Effect of Ceftobiprole on Human Intestinal Microflora

Drug Resistance Clinical Trial

Official title:

Effect of Ceftobiprole on the Intestinal Human Microflora Following Multiple-dose Administration in Healthy Female and Male Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00965042
• Other study ID #: CR016306
• Secondary ID: BAC-1002
• Status: Completed
• Phase: Phase 1
• First received: August 21, 2009
• Last updated: July 27, 2012
• Start date: April 2009
• Est. completion date: June 2009

Study information

• Verified date: July 2012
• Source: Basilea Pharmaceutica
• Contact: n/a
• Is FDA regulated: No
• Health authority: Belgium: Ministry of Social Affairs, Public Health and the EnvironmentSweden: Medical Products Agency
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to investigate the effect of ceftobiprole treatment on intestinal microflora in healthy volunteers.

Description:

This is an open-label, single center study to investigate the effect on human intestinal microflora of multiple doses of ceftobiprole treatment administered at 8 hours intervals for 7 consecutive days. Careful investigation of the effect of Ceftobiprole treatment on the intestinal microflora is of importance since alteration of the intestinal microflora balance may facilitate colonization by pathogenic bacteria strains or enable microorganisms already present in the normal microflora to develop resistance. A total of 7 fecal samples will be collected on day 2, 4, 7, 10, 14 and 21 for determination of ceftobiprole concentration in fecal, intestinal microflora pattern and measuring the susceptibility for Ceftobiprole of isolated bacterial strains. A total of 13 plasma samples will be collected on day 1, 4, 7, 10, 14 and 21 for determination of ceftobiprole concentration in plasma. Safety evaluations including physical examination, vital signs, clinical laboratory tests, electrocardiogram and adverse event monitoring will be performed throughout the study. 500 mg ceftobiprole, intravenous infusion over 120 minutes, every 8 hours for 7 consecutive days

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: June 2009
• Est. primary completion date: May 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Healthy volunteers with body weight >= 50 kg and body mass index between 18 and 30

• Agree to remain hospitalized at the trial unit during the 7-day drug administration period and will only leave the trial unit under supervision of a study nurse twice a day for one hour maximum

• Refrain from excessive jogging and any strenuous exercise during the study

• Be able to adhere to the dietary, fluid and smoking restrictions during the study

• Have negative pregnancy test result at the screening and agree to use adequate contraception method and not to become pregnant or donate sperm throughout the study

Exclusion Criteria:

• No clinically significant medical illness, abnormal findings in physical examination, vital signs, laboratory tests and electrocardiogram, or known allergy to the study drug, cephalosporins, beta-lactam antibiotics or other clinically significant allergies requiring treatment

• No antibiotic treatment within the last 3 months

• No drug or alcohol abuse within the last 5 years

• No blood donation or substantial loss of blood of more than 500 ml within the last 3 months or intention to donate blood during the study or within 1 month after study completion

• No history of smoking of more than 10 cigarettes , or 2 cigars, or 2 pipes of tobacco or 5 sniffs per day within the last 3 months

Study Design

Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Antimicrobial Agent
• Cephalosporins
• Drug Resistance

Intervention

Drug:
• Ceftobiprole
ceftobiprole 500 mg by intravenous infusion every 8 hours for 7 days

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Basilea Pharmaceutica

References & Publications (1)

Bäckström T, Panagiotidis G, Beck O, Asker-Hagelberg C, Rashid MU, Weintraub A, Nord CE. Effect of ceftobiprole on the normal human intestinal microflora. Int J Antimicrob Agents. 2010 Dec;36(6):537-41. doi: 10.1016/j.ijantimicag.2010.07.021. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bacterial strains and numbers in feces; Minimum inhibitory concentrations for ceftobiprole for isolated resistant strains		Day 2, 4, 7, 10, 14 and 21	No
Secondary	Fecal concentration of ceftobiprole		Day 2, 4, 7, 10, 14 and 21	No
Secondary	Plasma Concentration of ceftobiprole		Day 1, 4, 7, 10, 14, and 21	No