- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02319057
Pharmacokinetic Study of Single Doses of ORM-12741 (Nebula PK 1)
Pharmacokinetic Study of Modified Release Formulations and an Immediate Release Formulation of ORM-12741 After Single Oral Doses
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
-
-
-
Turku, Finlandia
- Clinical Research Services Turku, CRST
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Written informed consent (IC) obtained.
- Good general health ascertained by detailed medical history and physical examination.
- Females and males between 18 and 65 years of age (inclusive).
- Body mass index (BMI) between 18-30 kg/m2 (inclusive, BMI = weight/height2).
- Weight of 50-100 kg (inclusive).
- Regular intestinal transit (no recent history of recurrent constipation, diarrhoea, or other intestinal problems).
Exclusion Criteria:
- Predicted poor compliance or inability to communicate well with the investigator or the study centre personnel.
- Veins unsuitable for repeated venipuncture or cannulation.
- Evidence of clinically significant cardiovascular, renal, hepatic, haematological, gastrointestinal, pulmonary, metabolic-endocrine, neurological, urogenital or psychiatric disease as judged by the investigator.
- 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.
- Susceptibility to severe allergic reactions.
- 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.
- 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).
- Current use of nicotine-containing products more than 5 cigarettes or equivalent/day.
- Inability to refrain from using nicotine-containing products during the stay at the study centre.
- 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.
- Blood donation or loss of significant amount of blood within 3 months prior to the first study treatment administration.
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.
- HR < 45 beats/minute or > 100 beats/minute after a 10-minute rest in supine position at the screening visit.
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.
- 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.
- History of drug abuse or positive result in drug abuse test.
- Positive serology to human immunodeficiency virus antibodies (HIVAgAb), hepatitis C virus antibodies (HCVAb) or hepatitis B surface antigen (HBsAg).
- 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).
- 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.
- 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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: Panel 1
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Sperimentale: Panel 2
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Sperimentale: Panel 3
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Sperimentale: Panel 4
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Sperimentale: Panel 5
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Sperimentale: Panel 6
Adaptive design: Each subject will receive 1-4 single doses of ORM-12741 including various dose levels of ORM-12741 MR A, ORM-12741 MR B, ORM-12741 IR or combination of these
|
Formulazione a rilascio modificato di ORM-12741
Formulazione a rilascio modificato di ORM-12741
Immediate release formulation of ORM-12741
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Pharmacokinetics
Lasso di tempo: Blood samples collected frequently on day 1 and once or twice a day for 4 days
|
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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Safety measures, i.e. assessing adverse events, vital signs, ECG, safety laboratory values
Lasso di tempo: 24 hours per period
|
adverse events, vital signs, ECG, safety laboratory values
|
24 hours per period
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- 3098011
- 2014-000193-19 (Numero EudraCT)
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su ORM-12741 SIGNOR A
-
Orion Corporation, Orion PharmaCompletato
-
Orion Corporation, Orion PharmaCompletato
-
Orion Corporation, Orion PharmaCompletato
-
Orion Corporation, Orion PharmaCompletato
-
Orion Corporation, Orion PharmaJanssen PharmaceuticalsCompletatoIl morbo di AlzheimerFinlandia
-
Orion Corporation, Orion PharmaCompletato
-
Orion Corporation, Orion PharmaCompletatoVolontari maschi saniOlanda
-
Orion Corporation, Orion PharmaCompletato
-
University of Cape TownUniversity of Oxford; Orion Corporation, Orion PharmaCompletatoVolontariato sanoSud Africa