Pharmacokinetic Study of Single Doses of ORM-12741

Healthy Clinical Trial

— Nebula PK 1  

Official title:

Pharmacokinetic Study of Modified Release Formulations and an Immediate Release Formulation of ORM-12741 After Single Oral Doses

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02319057
• Other study ID #: 3098011
• Secondary ID: 2014-000193-19
• Status: Completed
• Phase: Phase 1
• First received: October 6, 2014
• Last updated: May 5, 2015
• Start date: September 2014
• Est. completion date: February 2015

Study information

• Verified date: May 2015
• Source: Orion Corporation, Orion Pharma
• Contact: n/a
• Is FDA regulated: No
• Health authority: Finland: Finnish Medicines Agency
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate ORM-12741 concentrations in the blood after different study drug formulations

Description:

The purpose of this study is to evaluate the pharmacokinetics and safety of single doses of modified release formulations and a immediate release formulation of ORM-12741

Recruitment information / eligibility

• Status: Completed
• Enrollment: 23
• Est. completion date: February 2015
• Est. primary completion date: February 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Written informed consent (IC) obtained.

2. Good general health ascertained by detailed medical history and physical examination.

3. Females and males between 18 and 65 years of age (inclusive).

4. Body mass index (BMI) between 18-30 kg/m2 (inclusive, BMI = weight/height2).

5. Weight of 50-100 kg (inclusive).

6. Regular intestinal transit (no recent history of recurrent constipation, diarrhoea, or other intestinal problems).

Exclusion Criteria:

1. Predicted poor compliance or inability to communicate well with the investigator or the study centre personnel.

2. Veins unsuitable for repeated venipuncture or cannulation.

3. Evidence of clinically significant cardiovascular, renal, hepatic, haematological, gastrointestinal, pulmonary, metabolic-endocrine, neurological, urogenital or psychiatric disease as judged by the investigator.

4. Any condition requiring regular concomitant treatment (including vitamins and herbal products) or likely to need any concomitant treatment during the study. Hormonal contraception and hormone replacement therapy are allowed.

5. Susceptibility to severe allergic reactions.

6. Intake of any medication that could affect the outcome of the study, within 2 weeks prior to the first study treatment administration or less than 5 times the half-life of the medication. Possible enzyme inducing drugs will be discussed case-by-case with the sponsor.

7. Regular consumption of more than 21 units of alcohol per week for males and 16 units per week for females (1 unit = 4 cl spirits, about 13 g of alcohol).

8. Current use of nicotine-containing products more than 5 cigarettes or equivalent/day.

9. Inability to refrain from using nicotine-containing products during the stay at the study centre.

10. Inability to refrain from consuming caffeine-containing beverages during the stay at the study centre, e.g. propensity to develop headaches when refraining from caffeine-containing beverages.

11. Blood donation or loss of significant amount of blood within 3 months prior to the first study treatment administration.

12. Any clinically significant 12-lead electrocardiogram (ECG) abnormality after a 10-minute rest in supine position at the screening visit, as judged by the investigator. For example:

• QTc (calculated with the Bazett's formula) > 470 msec for females and 450 msec for men.

13. HR < 45 beats/minute or > 100 beats/minute after a 10-minute rest in supine position at the screening visit.

14. At the screening visit systolic blood pressure (BP) < 90 mmHg or > 150 mmHg after a 10- minute rest in supine position, diastolic BP < 50 mmHg or > 90 mmHg after a 10-minute rest in supine position, or symptomatic orthostatic hypotension, or

• decrease of = 20 mmHg of systolic BP or

• decrease of = 10 mmHg of diastolic BP after 3 minutes in standing position.

15. Any abnormal value in laboratory tests, or vital signs, or physical examination finding, which in the opinion of the investigator could interfere with the interpretation of the test results or cause a health risk for the subject if he takes part in the study.

16. History of drug abuse or positive result in drug abuse test.

17. Positive serology to human immunodeficiency virus antibodies (HIVAgAb), hepatitis C virus antibodies (HCVAb) or hepatitis B surface antigen (HBsAg).

18. Females of childbearing potential if they are not using proper contraception (hormonal contraception, intrauterine device [IUD] or surgical sterilization, spermicidal foam in conjunction with condom on male partner) during the study. Use of oral/hormonal contraception alone is not acceptable. (Note: women of childbearing potential with no current heterosexual relationship can be included without contraception according to the judgement of the investigator).

19. Any other condition that in the opinion of the investigator would interfere with the evaluation of the results or constitute a health risk for the study subject.

20. Participation in a clinical drug study within 3 months prior to the first study treatment administration of this study or earlier participation in a clinical study with ORM-12741.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• ORM-12741 MR A
Modified release formulation of ORM-12741
• ORM-12741 IR
Immediate release formulation of ORM-12741
• ORM-12741 MR B
Modified release formulation of ORM-12741

Locations

Country	Name	City	State
Finland	Clinical Research Services Turku, CRST	Turku

Sponsors (1)

Lead Sponsor	Collaborator
Orion Corporation, Orion Pharma

Country where clinical trial is conducted

Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pharmacokinetics	Explore the PK profile (e.g. Cmax, tmax, AUC, t1/2) and determine protein binding	Blood samples collected frequently on day 1 and once or twice a day for 4 days	No
Secondary	Safety measures, i.e. assessing adverse events, vital signs, ECG, safety laboratory values	adverse events, vital signs, ECG, safety laboratory values	24 hours per period	Yes