- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01293630
A Dose-escalation Study of Ombrabulin in Combination With Paclitaxel and Carboplatin in Patients With Advanced Solid Tumors
An Open-label, Dose-escalation, Safety and Pharmacokinetics Phase I Study of Ombrabulin in Combination With Paclitaxel and Carboplatin Every 3 Weeks in Patients With Advanced Solid Tumors
The primary objective of the study is to determine the maximum tolerated dose (MTD) based on the incidence of dose limiting toxicity (DLT) and the maximum administered dose (MAD) of ombrabulin combined with paclitaxel and carboplatin administered every 3 weeks in patients with advanced solid tumors.
Secondary Objectives:
- To assess the overall safety profiles of the combination therapy
- To characterize the pharmacokinetic profile of ombrabulin, its active metabolite RPR 258063, paclitaxel, and carboplatin when used in combination
- To document the objective tumor response
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Faktiske)
Fase
- Fase 1
Kontakter og plasseringer
Studiesteder
-
-
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Akashi-Shi, Japan
- Investigational Site Number 392002
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Hidaka-Shi, Japan
- Investigational Site Number 392001
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-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion criteria:
- Patients with advanced solid tumor for which the combination paclitaxel and carboplatin is potentially effective such as lung cancer, epithelial ovarian cancer.
- Patients who have signed and dated an Institutional Review Board (IRB)-approved patient informed consent form prior to study enrollment or performance of any study-specific procedures.
Exclusion criteria:
- Less than 20 or above 75 years of age ECOG performance status ≥2.
- Patients with more than 1 line of previous chemotherapy for advanced or metastatic disease (adjuvant/neoadjuvant and targeted agents [eg gefitinib] excluded)
- Concurrent treatment with any other anticancer therapy (except palliative radiotherapy),
- Women of childbearing potential who does not agree with contraception.
- Washout period of less than 28 days from prior anticancer therapies
- Symptomatic brain metastases and carcinomatous leptomeningitis.
- Other serious illness or medical conditions
- Current peripheral neuropathy ≥grade 2 and ototoxicity,
- Absolute neutrophils counts<1.5 x 10E9/L. - Platelets count<100 x 10E9/L. - hemoglobin <9.0 g/dL (without red blood cell transfusion within 28 days before the test). - Creatinine Clearance<55 mL/min. - Total bilirubin >upper normal limits of the institutional norms. - ALT/AST >1.5 times the upper normal limits of the institutional norms. - AP>2.5 times the upper normal limits of the institutional norms.
- Medical history of myocardial infarction, angina pectoris, congestive heart failure, coronary artery bypass graft , arrhythmia , stroke or history of arterial or venous thrombo-embolism within the past 180 days requiring anticoagulants.
- Patient with a LVEF <50% by echocardiography.
- Patient with uncontrolled hypertension and patient with organ damage related to hypertension such as left ventricular hypertrophy or grade 2 ocular fundoscopic changes or kidney impairment.
- Hypertension defined as systolic BP >140 mmHg or diastolic BP >90 mmHg on two repeated measurements at 30 minutes interval.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Cohort - 1 through 5
AVE8062 combined with paclitaxel and carboplatin will be administered once every 3 weeks
|
Farmasøytisk form: løsning Administrasjonsvei: intravenøs Farmasøytisk form: løsning Administrasjonsvei: intravenøs Farmasøytisk form: løsning Administrasjonsvei: intravenøs |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The number of of drug related adverse events meeting the defined dose limiting toxicity at Cycle 1
Tidsramme: 3 weeks
|
3 weeks
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The number of treatment emergent adverse events
Tidsramme: 30 days after the last injection
|
30 days after the last injection
|
|
The number of serious adverse events
Tidsramme: 30 days after the last injection
|
30 days after the last injection
|
|
The number of laboratory abnormalities
Tidsramme: 30 days after the last injection
|
30 days after the last injection
|
|
Pharmacokinetic parameter of ombrabulin: Cmax
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: tmax
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: Cmax
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): Cmax
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Investigator determination of response
Tidsramme: 30 days after the last injection
|
30 days after the last injection
|
|
Pharmacokinetic parameter of ombrabulin: AUC
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: CL
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: Vss
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: t 1/2
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: Cmax
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: AUC
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: t 1/2
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: Metabolic Ratio
Tidsramme: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: AUC
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: CL
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: Vss
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: t 1/2
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): AUC
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): CL
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): Vss
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): t 1/2
Tidsramme: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- TCD11270
- U1111-1115-2568 (Annen identifikator: UTN)
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