Pharmacoscintigraphic Investigation Into the Absorption of Nevirapine When Released Into Different Parts of the Gastro-intestinal Tract in Healthy Males

NCT ID: NCT02191189

Last Updated: 2014-07-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-05-31

Brief Summary

Study to determine the absorption of Nevirapine from different regions of the Gastro Intestinal tract.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment A, p.o.

50 mg Nevirapine administered orally in 100 mL water

Group Type: ACTIVE_COMPARATOR

Nevirapine suspension

Intervention Type: DRUG

Treatment B, ascending colon

50 mg Nevirapine administered to the ascending colon via Enterion™ capsule

Group Type: EXPERIMENTAL

Nevirapine suspension, into Enterion™ capsule

Intervention Type: DRUG

Treatment C, jejunum

50 mg Nevirapine administered to the jejunum via Enterion™ capsule

Group Type: EXPERIMENTAL

Nevirapine suspension, into Enterion™ capsule

Intervention Type: DRUG

Treatment D, ileum

50 mg Nevirapine administered to the ileum via Enterion™ capsule

Group Type: EXPERIMENTAL

Nevirapine suspension, into Enterion™ capsule

Intervention Type: DRUG

Treatment E, descending colon

50 mg Nevirapine administered to the descending colon via Enterion™ capsule

Group Type: EXPERIMENTAL

Nevirapine suspension, into Enterion™ capsule

Intervention Type: DRUG

Interventions

Nevirapine suspension, into Enterion™ capsule

Intervention Type: DRUG

Nevirapine suspension

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Healthy males according to the following criteria: complete medical history, including the physical examination, vital signs (Blood Pressure (BP), Pulse Rate (PR)), 12-lead electrocardiogram (ECG), clinical laboratory tests
• Aged 18-65 years
• Body Mass Index of between 18 and 35 kg/m2
• Subjects must be able to demonstrate ability to swallow an empty size 000 gelatin capsule
• Must be willing and able to participate in the whole study
• Must be able to provide signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local legislation

Exclusion Criteria

• Participation in a clinical research study involving investigational drugs or dosage forms within the previous 3 months
• Those who are unable/unwilling to consume all the components of a standard meal or gelatine
• Subjects who have ever self referred or who have been referred to a physician or counsellor for abuse or misuse of alcohol, non-medical, medicinal drugs or other substance abuse e.g. solvents
• Any current or previous use of Class A drugs such as opiates, cocaine, ecstasy, lysergic acid diethylamide (LSD), and amphetamines (Class B unless prepared for injection, in which case amphetamines are Class A)
• Volunteers that admit to occasional past use of cannabis will not be excluded as long as they have a negative drugs of abuse test and have been abstinent for at least 12 months
• Positive drugs of abuse test result
• Regular alcohol consumption in males >= 21 units per week. (1 Unit = ½ pint beer, a 25 mL shot of 40% spirit or a 125 mL glass of wine)
• Smoking of more than 10 cigarettes per day or equivalent (e.g. pipe, cigar, chewing tobacco)
• A breath carbon monoxide reading of greater than 20 ppm
• Inability to refrain from smoking for the duration of each study period
• Radiation exposure from clinical trials, including that from the present study and from diagnostic X-rays but excluding background radiation, exceeding 5 Millisieverts (mSv) in the last twelve months or 10 mSv in the last five years. No occupationally exposed worker, as defined in the Ionising Radiation Regulations 1999, shall participate in the study
• Clinically significant abnormal biochemistry, haematology or urinalysis, as judged by the Investigator
• Liver function laboratory test (LFT) results outside the upper normal range. Subjects with LFTs > grade 1 will not be included
• History of gastrointestinal surgery, with the exception of appendicectomy unless it was performed within the previous 12 months
• History of clinically significant cardiovascular, renal, hepatic, respiratory and particularly gastrointestinal disease, especially peptic ulceration, gastrointestinal bleeding, ulcerative colitis, Crohn's disease or Irritable Bowel Syndrome
• History of chronic or acute infections
• Diseases of the central nervous system (such as epilepsy) and psychiatric or neurological disorders
• Acute diarrhoea or constipation in the 7 days before the predicted first study day. If screening occurs >14 days before first study day, this criterion to be determined on first study day. Diarrhoea will be defined as the passage of liquid faeces and/or a stool frequency of greater than three times per day. Constipation will be defined as a failure to open the bowels more frequently than every other day
• Donation of blood within the previous three months
• Presence of non-removable metal objects such as metal plates, screws etc, in the abdominal region of the body
• Subjects will be excluded from the study if they are considered by the investigator to be at risk of transmitting through blood and other body fluids the agents responsible for AIDS (Acquired Immunodeficiency Syndrome) or other sexually transmitted disease or hepatitis. This will be achieved by the use of a card (similar to that used by the National Blood Transfusion Service), which asks a potential subject if they have reason to believe that they may fall into any category included on the card. If the verbal answer is in the affirmative then they will be excluded from the study.
• Positive hepatitis B virus (HBV), hepatitis C virus (HCV) or HIV test results
• Subjects receiving prohibited medication. Subjects must not stop taking a prescribed medication for the purpose of entering the study.
• Failure to satisfy the Principal Medical Investigator of fitness to participate for any other reason

As a precaution, male subjects will be instructed to use appropriate barrier method contraception (e.g. condoms and spermicide) during the time interval between taking the first dose and three months following the last dose. Subjects will be advised to inform Pharmaceutical Profiles if their partner becomes pregnant within three months of them receiving the last dose of the study drug. Pharmaceutical Profiles will monitor the pregnancy to conclusion.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Boehringer Ingelheim

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

1100.1484

Identifier Type: -

Identifier Source: org_study_id