Pharmacokinetics of Single and Repeat Oral Doses of Trametinib in Chinese Subjects With Solid Tumours

Cancer Clinical Trial

Official title:

A Phase I Study to Evaluate the Pharmacokinetics and Safety of Single and Repeat Oral Doses of Trametinib in Chinese Subjects With Solid Tumours

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02939846
• Other study ID #: 201021
• Status: Withdrawn
• Phase: Phase 1
• Start date: May 2017
• Est. completion date: December 2018

Study information

• Verified date: January 2017
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Present clinical study will be conducted in China to evaluate the pharmacokinetics of single and repeat oral doses of trametinib, the safety profile and the clinical activity in Chinese subjects with solid tumor. Approximately 10 evaluable subjects will be enrolled in the study, Subjects will receive trametinib 2 mg once daily (QD). Study treatment will continue until disease progression, death or unacceptable toxicity. The study will be completed after all subjects have discontinued from study treatment or last enrolled subject has had at least 16 weeks of follow-up, whichever occurs first.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2018
• Est. primary completion date: August 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Provided signed written informed consent

• Males and females =18 years of age (at the time consent is obtained).

• Histologically or cytologically confirmed diagnosis of locally advanced or metastatic solid tumours, melanoma subjects will be eligible if BRAF V600 mutation was confirmed in the tumour tissue by qualified clinical laboratories. The disease is not responsive to standard therapies, or for which there is no approved or curative therapy.

• Performance Status score of 0 or 1 according to the Eastern Cooperative Oncology Group (ECOG) scale.

• Adequate baseline organ function defined by: Absolute neutrophil count (ANC): >=1,200 /microliter (uL); Hemoglobin: >=9 grams (g)/deciliter (dL); Platelets: >=75,000 /uL; Prothrombin time/ International normalization ratio and activated partial thromboplastin time: <=1.5 x Upper Limit of Normal (ULN); Total bilirubin: <=1.5 x ULN; Aspartate aminotransferase and Alanine aminotransferase: <=2.5 x ULN; Calculated creatinine clearance (Calculate creatinine clearance using standard Cockcroft-Gault formula): >=50 milliliter (mL)/ minute (min) or 24-hour urine creatinine clearance>=50 mL/min; Left ventricular Ejection fraction (LVEF): >/= 50% LVEF in case there is no established Lower limit of normal (LLN) for a given institution.

• Able to swallow and retain orally administered medication and does not have any clinically significant gastrointestinal abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach or bowels. Subjects with prior Whipple procedure (pancreaticoduodenectomy) are eligible (if meeting above criteria).

• Men with a female partner of childbearing potential must have either had a prior vasectomy or agree to use effective contraception from the time of the first dose of trametinib until 16 weeks after the last dose of trametinib.

• Women of child-bearing potential must have a negative serum pregnancy test within 7 days of first dose of study treatment and agree to use effective contraception from 14 days prior to enrolment, throughout the treatment period and for 4 months after the last dose of study treatment.

Exclusion Criteria:

• Pregnant or Lactating female.

• History of another malignancy. Exception: Subjects who have been disease-free for 5 years, or subjects with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible.

• Use of an investigational drug within 28 days or five half-lives, whichever is longer preceding the first dose of trametinib.

• Previous treatment with a MEK inhibitor.

• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or sub-investigator, contraindicates their participation.

• History of interstitial lung disease or pneumonitis.

• Current use of a prohibited medication as described in Section 10.2.

•Colony-stimulating factors like filgrastim are prohibited during treatment as a prophylactic management.

• Any major surgery, radiotherapy, or immunotherapy within 21 days before initiation of trametinib. Chemotherapy regimens with delayed toxicity within 21 days before initiation of trametinib (42 days for prior nitrosourea or mitomycin C). Chemotherapy regimens given continuously or on a weekly basis with limited potential for delayed toxicity within the two weeks before initiation of trametinib.

Note: Use of bisphosphonates is considered supportive care and their use is permitted.

• History or current evidence / risk of retinal vein occlusion (RVO) or central serous retinopathy (CSR):

• Uncontrolled glaucoma or ocular hypertension, uncontrolled systemic disease such as hypertension, diabetes mellitus, or history of hyperviscosity or hypercoagulability syndromes).

• Visible retinal pathology as assessed by ophthalmic exam that is considered a risk factor for RVO or CSR such as:

• Evidence of new optic disc cupping

• Evidence of new visual field defects on automated perimetry

• Intraocular pressure > 21mm Hg as measured by tonography

• Symptomatic or uncontrolled leptomeningeal or brain metastases or spinal cord compression.

• Subjects previously treated for these conditions that have had stable central nervous system (CNS) disease are asymptomatic and off corticosteroids, or are on stable dose of corticosteroids for at least 1 month prior to study Day 1 are eligible.

• Subjects are not eligible to receive enzyme inducing anti-epileptic drugs (EIAEDs).

• QTc B = 480 msecs.

• History of acute coronary syndromes (including unstable angina), coronary angioplasty, or stenting within the past 24 weeks.

• History or evidence of current = Class II congestive heart failure as defined by New York Heart Association.

• History or evidence of current clinically significant uncontrolled arrhythmias.

• Subjects with controlled atrial fibrillation for >1 month prior to study Day 1 are eligible.

• History of Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection.

• Subjects with laboratory evidence of cleared HBV and/or HCV will be permitted, which defined as HBs antigen negative and HBV DNA negative(HBV DNA result is mandatory if both or either HBc and HBs antibody is positive); and HCV antibody is negative.

• History of HIV infection.

• Evidence of severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory, hepatic, renal, or cardiac disease).

• Have a known immediate or delayed hypersensitivity reaction or idiosyncrasy to dimethyl sulfoxide (DMSO).

• Any serious or unstable pre-existing medical conditions (aside from malignancy exceptions specified above), psychiatric disorders, or other conditions that could interfere with the subject's safety, obtaining informed consent, or compliance with study procedures.

Related Conditions & MeSH terms

• Cancer

Intervention

Drug:
• Trametinib
Trametinib study will be provided as 0.5 mg and 2.0 mg tablets. Each tablet will contain 0.5 mg or 2.0 mg of trametinib parent (present as the DMSO solvate)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): Cmax		At Day 1:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): Tmax		At Day 1:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): AUC (0-24h)		At Day 1:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): Cmin.ss		At Day 22:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): Cmax.ss		At Day 22:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): Cavg.ss		At Day 22:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	PK parameters of trametinib following single and repeat dose(2mg QD): AUC(0-24h)		At Day 22:Pre-dose, 0.5hr,1hr, 2hr,3hr,4hr, 6hr,10hr,24hr
Primary	Accumulation ratio of trametinib following single and repeat dose(2mg QD)		At Day 22
Primary	Effective half-life of trametinib following single and repeat dose(2mg QD)		At Day 22
Secondary	Composite of Physical examination assessment	Physical examination will include assessments of eyes, neurological and cardiovascular systems, lungs, abdomen, head, neck, ears, nose, mouth, throat, thyroid, lymph nodes, extremities, and skin, genitourinary (pelvic) and rectal exams.	Up to 30 days of the subject's last dose
Secondary	Composite of Safety and tolerability as assessed by vital signs assessment: blood pressure, temperature and pulse rate	Vital sign measurements will include systolic and diastolic blood pressure, body temperature and pulse rate.	Up to 30 days of the subject's last dose.
Secondary	Electrocardiogram (ECG) assessment	12-lead ECGs will be obtained at each time point using an ECG machine that automatically to calculate the heart rate and measures PR, QRS, QT and corrected QT interval duration (QTc intervals).	Every week in the 1st month, week 8, and then every 8 weeks until treatment discontinuation up to 30 days of the subject's last dose (assessed up to 5 years)
Secondary	Echocardiogram (ECHO) assessment	ECHO assessment will include an evaluation for left ventricular ejection fraction.	At week 4, week 8, and then every 8 weeks until treatment discontinuation up to 5 years
Secondary	Eye exams assessment		At screening, and when clinical indicated until treatment discontinuation up to 5 years
Secondary	Chemistry laboratory values assessment		Up to 30 days of the subject's last dose.
Secondary	Number of subjects with Adverse events (AEs)		Up to 30 days of the subject's last dose.
Secondary	Number of subjects with Serious Adverse events (SAEs)		Up to 30 days of the subject's last dose.
Secondary	Objective response rate (ORR)	ORR defined as the percentage of subjects with evidence of a confirmed complete response (CR) or partial response (PR) as per Response Evaluation	Every 2 months until disease progression up to 5 years
Secondary	Progression free survival(PFS)	PFS defined as the time from first dose of study treatment until the first date of either objective disease progression or death due to any cause	Every 2 months until disease progression up to 5 years
Secondary	Hematology laboratory values assessment		Up to 30 days of the subject's last dose
Secondary	Urinalysis laboratory values assessment		Up to 30 days of the subject's last dose