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Clinical Trial Details

Trial ID: L6644
Source ID: NCT01293461
Associated Drug: Cbx129801
Title: Safety and Pharmacokinetics of CBX129801 in Patients With Type 1 Diabetes
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 1 Diabetes|Diabetes Mellitus|Peripheral Diabetic Neuropathy
Interventions: DRUG: CBX129801|DRUG: Placebo
Outcome Measures: Primary: To assess the single and multiple dose pharmacokinetics of plasma CBX129801 after subcutaneous (SC) administration of CBX129801 by estimating parameters of Cmax, Tmax, Cmin, AUClast, AUCinf, Tlag, Cav, CL/F, Vz/F, and half life., Plasma CBX129801 will be used to assess the concentration versus time profiles and PK of CBX129801., For duration of study / 16 months|To assess the safety and tolerability of CBX129801 when administered SC by adverse events, injection site assessments, clinical laboratory tests, vital signs, physical examinations, and electrocardiograms., For duration of study / 16 months | Secondary: To evaluate the technique of sensory nerve conduction velocity (SNCV) in the sural nerves in patients with type 1 diabetes mellitus., Predose and 6 and 12 weeks postdose|To assess the immunogenicity of CBX129801 by occurrence of anti-CBX129801 antibody formation., For duration of study / 16 months|To evaluate the technique of motor nerve conduction velocity (MNCV) in the peroneal nerves in patients with type 1 diabetes mellitus., Predose and 6 and 12 weeks postdose|To evaluate the technique of vibration perception threshold (VPT) in patients with type 1 diabetes (Part 2 only), Predose and 12 weeks postdose
Sponsor/Collaborators: Sponsor: Cebix Incorporated
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1|PHASE2
Enrollment: 72
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2011-04
Completion Date: 2012-10
Results First Posted:
Last Update Posted: 2013-03-01
Locations: Escondido, California, United States|Tustin, California, United States|Walnut Creek, California, United States|Aurora, Colorado, United States|Butte, Montana, United States|San Antonio, Texas, United States|Olympia, Washington, United States|Renton, Washington, United States
URL: https://clinicaltrials.gov/show/NCT01293461