprietary Probiotic Dietary Supplement) in Chronic Kidney Failure Patients, in Conjunction With Standardized Care of Treatment

Resource links provided by NLM:

Further study details as provided by Kibow Biotech Inc.:

Primary Outcome Measures:
  • 15-20% Changes in BUN. [ Time Frame: Baseline, 1 month, 2 months, 3 months, 4 months, 6 months. ]
  • 15-20% Change in Creatinine [ Time Frame: Baseline, 1 month, 2 months, 3 months, 4 months, 6 months ]

Secondary Outcome Measures:
  • Quality of life outcome based on questionnaire. [ Time Frame: Baseline, 1 month, 2 months, 3 months, 4 months, 6 months ]
  • To observe inflammatory and oxidative stress biomarkers. [ Time Frame: Baseline, 1 month, 2 months, 3 months, 4 months, 6 months ]
    Observe inflammatory and stress markers in metabolites from blood serum.

  • Observation and analysis of patient fecal matter. [ Time Frame: Baseline, 1 month, 2 months, 3 months, 4 months, 6 months ]
    Observation and analysis of patient fecal matter to determine bacterial flora levels that are present in the stool.

Biospecimen Retention:   Samples With DNA
Blood plasma and serum

Estimated Enrollment: 30
Study Start Date: July 2011
Estimated Study Completion Date: October 2012
Estimated Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Chronic Kidney Failure 3/4 Dietary Supplement: Kibow Biotics/Renadyl
Month 1, one capsule three times daily (90 colony forming units); Month 2, two capsules three times daily (180 CFU's); Month 3 & 4, three capsules three times daily (270 CFU's). Months 5 & 6 are washout periods, in which the patient receives no product. All parameters are still monitored by the study site during months 5 & 6. All medical, physical, clinical, QOL and other parameters will be monitored as well.
Other Name: Kibow Biotics

Detailed Description:

Probiotics are increasingly utilized clinically. As their safety and health benefits are established, it is reasonable to anticipate that probiotic bacteria will be incorporated into a growing number of clinical regimens, as a dietary supplement.

Extensive in vitro R&D investigations in Kibow's laboratories

Bacterial strains studied were a mixture of patented and proprietary strains of Streptococcus thermophilus (KB27), Lactobacillus acidophilus (KB31) and Bifidobacterium longum (KB35).

Oral administration of these bacterial formulations, tested in the 5/6th nephrectomized rat model (at Thomas Jefferson University, Phila., PA) and minipig model (at Indiana University, Indianapolis, IN), decreased both blood urea nitrogen (BUN) and serum creatinine (Scr) levels.

Two independent veterinarians investigated the effect of Kibow Biotics® in cats and dogs (of both genders and varying body weights) with moderate to severe kidney failure. Based on positive results, this formulation, marketed and distributed as AzodylTM, is currently licensed for veterinary applications to Vetoquinol USA.

Pilot scale studies, double blind, placebo controlled, cross-over studies for six months conducted in 45 patients in USA, Canada, Argentina, and Nigeria demonstrates reduction of BUN (P>95%) and improved quality of life (P>95%). Decrease in creatinine and uric acid levels were also observed. However, these studies were based on correlating the age of geriatric cats and dogs with moderate to significant kidney failure to human geriatric conditions. The proposed current study is being reevaluated based on correlating the weight basis of animal to human conditions. Hence, this is a does escalation study on ingestion of 1x (90 billion CFU/day), 2x (180 billion CFU/day), and 3x (270 billion CFU/day) dosages.


Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Outpatient hospital setting.

Inclusion Criteria:

  • Age 18 to 75 years
  • CKD Stages 3 and 4 as documented by prior medical history
  • Serum Creatinine >2.5 mg/dL
  • Stable and on CKD status 3 and 4 at least for a year or more

Exclusion Criteria:

  • Pregnant or nursing women
  • Refusal to sign the informed consent form
  • Documented to have HIV/AIDS/Liver disease
  • Active dependency on drugs or alcohol
  • Any non-related medical, debilitating disease/disorder that would interfere with adherence to this study
  • Currently on anticoagulant therapy
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01450657

Contact: Stephanie DeLoach, M.D. 215-955-1301
Contact: Bonita Falkner, M.D. 215-503-2500

United States, Pennsylvania
Thomas Jefferson University Recruiting
Philadelphia, Pennsylvania, United States, 19107
Contact: Stephanie DeLoach, M.D.    215-955-1301   
Principal Investigator: Stephanie DeLoach, M.D.         
Sub-Investigator: Bonita Falkner, M.D.         
Sponsors and Collaborators
Kibow Biotech Inc.
Thomas Jefferson University
Principal Investigator: Stephanie DeLoach, M.D. Thomas Jefferson University, Philadelphia, PA
  More Information

Responsible Party: Kibow Biotech Inc. Identifier: NCT01450657     History of Changes
Other Study ID Numbers: KIB002
Study First Received: September 26, 2011
Last Updated: May 2, 2012

Keywords provided by Kibow Biotech Inc.:
Chronic Kidney failure stage three and four
Kibow Biotics
Gut based uremic toxin removal

Additional relevant MeSH terms:
Renal Insufficiency
Kidney Failure, Chronic
Kidney Diseases
Urologic Diseases
Renal Insufficiency, Chronic processed this record on April 28, 2017