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

26. september 2014 oppdatert 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.

Studieoversikt

Status

Suspendert

Intervensjon / Behandling

Detaljert beskrivelse

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

Intervensjonell

Registrering (Forventet)

70

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 90 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum tolerated dose
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Antall personer med uønskede hendelser
Tidsramme: Inntil sykdomsprogresjon eller uakseptabel toksisitet (forventet å være 4-6 måneder)
De toksiske effektene av stoffet vil bli vurdert ut fra uønskede hendelser, vitale tegn og ved klinisk signifikante endringer i laboratorieevalueringene.
Inntil sykdomsprogresjon eller uakseptabel toksisitet (forventet å være 4-6 måneder)
Objektiv respons
Tidsramme: Inntil sykdomsprogresjon eller uakseptabel toksisitet (forventet å være 4-6 måneder)
Evaluering av respons: Klinisk respons vil bli presentert pasientmessig for ulike dosenivåer.
Inntil sykdomsprogresjon eller uakseptabel toksisitet (forventet å være 4-6 måneder)
Pharmacokinetic profile(Cmax,Tmax and AUC)
Tidsramme: 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
Tidsramme: 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)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

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

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. desember 2012

Primær fullføring (Forventet)

1. november 2014

Studiet fullført (Forventet)

1. desember 2014

Datoer for studieregistrering

Først innsendt

28. januar 2013

Først innsendt som oppfylte QC-kriteriene

28. januar 2013

Først lagt ut (Anslag)

30. januar 2013

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

29. september 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. september 2014

Sist bekreftet

1. september 2014

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • PL225B/71/11

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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