Pharmacokinetics in Subjects With Renal Impairment

Renal Impairment Clinical Trial

Official title:

A Phase I, Open-label, Parallel-group, Mono-center Trial to Investigate the Pharmacokinetics of a Single Intravenous Dose of Cilengitide in Subjects With Mild, Moderate or Severe Renal Impairment Compared to Subjects With Normal Renal Function

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01504165
• Other study ID #: EMR062041_016
• Secondary ID: 2011-002389-19
• Status: Completed
• Phase: Phase 1
• First received: January 3, 2012
• Last updated: February 3, 2014
• Start date: January 2012
• Est. completion date: April 2012

Study information

• Verified date: February 2014
• Source: Merck KGaA
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationGermany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

This is an open-label, non-randomized, parallel-group, mono-center, single intravenous dose, Phase I trial to investigate the Pharmacokinetic (PK) and safety of cilengitide in subjects with different grades of renal impairment as compared to subjects with normal renal function.

Description:

Subjects with impaired renal function will be screened and will be stratified by their estimated glomerular filtration rate (GFR) according to the Modification of Diet in Renal Disease (MDRD) equation and assigned to one of the stratification groups defined below:

Group Number/Renal function/Creatinine Clearance (GFR according to MDRD)

1. Normal renal function (≥ 90 mL/min)

2. Mild renal impairment (60 - 89 mL/min)

3. Moderate renal impairment (30 - 59 mL/ min) 4a: Severe renal impairment (< 30 mL/min) - no dialysis required 4b: (if applicable) Severe renal impairment (< 30 mL/min) - no dialysis required

Subjects in Groups 2 and 3 will receive a single dose of 2000mg of cilengitide as 1-hour i.v. infusion. Subjects from group 4a will receive a single dose of 1000mg of cilengitide as 1-hour i.v. infusion . PK samples will be collected and basic PK parameters will be calculated. The safety, tolerability, and PK will be evaluated by the Safety Monitoring Committee (SMC). If the SMC has no concerns, Group 4b will be treated with a higher dose (up to 2000mg) of cilengitide. Then, Group 1 (healthy subjects) will be started after the last subject with renal impairment (in either Group 2, 3, or 4a; or in Group 4b, if applicable) has completed all activities on Day 3. They will also receive a single dose of 2000mg of cilengitide as 1-hour i.v. infusion.

The duration of the trial from the first subject enrolled to the last subject last visit will be approximately 6 months (approximately 8 months, in case Group 4b is included). Each subject will participate in the trial for up to 35 days, including screening and the end of trial examination.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: April 2012
• Est. primary completion date: April 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Body mass index (BMI): = 18 kg/m² and = 35 kg/m²

For subjects with normal renal function:

• Vital signs (pulse rate and blood pressure) within the normal range or showing no clinically relevant deviation

• Estimated creatinine clearance according to the MDRD equation of = 90 mL/min at Screening

For subjects with impaired renal function:

• Laboratory parameters should be within acceptable range for subjects with renal impairment,

• Vital signs: Pulse rate within the normal range of 45-100 beats/minute in supine position after 5 minutes of rest. Blood pressure diastolic below 100 mmHg, and systolic below 160 mmHg for Groups 1-3 and below 180 mmHg for Group 4a and 4b, in supine position after 5 minutes of rest

• Calculated creatinine clearance according to the MDRD equation of < 90 mL/min at Screening and the possibility of stratification to one of the Groups.

Exclusion Criteria:

• History of malignant disease within the last 5 years or acute malignant disease

• Medical history of wound healing problems and/or any current open wounds

• Current or history of bleeding disorders and/or history of thromboembolic events (considering family history as well); thrombolytics or oral or parenteral anticoagulants within 30 days prior to Day 1

• Electrocardiogram recording (12-lead ECG) with signs of clinically relevant pathology as judged by the Investigator

For subjects with impaired renal function:

• Chronic heart failure non stabilized (New York Heart Association [NYHA] class III and IV)

• Acute renal failure of any etiology (including viral, toxic, or drug induced)

• Requiring dialysis

• History of renal transplantation

• Uncontrolled diabetes mellitus as judged by the Investigator

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Renal Impairment
• Renal Insufficiency

Intervention

Drug:
• cilengitide 2000mg
A single dose of cilengitide 2000mg (250mL) will be administered as 1-hour i.v. infusion on Day 1
• cilengitide 2000mg
A single dose of cilengitide 2000mg (250mL) will be administered as 1-hour i.v. infusion on Day 1
• cilengitide 2000mg
A single dose of cilengitide 2000mg (250mL) will be administered as 1-hour i.v. infusion on Day 1
• cilengitide 1000mg
A single dose of cilengitide 1000mg (125mL) will be administered as 1-hour i.v. infusion on Day 1
• cilengitide > 1000mg and up to 2000mg
A single dose of cilengitide > 1000mg and up to 2000mg will be administered as 1-hour i.v. infusion on Day 1 if applicable, based on Safety Monitoring Committee decision

Locations

Country	Name	City	State
Germany	For Research Sites contact Merck KGaA Communication Center in	Darmstadt
Germany	CRS Clincial Research Services Kiel GmbH	Kiel

Sponsors (1)

Lead Sponsor	Collaborator
Merck KGaA

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Peak Plasma Concentration (Cmax) of cilengitide in plasma	Cmax of cilengitide in plasma after single dose in groups of subjects with different grades of renal function compared to subjects with normal renal function.	48 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Primary	Area under the plasma concentration versus time curve (AUC) of cilengitide in plasma	AUC of cilengitide in plasma after single dose in groups of subjects with different grades of renal function compared to subjects with normal renal function.	48 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Terminal half life t1/2 of cilengitide		48 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Plasma clearance of cilengitide (CL)		48 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Cilengitide volume of distribution (Vz) in plasma		48 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Absolute and relative amount of cilengitide excreted into urine (Ae0-8)		24 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Renal clearance of cilengitide (CLR)		24 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No
Secondary	Plasma-protein-binding: Fraction unbound of cilengitide		2 hours after start of infusion of 1 single dose of cilengitide administered as 1-hour intravenous infusion	No