Back to resultsA Study to Evaluate Bioavailability and Food Effect of Selumetinib (AZD6244) in Healthy Male Participants
Primary Purpose
Neurofibromatosis Type 1 (NF1)-Related Plexiform Neurofibromas (PNs), Healthy Participants
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Treatment A
Treatment B
Treatment C
Treatment D
Acetaminophen
Sponsored by
About this trial
This is an interventional treatment trial for Neurofibromatosis Type 1 (NF1)-Related Plexiform Neurofibromas (PNs) focused on measuring MEK Inhibitor, Selumetinib capsule, Selumetinib granule, PK, Bioavailibilty, Crossover study, Open-label, Food effect
Eligibility Criteria
Inclusion Criteria
- Provision of signed and dated, written informed consent before any study-specific procedures.
- Healthy male participants aged 18 to 45 years (inclusive) with suitable veins for cannulation or repeated venipuncture.
- Have a body mass index (BMI) between 18 and 30 kg/m2 inclusive and weigh at least 50 kg.
- Participants is able to consume a low-fat meal within a 30-minute period.
- Participants has a creatinine clearance (CRCL) greater than 50 mL/min using Cockcroft-Gault formula.
Participants is willing to comply with contraception requirements as described below:
- Male participants with sexual partners who can become pregnant (i.e., women of childbearing potential) must use 2 highly-effective methods of contraception, one of which must be a barrier method (condom with spermicide) from the time of the first administration of the IMP until 12 weeks after the last administration of the IMP to avoid pregnancy and/or potential adverse effects on the developing embryo.
- Participants with sexual partners who are pregnant must use an effective method of contraception (barrier method) from the time of the first administration of the IMP until 12 weeks after the last administration of the IMP.
- Participants must avoid sperm donation during the study and for 12 weeks after the last administration of the IMP.
- Reliable methods of contraception must be used consistently and correctly.
- Reliable methods of contraception for participants include: Use of barrier methods (condom and spermicide) for the duration of the study until 12 weeks after the last administration of the IMP.
Acceptable methods for participants partners include:
- Use of implants, injectables and combined oral contraceptives (must be used in combination with a barrier method of contraception)
- Use of intrauterine devices (must be used in combination with a barrier method of contraception)
Exclusion Criteria :
- Participants of Japanese, non-Japanese Asian or Indian ethnicity.
- Participants has any one parent or grandparent (maternal or paternal) that was Japanese or non-Japanese Asian (e.g., China, Taiwan, Korea, Philippines, Thailand, Vietnam and Malaysia) or Indian.
- History or presence of central serous retinopathy or retinal vein thrombosis, IOP greater than 21 mmHg or uncontrolled glaucoma.
- History of any clinically significant disease or disorder which, in the opinion of the PI, may put the participant at risk because of participation in the study, influence the result of the study or influence the participants ability to participate in the study.
Participant has ophthalmologic conditions as follows:
- Current or past history of central serous retinopathy/retinal pigment epithelial detachment or retinal vein occlusion.
- Intra-ocular pressure > 21 mmHg or uncontrolled glaucoma (irrespective of IOP).
Participant has any cardiac conditions as follows:
- Uncontrolled hypertension (BP ≥ 150/95 mmHg despite medical therapy).
- Acute coronary syndrome within 6 months before starting treatment.
- Uncontrolled Angina - Canadian Cardiovascular Society grade II-IV despite medical therapy.
- Symptomatic heart failure New York Heart Association (NYHA) Class II-IV, prior or current cardiomyopathy, or severe valvular heart disease.
Prior or current cardiomyopathy including but not limited to the following: 1) Known hypertrophic cardiomyopathy.
2) Known arrhythmogenic right ventricular cardiomyopathy. 3) Previous moderate or severe impairment of LVEF < 45% on echocardiography even if full recovery has occurred.
- Left ventricular ejection fraction below the lower limit of normal (LLN) or < 55% measured by ECHO at the Screening Visit.
- Severe valvular heart disease.
