- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02125578
A Multiple Dose Safety Study of PEG-IFN in Healthy Volunteers
25. april 2014 oppdatert av: Biogen
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Multiple-Dose, Dose-Ranging, Parallel-Group Study of PEGylated Interferon Beta-1a (BIIB017) in Healthy Volunteers
The primary objectives are to identify the highest safe and well-tolerated dose and frequency of BIIB017 (PEGylated Interferon Beta-1a) subcutaneous (SC), within the range of 63 to 188 mcg, when given every other week or every 4 weeks to healthy volunteers (HV).
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
69
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Arizona
-
Phoenix, Arizona, Forente stater
- Research Site
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 45 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Key Inclusion Criteria:
- Body Mass Index (BMI) of 18 to 35 kg/m2, inclusive, and a minimum body weight of 50.0 kg at screening.
- All male subjects and female subjects of child-bearing potential must be willing and able to practice effective birth control during the study and be willing and able to continue contraception for 30 days after their last dose of study treatment.
Key Exclusion Criteria:
- Abnormal screening and baseline blood and urine tests determined to be clinically significant by the Investigator.
- Hematologic or hepatic enzyme laboratory values that were outside the normal range.
- History of severe allergic or anaphylactic reactions.
- History of any clinically-significant (as determined by the Investigator) cardiac, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other major disease, and/or history of seizure disorder.
- A family history of MS in a first-degree relative.
- A fever (body temperature >38°C) or symptomatic viral or bacterial infection (including upper respiratory infection) within 1 week prior to Day 1.
- Abnormal ECG values as determined by the Investigator.
- Positive test result for hepatitis C antibody, hepatitis B surface antigen (HBsAg), or human immunodeficiency virus (HIV) antibody.
- Female subjects who are considering pregnancy, currently pregnant or breastfeeding.
- Subjects who received a tattoo or body piercing (including earring) within 60 days of baseline or subjects who are considering getting a tattoo or body piercing (including earring) in the next 60 days.
- Use of any prescription or non-prescription medication that could inhibit bone marrow or liver function.
- Any previous treatment with any interferon product.
- Participation in any other investigational drug study within the 4 weeks prior to Day 1 or within 5 half-lives of the investigational treatment, whichever is longer.
- Treatment with the Flu Vaccine within 1 week prior to Day 1.
NOTE: Other protocol-defined inclusion/exclusion Criteria May Apply
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: BIIB017 (PEGylated Interferon Beta-1a)
Varying doses (63 mcg up to 188 mcg) of BIIB017 will be administered SC every other week for a total of 6 weeks.
|
Each participant will receive BIIB017 every other week or every 4 weeks.
|
|
Eksperimentell: BIIB017 (PEGylated Interferon Beta-1a) and Placebo
Varying doses (63 mcg up to 188 mcg) of BIIB017 will be administered SC every 4 weeks for a total of 6 weeks.
To ensure blinding, each subject will receive placebo every other week.
|
Each participant will receive BIIB017 every other week or every 4 weeks.
Each participant will receive placebo every other week or every 4 weeks.
|
|
Placebo komparator: Placebo
Placebo dose will be administered SC every other week for a total of 6 weeks.
|
Each participant will receive BIIB017 every other week or every 4 weeks.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The number of participants that experience Adverse Events (AEs)
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
The number of participants that experience flu-like symptoms
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
Participant assessment of injection site pain as measured by scores on a scale of 0 to 10, where 0 is no pain and 10 is extremely painful.
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
Clinician assessment of the injection site for erythema as assessed by a scale 0 to 3, where 0 represents no erythema and 3 represents severe erythema
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
Clinician assessment of the injection site for induration as assessed by a scale 0 to 3, where 0 represents no induration and 3 represents severe induration
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
Clinician assessment of tenderness to digital pressure at the injection site will be assessed on a scale of 0 to 3, where 0 represents no tenderness and 3 represents severe tenderness
Tidsramme: Up to Day 71
|
Up to Day 71
|
|
Clinician assessment of temperature at the injection site will be assessed on a scale of 0 to 2, where 0 represents normal temperature and 2 represents hot.
Tidsramme: Up to Day 71
|
Up to Day 71
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
AUC168h, area under the concentration-time curve
Tidsramme: Up to 168 hours post dose
|
Up to 168 hours post dose
|
|
Cmax, observed maximum serum concentration
Tidsramme: Up to 336 hours post-dose
|
Up to 336 hours post-dose
|
|
Tmax, time to reach maximum serum concentration
Tidsramme: Up to 336 hours post-dose
|
Up to 336 hours post-dose
|
|
Terminal t½, half-life of the terminal phase
Tidsramme: Up to 336 hours post-dose
|
Up to 336 hours post-dose
|
|
EAUC-336h, area under the concentration-time curve from time zero to 336 hours post-dose
Tidsramme: Up to 336 hours post-dose
|
Up to 336 hours post-dose
|
|
Emax, the peak concentration observed minus baseline concentration
Tidsramme: Day 1 and Day 29
|
Day 1 and Day 29
|
|
PD parameters of serum concentrations of neopterin
Tidsramme: Day 1 and Day 29
|
Day 1 and Day 29
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2008
Primær fullføring (Faktiske)
1. mai 2008
Studiet fullført (Faktiske)
1. mai 2008
Datoer for studieregistrering
Først innsendt
25. april 2014
Først innsendt som oppfylte QC-kriteriene
25. april 2014
Først lagt ut (Anslag)
29. april 2014
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
29. april 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
25. april 2014
Sist bekreftet
1. april 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 105HV102
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .