- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00813384
A Phase 1 Study of AMG 208 in Subjects With Advanced Solid Tumors
A Phase 1, First-In-Human Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 208 in Adult Subjects With Advanced Solid Tumors
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
-
-
California
-
Beverly Hills, California, États-Unis, 90211
- Research Site
-
-
Missouri
-
St Louis, Missouri, États-Unis, 63110
- Research Site
-
-
Texas
-
Houston, Texas, États-Unis, 77030
- Research Site
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Men or women ≥ 18 years old
- Subjects must have a pathologically documented, definitively diagnosed, advanced solid tumor that is refractory to standard treatment, for which no standard therapy is available or the subject refuses standard therapy
- Measurable disease per RECIST guidelines (subjects with non-measurable, but evaluable disease are also eligible for Part 1 of the study)
- Eastern Cooperative Oncology Group (ECOG) Performance Status of ≤ 2
- Life expectancy of > 3 months, in the opinion of the investigator
- Female subjects who are post-menopausal (no menstrual period for a minimum of 12 months), or surgically sterilized. Female subjects of child bearing potential must remain abstinent or use double-barrier birth control method during the period of therapy and must be willing to use contraception 2 weeks following the last study drug administration and have a negative serum pregnancy test upon entry into this study
- Male subject is willing to use contraception upon enrollment, during the course of the study and for 12 weeks following the last study drug administration
- Willing to provide tumor samples and / or slides
- Competent to sign and date an Institutional Review Board approved informed consent form
- Hematological function, as follows:
Absolute neutrophil count (ANC) ≥ 1.5 x 109/L Platelet count ≥ 100 x 109/L Hemoglobin > 9 g/dL Prothrombin time (PT) or partial thromboplastin time (PTT) < 1.5 x institutional upper limit of normal (IULN)
- Renal function, as follows:
Serum creatinine < 2.0 mg/dL
- Hepatic function, as follows:
AST/ALT < 3x ULN and total bilirubin < 1.5x ULN in all subjects Alkaline phosphatase < 2.0 x ULN (if liver or bone metastases are present, ≤ 5 x ULN)
Exclusion Criteria:
- Any disorder that compromises the ability of the subject to give written informed consent and/or to comply with the study procedures.
- Primary central nervous system (CNS) tumors or metastases
- History of bleeding diathesis
- Myocardial infarction within 6 months of study day 1, symptomatic congestive heart failure (New York Heart Association > class II), unstable angina, or unstable cardiac arrhythmia requiring medication, or uncontrolled hypertension in the opinion of the investigator
- A baseline ECG QTc > 480 ms
- Active infection within 2 weeks of study enrollment (day 1)
- Significant gastrointestinal disorder(s), in the opinion of the investigator, (e.g. Crohn's disease, ulcerative colitis, extensive gastrointestinal resection) that may influence drug absorption
- Known positive test for HIV
- Known acute or chronic hepatitis B or hepatitis C infection, determined by serologic tests
- Unresolved toxicities from prior anti-tumor therapy, defined as not having resolved to CTCAE grade 0 or 1, or to levels dictated in the eligibility criteria with the exception of alopecia
- Anti-tumor therapy (chemotherapy, antibody therapy, molecular targeted therapy, retinoid therapy, hormonal therapy, or investigational agent) within 28 days of study day 1 (six weeks for nitrosureas, mitomycin C, or antibody or molecular targeted agents with t1/2 > 10 days); concurrent use of hormone deprivation therapy for hormone-refractory prostate cancer or breast cancer is permitted
- Treatment with immune modulators including, but not limited to, systemic corticosteroids, cyclosporine and tacrolimus within two weeks prior to enrollment
- Therapeutic or palliative radiation therapy within 2 weeks of study day 1
- Concurrent or prior (within 7 days of study day 1) anticoagulation therapy (low-dose warfarin [≤ 2 mg/day] or low molecular weight heparins for prophylaxis against central venous catheter thrombosis or aspirin [81 mg/day] is allowed)
- Prior participation in an investigational study and/or procedure within 28 days of study day 1
- Major surgery within 30 days of study day 1
- Any co-morbid medical disorder that may increase the risk of toxicity, in the opinion of the investigator or sponsor
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Dose Escalation
The dose escalation part of the study is aimed at determining the maximum tolerated dose (MTD), if feasible, and evaluating the safety, tolerability, pharmacokinetics and pharmacodynamics of AMG 208.
|
AMG 208 is a small molecule inhibitor of c-Met which is a well-characterized receptor tyrosine kinase expressed on the surface of epithelial cells.
C-Met receptor signaling has been shown to play a key role in the survival of cancer cells.
AMG 208 inhibits both ligand-dependent and ligand-independent c-Met cellular growth regulation.
Inhibition of c-Met signaling with AMG 208 provides a potential mechanism for blocking tumor growth and survival.
|
|
Expérimental: Dose Expansion
The dose expansion will consist of up to 30 subjects and the dose level of AMG 208 will be dependent upon emerging safety and PK data from the dose escalation part of the study.
|
AMG 208 is a small molecule inhibitor of c-Met which is a well-characterized receptor tyrosine kinase expressed on the surface of epithelial cells.
C-Met receptor signaling has been shown to play a key role in the survival of cancer cells.
AMG 208 inhibits both ligand-dependent and ligand-independent c-Met cellular growth regulation.
Inhibition of c-Met signaling with AMG 208 provides a potential mechanism for blocking tumor growth and survival.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
To determine the maximum tolerated dose (MTD) of AMG 208, if possible
Délai: 3.5 years
|
3.5 years
|
|
To evaluate for clinical responses associated with AMG 208 treatment in subjects (Dose Expansion) with advanced solid malignancies according to RECIST criteria
Délai: 3.5 years
|
3.5 years
|
|
To characterize the pharmacokinetic (PK) exposure of AMG 208 when administered orally to subjects with advanced solid malignancies
Délai: 3.5 years
|
3.5 years
|
|
To evaluate the safety and tolerability of AMG 208 in subjects with advanced solid malignancies
Délai: 3.5 years
|
3.5 years
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
To evaluate for a decrease in tumor cell proliferation associated with AMG 208 treatment in subjects with advanced solid malignancies according to FLT-PET scanning
Délai: 3.5 years
|
3.5 years
|
|
To assess tumor volume changes after AMG 208 treatment by computed tomography (CT) or magnetic resonance imaging (MRI)
Délai: 3.5 years
|
3.5 years
|
|
To assess skin specimens for potential biomarkers
Délai: 3.5 years
|
3.5 years
|
|
To determine whether c-Met expression, mutation, or amplification in tumor specimens correlates with a response to AMG 208
Délai: 3.5 years
|
3.5 years
|
Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 20080895
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .