PK/PD Study of Subcutaneous Cenderitide Infusion in CHF Patients

Phase 1

Completed

• Conditions: Heart Failure; ADHF; Chronic Heart Failure; CHF
• Interventions: Other: Placebo; Drug: Cenderitide

• Registration Number: NCT01316432
• Lead Sponsor: Nile Therapeutics

Brief Summary

The purposed of the study is to evaluate the pharmacokinetics (PK) response of continuous subcutaneous (SQ) infusion of cenderitide, as compared with a single SQ bolus.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2011-03-14
• Study First Submitted QC: 2011-03-15
• Study First Posted: 2011-03-16
• Study Start: 2011-05
• Primary Completion: 2011-10
• Study Completion: 2011-11
• Status Verified: 2012-10
• Last Update Submitted: 2012-10-16
• Last Update Posted: 2012-10-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 58

Inclusion Criteria

• Male or female ≥ 18 years of age.
• Documented systolic heart failure with ejection fraction (EF) ≤ 40%
• Clinical evidence of volume overload
• Systolic blood pressure ≥ 120 mmHg and ≤ 200 mmHg and diastolic blood pressure > 60 mmHg and < 110 mmHg at the time of screening.
• Stable doses of oral medication at least 24 hours prior to screening
• No known allergy or contraindication to furosemide (Lasix®)
• Female patients must be post-menopausal or surgically sterile. A woman may be considered to be surgically sterilized if she has had a bilateral tubal ligation (for at least 6 months), bilateral oophorectomy or complete hysterectomy.
• Be adequately informed of the nature and risks of the study and give written informed consent prior to receiving study medication.

Exclusion Criteria

• Acute or suspected acute myocardial infarction (AMI) or troponin levels > 5X the upper limit of normal at the institution's local laboratory and accompanied by dynamic ECG changes consistent with AMI
• Clinical diagnosis of acute coronary syndrome (ACS) within 30 days prior to screening.
• Evidence of uncorrected volume or sodium depletion (NA ≤ 130) or other condition that would predispose the patient to adverse events.
• Clinically significant aortic or mitral valve stenosis.
• Temperature > 38°C (oral or equivalent), sepsis or active infection requiring IV anti-microbial treatment.
• ADHF associated with significant arrhythmias (ventricular tachycardia, bradyarrhythmias with ventricular rate < 45 beats per minute or atrial fibrillation/flutter with ventricular response of > 160 beats per minute).
• Severe renal failure defined as creatinine clearance < 30 mL/min as estimated by both the Cockcroft-Gault and the Modification of Diet in Renal Disease (MDRD) equations.
• Significant pulmonary disease (history of oral daily steroid dependency, history of CO2 retention or need for intubation for acute exacerbation, or currently receiving IV steroids).
• Any organ transplant recipient, currently listed (anticipated in the next 60 days) for transplant, or admitted for cardiac transplantation.
• Major surgery within 30 days.
• Major neurologic event, including cerebrovascular events in the prior 60 days.
• Acute myocarditis or hypertrophic obstructive, restrictive, or constrictive cardiomyopathy (not including restrictive mitral filling patterns).
• Known hepatic impairment
• Received an investigational drug within 30 days prior to screening.
• Women who are pregnant or breastfeeding.
• Known hypersensitivity or allergy to natriuretic peptide or its components, nesiritide, other natriuretic peptides or related compounds.
• Any condition which, in the opinion of the Investigator, could interfere with, or for which the treatment might interfere with the conduct of the study, or which would unacceptably increase the risk of the patient's participation in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	24 hrs of SQ placebo infusion
SQ Bolus Cenderitide	Cenderitide	-
SQ Infusion Cenderitide	Cenderitide	24 hour SQ infusion of cenderitide

Primary Outcome Measures

Name	Time	Method
Pharmacokinetics (PK)	Up to 36 hours	Pharmacokinetic measurements of subcutaneous cenderitide infusion compared with a subcutaneous bolus administration

Secondary Outcome Measures

Name	Time	Method
Pharmacodynamics (PD)	Up to 36 hours	Pharmacodynamics, safey and tolerability will be measured by BP, heart rate, and plasma cGMP after administration.

Trial Locations

Locations (5)

Analab Clinical Research, Inc.; 🇺🇸 Lenexa, Kansas, United States

Hennepin County Medical Center; 🇺🇸 Minneapolis, Minnesota, United States

Orange County Research Center; 🇺🇸 Tustin, California, United States

Jacksonville Center for Clinical Research; 🇺🇸 Jacksonville, Florida, United States

Benchmark Research; 🇺🇸 Metairie, Louisiana, United States