- Atrial fibrillation with a ventricular rate > 100 beats per minute (bpm) on ECG at rest.
- QTcF > 450 ms or other factors that increase the risk of QT prolongation.
- Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the first administration of IMP.
- Any clinically relevant abnormal findings in physical examination, hematology, clinical chemistry, urinalysis, vital signs or ECG at the Screening Visit, which in the opinion of the PI, may put the participant at risk because of his participation in the study. Test may be repeated twice at the discretion of the Investigator if abnormal.
- Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody, and human immunodeficiency virus (HIV) antibody.
- A suspected/manifested infection according to the International Air Transport Association (IATA) Categories A and B infectious substances.
- History of, or current alcohol or drug abuse, as judged by the principal investigator (PI).
- Participation in another clinical study (investigational product administered within 30 days before the Screening Visit, or participation in a method development study [no drug] 30 days before the Screening Visit). Participation is defined as the completion of a treatment related visit.
- Planned in-patient surgery, dental procedure or hospitalization during the study.
- Plasma donation within 30 days of the Screening Visit or any blood donation/loss more than 500 mL during the 90 days before the Screening Visit.
- A definite or suspected personal history of intolerance or hypersensitivity to drugs and/or their excipients, judged to be clinically relevant by the PI.
- Known severe hypersensitivity to selumetinib or acetaminophen or any excipient of these medicinal products or history of allergic reactions attributed to compounds of similar chemical or biologic composition to selumetinib.
- Current smokers or those who have smoked or used nicotine products (including e-cigarettes) within the 90 days before the Screening Visit.
- Positive screen for drugs of abuse, alcohol or cotinine at the Screening Visit or on each admission to the Clinical Unit or positive screen for alcohol on each admission to the Clinical Unit.
- Use of drugs with enzyme-inducing properties such as St John's Wort within 4 weeks before the first administration of IMP.
- Use of any prescribed medicine and over-the-counter (OTC) drugs (including herbal remedies, vitamins and minerals) within 2 weeks or 5 times the half-life, whichever is the longer, of the respective drug before Day -1 or Treatment Period 1. No medications known to prolong the QT/QTc interval are allowed.
- Excessive intake of caffeine-containing drinks or food e.g., coffee, tea, chocolate, Red Bull or cola (more than 6 units of caffeine per day). One caffeine unit is contained in the following items: 1 (6 oz) cup of coffee, 2 (12 oz) cans of cola, 1 (12 oz) cup of tea, ½ (4 oz) cup of energy drink (e.g., Red Bull) or 3 oz of chocolate.
- Known or suspected history of alcohol or drug abuse or excessive intake of alcohol as judged by the PI.
- Involvement of any AstraZeneca, PAREXEL or Clinical Unit employee or their close relatives.
- Participants who have previously been randomized to treatment in the current study.
- Judgment by the PI that the participant should not participate in the study if they have any ongoing or recent (i.e., during the screening period) minor medical complaints that may interfere with the interpretation of study data or are considered unlikely to comply with study procedures, restrictions and requirements.
- Vulnerable participants , e.g., kept in detention, protected adults under guardianship, trusteeship, or committed to an institution by governmental or juridical order.
