- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 1
Kontakter og lokationer
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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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
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 undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Cohort - 1 through 5
AVE8062 combined with paclitaxel and carboplatin will be administered once every 3 weeks
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Lægemiddelform: opløsning Administrationsvej: intravenøs Lægemiddelform: opløsning Administrationsvej: intravenøs Lægemiddelform: opløsning Administrationsvej: intravenøs |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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The number of of drug related adverse events meeting the defined dose limiting toxicity at Cycle 1
Tidsramme: 3 weeks
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3 weeks
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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The number of treatment emergent adverse events
Tidsramme: 30 days after the last injection
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30 days after the last injection
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The number of serious adverse events
Tidsramme: 30 days after the last injection
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30 days after the last injection
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The number of laboratory abnormalities
Tidsramme: 30 days after the last injection
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30 days after the last injection
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Pharmacokinetic parameter of ombrabulin: Cmax
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of RPR258063: tmax
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of paclitaxel: Cmax
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of carboplatin (free and total platinum): Cmax
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Investigator determination of response
Tidsramme: 30 days after the last injection
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30 days after the last injection
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Pharmacokinetic parameter of ombrabulin: AUC
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of ombrabulin: CL
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of ombrabulin: Vss
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of ombrabulin: t 1/2
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of RPR258063: Cmax
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of RPR258063: AUC
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of RPR258063: t 1/2
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of RPR258063: Metabolic Ratio
Tidsramme: Day 1-2 at Cycle 1
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Day 1-2 at Cycle 1
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Pharmacokinetic parameter of paclitaxel: AUC
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of paclitaxel: CL
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of paclitaxel: Vss
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of paclitaxel: t 1/2
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of carboplatin (free and total platinum): AUC
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of carboplatin (free and total platinum): CL
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of carboplatin (free and total platinum): Vss
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Pharmacokinetic parameter of carboplatin (free and total platinum): t 1/2
Tidsramme: Day 1-3 at Cycle 1
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Day 1-3 at Cycle 1
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- TCD11270
- U1111-1115-2568 (Anden identifikator: UTN)
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Kliniske forsøg med Avancerede solide tumorer
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Novartis PharmaceuticalsAfsluttetcMET Dysegulation Advanced Solid TumorsØstrig, Danmark, Sverige, Det Forenede Kongerige, Spanien, Tyskland, Holland, Forenede Stater
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Shanghai Qilu Pharmaceutical Research and Development...Ikke rekrutterer endnuMSI-H eller dMMR Advanced Solid Tumors
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Suzhou Zelgen Biopharmaceuticals Co.,LtdRekrutteringKRAS G12C Mutant Advanced Solid TumorsKina
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D3 Bio (Wuxi) Co., LtdRekrutteringHER-2 Positive Advanced Solid TumorsAustralien, Forenede Stater, Kina
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AmgenAktiv, ikke rekrutterendeKRAS p.G12C Mutant Advanced Solid TumorsForenede Stater, Frankrig, Canada, Spanien, Belgien, Østrig, Australien, Ungarn, Grækenland, Japan, Brasilien, Tyskland, Schweiz, Portugal, Rumænien, Sydkorea
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Shanghai Pudong HospitalUTC Therapeutics Inc.Trukket tilbageMesothelin-positive Advanced Refractory Solid TumorsKina
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Krankenhaus NordwestAfsluttetHer2/Neu Positive Advanced Solid TumorsTyskland
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Memorial Sloan Kettering Cancer CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater
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Memorial Sloan Kettering Cancer CenterLincoln Medical and Mental Health CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater, Puerto Rico
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Memorial Sloan Kettering Cancer CenterLincoln Medical and Mental Health CenterRekrutteringSolid tumor | Solid tumor, voksen | Solid tumor, uspecificeret, voksenForenede Stater, Puerto Rico
Kliniske forsøg med Ombrabulin (AVE8062)
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SanofiAfsluttet
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SanofiAfsluttetNeoplasmerFrankrig, Italien, Schweiz
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SanofiAfsluttetSarkomBelgien, Ungarn, Forenede Stater, Brasilien, Frankrig, Indien, Italien, Serbien, Spanien, Det Forenede Kongerige
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SanofiAfsluttet
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SanofiAfsluttetIkke-småcellet lungekræftFrankrig, Rumænien, Polen, Kroatien, Korea, Republikken, Italien, Chile, Forenede Stater, Australien, Tyskland, Den Russiske Føderation, Serbien, Ukraine
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SanofiAfsluttet
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SanofiAfsluttet
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SanofiAfsluttet
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SanofiAfsluttetOvariekræft TilbagevendendeBelgien, Den Russiske Føderation, Polen, Spanien, Tjekkiet, Forenede Stater, Frankrig, Tyskland, Italien, Ukraine