- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT00457418
High-Dose PEG-Intron Pharmacokinetic Study in Patients With Melanoma (Study P04831 AM2)
A Pharmacokinetic Study of PEG-Intron, Administered Weekly in Subjects With High-Risk Melanoma
Přehled studie
Typ studie
Zápis (Aktuální)
Fáze
- Fáze 1
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
- Subjects at least 18 years of age, of either sex, and of any race.
- Cytologically or histologically-confirmed melanoma, arising from a cutaneous or unknown site of origin, at Stages IIB, IIC, IIIA, IIIB, IIIC according to the American Joint Committee on Cancer (AJCC) 2001 guidelines.
- Adequate hepatic, renal and bone marrow function within 4 weeks prior to initiation of study treatment.
- Subjects presenting with synchronous primary and regional melanoma must have had adequate surgical margins surrounding the primary lesion.
- Full lymphadenectomy must be performed within 90 days prior to initiation of study treatment.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Give informed consent according to International Conference on Harmonisation - Good Clinical Practice (ICH-GCP) and national/local policy.
- Be able to adhere to dose and visit schedules.
- Female subjects of childbearing potential must be using a medically accepted method of birth control prior to Screening and agree to continue its use during the study or be surgically sterilized.
- Female subjects of childbearing potential must have a negative serum pregnancy test at Screening.
Exclusion Criteria:
- Female subjects who are pregnant, intend to become pregnant, or are breastfeeding.
- Previous treatment with interferon alpha, chemotherapy or immunotherapy for melanoma.
- Ocular melanoma, or melanoma of the mucous membranes.
- Evidence of distant or non-regional lymph node metastases.
- In-transit melanoma, even if the lesion has been resected.
- Disease that cannot be completely surgically resected.
- Lack of recovery from recent surgery.
- Prior malignancy within the past 5 years, except surgically cured squamous cell carcinoma of the skin, successfully resected early stage cutaneous melanoma, or cervical carcinoma in situ.
- Severe cardiovascular disease.
- Thyroid dysfunction not responsive to therapy.
- Uncontrolled diabetes mellitus (in the opinion of the investigator).
- Active autoimmune disease.
- Active and/or uncontrolled infection.
- History of seropositivity for human immunodeficiency virus (HIV).
- Pre-existing psychiatric condition.
Clinical diagnosis of substance abuse of one or more of the following drugs within the following timeframes (excluding time spent in detoxification, hospitalization or incarceration):
- Alcohol, intravenous drug use, inhalational, psychotropics, narcotics, cocaine, prescription or over-the-counter drugs: within 1 year of the Screening visit.
- Methadone, buprenorphine hydrochloride (HCl), and/or butorphanol tartrate: within 1 year of Screening visit, unless subject has drug screen negative for other (non-narcotic) drugs documented in the past year and repeated negative within 2 months of Screening visit.
- Multi-drug abuse (2 or more substances in 16a and 16b): within 3 years of Screening visit.
Marijuana:
- If historic use is deemed excessive by the principal investigator (or medically qualified individual), or is interfering with the subject's life, then the subject is not eligible and should not be screened.
- If marijuana use is not deemed excessive by principal investigator and does not interfere with life, subject must discontinue any current use of marijuana prior to entry into study.
- Medical condition requiring chronic systemic corticosteroids.
- Known allergy to the drug substance or any of the excipients in the PEG-Intron formulation.
- Any situation or condition that, in the opinion of the investigator, may interfere with optimal participation in the study.
- Use of any investigational drugs within 30 days of study entry.
- Participation in other clinical studies of investigational treatments.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: PEG-Intron
6 ug/kg/week, SC (first 8 weeks) 3 ug/kg/week, SC (252 weeks [weeks 9-260], maintenance) |
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Area Under the Curve (AUC) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
AUC was defined as the actual body exposure to drug after administration of a dose of the drug.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
|
Maximum Serum Concentration (Cmax) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
Cmax was defined as observed maximum plasma concentration.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
|
Average Concentration Within the Dosing Interval (Cavg) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
Cavg was defined as average plasma concentration.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
|
Minimum Serum Concentration (Cmin) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
Cmin was defined as observed minimum plasma concentration.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
|
Observed Time to Achieve Cmax (Tmax) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
Tmax was defined as time of maximum plasma concentration.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
|
Apparent Clearance(CL/F) of PEG-Intron at 12 Weeks
Časové okno: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
CL/F was defined apparent clearance - the volume of plasma in the vascular compartment cleared of drug per unit of time and per kilogram of body weight by the processes of metabolism and excretion.
|
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Number of Participants Who Experienced an Adverse Event (AE)
Časové okno: Entire study duration (up to 5 years)
|
An adverse event (AE) was defined as any untoward medical occurrence or unfavorable and unintended sign in a subject administered a pharmaceutical product, biologic (at any dose), or medical device, whether or not considered related to the use of that product.
|
Entire study duration (up to 5 years)
|
Spolupracovníci a vyšetřovatelé
Sponzor
Publikace a užitečné odkazy
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
Další identifikační čísla studie
- P04831
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Popis plánu IPD
http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final_Updated%20July_9_2014.pdf
http://engagezone.msd.com/ds_documentation.php
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