Sites / Locations
- Research Site
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
Treatment Sequence 1
Treatment Sequence 2
Treatment Sequence 3
Treatment Sequence 4
Arm Description
Participants will receive Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 1, Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 2, Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 3, and Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Participants will receive Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 1, Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 2, Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 3 and Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Participants will receive Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 1, Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 2, Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 3 and Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Participants will receive Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 1, Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 2, Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 3 and Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Outcomes
Primary Outcome Measures
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized area under plasma concentration-time curve from time zero to infinity (AUC/D)
To compare the AUC/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized area under the plasma concentration-time curve from time zero to time of last quantifiable concentration (AUClast/D)
To compare the AUClast/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized maximum observed plasma concentration (Cmax/D)
To compare the Cmax/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Fraction of administered selumetinib granule dose systemically available relative to the capsule reference (Frel)
To compare the Frel. of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Secondary Outcome Measures
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under plasma concentration time curve from time zero to infinity (AUC)
To compare AUC of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under the plasma concentration time curve from time zero to time of last quantifiable concentration (AUClast)
To compare AUClast of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under the plasma concentration-time curve from zero to 12 hours post-dose [AUC(0-12)]
To compare AUC (0-12) of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Maximum observed plasma concentration (Cmax)
To compare Cmax of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Ratio of AUC in fed state to AUC in the fasted state (FRAUC)
To compare FRAUC of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Ratio of Cmax in fed state to Cmax in the fasted state (FRCmax)
To compare FRCmax of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Half-life associated with terminal slope (λz) of a semi-logarithmic concentration-time curve (t½λz)
To compare t½λz of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Time to reach maximum observed plasma concentration (tmax)
To compare tmax of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Terminal elimination rate constant (λz)
To compare λz of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib plasma PK parameters: Apparent total body clearance of drug from plasma after extravascular administration (parent drug only) (CL/F)
To compare CL/F of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib plasma PK parameters: Apparent volume of distribution during the terminal phase after extravascular administration (Vz/F)
To compare Vz/F of selumetinib capsule fasted versus capsule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUC
To compare AUC of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUClast
To compare AUClast of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUC(0-12)
To compare AUC (0-12) of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Cmax
To compare Cmax of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: FRAUC
To compare FRAUC of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: FRCmax
To compare FRCmax of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: t½λz
To compare t½λz of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: tmax
To compare tmax of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib and N-desmethyl selumetinib plasma PK parameter: λz
To compare λz of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib plasma PK parameters: CL/F
To compare CL/F of selumetinib granule fasted versus granule low-fat fed state.
Selumetinib plasma PK parameters: Vz/F
To compare Vz/F of selumetinib granule fasted versus granule low-fat fed state.
Taste questionnaire
To assess palatability of selumetinib granule formulation. The standardized questionnaire will be administered to participants within 10 minutes following intake of selumetinib granule. Questionnaire about taste include sweet, salty, sour, bitter, metallic, and hot/spicy. Where 0 indicates not at all and 10 indicates extremely.
Number of participants with adverse events (AEs)
To assess the safety and tolerability of single doses of selumetinib in healthy participants.
Vital signs (systolic blood pressure [BP])
To assess systolic BP as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest for at least 5 minutes before the measurements.
Vital signs (diastolic BP)
To assess diastolic BP as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest for at least 5 minutes before the measurements.
Pulse rate
To assess pulse rate as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Participants should be supine and at rest for at least 5 minutes before the measurements.
12-lead electrocardiogram (ECG)
To assess 12-lead ECG as variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest 10 minutes before recording the ECG.
Number of participants with abnormal findings in physical examination
To assess physical examination as a variable safety and tolerability of single doses of selumetinib in healthy participants.
Ophthalmic examinations
To assess ophthalmic examination as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Ophthalmic examination included best corrected visual acuity, intra-ocular pressure and slit-lamp fundoscopy.
Laboratory assessments: hematology - Hemoglobin (Hb)
To assess Hb as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: hematology - erythrocyte count
To assess erythrocyte count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: hematology: Platelet count
To assess platelet count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: hematology: leucocyte differential count (absolute count)
To assess leucocyte differential count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: hematology: leucocyte cell count
To assess leucocyte cell count as variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments:hematology - differential count
To assess differential count of neutrophils, lymphocytes, monocyets, eosinophils and basophils) as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry - electrolytes
To assess serum level of sodium, potassium, magnesium and phosphate as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry - urea nitrogen
To assess urea nitrogen as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry - creatinine
To assess creatinine as variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: albumin
To assess albumin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: Total Calcium
To assess total calcium as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: Total protein
To assess total protein as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: Total bilirubin
To assess total bilirubin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: Creatine phosphokinase (CPK)
To assess CPK as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry: Troponin (isoform as per institutional norm)
To assess troponin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Serum clinical chemistry - Liver enzymes
To assess serum of Alkaline phosphatase (ALP), Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) and Gamma glutamyl transpeptidase (GGT) as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Clinical urinalysis - glucose
To assess urine glucose as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Clinical Urinalysis - protein
To assess urine protein as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Laboratory assessments: Clinical Urinalysis - blood
To assess urine blood as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
If urinalysis is positive for blood, a microscopy test will be performed to assess RBC, white blood cell [WBC], casts [cellular, granular, hyaline]).
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03649165
Brief Title
A Study to Evaluate Bioavailability and Food Effect of Selumetinib (AZD6244) in Healthy Male Participants
Official Title
A Phase I, Open-label, Single-center Relative Bioavailability and Food Effect Randomized Crossover Study of New Granule and Capsule Formulations of Selumetinib (AZD6244) in Healthy Male Subjects
Study Type
Interventional
2. Study Status
Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
September 5, 2018 (Actual)
Primary Completion Date
October 21, 2018 (Actual)
Study Completion Date
October 21, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will evaluate bioavailability and food effect of selumetinib (AZD6244) in healthy male participants. A total of 24 healthy male participants will be included to ensure at least 20 evaluable participants. The study is divided in 2 study parts; the same participants will participate in both parts of the study. Part 1 of the study is to investigate the pharmacokinetics (PK) of the selumetinib granule compared to the PK of selumetinib capsule, when administered with water under the fasted conditions. Part 2 of the study is to investigate the PK of selumetinib granule and capsule under fed conditions. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration.
Detailed Description
This study will be a 2-part, open-label, single-center relative bioavailability and food effect randomized crossover study of new granule and capsule formulations of selumetinib. A total of 24 healthy male participants aged between 18 to 45 years (inclusive), will be included to ensure at least 20 evaluable participants. The study is divided in 2 study parts; the same participants will participate in both parts of the study.
Part 1 of the study is designed to investigate the PK of the selumetinib granule compared to the PK of selumetinib capsule, when administered with water under the fasted conditions. Part 2 of the study is designed to investigate the PK of selumetinib granule and capsule under fed conditions. Participants will consume a low-fat, low-calorie meal. Thirty minutes after the start of the meal, selumetinib will be administered to the participants. In all treatment periods, participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying. The study will also assess the palatability of the selumetinib granule in both parts of the study.
Each participant will receive the following treatments:
Treatment A: 25 mg granule, fasted state
Treatment B: 50 mg capsule, fasted state
Treatment C: 25 mg granule, fed state
Treatment D: 50 mg capsule, fed state Participant will be randomly assigned to 1 of 4 treatment sequences. In all cases the treatments in Part 1 will be administered before the treatments in Part 2. The study will comprise of a screening period of maximum 28 days. Four treatment periods during which participants will be resident from the day before dosing (Day -1) until at least 48 hours after dosing; discharged on the morning of Day 3. A follow-up visit, will be within 7 to 10 days after the last dose of investigational medicinal product (IMP). There will be a minimum washout period of at least 5 days between each IMP administration. Each participant will be involved in the study for approximately 8 to 9 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurofibromatosis Type 1 (NF1)-Related Plexiform Neurofibromas (PNs), Healthy Participants
Keywords
MEK Inhibitor, Selumetinib capsule, Selumetinib granule, PK, Bioavailibilty, Crossover study, Open-label, Food effect
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment Sequence 1
Arm Type
Experimental
Arm Description
Participants will receive Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 1, Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 2, Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 3, and Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Arm Title
Treatment Sequence 2
Arm Type
Experimental
Arm Description
Participants will receive Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 1, Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 2, Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 3 and Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Arm Title
Treatment Sequence 3
Arm Type
Experimental
Arm Description
Participants will receive Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 1, Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 2, Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 3 and Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Arm Title
Treatment Sequence 4
Arm Type
Experimental
Arm Description
Participants will receive Treatment B (selumetinib 50 mg capsule, fasted state) in Part 1, Period 1, Treatment A (selumetinib 25 mg granule, fasted state) in Part 1, Period 2, Treatment D (selumetinib 50 mg capsule, fed state) in Part 2, Period 3 and Treatment C (selumetinib 25 mg granule, fed state) in Part 2, Period 4. Participants will also receive a single 500 mg dose of acetaminophen at the same time as selumetinib administration where it will act as a marker for gastric emptying.
Intervention Type
Drug
Intervention Name(s)
Treatment A
Intervention Description
During Part 1 of the study, participants will receive single doses of selumetinib 25 mg granule under fasted conditions. The dose will be administered after an overnight fast of at least 10 hours. The IMP will be administered with approximately 240 mL of water. No food will be allowed for at least 4 hours post-dose.
Intervention Type
Drug
Intervention Name(s)
Treatment B
Intervention Description
During Part 1 of the study, participants will receive single doses of selumetinib 50 mg capsule under fasted conditions. The dose will be administered after an overnight fast of at least 10 hours. The IMP will be administered with approximately 240 mL of water. No food will be allowed for at least 4 hours post-dose.
Intervention Type
Drug
Intervention Name(s)
Treatment C
Intervention Description
During Part 2 of the study, participants will receive single doses of selumetinib 25 mg granule under fed conditions. Following an overnight fast of at least 10 hours, participants will start consumption of the recommended meal within 30 minutes before administration of the IMP. Participants will be required to consume the entire meal in 30 minutes or less; however, the IMP should be administered 30 minutes after start of the meal. The IMP will be administered with approximately 240 mL of water. No food will be allowed for at least 4 hours post-dose, where after a meal may be provided.
Intervention Type
Drug
Intervention Name(s)
Treatment D
Intervention Description
During Part 2 of the study, participants will receive single doses of selumetinib 50 mg capsule under fed conditions. Following an overnight fast of at least 10 hours, participants will start consumption of the recommended meal within 30 minutes before administration of the IMP. Participants will be required to consume the entire meal in 30 minutes or less; however, the IMP should be administered 30 minutes after start of the meal. The IMP will be administered with approximately 240 mL of water. No food will be allowed for at least 4 hours post-dose, where after a meal may be provided.
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Intervention Description
Participants will receive a single 500mg dose of acetaminophen at the same time.
Primary Outcome Measure Information:
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized area under plasma concentration-time curve from time zero to infinity (AUC/D)
Description
To compare the AUC/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose(Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized area under the plasma concentration-time curve from time zero to time of last quantifiable concentration (AUClast/D)
Description
To compare the AUClast/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose(Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Dose normalized maximum observed plasma concentration (Cmax/D)
Description
To compare the Cmax/D of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose(Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Fraction of administered selumetinib granule dose systemically available relative to the capsule reference (Frel)
Description
To compare the Frel. of the new selumetinib granule formulation with selumetinib capsule formulation in fasted state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose(Days -1 to 3)
Secondary Outcome Measure Information:
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under plasma concentration time curve from time zero to infinity (AUC)
Description
To compare AUC of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose(Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under the plasma concentration time curve from time zero to time of last quantifiable concentration (AUClast)
Description
To compare AUClast of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Area under the plasma concentration-time curve from zero to 12 hours post-dose [AUC(0-12)]
Description
To compare AUC (0-12) of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Maximum observed plasma concentration (Cmax)
Description
To compare Cmax of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Ratio of AUC in fed state to AUC in the fasted state (FRAUC)
Description
To compare FRAUC of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Ratio of Cmax in fed state to Cmax in the fasted state (FRCmax)
Description
To compare FRCmax of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Half-life associated with terminal slope (λz) of a semi-logarithmic concentration-time curve (t½λz)
Description
To compare t½λz of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Time to reach maximum observed plasma concentration (tmax)
Description
To compare tmax of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Terminal elimination rate constant (λz)
Description
To compare λz of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib plasma PK parameters: Apparent total body clearance of drug from plasma after extravascular administration (parent drug only) (CL/F)
Description
To compare CL/F of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib plasma PK parameters: Apparent volume of distribution during the terminal phase after extravascular administration (Vz/F)
Description
To compare Vz/F of selumetinib capsule fasted versus capsule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUC
Description
To compare AUC of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUClast
Description
To compare AUClast of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: AUC(0-12)
Description
To compare AUC (0-12) of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: Cmax
Description
To compare Cmax of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: FRAUC
Description
To compare FRAUC of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: FRCmax
Description
To compare FRCmax of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: t½λz
Description
To compare t½λz of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: tmax
Description
To compare tmax of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib and N-desmethyl selumetinib plasma PK parameter: λz
Description
To compare λz of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib plasma PK parameters: CL/F
Description
To compare CL/F of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Selumetinib plasma PK parameters: Vz/F
Description
To compare Vz/F of selumetinib granule fasted versus granule low-fat fed state.
Time Frame
At pre-dose, and 0.25, 0.5, 0.75, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 3, 3.5, 4, 5, 6, 8, 12, 24, 36 and 48 hours post-dose (Days -1 to 3)
Title
Taste questionnaire
Description
To assess palatability of selumetinib granule formulation. The standardized questionnaire will be administered to participants within 10 minutes following intake of selumetinib granule. Questionnaire about taste include sweet, salty, sour, bitter, metallic, and hot/spicy. Where 0 indicates not at all and 10 indicates extremely.
Time Frame
At Days -1 to 3 (within 10 minutes following intake of selumetinib granule)
Title
Number of participants with adverse events (AEs)
Description
To assess the safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
From the time of informed consent, throughout the treatment periods up to and including the Follow-up Visit (7 to 10 days after last dose)
Title
Vital signs (systolic blood pressure [BP])
Description
To assess systolic BP as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest for at least 5 minutes before the measurements.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Vital signs (diastolic BP)
Description
To assess diastolic BP as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest for at least 5 minutes before the measurements.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Pulse rate
Description
To assess pulse rate as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Participants should be supine and at rest for at least 5 minutes before the measurements.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
12-lead electrocardiogram (ECG)
Description
To assess 12-lead ECG as variable of safety and tolerability of single doses of selumetinib in healthy participants. Participants should be supine and at rest 10 minutes before recording the ECG.
Time Frame
From baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Number of participants with abnormal findings in physical examination
Description
To assess physical examination as a variable safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
From baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Ophthalmic examinations
Description
To assess ophthalmic examination as a variable of safety and tolerability of single doses of selumetinib in healthy participants. Ophthalmic examination included best corrected visual acuity, intra-ocular pressure and slit-lamp fundoscopy.
Time Frame
At screening Visit or on Day -1 of Treatment Period 1
Title
Laboratory assessments: hematology - Hemoglobin (Hb)
Description
To assess Hb as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: hematology - erythrocyte count
Description
To assess erythrocyte count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: hematology: Platelet count
Description
To assess platelet count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: hematology: leucocyte differential count (absolute count)
Description
To assess leucocyte differential count as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: hematology: leucocyte cell count
Description
To assess leucocyte cell count as variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments:hematology - differential count
Description
To assess differential count of neutrophils, lymphocytes, monocyets, eosinophils and basophils) as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry - electrolytes
Description
To assess serum level of sodium, potassium, magnesium and phosphate as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry - urea nitrogen
Description
To assess urea nitrogen as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry - creatinine
Description
To assess creatinine as variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: albumin
Description
To assess albumin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: Total Calcium
Description
To assess total calcium as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: Total protein
Description
To assess total protein as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: Total bilirubin
Description
To assess total bilirubin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: Creatine phosphokinase (CPK)
Description
To assess CPK as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry: Troponin (isoform as per institutional norm)
Description
To assess troponin as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Serum clinical chemistry - Liver enzymes
Description
To assess serum of Alkaline phosphatase (ALP), Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) and Gamma glutamyl transpeptidase (GGT) as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Clinical urinalysis - glucose
Description
To assess urine glucose as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Clinical Urinalysis - protein
Description
To assess urine protein as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
Title
Laboratory assessments: Clinical Urinalysis - blood
Description
To assess urine blood as a variable of safety and tolerability of single doses of selumetinib in healthy participants.
If urinalysis is positive for blood, a microscopy test will be performed to assess RBC, white blood cell [WBC], casts [cellular, granular, hyaline]).
Time Frame
Change from baseline up to follow-up/early termination visit (7 to 10 days after last dose)
10. Eligibility
Sex
Male
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria
Provision of signed and dated, written informed consent before any study-specific procedures.
Healthy male participants aged 18 to 45 years (inclusive) with suitable veins for cannulation or repeated venipuncture.
Have a body mass index (BMI) between 18 and 30 kg/m2 inclusive and weigh at least 50 kg.
Participants is able to consume a low-fat meal within a 30-minute period.
Participants has a creatinine clearance (CRCL) greater than 50 mL/min using Cockcroft-Gault formula.
Participants is willing to comply with contraception requirements as described below:
Male participants with sexual partners who can become pregnant (i.e., women of childbearing potential) must use 2 highly-effective methods of contraception, one of which must be a barrier method (condom with spermicide) from the time of the first administration of the IMP until 12 weeks after the last administration of the IMP to avoid pregnancy and/or potential adverse effects on the developing embryo.
Participants with sexual partners who are pregnant must use an effective method of contraception (barrier method) from the time of the first administration of the IMP until 12 weeks after the last administration of the IMP.
Participants must avoid sperm donation during the study and for 12 weeks after the last administration of the IMP.
Reliable methods of contraception must be used consistently and correctly.
Reliable methods of contraception for participants include: Use of barrier methods (condom and spermicide) for the duration of the study until 12 weeks after the last administration of the IMP.
Acceptable methods for participants partners include:
Use of implants, injectables and combined oral contraceptives (must be used in combination with a barrier method of contraception)
Use of intrauterine devices (must be used in combination with a barrier method of contraception)
Exclusion Criteria :
Participants of Japanese, non-Japanese Asian or Indian ethnicity.
Participants has any one parent or grandparent (maternal or paternal) that was Japanese or non-Japanese Asian (e.g., China, Taiwan, Korea, Philippines, Thailand, Vietnam and Malaysia) or Indian.
History or presence of central serous retinopathy or retinal vein thrombosis, IOP greater than 21 mmHg or uncontrolled glaucoma.
History of any clinically significant disease or disorder which, in the opinion of the PI, may put the participant at risk because of participation in the study, influence the result of the study or influence the participants ability to participate in the study.
Participant has ophthalmologic conditions as follows:
Current or past history of central serous retinopathy/retinal pigment epithelial detachment or retinal vein occlusion.
Intra-ocular pressure > 21 mmHg or uncontrolled glaucoma (irrespective of IOP).
Participant has any cardiac conditions as follows:
Uncontrolled hypertension (BP ≥ 150/95 mmHg despite medical therapy).
Acute coronary syndrome within 6 months before starting treatment.
Uncontrolled Angina - Canadian Cardiovascular Society grade II-IV despite medical therapy.
Symptomatic heart failure New York Heart Association (NYHA) Class II-IV, prior or current cardiomyopathy, or severe valvular heart disease.
Prior or current cardiomyopathy including but not limited to the following: 1) Known hypertrophic cardiomyopathy.
2) Known arrhythmogenic right ventricular cardiomyopathy. 3) Previous moderate or severe impairment of LVEF < 45% on echocardiography even if full recovery has occurred.
Left ventricular ejection fraction below the lower limit of normal (LLN) or < 55% measured by ECHO at the Screening Visit.
Severe valvular heart disease.
Atrial fibrillation with a ventricular rate > 100 beats per minute (bpm) on ECG at rest.
QTcF > 450 ms or other factors that increase the risk of QT prolongation.
Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the first administration of IMP.
Any clinically relevant abnormal findings in physical examination, hematology, clinical chemistry, urinalysis, vital signs or ECG at the Screening Visit, which in the opinion of the PI, may put the participant at risk because of his participation in the study. Test may be repeated twice at the discretion of the Investigator if abnormal.
Any positive result on screening for serum hepatitis B surface antigen, hepatitis C antibody, and human immunodeficiency virus (HIV) antibody.
A suspected/manifested infection according to the International Air Transport Association (IATA) Categories A and B infectious substances.
History of, or current alcohol or drug abuse, as judged by the principal investigator (PI).
Participation in another clinical study (investigational product administered within 30 days before the Screening Visit, or participation in a method development study [no drug] 30 days before the Screening Visit). Participation is defined as the completion of a treatment related visit.
Planned in-patient surgery, dental procedure or hospitalization during the study.
Plasma donation within 30 days of the Screening Visit or any blood donation/loss more than 500 mL during the 90 days before the Screening Visit.
A definite or suspected personal history of intolerance or hypersensitivity to drugs and/or their excipients, judged to be clinically relevant by the PI.
Known severe hypersensitivity to selumetinib or acetaminophen or any excipient of these medicinal products or history of allergic reactions attributed to compounds of similar chemical or biologic composition to selumetinib.
Current smokers or those who have smoked or used nicotine products (including e-cigarettes) within the 90 days before the Screening Visit.
Positive screen for drugs of abuse, alcohol or cotinine at the Screening Visit or on each admission to the Clinical Unit or positive screen for alcohol on each admission to the Clinical Unit.
Use of drugs with enzyme-inducing properties such as St John's Wort within 4 weeks before the first administration of IMP.
Use of any prescribed medicine and over-the-counter (OTC) drugs (including herbal remedies, vitamins and minerals) within 2 weeks or 5 times the half-life, whichever is the longer, of the respective drug before Day -1 or Treatment Period 1. No medications known to prolong the QT/QTc interval are allowed.
Excessive intake of caffeine-containing drinks or food e.g., coffee, tea, chocolate, Red Bull or cola (more than 6 units of caffeine per day). One caffeine unit is contained in the following items: 1 (6 oz) cup of coffee, 2 (12 oz) cans of cola, 1 (12 oz) cup of tea, ½ (4 oz) cup of energy drink (e.g., Red Bull) or 3 oz of chocolate.
Known or suspected history of alcohol or drug abuse or excessive intake of alcohol as judged by the PI.
Involvement of any AstraZeneca, PAREXEL or Clinical Unit employee or their close relatives.
Participants who have previously been randomized to treatment in the current study.
Judgment by the PI that the participant should not participate in the study if they have any ongoing or recent (i.e., during the screening period) minor medical complaints that may interfere with the interpretation of study data or are considered unlikely to comply with study procedures, restrictions and requirements.
Vulnerable participants , e.g., kept in detention, protected adults under guardianship, trusteeship, or committed to an institution by governmental or juridical order.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald Goldwater, MD
Organizational Affiliation
PAREXEL Early Phase Clinical Unit Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Site
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21225
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35410754
Citation
Cohen-Rabbie S, Mattinson A, So K, Wang N, Goldwater R. A Phase I, Open-label, Randomized, Crossover Study of the Relative Bioavailability of Capsule and Granule Formulations of Selumetinib. Clin Ther. 2022 Apr;44(4):565-576. doi: 10.1016/j.clinthera.2022.02.009. Epub 2022 Apr 9.
Results Reference
derived
PubMed Identifier
35170228
Citation
Cohen-Rabbie S, Mattinson A, So K, Wang N, Goldwater R. Effect of food on capsule and granule formulations of selumetinib. Clin Transl Sci. 2022 Apr;15(4):878-888. doi: 10.1111/cts.13209. Epub 2022 Feb 15.
Results Reference
derived
Learn more about this trial
A Study to Evaluate Bioavailability and Food Effect of Selumetinib (AZD6244) in Healthy Male Participants
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