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- Klinische proef NCT01779336
Clinical Study of Oral IGF-1R Inhibitor in Subjects With Advanced Refractory Solid Tumors
26 september 2014 bijgewerkt door: Piramal Enterprises Limited
An Open Label Multicentre Phase 1 Study of Oral IGF-1R Inhibitor PL225B in Subjects With Advanced Refractory Solid Tumors.
Clinical study of oral IGF-1R inhibitor PL225B in subjects with advanced refractory solid tumors.
The primary objective is to determine the maximum tolerated dose and dose limiting toxicity (ies) of oral IGF-1R inhibitor PL225B in subjects with advanced refractory solid tumors.
Studie Overzicht
Toestand
Geschorst
Interventie / Behandeling
Gedetailleerde beschrijving
An open label multicentre Phase 1 study of oral IGF-1R inhibitor PL225B in subjects with advanced refractory solid tumors.
This is a dose-finding trial using the modified Accelerated Titration Design with 3 new subjects per cohort and 100% dose increments in the accelerated phase followed by standard phase with 40% dose increments.Subjects will receive study drug on a daily basis for twenty-one (21) days according to the dose and schedule specified for a particular cohort of therapy.
Toxicity profile of the drug will be assessed during Cycle 1 of subject treatment in each cohort for determination of Maximum Tolerated Dose (MTD) according to the schedule given below.
Studietype
Ingrijpend
Inschrijving (Verwacht)
70
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Maharashtra
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Nagpur, Maharashtra, Indië, 440010
- Central India Cancer Research Institute
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Nashik, Maharashtra, Indië, 422004
- Curie Manavata Cancer Centre
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Pune, Maharashtra, Indië, 411001
- Ruby Hall Clinic
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Tamil Nadu
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Madurai, Tamil Nadu, Indië, 625107
- Meenakshi Mission Hospital and Research Centre
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California
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Los Angeles, California, Verenigde Staten, 90033
- USC Norris Comprehensive Cancer Center
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 90 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Subjects having histologically and/or cytologically confirmed non-haematological malignancy that is metastatic or unresectable and for which standard curative or palliative treatment does not exist or is no longer effective
- Subjects should have measurable or evaluable disease
- Subjects of either sex, of all races and ethnic groups, and ≥18 years of age
- ECOG (Eastern Cooperative Oncology Group) performance status 0-1
- Subjects with life expectancy of at least 4 months
- Subjects with fasting plasma glucose ≤ 125 mg/dL and HbA1c < 6.5 % at screening Subjects with fasting plasma glucose ≤150 mg/dL and HbA1c ≤ 7.0 % at screening for the Diabetes Expansion Cohort.
- For the Diabetes Expansion Cohort - Subjects with known history of type 2 diabetes mellitus that are well-controlled on a stable dose of oral anti-diabetic agents such as metformin and/or sulfonylureas for 4 weeks prior to screening.
Subjects must have normal organ and marrow function as defined below:
- Absolute neutrophil count ≥ 1500/cmm
- Platelets ≥ 100,000/cmm
- Total bilirubinwithin normal limits of the institution
- AST/ALT ≤ 2.5 X institutional upper limit of normal (ULN) or ≤ 5 X institutional upper limit of normal (ULN) in the presence of liver metastases
- Creatinine ≤ 1.5 X institutional upper limit of normal (ULN)
- Subjects willing for repeat oral dosing and follow-up, including pharmacokinetic sampling
- Women of childbearing potential and men willing to agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, during the duration of study participation and for at least 4 weeks after withdrawal from the study, unless they are surgically sterilised
- Ability to understand and the willingness to provide a written informed consent document
Exclusion Criteria
- Subjects who have received any prior chemotherapy, radiotherapy, biologic/targeted anti-cancer therapy or surgery within 4 weeks (6 weeks for monoclonal antibodies, radioactive monoclonal antibodies or any radio- or toxin- immunoconjugates) before the first study drug administration and have not recovered (to AEs < Grade 2) from the toxic effects from any prior therapy
- Subjects having received any other investigational agents within 4 weeks prior to the first study drug administration and have not recovered completely (to AEs < Grade 2) from the side effects of the earlier investigational agent
- Subjects with documented history of diabetes mellitus except for the Diabetes Expansion Cohort
- For the Diabetes Expansion Cohort - Subjects who have type 1 diabetes mellitus, maturity onset diabetes of the young, hyperglycemia due to reasons other than type 2 diabetes mellitus.
- For the Diabetes Expansion Cohort - Subjects who currently require insulin, thiazolidinediones, dual proliferator-activated receptors (PPAR) agonists, glucagon-like peptide (GLP-1) analogues, dipeptidyl peptidase (DPP-IV) inhibitors or have received the same in the 4 weeks prior to screening.
- Subjects with known complications of diabetes like diabetic nephropathy or diabetic retinopathy
- Subjects with known brain metastases
- Subjects with gastrointestinal abnormalities including inability to take oral medication, malabsorption or other conditions like chronic inflammatory bowel disease that may affect absorption.
- Subjects with a history of myocardial infarction or uncontrolled cardiac dysfunction during the previous 6 months
- Subjects with baseline QTc interval >470 msec at screening
- Subjects on warfarin. Prophylactic anticoagulation with low molecular weight heparin is allowed
- Subjects with history of anaphylaxis or angioedema, bronchial asthma, peptic ulcer and clinically significant food or drug allergy
- Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Women who are pregnant or nursing
- Subjects with known seropositivity to human immunodeficiency virus (HIV), positive for Hepatitis B, positive for Hepatitis C (antigen positive), or known hepatic cirrhosis
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
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 |
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Experimenteel: PL225B
Patients will receive study drug on a daily basis until disease progression or unacceptable toxicity in sequential cohorts following accelerated titration design.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Maximum tolerated dose
Tijdsspanne: End of Cycle 1 (i.e. 21 Days)
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Subjects will receive study drug on a daily basis for twenty-one (21) days according to the dose and schedule specified for a particular cohort of therapy.Toxicity profile of the drug will be assessed during Cycle 1 of subject treatment in each cohort for determination of Maximum Tolerated Dose (MTD).
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End of Cycle 1 (i.e. 21 Days)
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Nummer van proefpersoon met bijwerkingen
Tijdsspanne: Tot ziekteprogressie of onaanvaardbare toxiciteit (naar verwachting 4-6 maanden)
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De toxische effecten van het medicijn zouden worden beoordeeld aan de hand van bijwerkingen, vitale functies en door klinisch significante veranderingen in de laboratoriumevaluaties.
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Tot ziekteprogressie of onaanvaardbare toxiciteit (naar verwachting 4-6 maanden)
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Objectieve reactie
Tijdsspanne: Tot ziekteprogressie of onaanvaardbare toxiciteit (naar verwachting 4-6 maanden)
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Evaluatie van de respons: Klinische reacties zullen patiëntgewijs worden gepresenteerd voor verschillende dosisniveaus.
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Tot ziekteprogressie of onaanvaardbare toxiciteit (naar verwachting 4-6 maanden)
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Pharmacokinetic profile(Cmax,Tmax and AUC)
Tijdsspanne: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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The following PK parameters will be calculated: Cmax (peak plasma concentration), Tmax (time to peak plasma concentration), AUC0-t (area under the plasma concentration curve from time zero to time of last quantifiable concentration), AUC0-12, AUC0-inf (area under the plasma concentration curve from time zero extrapolated to infinity), percent AUC extrapolated, kel (elimination rate constant), t1/2 (elimination half-life), CL/F (oral clearance), Vz/F (oral apparent volume of distribution) and Racc (accumulation ratio).
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Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Activity of PL225B based on selected biomarkers
Tijdsspanne: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Plasma samples will be used for analysis of circulating exploratory biomarkers which are likely to change in response to PL225B administration.
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Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Dr Anthony El-Khoueiry, MD, University of Southern California
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 december 2012
Primaire voltooiing (Verwacht)
1 november 2014
Studie voltooiing (Verwacht)
1 december 2014
Studieregistratiedata
Eerst ingediend
28 januari 2013
Eerst ingediend dat voldeed aan de QC-criteria
28 januari 2013
Eerst geplaatst (Schatting)
30 januari 2013
Updates van studierecords
Laatste update geplaatst (Schatting)
29 september 2014
Laatste update ingediend die voldeed aan QC-criteria
26 september 2014
Laatst geverifieerd
1 september 2014
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- PL225B/71/11
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 .