- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT01886287
P:II Above-Label Octreotide-LAR With Insufficiently Controlled Carcinoid Syndrome
Phase II Study of Above-Label Octreotide-LAR in Patients With Insufficiently Controlled Carcinoid Syndrome
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The study population will consist of patients with advanced (metastatic or unresectable) neuroendocrine tumors with suboptimally controlled carcinoid syndrome. While the majority of patients will have primary tumors of the ileocecum (midgut), any serotonin-producing neuroendocrine tumors will be eligible (including pancreatic, lung and unknown primary).
All patients will be followed for adverse events and serious adverse events for 28 days following the last dose of above-label octreotide, or until resolution or stabilization of the event, whichever comes first.
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 2
Contacten en locaties
Studie Locaties
-
-
Florida
-
Tampa, Florida, Verenigde Staten, 33612
- H. Lee Moffitt Cancer Center and Research Institute
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Metastatic neuroendocrine tumors that are considered well or moderately differentiated (or low to intermediate grade). Patients with poorly differentiated neuroendocrine carcinomas or small cell carcinomas are excluded from the study.
- Elevated urine 5-hydroxyindoleacetic acid (5-HIAA)
- More than 2 bowel-movements per day OR more than 4 flushing episodes per week on average
- Patient currently on octreotide LAR 30mg every 3 or 4 weeks (for at least 3 cycles prior to screening)
- Age ≥ 18 years
- Minimum of four weeks since any major surgery, liver-directed therapy (embolization, etc.) or systemic cancer treatment other than octreotide LAR
- Eastern Cooperative Oncology Group (ECOG) performance status ≤2
- Life expectancy > 12 weeks
- Reliable contraception should be maintained throughout the study and for 3 months after study drug discontinuation.
- Signed informed consent to participate in the study must be obtained from patients after they have been fully informed of the nature and potential risks by the investigator (or his/her designee) with the aid of written information.
Exclusion Criteria:
- Known hypersensitivity to somatostatin analogues
- Patients with poorly differentiated neuroendocrine cancers
- Patients with liver cirrhosis
- Patients receiving hemodialysis or peritoneal dialysis
- Patients with cachexia who, in the opinion of the investigator, may have difficulty tolerating intramuscular injection
- Patients with symptomatic cholelithiasis or biliary events within past five years (who have not undergone cholecystectomy)
- Patients with recent history (within 5 years) of pancreatitis
- Patients with uncontrolled diabetes (HgA1c >8.0 despite adequate therapy)
- Women of child-bearing potential, UNLESS they are using two birth control methods
- Women who are pregnant or lactating
- HIV positive patients
- History of sustained ventricular tachycardia, ventricular fibrillation, advanced heart block, idiopathic syncope thought to be related to ventricular arrhythmia, or congenital long QT syndrome
- Risk factors for Torsades de Pointes such as cardiac failure, clinically significant/symptomatic bradycardia
- Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study
- History of noncompliance to medical regimens or unwillingness to comply with the protocol
- Patients who were unable to tolerate or did not benefit from above-label dose octreotide (>30mg) in the past
- Concomitant use of other cancer treatments or carcinoid syndrome treatments (whether standard or experimental). Patients should discontinue any concomitant cancer medications more than two weeks prior to screening.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Octreotide Long-acting Release (LAR)
Octreotide LAR will be administered at a dose of 60 mg intramuscularly (IM) every 4 weeks.
|
Octreotide LAR as outlined in Treatment Arm.
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of Participants With Improved Frequency of Diarrhea
Tijdsspanne: At 12 weeks
|
The frequencies of flushing, diarrhea, and carcinoid syndrome control rating (scale 1-5) will be measured and compared at week 0 and week 12 .
These measurements will be compared using two-sided non-parametric paired Wilcoxon signed-rank.
|
At 12 weeks
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Rate of Progression Free Survival (PFS) at 6 Months
Tijdsspanne: At 6 months
|
Progression-free survival, defined as rate of patients alive and free of progression from the date of first study treatment to the end of trial at 6 months.
Progressive disease (PD): at least a 20% increase in the sum of the longest diameter of target lesions, taking as reference the smallest sum longest diameter recorded since the treatment started or the appearance of one or more new lesions.
|
At 6 months
|
Medewerkers en onderzoekers
Medewerkers
Publicaties en nuttige links
Nuttige links
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Schatting)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Chemisch veroorzaakte aandoeningen
- Neoplasmata per histologisch type
- Neoplasmata
- Adenocarcinoom
- Carcinoom
- Neoplasmata, glandulair en epitheel
- Neuro-ectodermale tumoren
- Neoplasmata, kiemcellen en embryonaal
- Neoplasmata, zenuwweefsel
- Neuro-endocriene tumoren
- Geneesmiddelgerelateerde bijwerkingen en bijwerkingen
- Carcinoom, neuro-endocrien
- Carcinoïde tumor
- Maligne carcinoïdsyndroom
- Serotonine syndroom
- Antineoplastische middelen
- Gastro-intestinale middelen
- Antineoplastische middelen, hormonaal
- Octreotide
Andere studie-ID-nummers
- MCC-17410
- CSMS995AUS64T (Andere identificatie: Novartis)
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .