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Clinical Study of Oral IGF-1R Inhibitor in Subjects With Advanced Refractory Solid Tumors

26 september 2014 uppdaterad av: 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.

Studieöversikt

Status

Upphängd

Intervention / Behandling

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Förväntat)

70

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • California
      • Los Angeles, California, Förenta staterna, 90033
        • USC Norris Comprehensive Cancer Center
    • Maharashtra
      • Nagpur, Maharashtra, Indien, 440010
        • Central India Cancer Research Institute
      • Nashik, Maharashtra, Indien, 422004
        • Curie Manavata Cancer Centre
      • Pune, Maharashtra, Indien, 411001
        • Ruby Hall Clinic
    • Tamil Nadu
      • Madurai, Tamil Nadu, Indien, 625107
        • Meenakshi Mission Hospital and Research Centre

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 90 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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:

    1. Absolute neutrophil count ≥ 1500/cmm
    2. Platelets ≥ 100,000/cmm
    3. Total bilirubinwithin normal limits of the institution
    4. 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
    5. 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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: PL225B
Patients will receive study drug on a daily basis until disease progression or unacceptable toxicity in sequential cohorts following accelerated titration design.
  • Patients 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.
  • This 21 day administration will define a treatment cycle.
  • Patients may receive consecutive treatment cycles until evidence of disease progression, intolerance of therapy, or withdrawal from the protocol as specified.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Maximum tolerated dose
Tidsram: End of Cycle 1 (i.e. 21 Days)
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).
End of Cycle 1 (i.e. 21 Days)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Antal försökspersoner med biverkningar
Tidsram: Tills sjukdomsprogression eller oacceptabel toxicitet (förväntas vara 4-6 månader)
De toxiska effekterna av läkemedlet skulle bedömas utifrån biverkningar, vitala tecken och genom kliniskt signifikanta förändringar i laboratorieutvärderingarna.
Tills sjukdomsprogression eller oacceptabel toxicitet (förväntas vara 4-6 månader)
Objektivt svar
Tidsram: Tills sjukdomsprogression eller oacceptabel toxicitet (förväntas vara 4-6 månader)
Utvärdering av svar: Kliniska svar kommer att presenteras patientmässigt för olika dosnivåer.
Tills sjukdomsprogression eller oacceptabel toxicitet (förväntas vara 4-6 månader)
Pharmacokinetic profile(Cmax,Tmax and AUC)
Tidsram: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
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).
Until disease progression or unacceptable toxicity (expected to be 4-6 months)
Activity of PL225B based on selected biomarkers
Tidsram: Until disease progression or unacceptable toxicity (expected to be 4-6 months)
Plasma samples will be used for analysis of circulating exploratory biomarkers which are likely to change in response to PL225B administration.
Until disease progression or unacceptable toxicity (expected to be 4-6 months)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Dr Anthony El-Khoueiry, MD, University of Southern California

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 december 2012

Primärt slutförande (Förväntat)

1 november 2014

Avslutad studie (Förväntat)

1 december 2014

Studieregistreringsdatum

Först inskickad

28 januari 2013

Först inskickad som uppfyllde QC-kriterierna

28 januari 2013

Första postat (Uppskatta)

30 januari 2013

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

29 september 2014

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

26 september 2014

Senast verifierad

1 september 2014

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • PL225B/71/11

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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