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A Study in Cancer Patients to Evaluate the Bioequivalence of Alternative Formulations of Lapatinib

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00996762
Recruitment Status : Completed
First Posted : October 16, 2009
Last Update Posted : November 13, 2017
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline

Tracking Information
First Submitted Date  ICMJE October 8, 2009
First Posted Date  ICMJE October 16, 2009
Last Update Posted Date November 13, 2017
Actual Study Start Date  ICMJE November 12, 2009
Actual Primary Completion Date September 18, 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: December 9, 2010)
The primary PK endpoints will be AUC(0-24) and Cmax of lapatinib [ Time Frame: Period 1 Day 7 and Period 2 Day 7 ]
Original Primary Outcome Measures  ICMJE
 (submitted: October 15, 2009)
The primary PK endpoints will be AUC(0-24) and Cmax of lapatinib [ Time Frame: Day 7 and Day 14 ]
Change History Complete list of historical versions of study NCT00996762 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: December 9, 2010)
  • The secondary PK endpoints will be Cmin, tmax, and tlag of lapatinib [ Time Frame: Period 1 Day 7 and Period 2 Day 7 ]
  • Safety and tolerability endpoints will consist of adverse events and changes in laboratory values. [ Time Frame: 2 wks ]
  • Response to questionnaire regarding taste, consistency, and subject acceptability of alternative formulations of lapatinib. [ Time Frame: Day 1 and Day 7 in either Period1 or Period 2 ]
Original Secondary Outcome Measures  ICMJE
 (submitted: October 15, 2009)
  • The secondary PK endpoints will be Cmin, tmax, and tlag of lapatinib [ Time Frame: Day 7 and Day 14 ]
  • Safety and tolerability endpoints will consist of adverse events and changes in laboratory values. [ Time Frame: 2 wks ]
  • Response to questionnaire regarding taste, consistency, and subject acceptability of alternative formulations of lapatinib. [ Time Frame: Days 1, 7, 8, & 14 ]
Current Other Outcome Measures  ICMJE Not Provided
Original Other Outcome Measures  ICMJE Not Provided
 
Descriptive Information
Brief Title  ICMJE A Study in Cancer Patients to Evaluate the Bioequivalence of Alternative Formulations of Lapatinib
Official Title  ICMJE An Open-label, Randomized, Adaptive Design, Two-period Crossover Study in Cancer Patients to Evaluate the Bioequivalence of Alternative Formulations of Lapatinib Compared to the Commercial Tablet
Brief Summary This study will assess alternative formulations of lapatinib for relative bioavailability and bioequivalence (BE) with the current commercial formulation (reference). Subjects will be dosed for at least one week (7 days) on each formulation and PK samples will be collected after each lapatinib formulation dosing Period on Period 1 Day 7 and Period 2 Day7 at pre-dose and up to 24 hrs post dose. The study may evaluate up to three alternative test formulations. After subjects complete the PK evaluation at the End of Study Visit, if they are eligible, they will have the option to enter EGF111767, an open-label, Phase Ib continuation study of lapatinib monotherapy or lapatinib in combination with other anti-cancer treatments.
Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase Phase 1
Study Design  ICMJE Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Neoplasms, Breast
Intervention  ICMJE Drug: lapatinib
1250 mg or 1500 mg lapatinib commercial tablet
Other Names:
  • 1250 mg alternative formulation 1
  • 1250 mg alternative formulation 3
  • 1250 mg alternative formulation 2
Study Arms Experimental: Part 1-3
2-period crossover, Period 1 (D1-7) will receive either the commercial formulation or the alternative formulation. Period 2 (D1-7) will receive the formulation not received in Period 1. There will be 3 parts with 3 different alternative formulations. Subjects will only participate in one part.
Intervention: Drug: lapatinib
Publications * Koch KM, Ferron-Brady G, Lemmon C, Cartee L, Hollyfield H, D'Amelio AM Jr, Piepszak A, Swaby RF, Curran D, Arya N. Bioequivalence study with lapatinib powder for oral suspension and the original tablet formulation in cancer patients. Clin Pharmacol Drug Dev. 2015 May-Jun;4(3):203-9. doi: 10.1002/cpdd.139. Epub 2014 Oct 27.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: November 8, 2017)
158
Original Estimated Enrollment  ICMJE
 (submitted: October 15, 2009)
432
Actual Study Completion Date September 18, 2012
Actual Primary Completion Date September 18, 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • Histologically or cytologically confirmed diagnosis of: Metastatic breast cancer that over-expresses ErbB2 (3+ by IHC; FISH or CISH positive)and the subject has received prior therapy including an anthracycline, a taxane, and trastuzumab OR Recurrent, advanced, or metastatic solid tumor malignancy (including breast cancer that does not over-express ErbB2) that is refractory to standard therapies, for which there is no approved therapy, or for which lapatinib in combination with one of the permitted anti-cancer regimens specified in the continuation study EGF111767 may provide clinical benefit.
  • Is at least 18 years of age.
  • A female is eligible to enter and participate in the study if she is of: Non-childbearing potential (i.e. physiologically incapable of becoming pregnant), including any female who is: Pre-menopausal with a documented bilateral oophorectomy (ovariectomy), bilateral tubal ligation, or hysterectomy. Post-menopausal defined as total cessation of menses for >/=12 months (in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) > 40 MlU/ml and estradiol < 40 pg/ml [< 140 pmol/L] is confirmatory). Childbearing potential, has a negative serum pregnancy test at Screening and agrees to one of the contraception methods listed in the protocol for the time period from 14 days prior to the first dose of study drug until 30 days post the last dose of study drug to sufficiently minimize the risk of pregnancy at that point.
  • Subject is a man with a female partner of childbearing potential who agrees to use contraception.
  • Is able to swallow and retain oral medication and does not have uncontrolled emesis regardless of etiology.

NOTE: If subject has a current or recent (within 14 days) history of nausea or emesis, the subject must be reviewed by the Investigator and the GSK medical monitor. Prophylactic antiemetic therapy may be appropriate.

  • ECOG performance status 0 to 1.
  • Adequate bone marrow function: Hemoglobin >/= 9 gm/dL, Absolute granulocyte count >/=1,500/mm3 (1.5 x 109/L), Platelets >/=75,000/mm3 (75 x 109/L). NOTE: Transfusions of blood and blood products as well as growth factor support are prohibited within 14 days prior to the first dose of study drug.
  • Calculated creatinine clearance (CrCl) >/= 50 ml/min based on Cockcroft and Gault.
  • Total bilirubin </= 1.5 X upper limit of normal (ULN).
  • Alanine transaminase (ALT) </= 3 times the upper limit of normal (ULN) with or without liver metastases.
  • Has a LVEF within the normal institutional range (or >/= 50%) based on ECHO or MUGA.
  • Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

Exclusion Criteria:

  • Is pregnant or lactating.
  • Has malabsorption syndrome, a disease affecting gastrointestinal function, a GI tract bypass in place, or has undergone a resection of the distal stomach and pylorus, small bowel, or ascending or transverse colon that could impact lapatinib absorption.

NOTE: Resection of the gastric antrum, the appendix, descending colon, sigmoid colon and rectum are permitted if there is no overt evidence of malabsorption.

  • Has acute or currently active (e.g.,requiring anti-viral therapy) hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment).
  • Has evidence of symptomatic or uncontrolled brain metastases or leptomeningeal disease. Subjects with brain metastases treated by surgery and/or radiotherapy are eligible if neurologically stable and do not require steroids or anticonvulsants for at least 28 days prior to the first dose of study drug.
  • Is considered medically unfit for the study by the investigator as a result of the medical interview, physical exam, or screening investigations.
  • Has a known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product such as gefitinib [IRESSA] and erlotinib [TARCEVA].
  • Has received anti-cancer therapy (including chemotherapy, radiation therapy, immunotherapy, biologic therapy, investigational therapy, surgery, or hormonal therapy) within 14 days prior to the first dose of lapatinib.

NOTE: Any ongoing potentially reversible toxicity from prior anti-cancer therapy that is > Grade 1 (except alopecia or Grade 2 neuropathy that has been stable for at least 4 weeks) or any toxicity from prior anti-cancer therapy that is progressing in severity will render the subject ineligible unless agreed to by the GSK Medical Monitor and the Investigator.

  • Is receiving any prohibited medication or consuming any food or beverage within the timeframe indicated on the prohibited medication list.
  • Has physiological, familial, sociological, or geographical conditions that do not permit compliance with the protocol.
  • Clinically significant ECG abnormality including baseline QTc prolongation >480msec.
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Korea, Republic of,   United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT00996762
Other Study ID Numbers  ICMJE 112930
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party GlaxoSmithKline
Study Sponsor  ICMJE GlaxoSmithKline
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Study Director: GSK Clinical Trials GlaxoSmithKline
PRS Account GlaxoSmithKline
Verification Date November 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP