- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning 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
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Inskrivning (Faktisk)
Fas
- Fas 1
Kontakter och platser
Studieorter
-
-
-
Akashi-Shi, Japan
- Investigational Site Number 392002
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Hidaka-Shi, Japan
- Investigational Site Number 392001
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
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
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Cohort - 1 through 5
AVE8062 combined with paclitaxel and carboplatin will be administered once every 3 weeks
|
Läkemedelsform: lösning Administreringssätt: intravenöst Läkemedelsform: lösning Administreringssätt: intravenöst Läkemedelsform: lösning Administreringssätt: intravenöst |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
The number of of drug related adverse events meeting the defined dose limiting toxicity at Cycle 1
Tidsram: 3 weeks
|
3 weeks
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
The number of treatment emergent adverse events
Tidsram: 30 days after the last injection
|
30 days after the last injection
|
|
The number of serious adverse events
Tidsram: 30 days after the last injection
|
30 days after the last injection
|
|
The number of laboratory abnormalities
Tidsram: 30 days after the last injection
|
30 days after the last injection
|
|
Pharmacokinetic parameter of ombrabulin: Cmax
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: tmax
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: Cmax
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): Cmax
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Investigator determination of response
Tidsram: 30 days after the last injection
|
30 days after the last injection
|
|
Pharmacokinetic parameter of ombrabulin: AUC
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: CL
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: Vss
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of ombrabulin: t 1/2
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: Cmax
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: AUC
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: t 1/2
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of RPR258063: Metabolic Ratio
Tidsram: Day 1-2 at Cycle 1
|
Day 1-2 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: AUC
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: CL
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: Vss
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of paclitaxel: t 1/2
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): AUC
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): CL
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): Vss
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
|
Pharmacokinetic parameter of carboplatin (free and total platinum): t 1/2
Tidsram: Day 1-3 at Cycle 1
|
Day 1-3 at Cycle 1
|
Samarbetspartners och utredare
Sponsor
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- TCD11270
- U1111-1115-2568 (Annan identifierare: UTN)
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